| Sr. No. | Title | Date | |
|---|---|---|---|
| 1 |
Kulkarni BP, Shanmukhaiah C, Ghargi K, Pandey P, Kharat S, Pawar P, Shinde S, Kawankar N, Shanbhag S Coincidental occurrence of severe factor XII deficiency in a case of mild hemophilia A: a unique coagulation laboratory diagnostic conundrum
Blood Coagul Fibrinolysis. 2025 Jan 27. doi: 10.1097/MBC.0000000000001346.
|
2025 | |
| 2 |
Tomar A, Devendra R, Parchure D, Kulkarni S Weak or partial D: Importance of molecular characterization of D variants
Transfus Apher Sci. 2025 Jan 11;64(2):104069. (IF:1.4)
|
2025 | |
| 3 |
Davidovich C, Erokhina K, Gupta CL, Zhu YG, Su JQ, Djordjevic SP, Wyrsch ER, Blum SE, Cytryn E Occurrence of "under-the-radar" antibiotic resistance in anthropogenically affected produce
ISME J. 2025 Jan 2;19(1):wrae261. (IF:10.8)
|
2025 | |
| 4 |
Saptarshi AN, Subramaniam K, Nemani S, More TA, Dongerdiye R, Kedar P Hematopoietic Stem Cell Transplant of a Congenital Dyserythropoietic Anemia Type II Patient: A Rare Report from the Indian Population
Indian J Hematol Blood Transfus. 2025 Jan;41(1):194-196. (IF:0.7)
|
2025 | |
| 5 |
Ghatanatti J, Dhangar S, Vundinti BR Variant Klinefelter Syndrome With Xq Trisomy (47,X,i(X)(q10),Y): A Case Report and Review of the Literature
Cureus. 2025 Jan 12;17(1):e77351. (IF:1.2)
|
2025 | |
| 6 |
Augustine M, Parchure D, Kshirsagar P, Bhembre S, Mallya MV, Adsule H, Sreekumar K, Kulkarni S Alloimmunization Due to Multiple Red Cell Antibodies in a RhD Positive Pregnancy: Lessons to be Learnt
Indian J Hematol Blood Transfus. 2025 Feb 19:1-4. (IF:0.7)
|
2025 | |
| 7 |
Govindarajan R, Jaganathasamy N, Krishnamoorthi R, Kumari K, Kumar A, Paulraj PS Risk factors of scrub typhus infection in children and adults in Kerala, south India
Asian Pac J Trop Med. 2025 Feb;18(2):84-92. (IF:1.9)
|
2025 | |
| 8 |
Asokan D, Mall A, Sankhe L, Jaganathasamy N, Pardeshi G Temporal Trends of Dog Bite Cases and their Correlation with Meteorological Factors in a Metropolitan City
Indian J Community Med. 2025 Feb;:10-4103. (IF:0.9)
|
2025 | |
| 9 |
Jose A, Bodade A, Madkaikar MR Assessing and managing iron deficiency anemia in sickle cell disease: Insights from a systematic review and meta-analysis
J Postgrad Med. 2025 Jan–Mar;71(1):33-40.
|
2025 | |
| 10 |
Kawankar N, Shanmukhaiah C, Kulkarni B Identification of a GFI1B variant associated with abnormal platelet function and normal platelet count
Br J Haematol. 2025 Feb;206(2):777-780.
|
2025 | |
| 11 |
Gupta M, Madkaikar M Predictive Markers for Response to Immunosuppressive Therapy in Aplastic Anaemia
Scand J Immunol. 2025 Mar;101(3):e70010. (IF:4.1)
|
2025 | |
| 12 |
Surve S, Thakor M, Madkaikar M, Kaur H, Desai S, Shanmugam R, Mohanty SS, Pandey A, Kerketta SA, Dave K, Gawit KG, Ramasamy LB, Warerkar O, Kedar P, Kulkarni R, Nair S, Rajamani N, Nadkarni A Protocol for a Multicentric Cohort Study on Neonatal Screening and Early Interventions for Sickle Cell Disease Among High-Prevalence States of India
Diagnostics (Basel). 2025 Mar 14;15(6):730. (IF:3.0)
|
2025 | |
| 13 |
Dhangar S, Shanmukhaiah C, Ghatanatti J, Sawant L, Maurya N, Vundinti BR Comprehensive analysis of tyrosine kinase domain mutations and imatinib resistance in chronic myeloid leukemia patients
Leuk Res. 2025 Mar 17;152:107679. (IF:2.1)
|
2025 | |
| 14 |
Paramasivam P, Jaganathasamy N, Ramalingam S, Mahalingam V, Nagarajan S, Shaik FA, Karuppasamy S, Bhaskar A, Srinivasan P, Manoharan T, Natesan A, Chinnaiyan P An Application for Spatial Frailty Models: An Exploration with Data on Fungal Sepsis in Neonates
Diseases. 2025 Mar 14;13(3):83. (IF:2.9)
|
2025 | |
| 15 |
Baysac K, Sun G, Nakano H, Schmitz EG, Cruz AC, Fisher C, Bailey AC; PLCG2-Immune Dysregulation Working Group; Mace E, Milner JD, Ombrello MJ PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants
J Allergy Clin Immunol. 2024 Jan;153(1):230-242. (IF:14.29)
|
2024 | |
| 16 |
Malhotra S, Roy M, Parchure D, Kaba M, Jain A, Kulkarni S, Bansal D, Sharma RR Autoimmune anti‐D in an RhD‐positive young infant: Learning from a rare case.
Vox Sanguinis. 2024 Jan;119(1):70-3. Short Report (IF:1.8)
|
2024 | |
| 17 |
Chougule A, Iyengar VV, Gowri V, Taur P, Madkaikar MR, Bodhanwala M, Desai MM Cleavage-resistant RIPK1-induced autoinflammatory syndrome-A report of three generations with periodic fever and clinical response to colchicine.
Int J Rheum Dis. 2024 Jan;27(1):e14837.(IF:2.4)
|
2024 | |
| 18 |
Khargekar N, Banerjee A, Athalye S, Mahajan N, Kargutkar N, Tapase P, Madkaikar M Role of hydroxyurea therapy in the prevention of organ damage in sickle cell disease: a systematic review and meta-analysis.
Syst Rev. 2024 Feb 8;13(1):60. Systematic Review & Meta Analysis (IF:6.3)
|
2024 | |
| 19 |
Athalye S, Patil A, Khargekar N, Shinde S, Chavan S, Dixit A, Shankarkumar A, Madkaikar M, Banerjee A Efficacy of combined HBsAg, anti-HBc and anti-HBs screening in minimizing transfusion transmission risk of hepatitis B infection in low resource setting.
Heliyon. 2024 Feb 3;10(3):e25805 (IF:3.4)
|
2024 | |
| 20 |
Gorivale M, Sawant P, Kargutkar N, Hariharan P, Thaker P, Chiddarwar A, Nadkarni A When a synonymous mutation breaks the silence in a thalassaemia patient.
Br J Haematol. 2024 Feb;204(2):677-682. (IF:5.1)
|
2024 | |
| 21 |
Dalvi A, Bargir UA, Natraj G, Shah I, Madkaikar M Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease.
Pathogens. 2024 Feb 25;13(3):203.(IF:3.3)
|
2024 | |
| 22 |
Kripa PK, Thanzeen PS, Nagaraj Jaganathasamy, Sangamithra Ravishankaran, Anupkumar R Anvikar, Alex Eapen Impact of climate change on temperature variations and extrinsic incubation period of malaria parasites in Chennai, India- Implications on its disease transmission potential.
Parasites Vectors. 2024 Mar 15;17(1):134.(IF:4.0)
|
2024 | |
| 23 |
Maurya N, Shanmukhaiah C, Dhangar S, Madkaikar M, Vundinti BR Comprehensive study of chromosomal CNVs and genomic variations predicting overall survival in Myelodysplastic syndromes.
Oncology. 2024 Mar;102(10):897-906. (IF:3.5)
|
2024 | |
| 24 |
Yadav RM, Gomare M, Gaikwad A, Waghmare U, Betodkar U, Vashi MD, Kamal VK, Thangaraj JWV, Bangar S, Bhatnagar T, Murhekar M Interplay of missed opportunity for vaccination and poor response to the vaccine led to measles outbreak in a slum area of Eastern Mumbai, India.
Epidemiol Infect. 2024 Mar 18;152:e56. (IF:2.5)
|
2024 | |
| 25 |
Patil R, Shanmukhaiah C, Gogtay NJ, Pandey P, Patil K, Jijina F, Madkaikar M Low-dose Emicizumab prophylaxis in severe haemophilia A patients -a retrospective study bringing new hope for our patients.
J Thromb Haemost. 2024 Apr;22(4):1024-1030. (IF:16.041)
|
2024 | |
| 26 |
Budukh AM, Pradhan S, Singh VB, Khanna D, Bagal SS, Chakravarti PS, Sharma AN, Vishwakarma RK, Shinde SS, Khargekar NC, Chaturvedi P, Dikshit RP, Shukla VK, Badwe RA Cancer pattern in Varanasi district from Uttar Pradesh state of India, a foundation for cancer control based on the first report of the population-based cancer registry.
Indian J Cancer. 2024 Apr 1;61(2):383-389. (IF:1.0)
|
2024 | |
| 27 |
Khargekar N, Takke A, Athalye S, Panale P, Rajamani N, Banerjee A Exploring factors influencing the perspective regarding HIV transmission and prevention among college students in India.
J Family Med Prim Care. 2024 Apr;13(4):1467-1472. (IF:1.1)
|
2024 | |
| 28 |
Jeffrey Pradeep Raj, Suraj Kallarakal Tomy, Amrutha Jose, Aadrika Kashyap, Joseph Varghese Kureethara, Tomy K Kallarakal Knowledge and perceptions about clinical research and its ethical conduct among college students from non-science background: a representative nation-wide survey from India.
BMJ Public Health 2024;2:e000748.
|
2024 | |
| 29 |
Asokan D, Mall A, Sankhe L, Jaganathasamy N, Pardeshi G Profile and geospatial analysis of dog bite cases attending the antirabies vaccine outpatient department at the tertiary level hospital of Mumbai.
Indian J Public Health. 2024 Apr 1;68(2):175-179. (IF:0.9)
|
2024 | |
| 30 |
Jain D, Gupta M, Madkaikar M, Jena RK, Khargekar N, Saraf SL, Krishnamurti L, Gupta K Sickle cell disease in India: current status and progress.
Lancet Haematol. 2024 May;11(5):e322-e323. (IF:15.4)
|
2024 | |
| 31 |
Yadav RM, Desai SS, Gupta M, Dalvi A, Bargir UA, Jodhawat N, Setia P, Shinde S, Parab A, Gada A, Taur P, Desai M, Madkaikar M Clinical Utility of Flow-Cytometry for Diagnosis and Genotype Phenotype Correlation in a Cohort of X-linked Agammaglobulinemia Patients.
Indian J Pediatr. 2024 Jun;91(6):638. (IF:4.3)
|
2024 | |
| 32 |
Jodhawat N, Bargir UA, Rawal G, Kamble P, Shinde-Vhatkar S, Dalvi A, Kulkarni S, Madkaikar M Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features.
J Clin Immunol. 2024 Jun 7;44(6):144. (IF:7.2)
|
2024 | |
| 33 |
Thaker P, Mahajan N, Mukherjee MB, Colah RB Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.
Int J Lab Hematol. 2024 Jun;46(3):434-450. (IF:2.2)
|
2024 | |
| 34 |
Anuradha R, Srinivas M, Satyavani M, Suresh K, Muralidhar MN, Rajender Rao K Preconceptional paternal caloric restriction of high-fat diet-induced obesity in Wistar rats dysregulates the metabolism of their offspring via AMPK/SIRT1 pathway
Lipids Health Dis. 2024 Jun 8;23(1):174. (IF:3.9)
|
2024 | |
| 35 |
Mohanty MC, Govindaraj G, Ahmad M, Varose SY, Tatkare M, Shete A, Yadav S, Joshi Y, Yadav P, Sharma D, Kumar A, Verma H, Patil AP, Edavazhipurath A, Dhanasooraj D, Othayoth Kandy S, Puthenpurayil JM, Chakyar K, Melarcode Ramanan K, Madkaikar M Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Excretion in an Infant with Severe Combined Immune Deficiency with Spillover to a Parent
Vaccines (Basel). 2024 Jul 9;12(7):759. (IF:7.8)
|
2024 | |
| 36 |
Banerjee A, Athalye S, Shingade P, Khargekar V, Mahajan N, Madkaikar M, Khargekar N Efficacy of daily versus intermittent oral iron supplementation for prevention of anaemia among pregnant women: a systematic review and meta-analysis
EClinicalMedicine. 2024 Jul 17;74:102742. (IF:9.9)
|
2024 | |
| 37 |
Banerjee A, Farci P Fibrosis and Hepatocarcinogenesis: Role of Gene-Environment Interactions in Liver Disease Progression
Int J Mol Sci. 2024 Aug 8;25(16):8641. (IF:4.9)
|
2024 | |
| 38 |
Gupta M, S C, Vundinti B, Jose A, Tiwari S, Bhowmick A, Madkaikar M Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Aug 13:uxae076. (IF:3.4)
|
2024 | |
| 39 |
Radhika R, Tullu MS, Karande S, Bargir UA Major Histocompatibility Complex (MHC) Class II Deficiency- A Case of Primary Immunodeficiency Disorder
Indian J Pediatr. 2024 Sep;91(9):967-969. (IF:2.1)
|
2024 | |
| 40 |
Kumar LS, Raghavendra PR, Nair S, et al. Silver hair in a neonate: a tale of 2 fatal cases
Oxf Med Case Reports. 2024;2024(9):omae106. (IF:N/A)
|
2024 | |
| 41 |
Gupta CL, Jaganathasamy N, Madkaikar M Microbiome in sickle cell disease: Pathophysiology and therapeutic insights
Br J Haematol. 2024 Oct;205(4):1279-1287. (IF:5.1)
|
2024 | |
| 42 |
Shinde-Vhatkar S, Bargir U, Madkaikar M Immunophenotypic Analysis of Patients with Pyogenic Liver Abscess for Underlying Inborn Errors of Immunity
Indian J Pediatr. 2024 Oct;91(10):1105. (IF:2.1)
|
2024 | |
| 43 |
Dongerdiye R, Kedar PS, Saptarshi A, Sampagar A, Shanmukhaiah C, Mudaliar S, Kanvinde P, Desai M, Madkaikar M Non-syndromic congenital sideroblastic anaemia; phenotype, and genotype of 15 Indian patients
Ann Hematol. 2024 Oct;103(10):3987-3998. (IF:3.0)
|
2024 | |
| 44 |
Khanna D, Shruti T, Tiwari M, Sharma P, Khan A, Ranjan S, Balasundaram P, Khargekar N, Chaturvedi P, Mishra A Prevalence of Oral Potentially Malignant Lesions, Tobacco use, and Effect of Cessation Strategies among Solid Waste Management workers in Northern India: a pre-post intervention study
BMC Oral Health. 2024 Oct 26;24(1):1292. (IF:2.6)
|
2024 | |
| 45 |
Shaikh R, Kanjaksha G, Kashivishwanath V, Kulkarni S, Jadhav S, Maru H, Gorakshakar A ACKR1 gene polymorphisms in Bombay blood group (O(h)) individuals of Indian origin
Transfus Apher Sci. 2024 Oct;63(5):103975. (IF:1.4)
|
2024 | |
| 46 |
Gupta M, S C, Vundinti B, Jose A, Tiwari S, Bhowmick A, Madkaikar M Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Nov 12;218(3):291-299. (IF:3.4)
|
2024 | |
| 47 |
Roshan Shaikh, Ghosh Kanjaksha, Ajit Gorakshakar Duffy Binding Protein Ligand (PvDBP) gene duplication in Indian P. Vivax Malaria isolates: implication for malaria research
Curr Genet. 2024 Nov 9;70(1):18. (IF:1.8)
|
2024 | |
| 48 |
Snigdha A, Majumdar V, Manjunath NK, Jose A Yoga-based lifestyle intervention for healthy ageing in older adults: a two-armed, waitlist randomized controlled trial with multiple primary outcomes
Geroscience. 2024 Dec;46(6):6039-6054. (IF:5.3)
|
2024 | |
| 49 |
Gaikwad P, Bargir UA, Jodhawat N, Dalvi A, Shinde S, Tamhankar P, Setia P, Kambli P, Dhawale A, Temkar L, Vedpathak D, Jose A, Gupta M, Yadav-Malik R, Dutta S, Bose K, Taur P, Gowri V, Iyengar V, Chougule A, Desai M, Sivasankaran M, Bhattad S, Balaji S, Mudaliar S, Kacha A, Subramanian G, Patel S, Sharma S, Sampagar A, Madkaikar M Mutational Landscape of Patients with Wiskott Aldrich Syndrome: Update from India
J Clin Immunol. 2024 Dec 17;45(1):56. (IF:7.2)
|
2024 | |
| 50 |
Roshan Shaikh, Ghosh Kanjaksha, Ajit Gorakshakar Whispers of the Genome: Unmasking SNP through Simple Modified PCR
Indian Journal of Anthropological Research. 2024 Dec;3(2):291-303.
|
2024 | |
| 51 |
Prabhakar Kedar, Rashmi Dongerdiye, Ritika Khurana, Sangeeta Mudaliar Rare red cell enzymopathies in the Indian population: A comprehensive review
Pediatric Hematology Oncology Journal. 2024 Dec;9(4):235-243.
|
2024 | |
| 52 |
Banerjee A, Athalye S, Khargekar N, Shingade P, Madkaikar M. Chronic Hepatitis B and Related Liver Diseases Are Associated with Reduced 25-Hydroxy-Vitamin D Levels: A Systematic Review and Meta-Analysis.
Biomedicines. 2023 Jan 5;11(1):135. doi: 10.3390/biomedicines11010135. PMID: 36672644; PMCID: PMC9855868. (IF:4.7)
|
2023 | |
| 53 |
Maurya N, Mohanty P, Panchal P, Shanmukhaiah C, Vundinti BR. Over expression of mTOR gene predicts overall survival in myelodysplastic syndromes
Mol Biol Rep. 2023 Jan;50(1):235-244. (IF:2.8)
|
2023 | |
| 54 |
Kulkarni V, Chellasamy SK, Dhangar S, Ghatanatti J, Vundinti BR Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
Mol Hum Reprod. 2023 Jan 31;29(2):gaad001.(IF:4.0)
|
2023 | |
| 55 |
Kargutkar N, Sawant-Mulay M, Hariharan P, Chandrakala S, Nadkarni A Role of microRNA in hydroxyurea mediated HbF induction in sickle cell anaemia patients.
Sci Rep. 2023 Jan 7;13(1):369. (IF:3.8)
|
2023 | |
| 56 |
Khargekar N, Shinde N, Banerjee A, Madkaikar M, Nadkarni A Impact of COVID-19 infection among indian sickle cell disease patients.A.
Indian J Public Health. 2023 Jan-Mar;67(1):112-116.(IF:1.7)
|
2023 | |
| 57 |
Vundinti BR, Korgaonkar S, Dhangar S, Jijina F, Shanmukhaiah C Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective study
J Cancer Res Ther. 2023 Jan-Mar;19(2):340-346.(IF:1.3)
|
2023 | |
| 58 |
Chougule A, Taur P, Gowri V; C. O. E. Consortium; Desai MM SPENCD Presenting with Evans Phenotype and Clinical Response to JAK1/2 Inhibitors-a Report of 2 Cases.
J Clin Immunol. 2023 Feb;43(2):331-334.(IF:9.1)
|
2023 | |
| 59 |
Roos D, van Leeuwen K, Madkaikar M, Kambli PM, Gupta M, Mathews V, Rawat A, Kuhns DB, Holland SM, de Boer M, Kanegane H, Parvaneh N, Lorenz M, Schwarz K, Klein C, Sherkat R, Jafari M, Wolach B, den Dunnen JT, Kuijpers TW, Köker MY Hematologically important mutations: Leukocyte adhesion deficiency (second update)
Blood Cells Mol Dis. 2023 Mar;99:102726.(IF:2.3)
|
2023 | |
| 60 |
Desai N, Pradhan V, Chougule D, Tiwari S, Mandke C, Yadav RM, Athvale A, Kawle J, Pai V, Pawaskar S, Kharkar H, Bhosale S, Parab A, Ansari S, Kumar KH, Mhashal S, Redkar N, Madkaikar M Perturbations of immune landscape in COVID-19 associated mucormycosis. M
Mycoses. 2023 Mar;66(3):226-236.(IF:4.9)
|
2023 | |
| 61 |
Lokhande AS, Panchal F, Munshi R, Madkaikar M, Malshe VC, Devarajan PV pH-responsive microparticles of rifampicin for augmented intramacrophage uptake and enhanced antitubercular efficacy.
Int J Pharm. 2023 Mar 25;635:122729.(IF:5.8)
|
2023 | |
| 62 |
More TA, Devendra R, Dongerdiye R, Warang P, Kedar P Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum
Mol Genet Genomics. 2023 Mar;298(2):427-439.(IF:3.1)
|
2023 | |
| 63 |
Kargutkar N, Hariharan P, Nadkarni A Dynamic interplay of microRNA in diseases and therapeutic A.
Clin Genet. 2023 Mar;103(3):268-276. (IF:3.5)
|
2023 | |
| 64 |
Chougule A, Taur P, Iyengar VV, Gowri V, Kulkarni BP, Madkaikar MR, Bodhanwala, M, Desai MM. Clinical features, laboratory and molecular findings of children with leukocyte adhesion deficiency type-III from a single center in India.
Pediatric Hematology Oncology Journal Volume 8, Issue 1, March 2023, Pages 4-9 (IF : 1.969)
|
2023 | |
| 65 |
Pandrowala A, Desai M, Madkaikar M, Kulkarni S, Shobhavat L, Mishra J, Jain S, Chandane P, Sehgal K, Chavan S, Karkera P, Bendre P, Thanky A, Rao S, Prabhu S, Bodhanwala M, Agarwal B, Hiwarkar P. Changing outcomes of stem cell transplantation in primary immunodeficiencies: Results from a tertiary-care charitable trust hospital in Mumbai.
J Allergy Clin Immunol Glob. 2023 Mar 29;2(3):100105. (IF: --)
|
2023 | |
| 66 |
Shah I, Shetty NS, Chigari P, Pradhan V, Chougule D, Poojari VS, Jaiswal A, Madkaikar M. Vitamin D receptor genetic polymorphisms in severe and recurrent tuberculosis in children
Indian J Tuberc. 2023 Apr;70(2):239-244.(IF:1.57)
|
2023 | |
| 67 |
Maru V, Madkaikar M, Gada A, Pakhmode V, Padawe D, Bapat S. Response of stem cells derived from human exfoliated deciduous teeth to Bio-C Repair and Mineral Trioxide Aggregate Repair HP: Cytotoxicity and gene expression assessment.
Dent Res J (Isfahan). 2023 Apr 26;20:55. eCollection 2023.(IF:1.23)
|
2023 | |
| 68 |
Parchure DS, Mishra GV, Kulkarni SS. Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population
Immunohematology. 2023 Apr 5;39(1):19-31.(IF:0.268)
|
2023 | |
| 69 |
Mohanty MC, Mohammad A, Verma H, Kumar A, Madkaikar MR, Desai M, Varose SY, Sawant U, Yadav RM, Taur P, Kathuria R, Tatkare M, Murhekar M, Haldar P, Abraham P Poliovirus surveillance in patients with primary immunodeficiencies, India
Bull World Health Organ. 2023 May 1;101(5):346-354.(IF:11.1)
|
2023 | |
| 70 |
Shete A, Deshpande S, Sawant J, Warthe N, Thakar M, Madkaikar M, Pradhan V, Rao P, Rohatgi S, Mukherjee A, Anand T, Satija A, Sharma Velamuri P, Das M, Deasi N, Kumar Tembhurne A, Yadav R, Pawaskar S, Rajguru C, Sankhe LR, Chavan SS, Panda S. Higher proinflammatory responses possibly contributing to suppressed cytotoxicity in patients with COVID-19 associated mucormycosis
Immunobiology. 2023 May;228(3):152384.(IF:3.152)
|
2023 | |
| 71 |
Dongerdiye R, Bokde M, More TA, Saptarshi A, Devendra R, Chiddarwar A, Warang P, Kedar P. Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
Ann Hematol. 2023 May;102(5):1029-1036.(IF:4.03)
|
2023 | |
| 72 |
Khadilkar P, Chougule D, Tipnis T, Khopkar U, Nadkar M, Rajadhyaksha A, Kini S, Kharkar V, Athvale A, Athvale T, Madkaikar M, Pradhan V A comparative study of modulatory interaction between cytokines and apoptotic proteins among Scleroderma patients with and without pulmonary involvement.
Cytokine 2023 Jun;166:156183.(IF:3.926)
|
2023 | |
| 73 |
Patil R, Singh SV, Mandlik JS, Jadhav A, Handa A, Jadhav A Evaluating the Efficacy of Certain Intermediate Irrigants in Preventing Precipitate Formed Due to Sodium Hypochlorite and Chlorhexidine Within the Root Canal System: An In Vitro Study.
Cureus 2023 Jun 2;15(6):e39871.(IF:1.2)
|
2023 | |
| 74 |
Dhangar S, Shanmukhaiah C, Sawant L, Ghatanatti J, Shah A, Mathan S LP, Vundinti BR. Synergetic effect of Azacitidine and Sorafenib in treatment of a case of myeloid neoplasm with sole chromosomal abnormality t(8;22)(p11.2;q11.2)/BCR-FGFR1 rearrangement
Cancer Genet. 2023 Jun;274-275:26-29. (IF:2.169)
|
2023 | |
| 75 |
Gowri V, Chougule A, Gupta M, Taur P, Iyengar VV, Sivasankaran M, Munirathnam D, Krishna S, Bargir UA, Dalvi A, Setia P, Jodhawat N, Shinde S, Prabhu SS, Bodhanwala M, Madkaikar MR, Desai MM Clinical, immunological and molecular findings of patients with DOCK-8 deficiency from India
Scand J Immunol. 2023 Jul;98(1):e13276. .(IF:3.889)
|
2023 | |
| 76 |
Satija A, Anand T, Mukherjee A, Velamuri PS, Singh KJ, Das M, Josten K, Keche AY, Nagarkar NM, Gupta P, Himanshu D, Mistry SN, Patel JD, Rao P, Rohatgi S, Ghosh S, Hazra A, Kindo AJ, Annamalai R, Rudramurthy SM, Singh MP, Shameem M, Fatima N, Khambholja JR, Parikh S, Madkaikar M, Pradhan VD, Bhargava A, Mehata R, Arora RD, Tigga R, Banerjee G, Sonkar V, Malhotra HS, Kumar N, Patil R, Raut CG, Bhattacharyya K, Arthur P, Somu L, Srikanth P, Shah PB, Panda NK, Sharma D, Hasan W, Ahmed A, Bathla M, Solanki S, Doshi H, Kanani Y, Patel N, Shah Z, Tembhurne AK, Rajguru C, Sankhe LR, Chavan SS, Yadav RM, Panda S. Satellite Epidemic of Covid-19 Associated Mucormycosis in India: A Multi-Site Observational Study.
Mycopathologia 2023 Oct;188(5):745-753.(IF:3.785)
|
2023 | |
| 77 |
Setia P, Bargir UA, Shanmukhaiah C, Jodhawat N, Gaikwad P, Vedpathak D, Dutta S, Kulkarni R, Kambli P, Dalvi A, Shinde S, Gupta M, Nambiar N, Sawant S, Shelar S, Dhawale A, Mohanty M, Yadav RM, Bose K, Madkaikar M. Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas-mediated apoptotic pathway.
Br J Haematol. 2023 Jul;202(2):e11-e15.(IF:8.615)
|
2023 | |
| 78 |
Mohanty MC, Desai M, Mohammad A, Aggarwal A, Govindaraj G, Bhattad S, Lashkari HP, Rajasekhar L, Verma H, Kumar A, Sawant U, Varose SY, Taur P, Yadav RM, Tatkare M, Fernandes M, Bargir U, Majumdar S, Edavazhippurath A, Rangarajan J, Manthri R, Madkaikar MR Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I.
Vaccines (Basel). 2023 Jul 6;11(7):1211. (IF:7.8)
|
2023 | |
| 79 |
Athalye S, Khargekar N, Shinde S, Parmar T, Chavan S, Swamidurai G, Pujari V, Panale P, Koli P, Shankarkumar A, Banerjee A Exploring risk factors and transmission dynamics of Hepatitis B infection among Indian families: Implications and perspective.
J Infect Public Health. 2023 Jul;16(7):1109-1114. (IF:7.537)
|
2023 | |
| 80 |
Saptarshi AN, Dongerdiye RK, More TA, Kedar PS. Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Ital J Pediatr. 2023 Jul 16;49(1):84.(IF:3.288)
|
2023 | |
| 81 |
Saptarshi AN, More TA, Dongerdiye R, Kedar P Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.
Indian J Pediatr. 2023 Aug;90(8):840. (IF:1.136)
|
2023 | |
| 82 |
Jodhawat N, Bargir UA, Setia P, Taur P, Bala N, Madkaikar A, Yadav RM, Dalvi A, Shinde S, Gupta M, Shelar S, Kambli P, Gowri V, Lokeshwar M, Satoskar P, Desai M, Madkaikar M Normative data for paediatric lymphocyte subsets: A pilot study from western India.
Indian J Med Res. 2023 Aug;158(2):161-174. (IF:5.274)
|
2023 | |
| 83 |
Shah A, Kumar C, Shanmukhaiah C, Rajendran A, Mudaliar S, Idicula-Thomas S, Vundinti BR. Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia.
Ann Hematol. 2023 Oct;102(10):2683-2693.(IF:3.5)
|
2023 | |
| 84 |
Venkatachari IV, Chougule A, Gowri V, Taur P, Bodhanwala M, Prabhu S, Madkaikar M, Desai M Monogenic inborn errors of immunity in autoimmune disorders
Immunol Res. 2023 Oct;71(5):771-780. (IF:4.4)
|
2023 | |
| 85 |
Shabrish S, Chandrakasan S, Madkaikar M Editorial: NK cell defects: diagnosis and treatment.
Front Immunol. 2023 Oct 31;14:1323793. doi: 10.3389/fimmu.2023.1323793. eCollection 2023.(IF:8.787)
|
2023 | |
| 86 |
Surve S, Chauhan S, Kulkarni R, Salvi N, Nadkarni A, Madkaikar M, Chaudhary K, Chavan A, Suryavanshi D, Thorat A, Kaur H. Challenges in screening for sickle cell disease among newborns from the tribal region of Palghar, Maharashtra during the COVID-19 pandemic.
Indian J Med Res. 2023 Oct 1;158(4):378-383. (IF:5.274)
|
2023 | |
| 87 |
Ghosh K, Shome DK, Kulkarni B, Ghosh MK, Ghosh K. Fibrosis and bone marrow: understanding causation and pathobiology
J Transl Med. 2023 Oct 9;21(1):703.(IF:8.448)
|
2023 | |
| 88 |
Gaikwad P, Bargir UA, Shinde S, Kini P, Chaurasia R, Yadav U, Dhawale A, George M, Jodhawat N, Setia P, Vedpathak D, Dalvi A, Parab A, Gupta M, Yadav RM, Goriwale M, Vundinti B, Bhat N, Sapra BK, Otiv M, Sharma R, Madkaikar M. A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case.
J Clin Immunol. 2023 Nov;43(8):1891-1902. (IF:8.542)
|
2023 | |
| 89 |
Ghosh K, Kinanka Ghosh and Bipin Kulkarni. HNF1 Associated Novel Missense Mutation Associated with MODY-3 and Type 2 Diabetes in an Indian Family
Am J Biomed Sci & Res. Nov 2023: 19(2) AJBSR.MS.ID.002574, DOI: 10.34297 AJBSR.2023.19.002574 (Impact factor: 1.628).
|
2023 | |
| 90 |
Kargutkar N, Nadkarni A Effect of hydroxyurea on erythrocyte apoptosis in hemoglobinopathy patients.
Expert Rev Hematol.2023 Jul-Dec;16(9):685-692. doi: 10.1080/17474086.2023.2231152. (IF: 2.8)
|
2023 | |
| 91 |
Dhangar S, Panchal P, Ghatanatti J, Suralkar J, Shah A, Vundinti BR. disability associated with chromosomal copy number variations.
BMC Med Genomics. 2022 Jan 3;15(1):2..Erratum in: BMC Med Genomics. 2022 Jan 18;15(1):11.(IF:2.931)
|
2022 | |
| 92 |
Kulkarni BP, Ghargi K, Shanmukhaiah C and Shetty SD. Rare Occurrence of Inhibitors in Von Willebrand Disease: A Case Report
Front. Med. 2022 Jan 11;8:807664. doi: 10.3389/fmed.2021.807664. (IF:5.091)
|
2022 | |
| 93 |
Shanmukhaiah C, Jijina F, Kannan S, Pai NG, Kulkarni B, Khuba SV, Shaikh M, Joshi A, Phatale R, Apte S. Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature.
Haemophilia. 2022 Jan;28(2):286-291. (IF: 4.287)
|
2022 | |
| 94 |
Kulkarni S, Mishra G, Maru H, Parchure D, Gupta D, Bajaj AK, Sindhwani SP, Chaphekar A, Shah R, Férec C, Madkaikar M, Fichou Y. Molecular characterization of rare D--/D-- variants in individuals of Indian origin
BloodTransfus. 2022 Jan;20(1):59-65.(IF:3.443)
|
2022 | |
| 95 |
Deorukhkar A, Kulkarni A, Kedar P. Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.
Mol Biol Rep. 2022 Jan;49(3):2141-2147 (IF: 2.316 )
|
2022 | |
| 96 |
Sampagar A, Gosavi M, Kedar P, Patel T, Dongerdiye R, Mahantashetti N. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.Int
J Hematol. 2022 Feb;115(2):255-262. (IF:2.49)
|
2022 | |
| 97 |
Thaker P, Colah RB, Patel J, Raicha B, Mistry A, Mehta V, Italia Y, Desai S, Dave K, Shanmugam R, Ghosh K and Mukherjee MB Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years.
Front Med (Lausanne)2022 Feb 15;8:731884. (IF :5.091)
|
2022 | |
| 98 |
Kawankar N, Shetty S, Kulkarni B. Novel RASGRP2 variants in platelet function defects: Indian study
Br J Haematol. 2022 Feb;197(3):377-380 (IF 6.998)
|
2022 | |
| 99 |
Shanmukhaiah C, Jijina F, Kannan S, Pai NG, Kulkarni B, Khuba SV, Shaikh M, Joshi A, Phatale R, Apte S. Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature.
Haemophilia. 2022 Mar;28(2):286-291. (IF: 4.287)
|
2022 | |
| 100 |
Iyengar VV, Chougule A, Gowri V, Taur P, Prabhu S, Bodhanwala M, Bargir UA, Madkaikar M, Desai MM XMEN saved by magnesium.
Scand J Immunol. 2022 Mar 9:e13154. doi: 10.1111/sji.13154. Online ahead of print.(IF : 3.487)
|
2022 | |
| 101 |
Deorukhkar A, Kulkarni A, Kedar P. Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.
Mol Biol Rep. 2022 Mar;49(3):2141-2147 (IF: 2.316 )
|
2022 | |
| 102 |
Lashkari HP, Madkaikar M, Dalvi A, Gupta M, Bustamante J, Sharma M, Rawat A, Bhatia P, Bhat KG, Rao S, Kamath N, Moideen F, Latour S, Winter S, Bhavani GS, Girisha KM. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India.
Indian J Pediatr. 2022 Mar;89(3):233-242 (IF:1.967)
|
2022 | |
| 103 |
Hariharan P, Sawant P, Sheth J, Nadkarni A. Rapid molecular identification of a rare β-globin gene deletion & its clinical implication.
Indian J Med Res. 2022 Mar;155(3&4):432-437.(IF:2.267)
|
2022 | |
| 104 |
Gangadharan H, Paul VJ, Ravi R etal. Gastrointestinal involvement ofcommon variable immunodeficiency: A diagnostic challenge to the physician.
J R Coll Physicians Edinb. 2022 Mar;52(1):34-38. doi: 10.1177/14782715221088963. PMID: 36146961 (IF 0.726)
|
2022 | |
| 105 |
Madathil Govindaraj G, Jain A, Edavazhippurath A, Bhoyar RC, Dhanasooraj D, Mishra A, Gupta V, Nair M, Shiny PM, Uppuluri R, Kumar A, Kashyap A, Ajith Kumar VT, Shankaran G, Senthivel V, Imran M, Kumar Divakar M, Sawant S, Dalvi A, Madkaikar M, Raj R, Sivasubbu S, Scaria V. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India
Hum Immunol. 2022 Apr;83(4):335-345. doi: 10.1016/j.humimm.2022.01.003. Epub 2022 Jan 21 (IF:2.85)
|
2022 | |
| 106 |
Iyengar VV, Gowri V, Taur P; COE consortium, Desai MM Vanishing Lymphocytes in a Case of Vanishing Bone Disease
J Clin Immunol. 2022 Apr 42(3): 706-708. (IF:8.317)
|
2022 | |
| 107 |
Madathil Govindaraj G, Jain A, Edavazhippurath A, Bhoyar RC, Dhanasooraj D, Mishra A, Gupta V, Nair M, Shiny PM, Uppuluri R, Kumar A, Kashyap A, Ajith Kumar VT, Shankaran G, Senthivel V, Imran M, Kumar Divakar M, Sawant S, Dalvi A, Madkaikar M, Raj R, Sivasubbu S, Scaria V. Clinical, immunological and genomic characteristics of children with X-linked gammaglobulinemia from Kerala, South India.
Hum Immunol. 2022 Jan 21:S0198-8859(22)00005-2. (IF: 2.85)
|
2022 | |
| 108 |
Maurya N, Mohanty P, Dhangar S, Panchal P, Jijina F, Mathan SLP, Shanmukhaiah C, Madkaikar M, Vundinti BR
Comprehensive analysis of genetic factors predicting overall survival in Myelodysplastic syndromes
Sci Rep. 2022 Apr 8;12(1):5925. doi: 10.1038/s41598-022-09864-9. (IF 4.379)
|
2022 | |
| 109 |
Madkaikar M, Desai MM. Iyengar VV, Chougule A, Gowri V, Taur P, Prabhu S, Bodhanwala M, Bargir UA, Scand J XMEN saved by magnesium.
Immunol. 2022 May;95(5):e13154. doi: 10.1111/sji.13154. Epub 2022 Mar 9. (IF:3.487)
|
2022 | |
| 110 |
Gowri V, Taur P, Chougule A; COE consortia, Desai M STAT 3 GOF with Polycythemia: a Twist to the Tale-First Case Report from India.
J Clin Immunol. 2022 May;42(4):866-868 (IF:8.317)
|
2022 | |
| 111 |
Kawankar N, Shetty S, Kulkarni B. Novel RASGRP2 variants in platelet function defects: Indian study
Br J Haematol. 2022 May;197(3):377-380 (IF 6.998)
|
2022 | |
| 112 |
Parchure D, Madkaikar M, Kulkarni S. Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experience.
Blood Transfus. 2022 May;20(3):235-244. doi: 10.2450/2021.0022-21. Epub 2021 Mar 31. (IF: 3.443)
|
2022 | |
| 113 |
Gorivale M, Hariharan P, Kargutkar N, Mehta P, Sawant P, Nadkarni A. Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton HBB c.320T C with pyrimidine 5 nucleotidase deficiency and the response to HU therapy
Blood Cells Mol Dis. 2022 May 7;96:102667. doi:10.1016/j.bcmd.2022.102667. Online ahead of print (IF :3.039)
|
2022 | |
| 114 |
Khargekar N, Singh A, Shruti T, Pradhan S. A Cross Sectional Assessment of the Profile of Risk Factors of Non-Communicable Diseases Among Health Care Staff of a Tertiary Cancer Hospital.
Lifestyle Med. 2022 May 31;12(2):98-103. doi: 10.15280/jlm.2022.12.2.98. PMID: 36157886; PMCID: PMC9490011. .(IF: 1.85)
|
2022 | |
| 115 |
Patil R, Shanbhag S, ShankarkumarA, Madkaikar M Antibody profile in post- vaccinated & SARS-CoV-2-infected individuals.
Indian J Med Res. 2022 May-Jun;155(5&6):538-545. (IF: 5.274)
|
2022 | |
| 116 |
Taur P, Madkaikar M, Desai M.Hiwarkar P, Bargir U, Pandrowala A, Bodhanwala M, Thakker N SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency
J Clin Immunol. 2022 Jul 15. doi: 10.1007/s10875-022-01323-4. Online ahead of print. (IF 8.317)
|
2022 | |
| 117 |
Gupta A, Jain M, Sheety T, Salunkhe L, Gorivale M, Nadkarni A Hemoglobin Reims- a rare alphgaglobin chain varinay and its interaction with beta thalassemia
Journal of Hematopathology. Received: 21 June 2022 / Accepted: 31 August 2022 doi.org/10.1007/s12308-022-00512-9 (IF :0.196)
|
2022 | |
| 118 |
Pankaj Kumar, Amit Bugalia
Pallavi Thaker, Manju Gorivale, Nighat Hussai,
Anita Nadkarni ,Nabhajit Mallik,
Co- inheritance of Hb Ottawa and HbS: a rare interaction leading to an interesting diagnostic challenge
Journal of Hematopathology. https://doi.org/10.1007/s12308-022-00514-7. Received: 15 July 2022 / Accepted: 6 September 2022 (IF:0.196)
|
2022 | |
| 119 |
Pandey A, Kaur H, Borah S, Khargekar N, Karra VK, Adhikari T, Jain D, Madkaikar M. A systematic review on hydroxyurea therapy for sickle cell disease in India.
Indian J Med Res. 2022 Aug;156(2):299-311. doi: 10.4103/ijmr.ijmr_3447_21. PMID: 36629190. .(IF: 5.274)
|
2022 | |
| 120 |
Warang PP, Shinde NS, Umare VD, Deshmukh PV, Ghosh K, Madkaikar MR, Colah RB, Mukherjee MB Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease.
Hemoglobin. 2022 Sep 8:1-5. doi: 10.1080/03630269.2022.2118603. Online ahead of print. (IF: 0.849)
|
2022 | |
| 121 |
Kargutkar N, Hariharan P, Nadkarni A. Dynamic interplay of microRNA in diseases and therapeutic.
Clinical Genetics. 2022 Oct 30. http://doi.org/10.1111/cge.14256 (IF: 5.422)
|
2022 | |
| 122 |
Takke A, Zarekar M, Muthuraman V, Ashar A, Patil K, Badhavkar A, Trivedi J, Khargekar N, Madkaikar M, Banerjee A. Comparative study of clinical features and vaccination status in Omicron and non-Omicron infected patients during the third wave in Mumbai, India.
J Family Med Prim Care. 2022 Oct;11(10):6135-6142. doi: 10.4103/jfmpc.jfmpc_430_22. Epub 2022 Oct 31. PMID: 36618147; PMCID: PMC9810849. (IF: 0.57)
|
2022 | |
| 123 |
Reetika Malik Yadav, Neha Jodhawat, Maya Gupta et al. Utility of HLA-DR in screening panel for errors of immunity.
Scandinavian Journal of Immunology. Published online 2022 Nov. https://doi.org/10.1111/sji.13238 (IF: 3.7)
|
2022 | |
| 124 |
Anand T, Mukherjee A, Satija A, Sharma Velamuri P, Singh J, Das M, Josten K, Yadav P, Sahay RR, Keche AY, Nagarkar NM, Gupta P, Himanshu D, Mistry SN, Pate JD, Rao P, Rohatgi S, Ghosh S, Hazra A, Kindo AJ, Annamalai R, Rudramurthy SM, Singh MP, Fatima MS, Khambholja JR, Parikh S, Madkaikar MR, Pradhan VD, Kataria S, Sharma P, Panda S, ICMR Mucormycosis group A case control investigation of Covid-19 associated mucormycosis in India.
BMC Infect Dis. 2022 Nov 16;22(1):856. (IF: 3.714)
|
2022 | |
| 125 |
Kedar P, Dongerdiye R, Chandrakala S, Bargir UA, Madkaikar M. Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family
Hematology. 2022 Dec;27(1):441-448. doi: 10.1080/16078454.2022.2058736. (IF :2.269)
|
2022 | |
| 126 |
Kondeti S, D M DY, Mn M, S M V K P, Nemani H, Kalashikam RR. Attenuation of FGF21 signalling might aggravate the impairment of glucose homeostasis during the high sucrose diet induced transition from prediabetes to diabetes in WNIN/GR-Ob rats.
Biomed Pharmacother. 2021 Jan 30;137:111252.(IF:7.5)
|
2021 | |
| 127 |
Seema A Korgaonkar, Durga Chougule, Uday Khopkar, Vidya Kharkar, Vikram Lahoria, Prasad Khadilkar, Manisha Madkaikar, Vandana Pradhan. Quantitative estimation of Antidesmoglein Autoantibodies by ELISA in Pemphigus patients and its correlation with disease activity.
Indian J Dermatol 2021 Jan; 66(1);98-9.
|
2021 | |
| 128 |
Fujii J, Homma T, Kobayashi S, Warang P, Madkaikar M, Mukherjee MB. Erythrocytes as a preferential target of oxidative stress in blood.
Free Radic Res. 2021 Jan 17:1-19. (IF:2.839).
|
2021 | |
| 129 |
Rawat A, Jindal AK, Suri D, Vignesh P, Gupta A, Saikia B, Minz RW, Banday AZ, Tyagi R, Arora K, Joshi V, Mondal S, Shandilya JK, Sharma M, Desai M, Taur P, Pandrowala A, Gowri V, Sawant-Desai S, Gupta M, Dalvi AD, Madkaikar M, Aggarwal A, Raj R, Uppuluri Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.
Front Immunol. 2021 Jan 15;11:612323. doi: 10.3389/fimmu. (IF:6.429)
|
2021 | |
| 130 |
Shah A, George M, Dhangar S, Rajendran A, Mohan S, Vundinti BR. Severe telomere shortening in Fanconi anemia complementation group L.
Mol Biol Rep. 2021 Jan;48(1):585-593.(IF:1.402)
|
2021 | |
| 131 |
Vignesh P, Rawat A, Kumrah R, Singh A, Gummadi A, Sharma M, Kaur A, Nameirakpam J, Jindal A, Suri D, Gupta A, Khadwal A, Saikia B, Minz RW, Sharma K, Desai M, Taur P, Gowri V, Pandrowala A, Dalvi A, Jodhawat N, Kambli P, Madkaikar MR, Bhattad S, Ramprakas Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.
Front Immunol. 2021 Feb 8;11:619146. doi: 10.3389/fimmu.2020.619146. (IF:6.429)
|
2021 | |
| 132 |
More TA, Kedar PS. Genotypic analysis of SLC4A1 A858D mutation in Indian population associated with distal renal tubular Acidosis (dRTA) coupled with hemolytic anemia.
Gene. 2021 Feb 15;769:145241. doi: 10.1016/j.gene.2020.145241.
|
2021 | |
| 133 |
Rawat A, Vignesh P, Sudhakar M, Sharma M, Suri D, Jindal A, Gupta A, Shandilya JK, Loganathan SK, Kaur G, Chawla S, Patra PK, Khadwal A, Saikia B, Minz RW, Aggarwal V, Taur P, Pandrowala A, Gowri V, Desai M, Kulkarni M, Hule G, Bargir U, Kambli P, Madkaik Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India.
Front Immunol. 2021 Feb 25;12:625320. doi: 10.3389/fimmu.2021.625320.(IF:6.429)
|
2021 | |
| 134 |
Taur PD, Gowri V, Pandrowala AA, Iyengar VV, Chougule A, Golwala Z, Chandak S, Agarwal R, Keni P, Dighe N, Bodhanwala M, Prabhu S, George B, Fouzia NA, Edison ES, Arunachalam AK, Madkaikar MR, Dalvi AD, Yadav RM, Bargir UA, Kambli PM, Rawat A, Das J, Josh Clinical and Molecular Findings in Mendelian Susceptibility to Mycobacterial Diseases: Experience From India.
Front Immunol. 2021 Feb 25;12:631298. doi: 10.3389/fimmu.2021.631298.(IF:6.429)
|
2021 | |
| 135 |
Saikia B, Rawat A, Minz RW, Suri D, Pandiarajan V, Jindal A, Sahu S, Karim A, Desai M, Taur PD, Pandrowala A, Gowri V, Madkaikar M, Dalvi A, Yadav RM, Lashkari HP, Raj R, Uppuluri R, Swaminathan VV, Bhattad S, Cyril G, Kumar H, Shukla A, Kalra M, Govindar Clinical Profile of Hyper-IgE Syndrome in India.
Front Immunol. 2021 Feb 26;12:626593. doi: 10.3389/fimmu.2021.626593. (IF:6.429)
|
2021 | |
| 136 |
Yadav RM, Bargir UA, Ganapule A, Dalvi A, Gupta M, Madkaikar M. HLA-DR covers Bare Lymphocyte Syndrome.
Scand J Immunol. 2021 Feb;93(2):e12968. doi: 10.1111/sji.12968.(IF:2.717)
|
2021 | |
| 137 |
Bargir UA, Madkaikar M. Chalazia, A Late Manifestation of Primary Immunodeficiency Disorders.
Ocul Immunol Inflamm. 2021 Feb 17;29(2):264. (IF:2.112)
|
2021 | |
| 138 |
Renji S, Shah N, Madkaikar M. Heme Oxygenase-1 Deficiency.
Indian Pediatr. 2021 Feb 15;58(2):196. (IF:3.83)
|
2021 | |
| 139 |
Renji S, Shah N, Madkaikar M. Heme Oxygenase-1 Deficiency.
Indian Pediatr. 2021 Mar 15;58(3):290-291.(IF:3.83)
|
2021 | |
| 140 |
Bhave A , Iyer L, Kazi N , Gorivale M , Nadkarni A. Hemoglobin Olympia [ ? codon 20 (B2) G ?A, Val?Met]: a silent Hemoglobin variant
J Clin Diag Res. 2021 Mar; 15(3): EC19-EC21(IF:0.754)
|
2021 | |
| 141 |
Madkaikar M, Gupta N, Yadav RM, Bargir UA. Indias crusade against COVID-19.
Nat Immunol. 2021 Mar;22(3):258-259. doi: 10.1038/s41590-021-00876-7.(IF:20.4)
|
2021 | |
| 142 |
Shabrish S, Kelkar M, Yadav RM, Bargir UA, Gupta M, Dalvi A, Aluri J, Kulkarni M, Shinde S, Sawant-Desai S, Kambli P, Hule G, Setia P, Jodhawat N, Gaikwad P, Dhawale A, Nambiar N, Gowri V, Pandrowala A, Taur P, Raj R, Uppuluri R, Sharma R, Kini P, Sivasan The Spectrum of Clinical, Immunological, and Molecular Findings in FamilialHemophagocytic Lymphohistiocytosis: Experience From India.
Front Immunol. 2021 Mar 5;12:612583. doi: 10.3389/fimmu.2021.612583. (IF:6.429)
|
2021 | |
| 143 |
Hariharan P, Nadkarni A Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targets.
Blood Reviews 2021 Mar 6:100823. doi: 10.1016/j.blre.2021.100823. (IF: 6.6)
|
2021 | |
| 144 |
Sane M, Dighe V, Patil R, Hassan PA, Gawali S, Patravale V. Bivalirudin and sirolimus co-eluting coronary stent: Potential strategy for the prevention of stent thrombosis and restenosis.
Int J Pharm. 2021 May 1;600:120403. doi: 10.1016/j.ijpharm.2021.120403. Epub 2021 Mar 10. (IF : 5.875)
|
2021 | |
| 145 |
George M, Solanki A, Mohanty P, Dhangar S, Rajendran A, Mohan S, Vundinti BR. Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.
Mol Biol Rep. 2021 Mar 28. doi: 10.1007/s11033-021-06293-1.(IF:1.402)
|
2021 | |
| 146 |
Colah RB, Nadkarni AH, Gorakshakar AC, Sawant PM, Mehta PR, Gorivale MS, Hariharan P, Mohanty D, Ghosh K. The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades.
Hemoglobin. 2021 Mar;45(2):112-118. (IF:0.822)
|
2021 | |
| 147 |
Parchure D, Madkaikar M, Kulkarni S. Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experience.
Blood Transfus. 2022 May;20(3):235-244. doi: 10.2450/2021.0022-21. Epub 2021 Mar 31. (IF: 3.443)
|
2021 | |
| 148 |
Suri D, Rikhi R, Jindal AK, Rawat A, Sudhakar M, Vignesh P, Gupta A, Kaur A, Sharma J, Ahluwalia J, Bhatia P, Khadwal A, Raj R, Uppuluri R, Desai M, Taur P, Pandrowala AA, Gowri V, Madkaikar MR, Lashkari HP, Bhattad S, Kumar H, Verma S, Imai K, Nonoyama S, Ohara O, Chan KW, Lee PP, Lau YL, Singh S Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India.
Front Immunol. 2021 Apr 16;12:627651.eCollection 2021. (IF : 7.561)
|
2021 | |
| 149 |
Pradhan VD, Khadilkar PV, Nadkar MY, Kini SH, Roumenina LT, Rajadhyaksha AG, Khan TA, Chougule D, Ghosh K, Bayry J, Kaveri S Impact of Autoantibodies to Complement Components on the Disease Activity in SLE.
J Assoc Physicians India. 2021 Apr;69(4):11-12. (IF : 0.313)
|
2021 | |
| 150 |
Yadav RM, Dalvi A, Gupta M, Bargir UA, Shabrish S, Aluri J, Kulkarni M, Hule G, Kambli P, Setia P, Jodhawat N, Taur P, Desai M, Madkaikar MR. Spectrum of Inborn errors of immunity in a cohort of 90 patients presenting with complications to BCG vaccination in India.
Scand J Immunol. 2021 May;93(5):e13010. (IF : 3.487)
|
2021 | |
| 151 |
John R, Dalal B, Shankarkumar A, Devarajan PV Innovative BetulinNanosuspension exhibits enhanced anticancer activity in a Triple Negative Breast Cancer Cell line and Zebrafish angiogenesis model.
Int J Pharm. 2021 May 1;600:120511. (IF : 5.875)
|
2021 | |
| 152 |
Fujii J, Homma T, Kobayashi S, Warang P, Madkaikar M, Mukherjee MB. Erythrocytes as a preferential target of oxidative stress in blood.
Free Radic Res. 2021 May;55(5):562-580. (IF : 4.148)
|
2021 | |
| 153 |
Thakar M, Saxena V, Janakiram N, Ravi V, Desai A, Singh S, Shivanna N, Minz RY, Singh A, Chatterjee M, Madkaikar M, Bembalkar S, Mukherjee A, Mahesh V. Reference Ranges of Different Lymphocyte Subsets in Indian Children: A Multi-Centric Study.
Indian Pediatr. 2021 May 15;58(5):424-429. (IF : 1.411)
|
2021 | |
| 154 |
Sane M, Dighe V, Patil R, Hassan PA, Gawali S, Patravale V. Bivalirudin and sirolimus co-eluting coronary stent: Potential strategy for the prevention of stent thrombosis and restenosis.
Int J Pharm. 2021 May 1;600:120403. doi: 10.1016/j.ijpharm.2021.120403. Epub 2021 Mar 10.(IF:5.2)
|
2021 | |
| 155 |
Yadav RM, Madkaikar MR. Interpreting the impact of hydroxychloroquine prophylaxis on SARS-CoV-2 infection.
Indian J Med Res. 2021 May&Jun;153(5&6):564-565. (IF : 2.375)
|
2021 | |
| 156 |
Zian Z, Berry SPD, Bahmaie N, Ghotbi D, Kashif A, Madkaikar M, Bargir UA, Abdullahi H, Khan H, Azizi G. The clinical efficacy of Rituximab administration in autoimmunity disorders, primary immunodeficiency diseases and malignancies.
Int Immunopharmacol. 2021 Jun;95:107565. (IF:4.932)
|
2021 | |
| 157 |
Afroz T, Mishra G, Saleh AJM, Madkaikar M, Kulkarni S Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent.
TransfusApher Sci. 2021 Jun;60(3):103109. (IF: 1.285)doi: 10.1016/j.transci.2021.103109. Epub 2021 Mar 8. (IF : 1.764)
|
2021 | |
| 158 |
Setia P, Bargir UA, Aluri J, Sampagar A, Pandit A, Kumar V, Jodhawat N, Shabrish S, Sawant S, Kelkar M, Kambli P, Dalvi A, Madkaikar M. Novel CD3Z and CD3E Deficiency in Two Unrelated Females.
J ClinImmunol. 2021 Jul;41(5):1116-1118 (IF:8.317)
|
2021 | |
| 159 |
Kalantri M, Khopkar U, Shah A, Bargir UA, Hule G, Madkaikar M. A case of disseminated subcutaneous phaeohyphomycosis caused by Exserohilumrostratum with CARD9 mutation.
Indian J DermatolVenereolLeprol.2021 Jul 7:1-3. (IF : 2.545)
|
2021 | |
| 160 |
Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P. Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C?>?A, (Q101K), in the AK1 gene in an Indian family.
BMC Med Genomics. 2021 Jul 28;14(1):191. (IF : 2.931)
|
2021 | |
| 161 |
Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, de Boer M, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Garcia-Morato MB, Shephard JLV, Cagdas D, Tezcan I, Sherkat R, Mortaz E Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
Blood Cells Mol Dis. 2021 Jul 28;92:102596. doi: 10.1016/j.bcmd.2021.102596. Online ahead of print. (3.039)
|
2021 | |
| 162 |
Jain A, Govindaraj GM, Edavazhippurath A, Faisal N, Bhoyar RC, Gupta V, Uppuluri R, Manakkad SP, Kashyap A, Kumar A, Divakar MK, Imran M, Sawant S, Dalvi A, Chakyar K, Madkaikar M, Raj R, Sivasubbu S, Scaria V. Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.
PLoS One. 2021 Jul 12;16(7):e0254407. doi: 10.1371/journal.pone.0254407. eCollection 2021.(IF : 3.240)
|
2021 | |
| 163 |
Kelkar MG, Bargir UA, Malik-Yadav R, Gupta M, Dalvi A, Jodhawat N, Shinde S, Madkaikar MR. CD8 T Cells Exhibit an Exhausted Phenotype in Hemophagocytic Lymphohistiocytosis.
J ClinImmunol.2021 Aug 14.doi: 10.1007/s10875-021-01109-0. Online ahead of print. (IF : 8.317)
|
2021 | |
| 164 |
Karimi E, Mahmoudian F, Reyes SOL, Bargir UA, Madkaikar M, Artac H, Sabzevari A, Lu N, Azizi G, Abolhassani H. Approach to genetic diagnosis of inborn errors of immunity through next-generation sequencing.
MolImmunol. 2021 Sep;137:57-66. (IF : 4.407)
|
2021 | |
| 165 |
Yadav RM, Pate A, Shankarkumar A, Athalye S, Shinde S, Bargir UA, Pate M, Ganpule M, Pruthi M, Patil H, Madkaikar MR. Serosurvey for Health-Care Workers Provides Supportive Evidence for the Effectiveness of Hydroxychloroquine Prophylaxis against SARS-CoV-2 Infection.
J Epidemiol Glob Health. 2021 Sep;11(3):283-288. (IF : 1.56)
|
2021 | |
| 166 |
Panwar U, Mishra K, Patel P, Bharadva S, Vaniawala S, Shah A, Vundinti BR, Kothari SL, Ghosh K. Assessment of Long-Term in vitro Multiplied Human Whartons Jelly-Derived Mesenchymal Stem Cells prior to Their Use in Clinical Administration.
Cells Tissues Organs. 2021;210(4):239-249. doi: 10.1159/000517423. Epub 2021 Sep 14. (IF : 2.481)
|
2021 | |
| 167 |
George M, Solanki A, Chavan N, Rajendran A, Raj R, Mohan S, Nemani S, Kanvinde S, Munirathnam D, Rao S, Radhakrishnan N, Lashkari HP, Ghildhiyal RG, Manglani M, Shanmukhaiah C, Bhat S, Ramesh S, Cherian A, Junagade P, Vundinti BR. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
Hum Mutat. 2021 Dec;42(12):1648-1665. (IF : 4.878)
|
2021 | |
| 168 |
Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P, Kedar PS. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolyticanaemia with developmental delay in an Indian family.
J ClinPathol. 2021 Oct;74(10):620-624. (IF : 3.411)
|
2021 | |
| 169 |
Sampagar A, Gosavi M, Kedar P, Patel T, Dongerdiye R, Mahantashetti N. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.
Int J Hematol. 2021 Oct 27.doi: 10.1007/s12185-021-03240-5. Online ahead of print. ( IF : 2.49)
|
2021 | |
| 170 |
Lashkari HP, Madkaikar M, Dalvi A, Gupta M, Bustamante J, Sharma M, Rawat A, Bhatia P, Bhat KG, Rao S, Kamath N, Moideen F, Latour S, Winter S, Bhavani GS, Girisha KM. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India.
Indian J Pediatr. 2021 Nov;89(3):233-242 (IF:1.967)
|
2021 | |
| 171 |
Roos D, Madkaikar M, Kuhns DB et al. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
Blood Cells Mol Dis. 2021 Dec92:102596 (IF:2.40)
|
2021 | |
| 172 |
Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y,Raicha B, Serrao E. Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
Am J Clin Pathol. 2020 Jan 1;153(1):82-87.(IF 1.962)
|
2020 | |
| 173 |
Nadkarni AH, Ghosh K, Ghosh K, Agrawal R. Recent advances in screening and diagnosis of haemoglobinopathy.
Expert Rev Hematol. 2020 Jan;13(1):13-21. (IF: 2.505)
|
2020 | |
| 174 |
Solanki A, Rajendran A, Mohan S, Raj R, Vundinti BR Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia.
PLoS One. 2020 Jan 15;15(1):e0227603.eCollection 2020 (IF:2.776)
|
2020 | |
| 175 |
Deshpande R, Shanbhag S, Jadli A, Shetty S. A rare case of Glanzmanns thrombasthenia and factor VII deficiency due to a combination of pathogenic and non-pathogenic gene variants.
Haemophilia. 2020 Jan;26(1):e26-e27 (IF:3.590)
|
2020 | |
| 176 |
Ghosh K, Ghosh K, Agrawal R,Nadkarni AH. Recent advances in screening and diagnosis of hemoglobinopathy.
Expert Rev Hematol. 2020 Jan;13(1):13-21.
|
2020 | |
| 177 |
Devendra R, Gupta V, Biradar SS, Bhat P, Hegde S, Hoti SL, Mukherjee MB, Hegde HV. G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.
Ann Hum Biol. 2020 Feb;47(1):55-58 (IF:1.588)
|
2020 | |
| 178 |
Bargir UA, Hule GP, Kambli P, Kulkarni M, Donta AK, Taur P, Gorakshakar A, Desai M, Madkaikar MR. "FUT2" a potential genetic modifier in NCF1 deficiency.
J Allergy Clin Immunol Pract. 2020 Mar;8(3):1097-1099. (IF:7.55)
|
2020 | |
| 179 |
Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H,Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, Ramanagoudr-Bhojappa R, Smogorzewska A, Mohan S, Rajendran A, Auerbach AD, Takata M, Chandrasekharap A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat. 2020 Jan;41(1):122-128. (IF 4.453)
|
2020 | |
| 180 |
Chawla S, Gorakshakar A, Ghosh K, Madkaikar M, Devarajan P Fabrication of gelatin functionalized silver nanoparticles for blood group profiling.
Nanotechnology. 2020 Mar 26. doi: 10.1088/1361-6528/ab83b9
|
2020 | |
| 181 |
Krishnan VP, Taur P, Pandrowala A, Madkaikar MR, Desai M X-Linked Hyper IgM Syndrome Presenting with Recurrent Tuberculosis-a Case Report.
J Clin Immunol. 2020 Apr;40(3):531-533.(IF:6.780)
|
2020 | |
| 182 |
More TA, Dongerdiye R, Devendra R, Warang PP, Kedar PS. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
Ann Hematol. 2020 Apr;99(4):715-727
|
2020 | |
| 183 |
Gupta V, Kulkarni A, Warang P, Devendra R, Chiddarwar A, Kedar PS. Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia.
Hum Mutat. 2020 Apr;41(4):737-748.
|
2020 | |
| 184 |
Prabhudesai A,Sharma R,Shetty S,Phadnis A,Kulkarni B Congenital PAI-1 deficiency results in psoas hematoma in an Indian patient.
Thromb Res. 2020 Jun;190:35-38. [IF: 2.77].
|
2020 | |
| 185 |
Chawla SS, Gorakshakar AC, Ghosh KK, Madkaikar MR, Devarajan PV Fabrication of gelatin functionalized silver nanoparticles for blood group profiling.
Nanotechnology. 2020 May 1;31(29):295102. doi: 10.1088/1361-6528/ab83b9.(IF:3.551)
|
2020 | |
| 186 |
More TA, Dalal B, Devendra R, Warang P, Shankarkumar A, Kedar PS. Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.
Cytometry B Clin Cytom. 2020 May;98(3):238-249.
|
2020 | |
| 187 |
Purohit S, Srivastava S, Shankarkumar A, Raj A, Dalal B, Marathe N, Shende C. Prevalence of Vitamin D Deficiency Amongst Indian Orthopaedic Surgeons.
Indian J Orthop. 2020 May 14;54(Suppl 1):183-187.
|
2020 | |
| 188 |
Bargir UA,Madkaikar MR 2019 Update on Primary Immunodeficiency Disorders by the International Union of Immunological Societies.
Indian Pediatr. 2020 Jun 15;57(6):565-567.(IF:1.186)
|
2020 | |
| 189 |
Umare V, Pradhan V, Dadheech S, Rajadhyaksha A, Ghosh K, Nadkarni A Clinical implications of IL-10 promoter polymorphisms on disease susceptibility in Indian SLE patients.
Lupus. 2020 Jun; 29(6):587-598.(IF:2.924)
|
2020 | |
| 190 |
Hariharan P, Kishnani P, Sawant P, Gorivale M, Mehta P, Kargutkar N, Colah R, Nadkarni A Genotypic-phenotypic heterogeneity of ??-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India..
Ann Hematol. 2020 Jul;99(7):1475-1483.(IF 3.0)
|
2020 | |
| 191 |
Shabrish S, Karnik N, Gupta V, Bhate P, Madkaikar MR. Impaired NK cell activation during acute dengue virus infection: A contributing factor to disease severity.
Heliyon. 2020 Jul 4;6(7):e04320. doi: 10.1016/j.heliyon.2020.e04320. eCollection 2020
|
2020 | |
| 192 |
Kulkarni S & Harita Maru. Extended phenotyping of blood group antigens: Towards improved transfusion practices.
Global Journal of Transfusion Medicine 2020 Jul-Dec, 5: 120-5. (IF:-)
|
2020 | |
| 193 |
Vinod Umare, Sneha Dadheech, Vandana Pradhan, Anjali Rajadhyaksha, Kanjaksha Ghosh, Anita Nadkarni* Cytokine genes multi-locus analysis reveals synergistic influence on genetic susceptibility in Indian SLE - A multifactor-dimensionality reduction approach.
Cytokine 2020 Nov;135:155240. (IF 3.5)
|
2020 | |
| 194 |
Dhangar S, Ghatanatti J, Vundinti BR. array-CGH revealed gain of Yp11.2 in 49,XXXXY and gain of Xp22.33 in 48,XXYY karyotypes of two rare klinefelter variants.
Intractable Rare Dis Res. 2020 Aug;9(3):145-150.(IF:1.447)
|
2020 | |
| 195 |
Mehta P, Sawant P, Gorivale M, Nadkarni A, Colah R, Mukherjee MB. Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathies.
Int J Lab Hematol. 2020 Aug;42(4):482-491. (IF 2.2)
|
2020 | |
| 196 |
Mishra G, Sachan D, Krishna D, Parchure D, Madkaikar MR, Kulkarni S. Characterising Indian RhD variants by serological and molecular methods.
Transfus Med. 2020 Aug;30(4):324-326.(IF:2.159)
|
2020 | |
| 197 |
Vira HJ, Pradhan VD, Umare VD, Chaudhary AK, Rajadhyksha AG, Nadkar MY, Ghosh K, Nadkarni AH. Role of MMP-2 and its inhibitor TIMP-2 as biomarkers for susceptibility to systemic lupus erythematosus.
Biomark Med. 2020 Aug;14(12):1109-1119.
|
2020 | |
| 198 |
Smvk P, M N M, D M DY, Kondeti S, Kalashikam RR. Strain specific variation underlines the disparity in stress response of rats to calorie dense diets in the pathophysiology of obesity.
Steroids. 2020 Aug;160:108653. doi: 10.1016/j.steroids.2020.108653.
|
2020 | |
| 199 |
Vira HJ, Pradhan VD, Umare VD, Chaudhary AK, Rajadhyksha AG, Nadkar MY, Ghosh K, Nadkarni AH. Expression of the matrix metalloproteinases MMP-2 and MMP-9 and their inhibitors TIMP-1 and TIMP-2 in systemic lupus erythematosus patients.
Neth J Med. 2020 Sep;78(5):261-268.
|
2020 | |
| 200 |
Soni P, Shanmukhaiah C, Patil R, Shetty S. Differential response to FEIBA is strongly associated with the prothrombotic microparticles.
Blood Cells Mol Dis. 2020 Sep;84:102441. doi: 10.1016/j.bcmd.2020.102441.
|
2020 | |
| 201 |
Talukdar D; Gogoi, A, Doley, D, Marak R, Kakati S, Pradhan V, Nadkarni A, Baruah S. The clinical and immunological profile of SLE patients from Assam, North-East India.
Ind J Rheumatol 2020 Sep;15(3) :181-186(IF:0.327)
|
2020 | |
| 202 |
Kulkarni S, Choudhary B, Gogri H, Sharma J, Madkaikar MR. Red cell antigen phenotypes in blood donors & thalassaemia patients for creation of red cell antigen-matched inventory.
Indian J Med Res. 2020 Sep;152(3):273-279.
|
2020 | |
| 203 |
Agarwal A, Mukherjee A, Kumar G, Chatterjee P, Bhatnagar T, Malhotra P; PLACID Trial Collaborators Convalescent plasma in the management of moderate covid-19 in adults in India: open label phase II multicentre randomised controlled trial (PLACID Trial).
BMJ. 2020 Oct 22;371:m3939. doi: 10.1136/bmj.m3939.(IF:30.223)
|
2020 | |
| 204 |
Gupta AD, Daruwalla MR, Pawar R, Sidhwa K, Hariharan P, Nadkarni A, Hb Yaizu A rare beta-globin chain variant posing diagnostic dilemma in high- performance liquid chromatography.
Ind J Pathol Microbiol 2020 Oct-Dec ;63(4) 663-665.(IF:0.663)
|
2020 | |
| 205 |
Hariharan P, Chavan V, Nadkarni A Significance of Heme oxygenase -1 (HMOX-1) gene on fetal hemoglobin induction in sickle cell anemia patients
Scientific Reports. 2020 Oct 28;10(1):18506. (IF 4.0)
|
2020 | |
| 206 |
Ukirde V, Usulumarty D, Maru H, Billa V. Are weak blood groups important to look for in kidney transplantation? A case report on interchanging blood groups.
Indian J Transplant 2020 Oct-Dec; 14(4):355-357.(IF:0.13)
|
2020 | |
| 207 |
Kulkarni S, Mishra G, Maru H, Parchure D, Gupta D, Bajaj AK, Sindhwani SP, Chaphekar A, Shah R, Férec C, Madkaikar M, Fichou Y. Molecular characterization of rare D--/D-- variants in individuals of Indian origin.
Blood Transfus. 2020 Nov 27. doi: 10.2450/2020.0183-20.(IF:3.662)
|
2020 | |
| 208 |
Yadav RM, Gupta M, Dalvi A, Bargir UA, Hule G, Shabrish S, Aluri J, Kulkarni M, Kambli P, Uppuluri R, Seshadri S, Jagadeesh S, Suresh B, Raja J, Taur P, Malaischamy S, Ghosh P, Mahalingam S, Kadam P, Lashkari HP, Tamhankar P, Tamhankar V, Mithbawkar S, Bh Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.
Front Immunol. 2020 Dec 7;11:612316. doi: 10.3389/fimmu.2020.612316. eCollection 2020.(IF:6.429)
|
2020 | |
| 209 |
Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P, Kedar PS. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe hemolytic anemia with developmental delay in an Indian family.
J Clin Pathol. 2020 Dec 25:jclinpath-2020-206960. doi: 10.1136/jclinpath-2020-206960.(IF:3.4)
|
2020 | |
| 210 |
Devendra R, Gupta V, Shanmugam R, Singh MPSS, Patel P, Valecha N, Mishra N, Ahmed N, Hoti SL, Hegde HV, Warang P, Chiddarwar A, Kedar P, Mayekar P, Mukherjee MB. Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.
Infect Genet Evol. 2020 Dec;86:104597. doi: 10.1016/j.meegid.2020.104597.
|
2020 | |
| 211 |
Kambli PM, Bargir UA, Yadav RM, Gupta MR, Dalvi AD, Hule G, Kelkar M, Sawant-Desai S, Setia P, Jodhawat N, Nambiar N, Dhawale A, Gaikwad P, Shinde S, Taur P, Gowri V, Pandrowala A, Gupta A, Joshi V, Sharma M, Arora K, Pilania RK, Chaudhary H, Agarwal A, K Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India.
Front Immunol. 2020 Dec 16;11:612703. doi: 10.3389/fimmu.2020.612703. eCollection 2020.PMID: 33391282
|
2020 | |
| 212 |
Kedar PS, Gupta V, Dongerdiye R, Chiddarwar A, Warang P, Madkaikar MR Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.
J Clin Pathol. 2019 Jan;72(1):81-85.(IF:2.894)
|
2019 | |
| 213 |
Upadhye D, Jain D, Nadkarni A, Ghosh K, Colah R. Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India.
Indian J Hematol Blood Transfus. 2019 Jan;35(1):109-113. (IF: 0.474)
|
2019 | |
| 214 |
Vira H, Pradhan V, Umare V, Chaudhary A, Rajadhyksha A, Nadkar M, Ghosh K, Nadkarni A. Role of polymorphisms in MMP-9 and TIMP-1 as biomarkers for susceptibility to systemic lupus erythematosus patients.
Biomark Med. 2019 Jan; 13(1):33-43.(IF:2.346)
|
2019 | |
| 215 |
Aluri J, Desai M, Gupta M, Dalvi A, Terance A, Rosenzweig SD, Stoddard JL, Niemela JE, Tamankar V, Mhatre S, Bargir U, Kulkarni M, Shah N, Aggarwal A, Lashkari HP, Krishna V, Govindaraj G, Kalra M, Madkaikar MR Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India.
Front Immunol. 2019 Feb 4;10:23. eCollection 2019. (IF: 5.511)
|
2019 | |
| 216 |
Shabrish S, Desai M, Saxena V, Kelkar M, Madkaikar MR. IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections.
J Clin Immunol. 2019 Feb;39(2):135-137. (IF: 4.227)
|
2019 | |
| 217 |
Dhangar S, Korgaonkar S, Vundinti BR. Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.
Intractable Rare Dis Res. 2019 Feb;8(1):72-77
|
2019 | |
| 218 |
Aluri J, Gupta MR, Dalvi A, Mhatre S, Kulkarni M, Desai M, Shah NK, Madkaikar Lymphopenia and Severe Combined Immunodeficiency (SCID) - Think Before You Ink.
Indian J Pediatr. 2019 Mar 16.doi:10.1007/s12098-019-02904-9.[Epub ahead of print] (IF: 1.046 )
|
2019 | |
| 219 |
Desai SA, Martin SL, Nanavati RN, Colah RB, Ghosh K, Kabra N, Mukherjee MB. Red Cell Distribution Width (RDW): Normative Data in Indian Neonates.
J Pediatr Hematol Oncol. 2019 Mar;41(2): e119-e-121.(IF: 1.060)
|
2019 | |
| 220 |
Shabrish S, Kelkar M, Chavan N, Desai M, Bargir U, Gupta M, Mehta P, Chichra A, S C, Taur P, Saxena V, Vundinti BR, Madkaikar MR. Natural Killer Cell Degranulation Defect: A Cause for Impaired NK-Cell Cytotoxicity a and Hyperinflammation in Fanconi Anemia Patients.
Front Immunol. 2019 Mar 21;10:490. eCollection 2019 (IF: 3.35)
|
2019 | |
| 221 |
Ghosh K, Mishra K, Shah A, Patel P, Shetty S. Novel Deleterious Sequence Change in the NLRP12 Gene in a Child with the Autoinflammatory Syndrome, Joint Hypermobility and Cutis Laxa from India.
Mediterr J Hematol Infect Dis. 2019 Mar 1;11(1):e2019018.
|
2019 | |
| 222 |
Gaikwad T, Deshpande R, Shetty S. Anti-factor VIII inhibitors against A2 and C2 domains in hemophilia A patients from India.
Blood Cells Mol Dis. 2018 Mar;75:11-12.(IF:1.836)
|
2019 | |
| 223 |
Mohanty P, Jadhav P, Shanmukhaiah C, Kumar S, Vundinti BR. A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.
Int J Dermatol. 2019 Mar 13. doi: 10.1111/ijd.14424. [Epub ahead of print]
|
2019 | |
| 224 |
Umare V, Pradhan V, Nath S, Rajadhyaksha A, Ghosh K, Nadkarni AH. Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients.
Lupus. 2019 Apr;28(4):545-554
|
2019 | |
| 225 |
Nadkarni AH, Gorakshakar AC, Sawant PM, Italia KY, Upadhye DS, Gorivale MS, Mehta PR, Hariharan P, Ghosh K, Colah RB The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center.
Int J Lab Hematol. 2019 Apr;41(2):218-226. (IF:1.919)
|
2019 | |
| 226 |
Devendra R, Warang P, Gupta V, Chiddarwar A, Kedar PS, Agarwal MB, Mukherjee MB. A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.
Indian J Hematol Blood Transfus. 2019 Apr;35(2):399-401.
|
2019 | |
| 227 |
Sidhwa K, Daruwalla MR, Pawar R, Nadkarni A, Hariharan P, Mehta P, Gupta AD. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband.
Indian J Pathol Microbiol. 2019 Apr-Jun;62(2):323-325.
|
2019 | |
| 228 |
Korgaonkar S, Dhangar S, Kulkarni V, Kerketta L, Vundinti BR. Chromosomal Aberrations in Primary Amenorrhea: A Retrospective Study.
J Hum Reprod Sci. 2019 Apr-Jun;12(2):92-97.
|
2019 | |
| 229 |
Bandari AK, Bhat S, Archana MV, Yadavalli S, Patel K, Rajagopalan P, Madugundu AK, Madkaikar MR, Reddy K, Muthusamy B, Pandey A. Family-Based Next-Generation Sequencing Study Identifies an IL2RG Variant in an Infant with Primary Immunodeficiency.
OMICS. 2019 May;23(5):285-290. doi: 10.1089/omi.2018.0196.(IF:2.370)
|
2019 | |
| 230 |
Martin SL, Desai S, Nanavati R, Colah RB, Ghosh K, Mukherjee MB. Red cell distribution width and its association with mortality in neonatal sepsis.
J Matern Fetal Neonatal Med. 2019 Jun;32(12):1925-1930.
|
2019 | |
| 231 |
Dongerdiye R, Kamat P, Jain P, Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS. Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
J Clin Pathol. 2019 Jun; 72(6): 393-398.(IF: 2.894)
|
2019 | |
| 232 |
Madkaikar MR, Shabrish S, Kulkarni M, Aluri J, Dalvi A, Kelkar M, Gupta M. Application of Flow Cytometry in Primary Immunodeficiencies: Experience From India.
Front Immunol. 2019 Jun 11;10:1248. doi: 10.3389/fimmu.2019.01248. eCollection 2019. Review.(IF:6.429)
|
2019 | |
| 233 |
Jadli A, Ghosh K, Damania K, Satoskar P, Bansal V, Shetty S. Prediction of preeclampsia using combination of biomarkers at 18-23?weeks of gestation: A nested case-control study.
Pregnancy Hypertens. 2019 Jul;17:20-27.
|
2019 | |
| 234 |
Das Gupta A, Hariharan P, Daruwalla M, Sidhwa K, Pawar R, Nadkarni A. Hemoglobin Titusville [?2 Codon 94 G>A]: A Rare Alpha Globin Chain Variant Causing Low Oxygen Saturation.
Indian J Hematol Blood Transfus. 2019 Jul;35(3):593-595.
|
2019 | |
| 235 |
Mohanty MC, Madkaikar MR, Desai M, Aluri J, Varose SY, Taur P, Sharma DK, Nalavade UP, Rane SV, Gupta M, Shabarish S, Dalvi A, Deshpande JM. Natural Clearance of Prolonged VDPV Infection in a Child With Primary Immunodeficiency Disorder.
Front Immunol. 2019 Jul 23;10:1567.doi:10.3389/fimmu.2019.01567. eCollection(IF:6.429).
|
2019 | |
| 236 |
Hule GP, Bargir UA, Kulkarni M, Kambli P, Taur P, Desai M, Madkaikar MR. Does Pioglitazone Lead to Neutrophil Extracellular Traps Formation in Chronic Granulomatous Disease Patients?
Front Immunol. 2019 Jul 31;10:1739. doi: 10.3389/fimmu.2019.01739. eCollection (IF:6.429).
|
2019 | |
| 237 |
Nair R, Gogri H, Kulkarni S, Gupta D. Detection of a rare subgroup of A phenotype while resolving ABO discrepancy.
Asian J Transfus Sci. 2019 Jul-Dec;13(2):129-131
|
2019 | |
| 238 |
Dalal K, Dalal B, Bhatia S, Shukla A, Shankarkumar A Analysis of serum Haptoglobin using glycoproteomics and lectin immunoassay in liver diseases in Hepatitis B virus infection.
Clin Chim Acta. 2019 Aug;495:309-317.
|
2019 | |
| 239 |
Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar MR. Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.
Indian J Pediatr. 2019 Aug;86(8):692-699.(IF:1.181)
|
2019 | |
| 240 |
Bandari AK, Muthusamy B, Bhat S, Govindaraj P, Rajagopalan P, Dalvi A, Shankar S, Raja R, Reddy KS, Madkaikar MR, Pandey A. A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases.
Front Immunol. 2019 Aug 21;10:1964. doi: 10.3389/fimmu.2019.01964. eCollection 2019.(IF:6.429)
|
2019 | |
| 241 |
Khadilkar PV, Khopkar US, Nadkar MY, Rajadhyaksha AG, Chougule DA, Deshpande SD, Madkaikar MR, Pradhan VD. Fibrotic Cytokine Interplay in Evaluation of Disease Activity in Treatment Naïve Systemic Sclerosis Patients from Western India.
J Assoc Physicians India. 2019 Aug;67(8):26-30.(IF:0.47)
|
2019 | |
| 242 |
Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y, Raicha B, Serrao E. Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
Am J Clin Pathol. 2019 Aug 1. pii: aqz108. doi: 10.1093/ajcp/aqz108. [Epub ahead of print]\
|
2019 | |
| 243 |
Ghosh K, Ghosh K, Agrawal R, Nadkarni AH. Recent advances in screening and diagnosis of haemoglobinopathy.
Expert Rev Hematol. 2019 Aug 21. doi: 10.1080/17474086.2019.1656525. [Epub ahead of print]
|
2019 | |
| 244 |
Soni P, Mantri S, Prabhudesai A, Patil R, Shanmukhaiah C, Shetty S. Triple jeopardy: A case of Glanzmanns thrombasthenia with anti-GPIIb-IIIa antibodies and HPA incompatibility resulting in stillbirth.
Thromb Res. 2019 Sep;181:141-144
|
2019 | |
| 245 |
Bargir UA, Hule GP, Kambli P, Kulkarni M, Donta AK, Taur P, Gorakshakar A, Desai M, Madkaikar MR. "FUT2" a potential genetic modifier in NCF1 deficiency.
J Allergy Clin Immunol Pract. 2019 Sep 5. pii: S2213-2198(19)30758-5. doi: 10.1016/j.jaip.2019.08.035.(IF:7.550)
|
2019 | |
| 246 |
Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, Ramanagoudr-Bhojappa R, Smogorzewska A, Mohan S, Rajendran A, Auerbach AD, Takata M, Chandrasekhara A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat. 2019 Sep 12. doi: 10.1002/humu.23914. [Epub ahead of print]
|
2019 | |
| 247 |
Dhangar S, Shanbhag V, Shanmukhaiah C, Vundinti BR. Lack of association between functional polymorphism of DNA repair genes (XRCC1, XPD) and clinical response in Indian chronic myeloid leukemia patients.
Mol Biol Rep. 2019 Oct;46(5):4997-5003.
|
2019 | |
| 248 |
Prabhudesai A, Shetty S, Shanmukhaiah C, Kalantri S, Bhattacharyya M, Kulkarni B A rare cause of bleeding in two Indian families with congenital alpha-2-antiplasmin deficiency.
Haemophilia. 2019 Oct 2. doi: 10.1111/hae.13851. [Epub ahead of print]
|
2019 | |
| 249 |
Kedar PS, Harigae H, Ito E, Muramatsu H, Kojima S, Okuno Y, Fujiwara T, Dongerdiye R, Warang PP, Madkaikar MR. Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.
Int J Hematol. 2019 Nov;110(5):618-626.(IF:2.245)
|
2019 | |
| 250 |
More TA, Dalal B, Devendra R, Warang P, Shankarkumar A, Kedar PS Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.
Cytometry B Clin Cytom. 2019 Nov 21. doi: 10.1002/cyto.b.21857. [Epub ahead of print](IF: 2.891)
|
2019 | |
| 251 |
Hariharan P, Colah R, Ghosh K, Nadkarni A. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Genomics. 2019 Dec, 111(6):1771-1776.(IF: 2.910)
|
2019 | |
| 252 |
Mohanty P, Jadhav P, Shanmukhaiah C, Kumar S, Vundinti BR A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.
Int J Dermatol. 2019 Dec;58(12):1468-1471. (IF:1.794)
|
2019 | |
| 253 |
Pathak V, Colah R, Ghosh K Effect of inherited red cell defects on growth of Plasmodium falciparum: An in vitro study.
Indian J Med Res. 2018 Jan;147(1):102-109.(IF: 1.508)
|
2018 | |
| 254 |
Kerketta LS, Ghosh K. Circulating microfilariae in haematological malignancies: do they have a role in pathogenesis?
J Helminthol. 2018 Jan;92(1):125-127.(IF: 1.61)
|
2018 | |
| 255 |
Umare V, Pradhan V, Rajadhyaksha A, Ghosh K, Nadkarni A. Predisposition of IL-1? (-511 C/T) polymorphism to renal and hematologic disorders in Indian SLE patients.
Gene 2018 Jan 30;641:41-45.(IF: 3.191)
|
2018 | |
| 256 |
Patil R, Bajpai S, Ghosh K, Shetty S. Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop. 2018 Jan 31;181:21-24.(IF: 2.509)
|
2018 | |
| 257 |
Martin SL, Desai S, Nanavati R, Colah RB, Ghosh K, Mukherjee MB. Red cell distribution width and its association with mortality in neonatal sepsis.
J Matern Fetal Neonatal Med. 2018 Jan 8:1-6.(IF: 1.493)
|
2018 | |
| 258 |
Upadhye D, Das RS, Ray J, Acharjee S, Ghosh K, Colah RB, Mukherjee MB. Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
Hemoglobin. 2018 Jan;42(1):43-46. (IF: 0.67)
|
2018 | |
| 259 |
Gogri H, Ray S, Agrawal S, Aruna S, Ghosh K, Gorakshakar A. Heterogeneity of O blood group in India: Peeping through the window of molecular biology.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68. (IF: 1.06)
|
2018 | |
| 260 |
Pathak V, Colah R, Ghosh K Plasmodium falciparum malaria skews globin gene expression balance in in-vitro haematopoietic stem cell culture system: Its implications in malaria associated anemia.
Exp Parasitol. 2018 Feb;185:29-38.(IF: 1.821)
|
2018 | |
| 261 |
Aluri J, Gupta M, Dalvi A, Mhatre S, Kulkarni M, Hule G, Desai M, Shah N, Taur P, Vedam R, Madkaikar MR. Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India.
Front Immunol. 2018 Feb 16;9:188.(IF: 5.511)
|
2018 | |
| 262 |
Chougule D, Nadkar M, Rajadhyaksha A, Pandit-Shende P, Surve P, Dawkar N, Khadilkar P, Patwardhan M, Kaveri S, Ghosh K, Pradhan V. Association of clinical and serological parameters of systemic lupus erythematosus patients with Epstein-Barr virus antibody profile.
J Med Virol. 2018 Mar;90(3):559-563.(IF: 1.988)
|
2018 | |
| 263 |
Gaikwad T, Ghosh K, Avery P, Kamali F, Shetty S. Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.
Clin Appl Thromb Hemost. 2018 Mar;24(2):353-359.(IF: 2.096)
|
2018 | |
| 264 |
Patil RK, Ghosh K, Chandrakala S, Shetty S. A possible need for routine screening for Strongyloides stercoralis infection in Indian haemophilia patients.
Indian J Med Res. 2018 Mar;147(3):315-317 (IF: 1.508)
|
2018 | |
| 265 |
Kulkarni S, Parchure DS, Gopalkrishnan V, Madkaikar MR. Screening for DEL phenotype in RhD negative Indians.
J Clin Lab Anal. 2018 Mar;32(3). doi: 10.1002/jcla.22288. Epub 2017 Jun 23 (IF:1.303)
|
2018 | |
| 266 |
Prabhudesai A, Shetty S, Ghosh K, Kulkarni B. Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein Occlusion.
J Assoc Physicians India. 2018 Mar;66(3):76-78.(IF:0.37)
|
2018 | |
| 267 |
Gogri H, Ray S, Agrawal S, Aruna S, Ghosh K, Gorakshakar A Heterogeneity of O blood group in India: Peeping through the window of molecular biology.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68. (IF: --)
|
2018 | |
| 268 |
Kulkarni SS, Gogri H, Parchure D, Mishra G, Ghosh K, Rajadhyaksha S, Madkaikar MR, Férec C, Fichou Y. RHD-Positive Alleles among D- C/E+ Individuals from India.
Transfus Med Hemother. 2018 May;45(3):173-177. (IF: 2.152)
|
2018 | |
| 269 |
Patil R, Bajpai S, Ghosh K, Shetty S. Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop. 2018 May;181:21-24. (IF: 2.509)
|
2018 | |
| 270 |
Fichou Y, Parchure D, Gogri H, Gopalkrishnan V, Le Maréchal C, Chen JM, Férec C, Madkaikar MR, Ghosh K, Kulkarni S. Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Transfusion. 2018 Jun;58(6):1540-1549. (IF: 3.423)
|
2018 | |
| 271 |
Deshpande R, Pathare A, Alkindi S, Al Zadjali S, Ghosh K, Shetty S. A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.
Int J Lab Hematol. 2018 Jun;40(3):e49-e51. (IF: 1.919)
|
2018 | |
| 272 |
Gogri H, Pitale P, Madkaikar MR, Kulkarni S. Molecular genotyping of Indian blood group system antigens in Indian blood donors.
Transfus Apher Sci. 2018 Jun;57(3):388-390. (IF: --)
|
2018 | |
| 273 |
Gupta M, Aluri J, Desai M, Lokeshwar M, Taur P, Lenardo M, Bergerson J, Dalvi A, Mhatre S, Kulkarni M, Kambli P, Madkaikar MR. Clinical, Immunological, and Molecular Findings in Four Cases of B Cell Expansion With NF-?B and T Cell Anergy Disease for the First Time From India.
Front Immunol. 2018 Jun 14;9:1049. eCollection 2018. (IF: 3.35)
|
2018 | |
| 274 |
Vinod Gupta, Rati Devendra, Aruna Rajendran, Neeraj Sidharthan, Prashant Warang,Prabhakar Kedar. Two Novel C-Terminal Frame shift Mutations in the CYB5R3 Gene Lead to Global Growth and Methemoglobinemia Type II. Developmental Delay associated with Recessive Congenital
Journal of Medical Science and Clinical Research 2018 June;6(6):626-636.(IF:6.379)
|
2018 | |
| 275 |
Swati Yardi, Mehul Rajpurkar, Aruna Shankarkumar. A retrospective study of quality management system at National Reference Laboratory in Mumbai- highlighting quality in HIV testing.
International J Med Sci Public Health 2018 June; 7(10):1-6. Online First (IF:)
|
2018 | |
| 276 |
Colah R, Nadkarni A, Gorakshakar A, Sawant P, Italia K, Upadhye D, Gaikwad H, Ghosh K. Prenatal Diagnosis of HbE-?-Thalassemia: Experience of a Center in Western India.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):474-479 (IF:0.474)
|
2018 | |
| 277 |
Lad H, Yadav M, Mehta P, Patel P, Sawant P, Colah RB, Mukherjee MB, Shanmugam R. First Observation of Hb Lepore Hollandia in the Baiga Tribal Family.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):581-584.(IF:0.474)
|
2018 | |
| 278 |
Yabaji PM, Shankarkumar A, Shukla A, Bhatia S Hepatitis C virus infection in a tertiary care hospital in Mumbai, India: Identification of a mixed and novel genotype.
Indian J Med Microbiol. 2018 Jul-Sep;36(3):352-356.(IF: 1.157)
|
2018 | |
| 279 |
Martin SL, Desai S, Nanavati R, Colah RB, Ghosh K, Mukherjee MB. Innate immune gene polymorphisms and their association with neonatal sepsis.
Infect Genet Evol. 2018 Aug;62:205-210.(IF:2.545)
|
2018 | |
| 280 |
Hule GP, Kanvinde PR, Kulkarni MA, van Leeuwen K, de Boer M, Bargir UA, Taur PD, Desai MM, Madkaikar MRR p47phox-/- Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.
J Clin Immunol. 2018 Aug;38(6):638-641.(IF:4.227)
|
2018 | |
| 281 |
Warang P, Homma T, Pandya R, Sawant A, Shinde N, Pandey D, Fujii J, Madkaikar MR, Mukherjee MB Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
Br J Haematol. 2018 Aug;182(4):559-566. (IF: 5.128)
|
2018 | |
| 282 |
Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar MR. Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
Hematology. 2018 Sep;23(8):567-573.(IF: 1.315)
|
2018 | |
| 283 |
Dhangar S, C SK, S C, Vundinti BR. Imatinib resistance due to a novel and rare class of mutation at position S348 (1043nt C?A) of Bcr/Abl gene in a chronic myeloid leukemia patient.
Leuk Res. 2018 Sep;72:96-98.(IF:2.319)
|
2018 | |
| 284 |
Pradhan V, Pandit P, Surve P, Lecerf M, Rajadhyaksha A, Nadkar M, Khadilkar PV, Chougule DA, Naigaonkar AA, Lacroix-Desmazes S, Bayry J, Ghosh K, Kaveri SV. Catalytic antibodies in patients with systemic lupus erythematosus.
Eur J Rheumatol. 2018 Sep;5(3):173-178. (IF: --)
|
2018 | |
| 285 |
Warang P & Kedar PS. Hereditary elliptocytosis: A rare red cell membrane disorder.
Indian J Hematol Blood Transfus 2018 Oct;34(4):754-755.(IF:0.474)
|
2018 | |
| 286 |
Shukla P, Korgaonkar S, Kerketta L, Vundinti BR. Prevalence and Association of Dermatological Manifestations with Fanconi Anemia: A Retrospective Study.
Indian Dermatol Online J. 2018 Sep-Oct;9(5):341-342.(IF: --)
|
2018 | |
| 287 |
Gorakshakar AC, Breganza PV, Colaco SP, Shaikh RF, Bohra MY, Sawant PM, Nadkarni AH, Colah RB, Ghosh KK. Rare ?- and ?-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India.
Hemoglobin. 2018 Sep - Nov;42(5-6):297-301. (IF: 0.462)
|
2018 | |
| 288 |
Dash PM, Sahu PK, Patel S, Mashon RS, Kharat KR, Mukherjee MB. Effect of Assorted Globin Haplotypes and ?-Thalassemia on the Clinical Heterogeneity of Hb S-?-Thalassemia.
Hemoglobin. 2018 Nov 29:1-7.(IF:0.462)
|
2018 | |
| 289 |
Chougule D, Nadkar M, Venkataraman K, Rajadhyaksha A, Hase N, Jamale T, Kini S, Khadilkar P, Anand V, Madkaikar MR, Pradhan V Adipokine interactions promote the pathogenesis of systemic lupus erythematosus.
Cytokine. 2018 Nov;111:20-27 (IF:3.514)
|
2018 | |
| 290 |
Kulkarni M, Hule G, de Boer M, van Leeuwen K, Kambli P, Aluri J, Gupta M, Dalvi A, Mhatre S, Taur P, Desai M, Madkaikar MR Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
J Clin Immunol. 2018 Nov;38(8):898-916. (IF: 4.227)
|
2018 | |
| 291 |
Rambhia KD, Kharkar V, Pradhan V, Patwardhan M, Ghosh K, Khopkar US. A study of prevalence of autoantibodies in patients with lichen planus from Mumbai, India.
Indian J Dermatol Venereol Leprol. 2018 Nov-Dec;84(6):667-671.(IF: 2.229)
|
2018 | |
| 292 |
Kulkarni S, Choudhary B, Gogri H, Patil S, Manglani M, Sharma R, Madkaikar MR. Molecular genotyping of clinically important blood group antigens in patients with thalassaemia.
Indian J Med Res. 2018 Dec;148(6):713-720. (IF: 1.508)
|
2018 | |
| 293 |
Chiddarwar AS, D'Silva SZ, Colah RB, Ghosh K, Mukherjee MB. Genetic lesions in the UGT1A1 genes among Gilberts syndrome patients from India.
Mol Biol Rep. 2018 Dec; 45(6):2733-2739.(IF:1.889)
|
2018 | |
| 294 |
Dalal K, Khorate P, Dalal B, Chavan R, Bhatia S, Kale A, Shukla P,Shankarkumar A. Differentially expressed serum host proteins in hepatitis B and C viral infections.
Virusdisease. 2018 Dec;29(4):468-477.(IF:0.364)
|
2018 | |
| 295 |
Patil R, S C, Parihar A, Mohite A, Shetty S. Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients.
Thromb Res. 2018 Dec;172:29-35.(IF:2.779)
|
2018 | |
| 296 |
Hariharan P, Colah R, Ghosh K, Nadkarni A. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Genomics. 2018 Dec 5. pii: S0888-7543(18)30542-1. doi: 10.1016/j.ygeno.2018.11.032.[Epub ahead of print] (IF: 2.910)
|
2018 | |
| 297 |
Hockham C, Bhatt S, Colah R, Mukherjee MB, Penman BS, Gupta S, Piel FB. The spatial epidemiology of sickle-cell anaemia in India.
Sci Rep. 2018 Dec 6;8(1):17685.(IF:4.122)
|
2018 | |
| 298 |
Patil R, Mukaddam A, Ghosh K, Shetty S. Management of pregnancy in dysfibrinogenemia cases: a dilemma.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):91-93. (IF: 1.367)
|
2017 | |
| 299 |
Ali S, Shetty S, Ghosh K. A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):94-95.(IF: 1.367)
|
2017 | |
| 300 |
Deshpande R, Ghosh K, Shetty S. Synergistic effect of factor VII gene polymorphisms causing mild factor VII deficiency in a case of severe factor X deficiency.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):105-106.(IF: 1.367)
|
2017 | |
| 301 |
Chiddarwar AS, D'Silva SZ, Colah RB, Ghosh K, Mukherjee MB. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults.
Ann Hum Genet. 2017 Jan;81(1):11-19.(IF: 1.659)
|
2017 | |
| 302 |
Gupta AD, Nadkarni A, Mehta P, Goriwale M, Ramani M, Chaudhary P, Mehrotra V, Colah R. Phenotypic expression of HbO Indonesia in two Indian families and its interaction with sickle hemoglobin.
Indian J Pathol Microbiol. 2017 Jan-Mar;60(1):79-83.(IF: 0.616)
|
2017 | |
| 303 |
Solanki A, Kumar Selvaa C, Sheth F, Radhakrishnan N, Kalra M, Vundinti BR. Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.
Leuk Res. 2017 Feb;53:50-56. (IF: 2.501)
|
2017 | |
| 304 |
Umare VD, Pradhan VD, Rajadhyaksha AG, Patwardhan MM, Ghosh K, Nadkarni AH. Impact of TNF-? and LT? gene polymorphisms on genetic susceptibility in Indian SLE patients.
Hum Immunol. 2017 Feb;78(2):201-208. (IF: 2.311)
|
2017 | |
| 305 |
Bacchelli C, Moretti FA, Carmo M, Adams S, Stanescu HC, Pearce K, Madkaikar M, Gilmour KC, Nicholas AK, Woods CG, Kleta R, Beales PL, Qasim W, Gaspar HB. Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency.
J Allergy Clin Immunol. 2017 Feb;139(2):634-642.e5. (IF: 13.081)
|
2017 | |
| 306 |
Madkaikar M, Gupta M, Dixit A, Patil V. Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W).
J Pediatr Hematol Oncol. 2017 Mar;39(2):143-146. (IF: 1.076)
|
2017 | |
| 307 |
Doley D, Kakati S, Saikia L, Rajadhyaksha A, Nadkar M, Khadilkar P, Patwardhan M, Pradhan V. A Comparitive Study of Anticardiolipin Antibodies among Systemic Lupus Erythematosus Patients from Western and Eastern India.
J Assoc Physicians India. 2017 Mar;65(3):14-19. (IF: 0.37)
|
2017 | |
| 308 |
R Devendra, R Shanmugam, MPSS Singh, CP Vishwakarma, S Godbhole, N Singh, V Gupta, P Kedar, MB Mukherjee. Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, India.
Meta Gene, 2017 Mar; 12:130-133. (IF: 1.27)
|
2017 | |
| 309 |
Kerketta LS, Ghosh K, Nadkarni A, Madkaikar M, Vundinti BR. Centrosome Aberration Frequency and Disease Association in B-Acute Lymphoblastic Leukemia.
In Vivo. 2017 Mar-Apr;31(2):215-220. (IF: 0.953)
|
2017 | |
| 310 |
Mehta P, Upadhye D, Hariharan P, Italia K, Sawant P, Nadkarni A, Subramanian G,Mukherjee MB. Identification of high oxygen affinity hemoglobin (Hb Andrew-Minneapolis) in an Indian family.
|
2017 | |
| 311 |
Warang P, Roshan Colah , Kedar PS. Lead poisoning induced severe hemolytic anemia, basophilic stippling, mimicking erythrocyte pyrimidine 5’-nucleotidase deficiency in Beta thalassemia minor.
J Clin Toxicol 2017 Apr; 7(2):1-3. (IF: 3.677)
|
2017 | |
| 312 |
Umare V, Nadkarni A, Nadkar M, Rajadhyksha A, Khadilkar P, Ghosh K, Pradhan VD Do high sensitivity C-reactive protein and serum interleukin-6 levels correlate with disease activity in systemic lupus erythematosuspatients?
J Postgrad Med. 2017 Apr-Jun;63(2):92-95. (IF: 0.912)
|
2017 | |
| 313 |
Kedar P, Desai A, Warang P, Colah R. A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia.
Hematology. 2017 May;22(4):252-257 (IF: )
|
2017 | |
| 314 |
Hariharan P, Gorivale M, Colah R, Ghosh K, Nadkarni A. Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?
Ann Hum Genet. 2017 May;81(3):125-128. (IF: 1.659)
|
2017 | |
| 315 |
Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K. Effect of the Hemochromatosis Mutations on Iron Overload among the Indian ? Thalassemia Carriers.
J Clin Lab Anal. 2017 May;31(3).(IF: 1.521)
|
2017 | |
| 316 |
Prabhudesai A, Shetty S, Ghosh K, Kulkarni B. Dysfunctional fibrinolysis and cerebral venous thrombosis.
Blood Cells Mol Dis. 2017 Jun;65:51-55. (IF: 1.882)
|
2017 | |
| 317 |
Aluri J, Italia K, Gupta M, Dalvi A, Bavdekar A, Madkaikar M. Low T cell receptor excision circles (TRECs) in a case of ZAP 70 deficient severe combined immunodeficiency (SCID) with a novel mutation from India.
Blood Cells Mol Dis. 2017 Jun;65:95-96. (IF: 1.882)
|
2017 | |
| 318 |
Warang P, Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M. Does novel P5N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
Blood Cells Mol Dis. 2017 Jul;66:8-10. (IF: 1.882)
|
2017 | |
| 319 |
Das S, Chiddarwar A, Warang P and Kedar P. Association of Heme Oxygenase-1 (Number of GT Repeats) with the methemoglobin levels in recessive congenital methemoglobinemia in Indian population.
J Molecular Genet Medicine 2017 Jul; 11(3):1-5 (IF: 2.20)
|
2017 | |
| 320 |
Kulkarni SS, Vasantha K, Gogri H, Parchure D, Madkaikar M, Férec C, Fichou Y. First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms.
Transfusion. 2017 Aug;57(8):1944-1948 (IF: 3.386)
|
2017 | |
| 321 |
Gaikwad T, Ghosh K, Shetty S. Dosing algorithms for vitamin K antagonists across VKORC1 and CYP2C9 genotypes: comment.
J Thromb Haemost. 2017 Aug; 15(8):1708. (IF: 5.287)
|
2017 | |
| 322 |
Patil R, Ghosh K, Shetty S. Mortality caused by intracranial bleeding in non-severe hemophilia A patients: comment.
J Thromb Haemost. 2017 Aug; 15(8):1709-10. (IF: 5.287)
|
2017 | |
| 323 |
Umare VD, Pradhan VD, Rajadhyaksha AG, Ghosh K, Nadkarni AH. A functional SNP MCP-1 (-2518A/G) predispose to renal disorder in Indian Systemic Lupus Erythematosus patients.
Cytokine. 2017 Aug;96:189-194. (IF: 3.488)
|
2017 | |
| 324 |
Vira H, Pradhan V, Umare V, Chaudhary A, Rajadhyksha A, Nadkar M, Ghosh K, Nadkarni A. Role of MMP-7 in the pathogenesis of systemic lupus erythematosus (SLE).
Lupus. 2017 Aug;26(9):937-943. (IF: 2.454)
|
2017 | |
| 325 |
Prabhudesai A, Shetty S, Ghosh K, Kulkarni B Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.
Eur J Haematol. 2017 Sep; 99(3):249-254. (IF: 2.653)
|
2017 | |
| 326 |
Kedar PS. Next-generation sequencing: emerging technology in the area of hematology and blood disorder.
Hematol Blood Disord 2017 Sep;1(1):1-2. (IF: )
|
2017 | |
| 327 |
Prabhudesai A, Shanbhag S, Mirgal D, Kawankar N, Shetty S. A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.
Haemophilia. 2017 Sep;23(5):e477-e479. (IF: 3.569)
|
2017 | |
| 328 |
Gorakshakar A, Gogri H, Ghosh K. Evolution of technology for molecular genotyping in blood group systems.
Indian J Med Res. 2017 Sep;146(3):305-315.(IF:1.532)
|
2017 | |
| 329 |
Mohanty MC, Madkaikar MR, Desai M, Taur P, Nalavade UP, Sharma DK, Gupta M. Dalvi A, Shabrish S, Kulkarni M, Aluri J, Deshpande JM Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India.
Emerg Infect Dis. 2017 Oct;23(10):1664-1670. (IF: 8.222)
|
2017 | |
| 330 |
Jadli A, Ghosh K, Satoskar P, Damania K, Bansal V, Shetty S. Combination of copeptin, placental growth factor and total annexin V microparticles for prediction of preeclampsia at 10-14 weeks of gestation.
Placenta. 2017 Oct;58:67-73. (IF: 2.759)
|
2017 | |
| 331 |
Shanbhag S, Ghosh K, Shetty S. Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories.
Thromb Res. 2017 Oct;158:138-139. (IF: 2.65)
|
2017 | |
| 332 |
Priya Hariharan, Madhavi Sawant, Manju Gorivale, Ruma Manchanda, Roshan Colah, Ghosh, Anita Nadkarni. Synergistic effect of two ??globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Mol Biol Rep 2017 Oct;44(5):413-417. (IF: 1.828)
|
2017 | |
| 333 |
Pranatharthiharan S, Patel MD, Malshe VC, Pujari V, Gorakshakar A, Madkaikar MR, Ghosh K, Devarajan PV. Asialoglycoprotein receptor targeted delivery of doxorubicin nanoparticles for hepatocellular carcinoma.
Drug Deliv. 2017 Nov;24(1):20-29(IF: 6.402)
|
2017 | |
| 334 |
Yadav S, Shetty S, Kulkarni B A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.
Transfusion. 2017 Nov;57(11):2712-2714. (IF: 3.386)
|
2017 | |
| 335 |
Kedar PS, Parmar V, Devendra R, Gupta V, Warang P, Madkaikar MR Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
Ann Hematol. 2017 Dec;96(12):2135-2139. (IF: 3.083)
|
2017 | |
| 336 |
Kulkarni M, Gupta M, Madkaikar MR Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in The Absence Of Molecular Diagnosis.
Scand J Immunol. 2017 Dec;86(6):486-490. (IF: 2.314)
|
2017 | |
| 337 |
Zaidi AU, Kedar PS, Koduri PR, Goyette GW Jr, Buck S, Paglia DE, Ravindranath Y Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.
Pediatr Hematol Oncol. 2017 Dec 11:1-6. (IF: 1.12)
|
2017 | |
| 338 |
Solanki A, Mohanty P, Shukla P, Rao A, Ghosh K, Vundinti BR. FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients.
PLoS One. 2016 Jan 22;11(1):e0147016.(IF: 2.806)
|
2016 | |
| 339 |
Upadhye DS, Jain DL, Trivedi YL, Nadkarni AH, Ghosh K, Colah RB Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.
PLoS One. 2016 Jan 19;11(1):e0147081.(IF: 2.806)
|
2016 | |
| 340 |
Pinto P, Shetty S, Lacroix-Desmazes S, Bayry J, Kaveri S, Ghosh K. Antibody profile in Indian severe haemophilia A patients with and without FVIII inhibitors
Immunol Lett. 2016 Jan;169:93-7.(IF: 2.86)
|
2016 | |
| 341 |
Joshi D, Korgaonkar S, Shanmukhaiah C, Vundinti BR. Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome.
Ann Hematol. 2016 Jan;95(1):79-85.(IF: 3.083)
|
2016 | |
| 342 |
Gorakshakar AC, Ghosh K. Use of lectins in immunohematology.
Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF: 1.06)
|
2016 | |
| 343 |
Patil R, Ghosh K, Shetty S. Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.
Ann Hematol. 2016 Feb;95(3):533-4.(IF: 3.083)
|
2016 | |
| 344 |
Pathak VA, Ghosh K. Erythropoiesis in Malaria Infections and Factors Modifying the Erythropoietic Response.
Anemia. 2016;2016:9310905. Epub 2016 Feb 29. Review. (IF: 3.00)
|
2016 | |
| 345 |
Garg S, Shanmukhaiah C, Marathe S, Mishra P, Babu Rao V, Ghosh K, Madkaikar MR. Differential antigen expression and aberrant signaling via PI3/AKT, MAP/ERK, JAK/STAT, and Wnt/? catenin pathways in Lin-/CD38-/CD34+ cells in acute myeloid leukemia.
Eur J Haematol. 2016 Mar;96(3):309-17.(IF: 2.653)
|
2016 | |
| 346 |
Shanbhag S, Ghosh K, Shetty S. Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.
Blood Cells Mol Dis. 2016 Mar;57:81-4.(IF: 1.882)
|
2016 | |
| 347 |
Jadli A, Ghosh K, Shetty S. Prediction of small-for-gestational-age at 35-37 weeks of gestation: too late for management?
Ultrasound Obstet Gynecol. 2016 Mar;47(3):385.(IF: 4.71)
|
2016 | |
| 348 |
Shetty S, Sharma N, Ghosh K. Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.
Crit Rev Oncol Hematol. 2016 Mar;99:129-33.(IF: 4.971)
|
2016 | |
| 349 |
Patil R, Ghosh K, Mukherjee S, Shetty S. Does consumption of platelet-derived microparticles in the fibrin clot explain the decrease in their percentage during pregnancy?
Blood Cells Mol Dis. 2016 Mar;57:115-7.(IF: 1.882)
|
2016 | |
| 350 |
Mahadik K, Shaikh R, Mahajan N, Pandit A, Shinde S, Kanjaksha Ghosh, Ajit C.Gorakshakar. Analysis of Complement Recepter Type I(CR1) Polymorphisms and Its Association with Malaria in Rural Population of Maharashtra.
World J Res Review. 2016 Mar;2(3):13-17.(IF: )
|
2016 | |
| 351 |
Chaudhary AK, Chaudhary S, Ghosh K, Shanmukaiah C, Nadkarni AH. Secretion and Expression of Matrix Metalloproteinase-2 and 9 from Bone Marrow Mononuclear Cells in Myelodysplastic Syndrome and Acute Myeloid Leukemia.
Asian Pac J Cancer Prev. 2016 Mar;17(3):1519-29.(IF: 2.39 )
|
2016 | |
| 352 |
Pinto P, Ghosh K, Shetty S. F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association.
Mutat Res. 2016 Apr;786:27-33.(IF: 5.5)
|
2016 | |
| 353 |
Jacob S, Nayak S, Kakar R, Chaudhari UK, Joshi D, Vundinti BR, Fernandes G, Barai RS, Kholkute SD, Sachdeva G. A triad of telomerase, androgen receptor and early growth response 1 in prostate cancer cells.
Cancer Biol Ther. 2016 Apr 2;1(4):439-48.(IF: 3.294)
|
2016 | |
| 354 |
Patil R, Ghosh K, Shetty S. A simple clot based assay for detection of procoagulant cell-derived microparticles.
Clin Chem Lab Med. 2016 Apr 1;54(5):799-803.(IF: 3.432)
|
2016 | |
| 355 |
Patil R, Ghosh K, Shetty S. Re: Does low-molecular-weight heparin influence fetal growth or uterine and umbilical arterial Doppler in women with a history of early-onset uteroplacental insufficiency and an inheritable thrombophilia? Secondary randomised controlled trial results LMWH
BJOG. 2016 Apr;123(5):844.(IF: 5.051)
|
2016 | |
| 356 |
Jadli AS, Ghosh K, Shetty S. Preeclampsia: simplified or still miles to go?
Am J Obstet Gynecol. 2016 May;214(5):668-9.(IF: 5.574)
|
2016 | |
| 357 |
Garg S, Ghosh K, Madkaikar MR. Antigen expression on a putative leukemic stem cell population and AML blast.
Int J Hematol. 2016 May;103(5):567-71.(IF: 1.61)
|
2016 | |
| 358 |
Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2016 May;2(4):381-5.(IF: 2.096)
|
2016 | |
| 359 |
Mohapatra R, Warang P, Ghosh K, Colah R. Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye.
Cytometry B Clin Cytom. 2016 May;90(3):279-84.(IF: 2.474)
|
2016 | |
| 360 |
Mirgal D, Ghosh K, Mahanta J, Dutta P, Shetty S. Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.
Trans R Soc Trop Med Hyg. 2016 May;110(5):294-8.(IF: --)
|
2016 | |
| 361 |
Shetty S, Ghosh K. Why should hemophilia B be milder than hemophilia A?
Haematologica. 2016 May;101(5):e213. (IF: 7.702)
|
2016 | |
| 362 |
Pradhan V, Pandit P, Rajadhyaksha A, Patwardhan M, Surve P, Kamble P, Lecerf M, Bayry J, Kaveri S, Ghosh K, Nadkar MY. Association of Serum Ferritin Levels with Hematological Manifestations in Systemic Lupus Erythematosus Patients from Western India.
J Assoc Physicians India. 2016 May;64(5):14-18.(IF: 0.37)
|
2016 | |
| 363 |
Madkaikar MR, Shabrish S, Desai M. Current Updates on Classification, Diagnosis and Treatment of Hemophagocytic Lymphohistiocytosis (HLH).
Indian J Pediatr. 2016 May;83(5):434-43.(IF: 0.945)
|
2016 | |
| 364 |
Fleisher TA, Madkaikar MR, Rosenzweig SD. Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies.
Indian J Pediatr. 2016 May;83(5):444-9.(IF: 0.945)
|
2016 | |
| 365 |
Madkaikar MR, Aluri J, Gupta S. Guidelines for Screening, Early Diagnosis and Management of Severe Combined Immunodeficiency (SCID) in India.
Indian J Pediatr. 2016 May;83(5):455-62 (IF: 0.945)
|
2016 | |
| 366 |
Disha S Parchure, Kulkarni SS Noninvasive fetal RHD genotyping from maternal plasma
Global Journal of Transfusion Science 2016 Jan-Jun;1(1): 21-28.(IF:--)
|
2016 | |
| 367 |
Upadhye D, Jain D, Trivedi Y, Nadkarni A, Ghosh K, Colah R. Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients.
Ann Hematol. 2016 Jun;95(7):1201-3.(IF: 3.083)
|
2016 | |
| 368 |
Pathak V, Colah R, Ghosh K. Correlation between 'H' blood group antigen and Plasmodium falciparum invasion.
Ann Hematol. 2016 Jun;95(7):1067-75.(IF: 3.083)
|
2016 | |
| 369 |
Gogri H, Kulkarni SS, Vasantha K, Jadhav S, Ghosh K, Gorakshakar A. Partial matching of blood group antigens to reduce alloimmunization in Western India.
Transfus Apher Sci. 2016 Jun;54(3):390-5.(IF: 1.3)
|
2016 | |
| 370 |
Patil R, Ghosh K, Shetty S. Could procoagulant cell-derived microparticles have a more crucial role in pregnancy complications rather than exosomes?
Am J Obstet Gynecol. 2016 Jun;214(6):765-6. (IF: 5.574)
|
2016 | |
| 371 |
Patil R, Ghosh K, Shetty S. Annexin A5 levels or circulating microparticles: what we see depends mainly on what we look for.
J Intern Med. 2016 Jun;279(6):608. (IF: 7.598)
|
2016 | |
| 372 |
Colah RB, Nadkarni A, Gorakshakar A, Sawant P, Gorivale M, Mehta P, Sawant M, Ghosh K. Five Rare ? Globin Chain Hemoglobin Variants in India.
Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):282-6.(IF: 0.403
|
2016 | |
| 373 |
Sawant M, Chandrakala S, Colah R, Ghosh K, Nadkarni A. Does HbF induction by hydroxycarbamide work through MIR210 in sickle cell anaemia patients?
Br J Haematol. 2016 Jun;173(5):801-3. (IF: 5.67)
|
2016 | |
| 374 |
Kulkarni B, Gorakshakar A, Singh V, Parihar A, Donta A, Gogri H, Jadhav S, Ghosh K, Shetty S. Indian Bombay phenotype: it is different!
Blood Transfus. 2016 Jun 24;15(1):74-76. (IF: 1.607)
|
2016 | |
| 375 |
Shabrish S, Gupta M, Madkaikar MR A Modified NK Cell Degranulation Assay Applicable for Routine Evaluation of NK Cell Function.
J Immunol Res. 2016;2016:3769590.(IF: 4.856)
|
2016 | |
| 376 |
Mohanty P, Korgaonkar S, Shanmukhaiah C, Ghosh K, Vundinti BR. Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.
Blood Cells Mol Dis. 2016 Jul;59:52-7.(IF: 1.882)
|
2016 | |
| 377 |
Deshpande R, Kulkarni B, Ghosh K, Shetty S. A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis.
Thromb Res. 2016 Jul;143:1-2.(IF: 2.65)
|
2016 | |
| 378 |
Patil R, Ghosh K, Shetty S. Comment on Salomon et al. Gestational Diabetes Mellitus Is Associated With Changes in the Concentration and Bioactivity of Placenta-Derived Exosomes in Maternal Circulation Across Gestation. Diabetes 2016;65:598-609.
Diabetes. 2016 Jul;65(7):e24-5.(IF: 8.684)
|
2016 | |
| 379 |
Italia K, Chandrakala S, Ghosh K, Colah R. Can hydroxyurea serve as a free radical scavenger and reduce iron overload in ?-thalassemia patients?
Free Radic Res. 2016 Jul; 27:1-7.(IF: 3.188)
|
2016 | |
| 380 |
Ali S, Ghosh K, Daly ME, Hampshire DJ, Makris M, Ghosh M, Mukherjee L, Bhattacharya M, Shetty S. Congenital macrothrombocytopenia is a heterogeneous disorder in India.
Haemophilia. 2016 Jul; 2(4):570-82.(IF: 3.569)
|
2016 | |
| 381 |
Chaudhary AK, Chaudhary S, Ghosh K, Nadkarni A. Pleiotropic Roles of Metalloproteinases in Hematological Malignancies: an Update.
Asian Pacific J. of Cancer Prevention 2016 Jul; 17(7):3043-51.(IF: 2.39)
|
2016 | |
| 382 |
Kulkarni SS, Vasantha K, Ghosh K. Antigen negative red blood cell inventory of Indian blood donors.
Transfus Apher Sci. 2016 Aug;55(1):131-5. (IF: 1.3)
|
2016 | |
| 383 |
Gupta M, Aluri J, Terrance A, Madkaikar MR. Adenosine Deaminase Deficiency with a Novel Gene Mutation.
Indian J Pediatr. 2016 Aug;83(8):875-6. (IF: 0.945)
|
2016 | |
| 384 |
Ghosh K Management of Haemophilia in Developing Countries: Challenges and Options.
Indian J Hematol Blood Transfus. 2016 Sep;32(3):347-55.(IF: 0.403)
|
2016 | |
| 385 |
Garg S, Shanmukhaiah C, Ghosh K, Madkaikar MR. Cell signaling in putative leukemic stem cells and blast population in acute myeloid leukemia.
Leuk Lymphoma. 2016 Sep;57(9):2195-8. (IF: 2.755)
|
2016 | |
| 386 |
Shanbhag S, Ghosh K, Shetty S. First trimester prenatal diagnosis of severe FXIII deficiency.
Haemophilia. 2016 Sep;22(5):e443-4. (IF: 3.569)
|
2016 | |
| 387 |
Ali S, Shetty S, Ghosh K. Bengal macrothrombocytopenia is not totally an innocuous condition.
Blood Cells Mol Dis. 2016 Sep;60:3-6.(IF: 1.882)
|
2016 | |
| 388 |
Italia K, Dabke P, Sawant P, Nadkarni A, Ghosh K, Colah RB. Hb E-?-Thalassemia in Five Indian States.
Hemoglobin. 2016 Sep;40(5):310-315.(IF: 0.77)
|
2016 | |
| 389 |
Kawankar N, Rathi J, Ghosh K, Shetty S. Clinical and molecular epidemiology of factor XI deficiency in India.
Thromb Res. 2016 Nov;147:85-87.(IF: 2.65)
|
2016 | |
| 390 |
Kulkarni M, Desai M, Gupta M, Dalvi A, Taur P, Terrance A, Bhat S, Manglani M, RajR, Shah I, Madkaikar M. Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families.
J Clin Immunol. 2016 Nov;36(8):774-784. (IF: 3.253)
|
2016 | |
| 391 |
Patil R, Ghosh K, Shetty S. Betrixaban in Acutely Ill Medical Patients.
N Engl J Med. 2016 Dec 15;375(24):e50.(IF: 72.406)
|
2016 | |
| 392 |
P Hariharan, S Colaco, R Colah, K Ghosh A Nadkarni Do b-globin gene variants contribute in substantial reduction in HbA2 levels?
Int. J. Lab Hematol 2016 Dec;38(6):610-615.(IF: 2.03)
|
2016 | |
| 393 |
Italia K, Kangne H, Shanmukaiah C, Nadkarni AH, Ghosh K, Colah RB. Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype.
Br J Haematol. 2015 Jan;168(1):156-9. (IF: 5.812)
|
2015 | |
| 394 |
Warang PP, Kedar PS, Shanmukaiah C, Ghosh K, Colah RB Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
Clin Genet. 2015 Jan;87(1):62-7. (IF: 3.892)
|
2015 | |
| 395 |
Vaidya S, Vundinti BR, Shanmukhaiah C, Chakrabarti P, Ghosh K. Evolution of BCR/ABL gene mutation in CML is time dependent and dependent on the pressure exerted by tyrosine kinase inhibitor
PLoS One. 2015 Jan 28;10(1):e0114828. eCollection 2015. (IF: 3.057)
|
2015 | |
| 396 |
Warang P, Devendra R, DSilva S, Chiddarwar A, Kedar PS, Ghosh K, Colah R, Mukherjee MB Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
Ann Hematol. 2015 Jan;94(1):169-71. (IF: 3.022)
|
2015 | |
| 397 |
Mishra A, Italia K, Gupta M, Desai M, Madkaikar MR Syndrome due to CD40 Deficiency: Possibly the first case from India.
Journal of Postgraduate Medicine. 2015 Jan-Mar; 61:41-48. (IF: 0.87 )
|
2015 | |
| 398 |
Vandana VP, Surve P, Rajadhyaksha A, Rajendran V, Patwardhan M, Umare V, Ghosh K, Nadkarni A Mannose binding lectin (MBL) 2 gene polymorphism & its association with clinical manifestations in systemic lupus erythematosus (SLE) patients from western India.
Indian J Med Res. 2015 Feb;141(2):199-204. (IF: 1.446)
|
2015 | |
| 399 |
Kangne HK, Jijina FF, Italia YM, Jain DL, Nadkarni AH, Ghosh KK, Colah RB. The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Sickle Cell Disease in Western India. Mutations in
Clin Appl Thromb Hemost. 2015 Mar;21(2):186-9.(IF: 1.973)
|
2015 | |
| 400 |
Italia K, Krishnamurti L, Mehta V, Raicha B, Italia K, Mehta P, Ghosh K, Colah R. Feasibility of a Newborn screening and follow-up programme for sickle cell disease among South Gujarat (India) tribal populations.
J Med Screen 2015 Mar;22(1):1-7 (IF: 1.75)
|
2015 | |
| 401 |
Vandana VP, Patwardhan M, Rajadhyaksha A, Dhawale N, Ghosh K Neuropsychiatric manifestations and associated autoantibodies in systemic lupus erythematosus patients from Western India.
Rheumatol Int. 2015 Mar;35(3):541-5. (IF: 1.702)
|
2015 | |
| 402 |
Warang P, Kedar PS, Ghosh K, Colah RB. Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience.
Clin Chem Lab Med 2015 Mar1;53(4):e105-8. (IF: 3.017 )
|
2015 | |
| 403 |
Shetty S, Ghosh K Novel therapeutic approaches for haemophilia.
Haemophilia 2015 Mar;21(2):152-61. (IF: 2.673 )
|
2015 | |
| 404 |
Shetty S, Ghosh K Challenges and open issues in the management of acquired hemophilia A (AHA).
Blood Cells Mol Dis. 2015 Mar;54(3):275-80.Review.(IF: 2.731)
|
2015 | |
| 405 |
Deb S, Ghosh K, Shetty SD. Nanoimaging in cardiovascular diseases: Current state of the art.
Indian J Med Res. 2015 Mar;141(3):285-98. (IF: 1.446 )
|
2015 | |
| 406 |
Madkaikar MR, Italia K, Gupta M, Chavan S, Mishra A, Rao M, Mhatre S, Desai M, Manglani M, Singh S, Suri D, Agrawal A, Ghosh K Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.
Blood Cells Mol Dis. 2015 Mar;54(3):217-23. (IF: 2.731)
|
2015 | |
| 407 |
Mhatre S, Madkaikar MR, Desai M, Ghosh K. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India
Blood Cells Mol Dis. 2015 Mar;54(3):250-7. (IF: 2.731 )
|
2015 | |
| 408 |
Koduri PR, Kedar PS, Warang P. Erythrocytosis, methemoglobinemia, and the saturation gap.
Ann Hematol. 2015 Mar;94(3):509-10.(IF: 3.022)
|
2015 | |
| 409 |
Mohanty D, Mukherjee MB, Colah RB, Wadia M, Ghosh K, Chottray GP, Jain D, Italia Y, Ashokan KS, Kaul R, Shukla DK, Muthuswamy V. Spectrum of Hemoglobinopathies Among the Primitive Tribes: A Multicentric Study in India.
Asia Pac J Public Health. 2015 Mar;27(2):NP562-71 (IF: 1.05)
|
2015 | |
| 410 |
Ghosh K. Sickle cell anaemia: The need for new approaches in management.
Natl Med J India. 2015 Mar-Apr;28(2):90-3. (IF: 0.907)
|
2015 | |
| 411 |
Shanbhag S, Pai N, Ghosh K, Shetty S. Prenatal diagnosis in a family with purfura fulminans.
Blood Coagul Fibrinolysis. 2015 Apr;26(3):350. (IF: 1.242 )
|
2015 | |
| 412 |
Upadhye D, Koduri P, Tarakeshwari S, Mehta P, Surve R, Warang P, Kedar PS, Nadkarni A, Ghosh K, Colah R. Hb M Hyde Park and Hb M Boston in two Indian families - a rare cause of methaemoglobinemia.
Int J Lab Hematol. 2015 Apr;37(2):e40-3. (IF: 2.401)
|
2015 | |
| 413 |
Patil AS, Shankarkumar A. Hepatitis B Diagnosis in Blood Bank: Evaluation and Challenges
MGM J Med Sci 2015 Apr-Jun; 2 (2) : 83-89 (IF: )
|
2015 | |
| 414 |
Mukherjee MB, Colah RB, Martin S, Ghosh K. Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario.
Indian J Med Res. 2015 May;141(5):516-20. (IF: 1.446)
|
2015 | |
| 415 |
Colah RB, Mukherjee MB, Martin S, Ghosh K. Sickle cell disease in tribal populations in India.
Indian J Med Res. 2015 May;141(5):509-15. (IF: 1.446 )
|
2015 | |
| 416 |
Ghosh K, Colah RB, Mukherjee MB. Haemoglobinopathies in tribal populations of India.
Indian J Med Res. 2015 May;141(5):505-8. (IF: 1.446)
|
2015 | |
| 417 |
Madkaikar MR, Italia K, Gupta M, Desai M, Aggarwal A, Singh S, Suri D, Mishra A, Chavan S, Ghosh K, Sarangal R, Dogra S. Leukocyte adhesion deficiency-I with a novel intronic mutation presenting with pyoderma gangrenosum- like lesions.
J Clin Immunol. 2015 May;3(4):431-4. (IF: 3.094 )
|
2015 | |
| 418 |
Mukaddam A, Patil R, Jadli A, Chandrakala S, Ghosh K, Shetty S Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
Am J Clin Pathol. 2015 May;143(5):755-. (IF: 2.278)
|
2015 | |
| 419 |
Shanbhag S, Lulla C, Ghosh K, Shetty S. Prenatal diagnosis in a haemophilia carrier with triplet pregnancy.
Haemophilia. 2015 May;21(3):e228-30. (IF: 2.673 )
|
2015 | |
| 420 |
Korgaonkar S, Vundinti BR. Tetrasomy X in a Child with Upper Limb Deformity.
Indian Pediatr. 2015 May;52(5):439. (IF: 0.972 )
|
2015 | |
| 421 |
Ghosh K Factors Modulating Blood HbA1C Level and Diabetic Retinopathy.
J Assoc Physicians India. 2015 May;63(5):95-6. (IF: 0.37)
|
2015 | |
| 422 |
Ghosh K. Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Indian J Hematol Blood Transfus. 2015 Jun;31(2):314-6. (IF: 0.232)
|
2015 | |
| 423 |
Jadli A, Kulkarni B, Ghosh K, Shetty S. High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.
Indian J Med Res. 2015 Jul;142(1):85-7. (IF: 1.446)
|
2015 | |
| 424 |
Lobo V, Shetty S, Kulkarni B, Butera D, Magalhaes GS, Ghosh K Erratum to: A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2015 Jul;94(7):1259. (IF: 3.022)
|
2015 | |
| 425 |
Merchant R, Italia K, Ahmed J, Ghosh K, Colah RB. A successful twin pregnancy in a patient with HbE-?-thalassemia in western India.
J Postgrad Med. 2015 Jul-Sep;61(3):203-5. (IF: 0.87)
|
2015 | |
| 426 |
Vaidya S, Ghosh K, Shanmukhaiah C, Vundinti BR. Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Aug 21;765:124-130. (IF: 2.73 )
|
2015 | |
| 427 |
Pathak V, Colah R, Ghosh K. Tyrosine kinase inhibitors: New class of antimalarials on the horizon?
Blood Cells Mol Dis. 2015 Aug;55(2):119-26. (IF: 2.18)
|
2015 | |
| 428 |
Jadli A, Sharma N, Damania K, Satoskar P, Bansal V, Ghosh K, Shetty S. Promising prognostic markers of preeclampsia: new avenues in waiting.
Thromb Res. 2015 Aug;136(2):189-95. Review. (IF: 2.32)
|
2015 | |
| 429 |
Kasatkar P, Kulkarni B, Ghosh K, Shetty S. Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.
Ann Hematol. 2015 Aug;94(8):1409-10. (IF: 3.022)
|
2015 | |
| 430 |
Dalal K., Shankarkumar A. Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma.
Intl J Res Engg Applied Sci 2015Aug; 5(8): 76-89. (IF:)
|
2015 | |
| 431 |
Patil R, Ghosh K, Shetty S. Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss.
Ann Intern Med. 2015 Sep 15;163(6):483-4. (IF: 16.593)
|
2015 | |
| 432 |
Jadli A, Ghosh K, Shetty S. Is peripheral blood corin level clinically relevant for prediction of pre-eclampsia?
Ultrasound Obstet Gynecol. 2015 Sep;46(3):380. (IF: 4.254)
|
2015 | |
| 433 |
Patil R, Ghosh K, Shetty S. Tissue factor expressed by circulating cancer cell-derived microparticles drastically increases the incidence of deep vein thrombosis in mice: comment.
J Thromb Haemost. 2015 Sep;13(9):1737-8. (IF: 5.565)
|
2015 | |
| 434 |
Korgaonkar S, Vundinti BR. Trisomy 8 Mosaicism in a Boy with Dysmorphic Features.
Indian Pediatr. 2015 Sep;52(9):812-3. (IF: 0.972)
|
2015 | |
| 435 |
Priya Madan Yabaji, Aruna Shankarkumar, and Kanjaksha Ghosh. A silent killer HCV (Hepatitis C virus) in India : A Review of prevalence from all available data
Intl J Curr Res, 2015 Sep; 7(9): 20193-20203. (IF: 0.08)
|
2015 | |
| 436 |
Pradhan V, Kemp EH, Nadkar M, Rajadhyaksha A, Lokhandwala K, Patwardhan M, Weetman AP, Nadkarni A, Ghosh K. Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to systemic lupus erythematosus in an Indian population.
Scand J Rheumatol. 2015 Oct;44(5):425-7. (IF: 2.307)
|
2015 | |
| 437 |
Italia K, Colah R, Ghosh K. Experimental animal model to study iron overload and iron chelation and review of other such models.
Blood Cells Mol Dis. 2015 Oct;55(3):194-9. (IF: 2.731)
|
2015 | |
| 438 |
Patil R, Ghosh K, Vora S, Shetty S. Inherited and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss.
Blood Cells Mol Dis. 2015 Oct;55(3):200-5. (IF: 2.731)
|
2015 | |
| 439 |
Sonawane Patil A, Shankarkumar Pawar A. Blood donation in Maharashtra: Prevalence of transfusion transmitted infections in blood donors.
Int J Pharm Bio Sci 2015 Oct; (4): (B) 981-987. (IF: 0.36)
|
2015 | |
| 440 |
Vaidya S, Ghosh K, Shanmukhaiah C, Vundinti BR Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Oct 15;765:124-30. (IF: 2.73)
|
2015 | |
| 441 |
Mukaddam A, Kulkarni B, Jadli A, Ghosh K, Shetty S. Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families.
Haemophilia. 2015 Nov;21(6):e519-23. (IF: 2.673)
|
2015 | |
| 442 |
Gorakshakar A, Donta A, Jadhav S, Vasantha K, Ghosh K. Molecular analysis of Bombay phenotype cases seen in India.
ISBT Science Series 2015 Nov; 10(2):100-105. (IF: 0.39)
|
2015 | |
| 443 |
Patil A and Shankar Kumar A. Hepatitis B screening accuracy in blood bank.
Intl J Recent Scient Res 2015 Nov; 6(11): 7345-7357 (IF: 0.13)
|
2015 | |
| 444 |
Pradhan V, Patwardhan M, Rajadhyksha A, Umare V, Khadilkar P, Kaveri SV, Ghosh K Association of clinical presentation with anti-nuclear antibody specificities among patients with systemic lupus erythematosus.
Indian J Nephrol. 2015 Nov-Dec;25(6):391-2 (IF: 0.55)
|
2015 | |
| 445 |
Gorivale M, Sawant P, Mehta P, Nadkarni A, Ghosh K, Colah R. Challenges in Prenatal Diagnosis of Beta Thalassaemia: Couples with Normal HbA2 in One Partner.
Prenat Diagn. 2015 Dec;35(13):1353-7. (IF: 3.043)
|
2015 | |
| 446 |
Ali S, Ghosh K, Shetty S. Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP).
Blood Cells Mol Dis. 2015 Dec;5(4):410-4. (IF: 2.731)
|
2015 | |
| 447 |
Mehta PR, Upadhye DS, Sawant PM, Gorivale MS, Nadkarni AH, Shanmukhaiah C, Ghosh K, Colah RB. Diverse phenotypes and transfusion requirements due to interaction of ?-thalassemias with triplicated ?-globin genes.
Ann Hematol. 2015 Dec;94(12):1953-8. (IF: 3.022)
|
2015 | |
| 448 |
Dalal B, Shankarkumar A, Ghosh K. Individualization of antiretroviral therapy Pharmacogenomic aspect.
Indian J Med Res. 2015 Dec;142(6):663-74. (IF: )
|
2015 | |
| 449 |
Patil R, Ghosh K, Damania K, Bansal V, Satoskar P, Darekar A, Shetty S. Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss.
Br J Haematol. 2015 Dec;171(5):892-6. (IF: 5.812)
|
2015 | |
| 450 |
Nadkarni A, Dabke P, Colah R, Ghosh K. Molecular understanding of Indian untransfused thalassemia intermedia.
Int J Lab Hematol. 2015 Dec;37(6):791-6. (IF: 2.401)
|
2015 | |
| 451 |
Kasatkar P, Ghosh K, Shetty S. Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
Indian J Med Res. 2015 Dec;142(6):759-62. (IF: 1.446)
|
2015 | |
| 452 |
Kulkarni B, Ghosh K, Shetty S. Second trimester prenatal diagnosis in Glanzmanns Thrombasthenia.
Haemophilia. 2015 Dec 28. [Epub ahead of print] (IF: 2.673)
|
2015 | |
| 453 |
Kasatkar P, Ghosh K, Shetty S. An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).
Ann Hematol. 2014 Jan; 93(1): 173-5. (IF:2.396)
|
2014 | |
| 454 |
Ray S, Gorakshakar AC, Vasantha K, Nadkarni A, Italia Y, Ghosh K. Molecular genotyping of ABO blood groups in some population groups from India.
Indian J Med Res 2014 Jan; 139(1): 105-111. (IF: 1.661)
|
2014 | |
| 455 |
Devadathan K, Sreedharan M, Sarasam S, Colah RB, Kunju Mohammed PA. Neurometabolic Disorder with Microcephaly, Dystonia and Central Cyanosis Masquerading as Cerebral Palsy
J Child Neurol 2014 Jan 1-4.(IF:1.717)
|
2014 | |
| 456 |
Kerketta LS, Baburao V, Ghosh K Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymphoblastic leukemia cases from India
Indian J Hum Genet. 2014 Jan;20(1):32-6. .(IF:--)
|
2014 | |
| 457 |
Ghosh K. Familial Mediterranean fever: An unusal disease enlightening the inflammation biology
Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--)
|
2014 | |
| 458 |
Merchant RH, Parekh D, Ahmed N, Madkaikar MR, Ahmed J X linked agammaglobulinemia: a single centre experience from India
Indian J Pediatr 2014 Jan; 81(1):92-4. (IF:0.919)
|
2014 | |
| 459 |
Colah R Thalassemias: can we reduce the national burden ?
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I43. (IF:2.66)
|
2014 | |
| 460 |
Shetty S. Haemophilia- diagnosis and management challenges
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I44. .(IF:2.66)
|
2014 | |
| 461 |
Vundinti BR. Chromosomal instability and molecular mutations in multi spectrum disease of Fanconi anemia
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I47. .(IF:2.66)
|
2014 | |
| 462 |
Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH. Masking of a ?-thalassemia determinant by a novel ??globin gene defect [Hb A2-Saurashtra or ?????G2)Pro®Ser; HBD: C.301C>T] in Cis
Hemoglobin 2014 Jan-Feb; 38(1):24-7. .(IF:0.955)
|
2014 | |
| 463 |
Kerketta LS, Rao VB, Ghosh K Chimeric Fusion Karyotypes in Childhood B-cell Acute Lymphoblastic Leukemia
Indian Pediatr. 2014 Feb 8;51(2):152-3.(IF:1.036)
|
2014 | |
| 464 |
Ray S, Gorakshakar AC, Vasantha K, Agarwal S, Nadkarni A, Ghosh K Molecular characterization of weaker variants of A and B in Indian population- the first report.
Tranf Apheresis Sci 2014 Feb; 50(1): 118-22.(IF:1.072)
|
2014 | |
| 465 |
Bhukhanvala DS, Sorathiya S, Surve R, Nair S, Italia K, Colah R, Ghosh K, Gupte SC Hemoglobin variants in Muslim community in South Gujarat, Western India.
Int J Lab Hematol. 2014 Feb;36(1):e15-7 (IF: 1.176)
|
2014 | |
| 466 |
Shetty S, Ghosh K. Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within
Haematologica. 2014 Mar;99(3):e30. (IF:5.868)
|
2014 | |
| 467 |
46 Kasatkar P, Shetty S, Ghosh K. Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients
PLoS One. 2014 Mar 27;9(3):e92575. (IF:3.534)
|
2014 | |
| 468 |
Pinto P, Ghosh K, Shetty S A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII inhibitor screening assay
Clin Chem.Lab Med. 2014 Mar;52(3):e39-41.(IF:2.955)
|
2014 | |
| 469 |
Gaikwad T, Jadli A, Ghosh K, Shetty S Delayed Vitamin K deficiency related bleeding: is it genetically linked?
Indian J Pediatr. 2014 Mar;81(3):310-1. (IF:0.919)
|
2014 | |
| 470 |
Ali S, Ghosh K, Shetty S Novel genetic abnormalities in Bernard-Soulier syndrome in India
Ann Hematol. 2014 Mar;93(3):381-4. (IF:2.396)
|
2014 | |
| 471 |
Parasannanavar DJ, Rajadhyaksha A, Ghosh K. Role of hla-B alleles and clinical presentation of b27 negative spondyarthritis patients from Mumbai, Western India
Autoimmune Dis. 2014;2014:327315. Epub 2014 Mar 6. (IF:--)
|
2014 | |
| 472 |
Nadkarni A, Dabke P, Colah RB, Ghosh K Fetal hemoglobin in sickle cell anemia
Blood Cells Mol Dis. 2014 Apr;52(4):175.(IF:2.331)
|
2014 | |
| 473 |
Kasatkar P, Shetty S, Ghosh K Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays
Prenat Diagn 2014 Apr; 34(4):377-81.(IF:3.296)
|
2014 | |
| 474 |
Italia K, Upadhye D, Dabke P, Kangane H, Colaco S, Sawant P, Nadkarni A, Gorakshakar A, Jain D, Italia Y, Ghosh K, Colah R Clinical and hematological presentation among Indian patients with common hemoglobin variants.
Clin Chim Acta 2014 Apr 20; 431:46-51.(IF:2.824)
|
2014 | |
| 475 |
Mishra A, Gupta M, Dalvi A, Ghosh K, Madkaikar MR Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID)
J Clin Immunol 2014 Apr; 34(3):316-22.(IF:3.184)
|
2014 | |
| 476 |
Ghosh K, Colah R, Manglani M, Choudhry VP, Verma I, Madan N, Saxena R, Jain D, Marwaha N, Das R, Mohanty D, Choudhary R, Agarwal S, Ghosh M, Ross C Guidelines for screening, diagnosis and management of hemoglobinopathies
Indian J Hum Genet. 2014 Apr;20(2):101-19. Review.
|
2014 | |
| 477 |
Swaminathan S, Garg S, Madkaikar MR, Gupta M, Jijina F, Ghosh K. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from
Indian J Hum Genet. 2014 Apr;20(2):160-5.
|
2014 | |
| 478 |
Vundinti BR. Methylenetetrahydrofolatereductase C677T polymorphism and folate metabolism in
Indian J Hum Genet. 2014 Apr;20(2):99-100
|
2014 | |
| 479 |
Gaikwad T, Ghosh K, Kulkarni B, Shetty S Factor V Leiden mutation modulates the bleeding phenotype in warfarin sensitive patients.
Thromb Res. 2014 May;133(5):955-6(IF:2.427)
|
2014 | |
| 480 |
Colah R, Mukherjee M, Ghosh K Sickle cell disease in India.
Curr Opin Hematol. 2014 May;21(3):215-23.(IF:4.053)
|
2014 | |
| 481 |
Nair PS, Shetty SD, Chandrakala S, Ghosh K Mutations in intron 1 and intron 22 inversion negative haemophilia a patients from Western India
PLoS One. 2014 May 20;9(5):e97337. eCollection 2014.(IF:3.534)
|
2014 | |
| 482 |
Prasannavar DJ, Yeola A, Vandana VP, Patwardhan M, Rajadhyaksha A, Ghosh K Distribution of HLA-DR?1 alleles among well-characterized rheumatoid arthritis patients from Western India.
Rheumatol Int. 2014 May;34(5):705-8.(IF:1.516)
|
2014 | |
| 483 |
Joshi D, Chandrakala S, Korgaonkar S, Ghosh K, Vundinti BR. Down-regulation of miR-199b associated with imatinib drug resistance in 9q34.1 deleted BCR/ABL positive CML patients.
Gene. 2014 Jun 1;542(2):109-12.(IF:2.082)
|
2014 | |
| 484 |
Warang P, Nair S, Nadkarni A, Kedar PS, Bhave A, Ghosh K, Colah R. Hb Koln [?98(FG5) [GTG ? ATG, Val ? Met]]: the first report from India.
Hematology. 2014 Jun;19(4):199-201.(IF:1.393)
|
2014 | |
| 485 |
Solanki A, Vundinti BR. Prenatal detection of Fanconi anemia.
Indian Pediatr. 2014 Jun;51(6):501
|
2014 | |
| 486 |
Shetty S, Shelar T, Mirgal D, Nawadkar V, Pinto P, Shabhag S, Mukaddam A, Kulkarni B, Ghosh K Rare coagulation factor deficiencies: a countrywide screening data from India.
Haemophilia. 2014 Jul; 20(4):575-81.(IF:3.170)
|
2014 | |
| 487 |
Vundinti BR, Kerketta L, Korgaonkar S, Vaidya S, Ghosh K Isodicentric Philadelphia [idic(Ph)] chromosome in a case of CML at chronic phase
Indian J Cancer. 2014 July-September;51(3):383-384.(IF:0.802)
|
2014 | |
| 488 |
D'Silva S, Colah RB, Ghosh K, Mukherjee MB Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates
Gene. 2014 Aug 15;547(1):18-22.(IF:2.443)
|
2014 | |
| 489 |
Maiti AK, Kim-Howard X, Motghare P, Vandana VP, Chua KH, Sun C, Arango-Guerrero MT, Ghosh K,Niewold TB, Harley JB, Anaya JM, Looger LL, Nath SK. Combined protein and nucleic acid-level effects of rs1143679(R77H), a lupus-predisposing variant within ITGAM.
Hum Mol Genet 2014 Aug 1; 23(15):4161-76.(IF:6.393)
|
2014 | |
| 490 |
Pinto P, Parasannanavar D, Ghosh K, Shetty S The association of HLA-DRB1 and HLA-DQB1 alleles with the development of factor VIII inhibitors in severe haemophilia A patients in India.
Tissue Antigens 2014 Aug; 84(2):235-7.(IF:2.35)
|
2014 | |
| 491 |
Ghosh K, Shetty S, Patil R. Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study: comment
J Thromb Haemost. 2014 Aug; 12(8):1377-8.(IF:5.72)
|
2014 | |
| 492 |
Ghosh K, Gorakshakar A. Dr. Bhatias legacy in the development of immunohematology research in the country
Asian J Transfus Sci. 2014;8(Suppl 1):S1-2.
|
2014 | |
| 493 |
Pinto P, Ghosh K, Shetty S Analysis of F8 inversions as risk factors for FVIII inhibitor development in Indian severe haemophilia A patients
Blood Cells Mol Dis 2014 Sep; 53(3):161-3.(IF:2.331)
|
2014 | |
| 494 |
Gaikwad T, Ghosh K, Shetty S VKORC1 and CYP2C9 genotype distribution in Asian countries.
Thromb Res. 2014 Sep; 134(3):537-44.(IF:3.133)
|
2014 | |
| 495 |
Madkaikar MR, Gupta M, Chavan S, Italia K, Desai M, Merchant R, Radhakrishnan N, Ghosh K X-linked hyper IgM syndrome: Clinical, immunological and molecular features in patients from India
Blood Cells Mol Dis. 2014 Sep; 53(3):99-104.(IF:2.331)
|
2014 | |
| 496 |
Pai N, Ghosh K, Shetty S Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).
Clin Appl Thromb Hemost. 2014 Sep;20(6):573-6 (IF: 1.332)
|
2014 | |
| 497 |
Shetty S, Ghosh K Paternal factor V Leiden and recurrent pregnancy loss: a new concept behind fetal genetics?: comment
J Thromb Haemost. 2014 Oct; 12(10):1758-9.(IF:5.72)
|
2014 | |
| 498 |
Dabke PS, Colah RB, Ghosh K, Nadkarni AH. Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients
Hematology 2014 Oct; 19(7):388-92.(IF:1.393)
|
2014 | |
| 499 |
Kulkarni B, Nair SB, Vijapurkar M, Mota L, Shanbhag S, Ali S, Shetty SD, Ghosh K. Molecular pathology of rare bleeding disorders (RBDs) in India: A systematic review.
PLos One 2014 Oct 2; 9(9):e108683.(IF:3.534)Review
|
2014 | |
| 500 |
Mhatre S, Madkaikar MR, Ghosh K, Desai M, Pujari V, Gupta M. Rapid flow cytometry based cytotoxicity assay for evaluation of NK cell function
Indian J Exp Biol 2014 Oct; 52(10):983-8.(IF:0.835)
|
2014 | |
| 501 |
Vandana VP, Rajadhyaksha A, Nadkar M, Pandit P, Surve P, Lecerf M, Bayry J, Kaveri S, Ghosh K Clinical and autoimmune profile of scleroderma patients from Western India
Int J Rheumatol. 2014;2014:983781. Epub 2014 Oct 19.(IF:1.469)
|
2014 | |
| 502 |
Mhatre S, Madkaikar MR, Jijina F, Ghosh K Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis Type-2.
J Pediat Hematol Oncol 2014 Nov; 36(8):e524-7.(iF:0.973)
|
2014 | |
| 503 |
Kedar PS, Warang P, Sanyal S, Devendra R, Ghosh K, Colah R Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.
Clin Chim Acta 2014 Nov1; 437:103-5.(IF:2.764)
|
2014 | |
| 504 |
Colaco S, Surve R, Sawant P, Nadkarni A, Ghosh K, Colah R. HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association.
Mediterr J Hematol Infect Dis. 2014 Nov 1;6(1):e2014072. eCollection 2014.(IF:-)
|
2014 | |
| 505 |
Mohapatra R, Warang P, Ghosh K, Colah R. Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye
Cytometry B Clin Cytom. 2014 Nov 24. [Epub ahead of print](IF:2.824)
|
2014 | |
| 506 |
Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2014 May;22(4):381-5.
|
2014 | |
| 507 |
Umare V, Vandana VP, Nadkar M, Rajadhyaksha A, Patwardhan M, Ghosh K, Nadkarni AH Effect of proinflammatory cytokines (IL-6, TNF-?, and IL-1?) on clinical manifestations in Indian SLE patients.
Mediators Inflamm. 2014;2014:385297.Epub 2014 Dec 7.
|
2014 | |
| 508 |
D Silva S, Colah RB, Ghosh K, Mukherjee MB. UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.
Gene. 2013 Jan 15;513(1):36-9.(IF:2.443)
|
2013 | |
| 509 |
Patil A, Poudyal BS, Kapali SM, Ghosh K, Shetty S Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
Ann Hematol. 2013 Jan;92(2):261-2. (IF: 2.615)
|
2013 | |
| 510 |
Kulkarni SS, Kasiviswanathan V, Ghosh K A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population
Blood Transfus. 2013 Jan;11(1):37-42. (IF: 2.099).
|
2013 | |
| 511 |
Mohanty D, Colah RB, Gorakshakar AC, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V. Prevalence of ?-thalassemia and other haemoglobinopathies in six cities in India: a
J Community Genet. 2013 Jan;4(1):33-42.
|
2013 | |
| 512 |
D Souza E, Sawant PM, Nadkarni AH, Gorakshakar A,Ghosh K, Colah RB. Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal
J Postgrad Med. 2013 Jan-Mar;59(1):15-20. (IF: 1.389)
|
2013 | |
| 513 |
Nair S, Nadkarni AH, Ghosh K, Colah R. Hemoglobin variants and high-performance liquid chromatography.
Int J Lab Hematol. 2013 Jan 11. [Epub ahead of print] .(IF: 1.176)
|
2013 | |
| 514 |
Pooja Dabke, Roshan Colah, Kanjaksha Ghosh, Anita Nadkarni Effect of Cis Acting Potential Regulators in the ? Globin Gene Cluster on the Production of HbF in Thalassemia Patients.
Mediterr J Hematol Infect Dis. 2013; 5(1): e2013012. Published online 2013 February 16.(IF: )
|
2013 | |
| 515 |
Magerus-Chatinet A, Stolzenberg MC, Lanzarotti N, Neven B, Daussy C, Picard C, Neveux N, Desai M, Rao M, Ghosh K, Madkaikar MR, Fischer A, Rieux-Laucat F Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation
J Allergy Clin Immunol. 2013 Feb;131(2):486-90.(IF: 11.003)
|
2013 | |
| 516 |
Gaikwad T, Ghosh K, Shetty S Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy
Eur J Clin Pharmacol. 2013 Feb;69(2):293-4.(IF: 2.845)
|
2013 | |
| 517 |
Nair S, Ghosh K. The myriad effects of cigarette smoke.
J Thromb Haemost. 2013 Feb;11(2):387-8.(IF: 5.731)
|
2013 | |
| 518 |
Ghosh K. Cytogenetics in paediatric aplastic anaemia: does it give an insight on the evolution of the disease?
Indian J Med Res. 2013 Mar;137(3):445-6.(IF: 1.837).
|
2013 | |
| 519 |
Vandana VP, Patwardhan M, Thakkar V, Kharkar V, Khopkar U, Ghosh K, Weetman AP, Gawkrodger DJ, Kemp EH. Vitiligo patients from India (Mumbai) show differences in clinical, demographic and autoantibody profiles compared to patients in western countries
J Eur Acad Dermatol Venereol. 2013 Mar;27(3):279-86.
|
2013 | |
| 520 |
Dabke P, Colah RB,Ghosh K, Nadkarni A. Effect of a group of genetic markers around the 5 regulatory regions of the ? globin gene cluster linked to high HbF on the clinical severity of ? thalassemia.
Blood Cells Mol Dis. 2013 Mar;50(3):156-60.(IF:2.361)
|
2013 | |
| 521 |
Vandana VP, Ghosh K Immunological disturbances associated with malarial infection
J Parasitic Dis 2013 Apr;37(1):11-15. Review.
|
2013 | |
| 522 |
Madkaikar MR, Mishra A, Desai M, Gupta M, Mhatre S, Ghosh K Comprehensive Report of Primary Immunodeficiency Disorders from a Tertiary Care Center in India
J Clin Immunol. 2013 Apr; 33(3):507-12.(IF:3.077)
|
2013 | |
| 523 |
Vandana VP,Patwardhan M, Rajadhyaksha A and Ghosh K Clinical and Immunological profile of systemic lupus erythematosus
Indian Pediatr 2013 Apr 8; 50(4): 405-7.(IF: 1.048)
|
2013 | |
| 524 |
Parasannanavar DJ, Yeola A, Vandana VP, Rajyadhaksha A,Ghosh K HLA-DR?1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients.
Rheumatol Int. 2013 Apr; 33(4): 867-70.(IF: 2.200)
|
2013 | |
| 525 |
Shukla P, Rao A, Ghosh K, Vundinti BR. Identification of a novel large intragenic deletion in a family with Fanconi Anemia: First
Gene. 2013 Apr 15; 518(2): 470-5. (IF:2.443)
|
2013 | |
| 526 |
Italia K, Jijina F, Merchant R, Swaminathan S, Nadkarni A, Gupta M,Ghosh K, Colah R. Comparison of in-vitro and in-vivo response to fetal hemoglobin production and ?-mRNA expression by hydroxyurea in Hemoglobinopathies
Indian J Hum Genet. 2013 Apr;19(2):251-8.
|
2013 | |
| 527 |
Bhukhanvala DS, Sorathiya SM, Sawant P, Colah R,Ghosh K, Gupte SC Antenatal screening for identification of couples for prenatal diagnosis of severe
J Obstet Gynaecol India. 2013 Apr;63(2):123-7.
|
2013 | |
| 528 |
Kasatkar P, Ghosh K, Shetty S Acquired von Willebrand syndrome: A rare disorder of heterogeneous etiology.
J Postgrad Med. 2013 Apr-Jun;59(2):98-101.(IF: 1.389)
|
2013 | |
| 529 |
Warang P, Kedar PS, Kar R, Ghosh K, Colah R New missense homozygous mutation (Q270Ter) in the pyrimidine 5 nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia
Ann Hematol. 2013 May;92(5):715-7. (IF: 2.615)
|
2013 | |
| 530 |
Ghosh K Multifactorial aetiology for bone disease in patients with haemophilia.
Eur J Haematol. 2013 May;90(5):435(IF:2.066)
|
2013 | |
| 531 |
Ghosh S,Ghosh K Maternal and neonatal outcomes in gestational diabetes mellitus
J Indian Med Assoc. 2013 May;111(5):330-1, 336.
|
2013 | |
| 532 |
Ankolkar M, Salvi V, Warke H, Vundinti BR, Balasinor NH. Methylation status of imprinted genes DLK1-GTL2, MEST (PEG1), ZAC (PLAGL1),
Fertil Steril. 2013 May;99(6):1668-73.
|
2013 | |
| 533 |
Nair SB, Nadkarni AH, Ghosh K, Colah RB Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal a TIndian (AATAAA>AATA- -) Mutation in Four Indian Families.
Hemoglobin. 2013 May-Jun; 37(3): 277-84.(IF: 1.304)
|
2013 | |
| 534 |
Patwardhan M, Vandana VP, Taylor LH, Thakkar V, Kharkar V, Khopkar U, Ghosh K, Gawkrodger DJ, Teare MD, Weetman AP, Kemp EH. The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian vitiligo patients: a case-control study and meta-analysis
Br J Dermatol. 2013 Jun; 168(6): 1195-1204.(IF: 3.666)
|
2013 | |
| 535 |
Vandana VP, Mahant G, Rajadhyaksha A, Surve P, Rajendran V, Patwardhan M, Nadkarni A, Dighe S, Ghosh K. A study on anti-mannose binding lectin (anti-MBL) antibodies and serum MBL levels in
Rheumatol Int 2013 Jun; 33(6): 1533-9.(IF: 1.885)
|
2013 | |
| 536 |
Gaikwad T, Ghosh K, Kulkarni B, Kulkarni V, Ross C, Shetty S Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over
Eur J Pharmacol. 2013 Jun 15;710(1-3):80-4.(IF:2.684)
|
2013 | |
| 537 |
Madkaikar MR, Mishra A, Ghosh K. Diagnostic approach to primary immunodeficiency disorders.
Indian Pediatr. 2013 Jun 8;50(6):579-86.(IF:1.044)
|
2013 | |
| 538 |
Pinto P, Ghosh K, Shetty S. Factor VIII haplotypes in severe hemophilia A patients in India
Ann Hematol. 2013 Jul; 92(7): 999-1000.(IF: 2.615)
|
2013 | |
| 539 |
Gupta M, Madkaikar MR, Rao VB, Mishra A, Govindaraj P, Thangaraj K, Ghosh K Mitochondrial DNA variations in myelodysplastic syndrome
Ann Hematol. 2013 Jul;92(7): 871-6. (IF: 2.615)
|
2013 | |
| 540 |
Patil R, Ghosh K, Shetty S Profibrinolytic microparticles are not adequately produced to compensate their
Haematologica. 2013 Jul;98(7):e69.(IF:5.868)
|
2013 | |
| 541 |
Gorakshakar AC, Kulkarni SS, Ghosh K. Molecular organization of Rh gene is likely to be heterogeneous across the world.
Asian J Transfus Sci. 2013 Jul;7(2):103-4.
|
2013 | |
| 542 |
Shetty S, Patil R, Ghosh K. Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review.
Eur J Obstet Gynecol Reprod Biol. 2013 Jul; 169(2):123-9.(IF:1.974)
|
2013 | |
| 543 |
Pai N, Ghosh K, Shetty S Hereditary thrombophilia in cerebral venous thrombosis: a study from India.
Blood Coagul Fibrinolysis. 2013 Jul; 24(5):540-3.(IF:1.238)
|
2013 | |
| 544 |
Chaudhary AK, Pandya S, Ghosh K, Nadkarni A. Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: An overview.
Mutat Res. 2013 Jul-Sep; 753(1):7-23.(IF: 3.680)
|
2013 | |
| 545 |
D Silva S, Colah RB, Ghosh K, Mukherjee MB. Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates
Curr Sci 2013 Aug; 105(4): 446-7. (IF: 0.933 )
|
2013 | |
| 546 |
Kasatkar P, Ghosh K, Shetty S. A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families
Ann Hematol. 2013 Aug; 92(8):1147-9. (IF: 2.615)
|
2013 | |
| 547 |
Kasatkar P, Ghosh K, Shetty S. The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal.
J Thromb Haemost. 2013 Sep; 11(9): 1784-5.(IF: 5.731)
|
2013 | |
| 548 |
Gorakshakar AC, Ghosh K. Transfusion transmitted infections in Indian thalassemics: a perspective
Indian J Hematol Blood Transfus. 2013 Sep;29(3):189-90.
|
2013 | |
| 549 |
Lugade AA, Bharali DJ, Vandana VP, Elkin G, Mousa SA, Thanavala Y Single low-dose un-adjuvanted HBsAg nanoparticle vaccine elicits robust , durable immunity.
Nanomedicine 2013 Oct; 9(7):923-34. (IF: 5.26)
|
2013 | |
| 550 |
Warang P, Kedar PS, Ghosh K, Colah R. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
Blood Cells Mol Dis. 2013 Oct;51(3): 133-7.(IF: 2.361)
|
2013 | |
| 551 |
Gaikwad T, Shetty S, Ghosh K Polymorphisms of warfarin metabolizing enzymes in an Indian population
Blood Cells Mol Dis. 2013 Oct; 51(3):203.(IF: 2.361)
|
2013 | |
| 552 |
Vaidya S, Joshi D, Ghosh K, Chakrabarti P, Vundinti BR A novel 5-way translocation t(9;11;13;19;22) in a case of chronic-phase chronic myeloid
Hum Pathol. 2013 Oct; 44(10):2365-9.(IF: 3.077)
|
2013 | |
| 553 |
Pinto P, Ghosh K, Shetty S. A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII
Clin Chem Lab Med. 2013 Oct 2:1-3.(2.955)
|
2013 | |
| 554 |
Jain DL, Apte M, Colah R, Sarathi V, Desai S, Gokhale A, Bhandarwar A, Jain HL, Ghosh K. Efficacy of Fixed Low Dose Hydroxyurea in Indian Children with Sickle Cell Anemia: A
Indian Pediatr. 2013 Oct;50(10):929-33 (IF :)
|
2013 | |
| 555 |
Garg S, Madkaikar MR, Ghosh K. Investigating cell surface markers on normal hematopoietic stem cells in three different
Int J Stem Cells. 2013 Nov;6(2):129-33.(IF:0.625)
|
2013 | |
| 556 |
Ali S, Ghosh K, Shetty S. Molecular pathology of Bernard-Soulier syndrome in Indian patients
Platelets. 2013 Nov; 24(7):571-3.(IF: 2.391)
|
2013 | |
| 557 |
Vandana VP, Rajadhyaksha A, Yadav K, Surve P, Patwardhan M, Dhavale N, Pandit P, Ghosh K Anti-C reactive protein antibodies in Indian patients with systemic lupus erythematosus
Indian J Nephrol 2013 Nov; 23(6): 434-7.
|
2013 | |
| 558 |
Shukla P, Solanki A, Ghosh K, Vundinti BR DNA interstrand cross-link repair: understanding role of Fanconi anemia pathway and
Eur J Haematol. 2013 Nov;91(5):381-93 (IF:2.066)
|
2013 | |
| 559 |
Bhukhanvala DS, Italia K, Sawant P, Colah R, Ghosh K, Gupte SC. Molecular characterization of ?-thalassemia in four communities in South Gujarat-codon
Ann Hematol. 2013 Nov;92(11):1473-6. (IF:2.615)
|
2013 | |
| 560 |
Ghosh K, Madkaikar MR, Gupta M, Jijina F. Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination
Turk J Haematol. 2013 Dec;30(4):366-70.(IF:0.34)
|
2013 | |
| 561 |
Ghosh K, Ghosh K. Pulmonary hydatidosis, strongyloidiasis and paragonimiasis in India.
J Assoc Physicians India. 2013 Dec;61(12):954-5
|
2013 | |
| 562 |
Parasannanavar DJ, Rajadhyaksha A, Ghosh K. Application of a Simple In-House PCR-SSP Technique for HLA-B* 27 Typing in Spondyloarthritis Patients.
Arthritis. 2013;2013:504109. doi: 10.1155/2013/504109. Epub 2013 Dec 19.
|
2013 | |
| 563 |
Kundu T, Shaikh A, Kutty A, Nalvade A, Kulkarni SS, Kulkarni R, Ghosh K. Homeopathic medicines substantially reduce the need for clotting factor concentrates in haemophilia patients: results of a blinded placebo controlled cross over trial.
Homeopathy. 2012 Jan;101(1):38-43.(IF: 1.141)
|
2012 | |
| 564 |
Datta S, Chowdhury A, Ghosh M, Das K, Jha P, Colah R, Mukherjee M, Majumder PP. A Genome wide search for Non-UGT1A1 markers associated with unconjugated bilirubin levels revelas significant association with a polymorphic marker near a gene of the Nucleoporin family
Ann.Hum.Genet. 2012 Jan; 76(1):33-41.(IF: 2.565)
|
2012 | |
| 565 |
Vijver Edith van de, Maddelena A, Sanal O, Holland SM, Uzel G, Madkaikar MR, Martin de Boer, Karin van Leeuwen, Koker MY, Parvaneh N, Fischer A, Law SK Alex, Klein N, Tezcan F IIhan, Unal E, Patiroglu T, Belohradsky BH, Schwartz K, Somech R, Kuijpers TW, R Hematologically important mutations: Leukocyte adhesion deficiency (first update)
Blood Cells Mol Dis 2012 Jan 15; 48(1):53-61.(IF: 2.351)
|
2012 | |
| 566 |
Vandana VP, Patwardhan M, Athavale A, Taushid S, Ghosh K. Mycobacterium tuberculosis triggers autoimmunity?
Indian J Tuberc. 2012 Jan;59(1):49-51.
|
2012 | |
| 567 |
Madkaikar MR, Currimbhoy Z , Gupta M, Desai M, Rao M, Ghosh K. Clinical Profile of Leukocyte Adhesion Deficiency Type I.
Indian Pediatr 2012 Jan; 49(1): 43-45.(IF:1.048)
|
2012 | |
| 568 |
Italia KY, Sawant PM, Nadkarni AH, Ghosh K, Colah RB Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of ?-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?
Hemoglobin. 2012 Feb; 36(2):114-23. (IF: 1.304)
|
2012 | |
| 569 |
Gupta S, Madkaikar MR, Singh S, Sehgal S. Primary immunodeficiencies in India: a perspective.
Ann N Y Acad Sci. 2012 Feb;1250:73-9.(IF: 3.155)
|
2012 | |
| 570 |
Kanani P, Poudyal BS, Shetty S, Kapali SM, Ghosh K. Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population.
Haemophilia. 2012 Mar;18(2):e44-5.(IF: 2.597)
|
2012 | |
| 571 |
Shukla P, Ghosh K and Vundinti BR Current and emerging therapeutic strategies for Fanconi anemia.
The Hugo J 2012 Mar; 6:1.(IF: )
|
2012 | |
| 572 |
Ghosh K, Ghosh K, Shetty S. Hemostasis Research in India: Past, Present, and Future.
Clin Appl Thromb Hemost. 2012 Mar-Apr;18(2):128-33.(IF: 1.332)
|
2012 | |
| 573 |
Mukherjee MB, Ghosh Kanjaksha Explaining anthropometric variations in sickle cell disease requires a multidimensional approach
Indian J Hum Genet. 2012 Jan-Apr;18(1): 1-2.
|
2012 | |
| 574 |
D Souza E, Nair S, Nadkarni A, Ghosh K, Colah RB SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India
Indian J Hum Genet 2012 Jan-Apr; 18(1): 87-90.
|
2012 | |
| 575 |
Nair PS, Shetty S, Ghosh K A homozygous female hemophilia A.
Indian J Hum Genet 2012 Jan-Apr; 18(1): 134-6.
|
2012 | |
| 576 |
Joshi SR, Vasantha K A profile of rare bloods in India and its impact in blood transfusion service.
Asian J Transf Sci 2012 Jan-Jun; 6(1): 42-43.
|
2012 | |
| 577 |
Nadkarni A, Italia K, Sawant P, Ghosh K, Colah R. Hemoglobin Lepore Hollandia in India.
Int J Lab Hematol. 2012 Apr;34(2):148-53. (IF: 1.176)
|
2012 | |
| 578 |
Gorakshakar A, Sathe P, Colah R, Nadkarni A, Ghosh K Hemoglobin Showa-Yakushiji: A Common ? Thalassemia Mutation Among the Agri Community from Western India.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 302-5.(IF; 1.110)
|
2012 | |
| 579 |
Vundinti BR, Korgaonkar S, Ghosh K. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Gene. 2012 Apr 25; 498(1):128-30.(IF: 2.443)
|
2012 | |
| 580 |
Vandana VP, Hire H and Ghosh K MicroRNA profile in understanding pathogenesis of systemic lupus erythematosus
Indian J Biotechnol 2012 Apr; 11:129-33.(IF: 0.55)
|
2012 | |
| 581 |
Kawankar N, Korgaonkar S, Kerketta L, Madkaikar MR, Jijina F, Ghosh K, Vundinti BR. DNA Copy Number Changes and Immunophenotype Pattern in Karyotypically Normal Acute Myeloid Leukemia Patients from Indian Population.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 265-70.(IF: 1.110)
|
2012 | |
| 582 |
Shetty S, Ghosh K. Malignancies in Indian haemophiliacs are mainly non viral associated
J Thromb Haemost. 2012 Apr 12.[Epub ahead of print](IF: 5.731)
|
2012 | |
| 583 |
Italia K, Sheth J, Sawant P, Nadkarni A, Ghosh K, Colah R. Prenatal diagnosis of HbE-Lepore and Hb Lepore-?-thalassemia: the importance of accurate genotyping of the couple at risk.
Prenat Diagn. 2012 Jul;32(7):703-7.(IF: 2.106)
|
2012 | |
| 584 |
Vaidya S, Sonawani A, Idicula-Thomas S, Vundinti BR, Ghosh K. Imatinib resistance due to a novel tri-nucleotide insertion in the SH2/C lobe interface of BCR/ABL kinase domain between position K357 and N358.
Leuk Res. 2012 May;36(5):e110-2.(2.472)
|
2012 | |
| 585 |
Pai N, Ghosh K, Shetty S Hereditary protein C deficiency in Indian patients with venous thrombosis.
Ann Hematol. 2012 Sep;91(9):1471-6.(IF: 2.615)
|
2012 | |
| 586 |
Warang P, Kedar PS, Ghosh K, Colah R. A new simple approach for the determination of pyrimidine 5-nucleotidase activity in human erythrocytes using an ELISA reader.
Int J Lab Hematol. 2012 Jun; 34(2): 232-4.(IF: 1.176)
|
2012 | |
| 587 |
Shetty S, Ghosh K. Cancers in patients with hemophilia: a retrospective study from the Italian Association of Hemophilia Centers: a rebuttal.
J Thromb Haemost. 2012 Jun;10(6):1200-1; author reply 1201-2. (IF: 5.731)
|
2012 | |
| 588 |
Ghosh K. Haematology research in India: past, present and future.
Indian J Hematol Blood Transfus. 2012 Jun;27(2):55-64. (IF: 0.056)
|
2012 | |
| 589 |
Pai N, Ghosh K, Shetty S Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups.
Blood Coagul Fibrinolysis. 2012 Jun;23(4):257-61.(IF: 1.25)
|
2012 | |
| 590 |
Lobo V, Shetty S, Kulkarni B, Ghosh K. A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2012 Jun; 91(6):917-21.(IF: 2.615)
|
2012 | |
| 591 |
Kulkarni SS, K Vasantha, Ghosh K A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.
Blood Transfus 2012 Jul; 12: 1-6. (IF: 2.099)
|
2012 | |
| 592 |
Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional ? gene variants identified in neonates during newborn screening for sickle cell disorders.
J Clin Pathol. 2012 Jul;65(7):654-9.(IF: 2.306)
|
2012 | |
| 593 |
Vandana VP, Das S, Surve P, Ghosh K Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus
Indian J Hum Genet 2012 May-Aug; 18(2): 155-60.
|
2012 | |
| 594 |
Ghosh K, Shetty S Malignancies in persons with haemophilia: 25-year data from India.
Natl Med J India. 2012 Jul-Aug;25(4):251.(IF: 0.595)
|
2012 | |
| 595 |
Jain DL, Sarathi V, Upadhye D, Gulhane R, Nadkarni AH, Ghosh K, Colah RB. Newborn screening shows a high incidence of sickle cell anemia in Central India.
Hemoglobin. 2012 Jul-Aug; 36(4):316-22.(IF: 1.304)
|
2012 | |
| 596 |
Gorakshakar AC, Ghosh K. Subclinical iron deficiency is a silent epidemic amongst voluntary blood donors.
Transfus Med. 2012 Aug;22(4):300-1. (IF:1.14)
|
2012 | |
| 597 |
Ghosh K, Shetty S. Bone health in persons with haemophilia (PWH): A review.
Eur J Haematol.2012 Aug;89(2):95-102.(IF: 2.614)
|
2012 | |
| 598 |
Warang P, Kedar P, Ghosh K, Colah RB Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
Int J Hematol. 2012 Aug;96(2):263-7. (IF: 1.268)
|
2012 | |
| 599 |
Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R. Variable haematological and clinical presentation of ?-thalassaemia carriers and homozygotes with the Poly A (T?C) mutation in the Indian population.
Eur J Haematol. 2012 Aug;89(2):160-4. (IF: 2.614)
|
2012 | |
| 600 |
D Silva S, Colah RB,Ghosh K, Mukherjee MB G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India.
J Matern Fetal Neonatal Med. 2012 Sep; 25(9):1833-4.(IF: 1.592)
|
2012 | |
| 601 |
Vandana VP, Rajadhyaksha A, Mahant G, Surve P, Patwardhan M, Dighe S,Ghosh K Anti-C1q antibodies and their association with complement components in Indian systemic lupus erythematosus patients
Indian J Nephrol. 2012 Sep;22(5):353-7.
|
2012 | |
| 602 |
Pinto P,Ghosh K, Shetty S. Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients
Haemophilia. 2012 Sep;18(5):794-7.(IF: 2.597)
|
2012 | |
| 603 |
Vandana VPD APO1/F as promoter polymorphism in systemic lupus erythematosus (SLE): significance in clinical expression of the disease
J Assoc Physicians India. 2012 Sep; 60:34-7.(IF:)
|
2012 | |
| 604 |
Vandana VPD, Dalvi H, Parsannavar D, Rajadhyaksha A, Patwardhan M, Ghosh K. Study of PTPN22 1858C/T polymorphism in rheumatoid arthritis patients from Western India.
Indian J Rheumatol 2012 Sep; 7(3):130-134.(IF: )
|
2012 | |
| 605 |
Kerketta LS, Rao VB, Ghosh K. Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection
Trop Med Int Health. 2012 Oct;17(10):1222-6.(IF: 2.795)
|
2012 | |
| 606 |
Kulkarni B, Kanakia S,Ghosh K, Shetty S. Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.
Ann Hematol. 2012 Oct;91(10):1667-8.(IF: 2.615)
|
2012 | |
| 607 |
Colaco S, Colah R,Ghosh K, Nadkarni A Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases
Clin Chim Acta. 2012 Oct 9;413(19-20):1705-7.(IF:2.661)
|
2012 | |
| 608 |
Jain D, Italia K, Sarathi V,Ghosh K, Colah R. Sickle Cell Disease from Central India: A Retrospective Analysis.
Indian Pediatr. 2012 Nov;49(11):911-3. (IF:1.048)
|
2012 | |
| 609 |
Jadli A, Kulkarni B, Ghosh K, Shetty S. Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases
Liver Int. 2012 Nov;32(10):1596-7.(IF: 3.824)
|
2012 | |
| 610 |
Ghosh K, Swaminathan S, Madkaikar MR, Gupta M, Kerketta L, Vundinti B. FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India.
Ann Hematol. 2012 Nov;91(11):1703-12. (IF: 2.615)
|
2012 | |
| 611 |
Shetty S,Ghosh K. APTT reagents for different coagulation tests: one size does not fit all
Am J Clin Pathol. 2012 Nov;138(5):757; author reply 757-8.
|
2012 | |
| 612 |
Adlbrecht C, Aigner E, Bellon JM, Bouloukaki I, Bouzas-Mosquera A, Carrilho AJ, Chang KC, Chattipakorn N, Chattipakorn SC, Chen YJ, Chung YC, Colah R,Datz C, Frokjaer JB, Fujimori S, Georgiadou P, Grion CM, Hsu CP, Hulsmann M, Hung MJ, Hung MY, Iliodromit Research update for articles published in EJCI in 2010
Eur J Clin Invest 2012 Nov; 42(11):1149-64.(If: 3.365)
|
2012 | |
| 613 |
Kedar PS, Warang P, Ghosh K, Colah R. Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family
Ann Hematol. 2012 Dec;91(12):1985-6. (IF: 2.615)
|
2012 | |
| 614 |
Madkaikar MRR, Gupta M, Rao M,Ghosh K Prenatal Diagnosis of LAD-I on Cord Blood by Flowcytometry.
Indian J Pediatr. 2012 Dec;79(12):1605-9.(IF: 0.521)
|
2012 | |
| 615 |
Patwardhan M, Vandana VP, Rajadhyaksha A, Umare V, Rajendran V, Surve P, Ghosh K Clinical and serological features of male Systemic Lupus Erythematosus patients from Western India
Indian J Rhematol 2012 Dec; 7(4):204-8.
|
2012 | |
| 616 |
Chalvam R, Colah RB,Mohanty D, Ghosh K, Mukherjee MB Restriction fragmentlength polymorphism (RFLP) of the X chromosome linked glucose-6- phosphate dehydrogenase (G6PD) locus in India.
Ann Hum Biol. 2011 Jan;38(1):106-9.(IF: 1.975)
|
2011 | |
| 617 |
Kanjaksha Ghosh, Roshan Colah. Phenotypic diversity of sickle cell disorders: a rebuttal
Curr Sci 2011 Jan; 100(2):149.(IF:0.897)
|
2011 | |
| 618 |
Shankarkumar U and Shankarkumar A. HLA-B17 Prevalence in HIV-1 infected patients under Antiretroviral treatment.
Int J Hum Genet 2011 Jan; 11(1):59-62.(IF:0.306)
|
2011 | |
| 619 |
D Silva S, Borse V, Colah RB, Ghosh K, Mukherjee MB. Association of (GT)n Repeats Promoter Polymorphism of Heme Oxygenase-1 Gene with Serum Bilirubin Levels in Healthy Indian Adults.
Genet Test Mol Biomarkers. 2011 Apr; 15(4):215-18. (IF: 1.110)
|
2011 | |
| 620 |
Warang P, Gupta M, Kedar PS, Ghosh K, Colah R Flow cytometric osmotic fragility-An effective screening approach for red cell membranopathies.
Cytometry Part B Clin Cytom 2011 May; 80(3):186-90.(IF: 2.525)
|
2011 | |
| 621 |
Basu A, Jain P, Sarkar P, Gangodkar S, Deshpande D, Ganti K, Shetty S, Ghosh K Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein
FEMS Immunol Med Microbiol. 2011 Jul; 62(2):140-7. (IF: 2.441)
|
2011 | |
| 622 |
Shanbhag S, Shetty S, Kulkarni B, Ghosh K. An improved, semi quantitative clot based assay for factor XIII
Haemophilia. 2011 Jul;17(4):718-20. (IF 2.597)
|
2011 | |
| 623 |
Kedar PS, Warang P, Ghosh K, Colah RB. Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH-cytochrome b5 reductase gene mutations.
Am J Hematol. 2011 Mar;86(3):327-9.(IF 3.476).
|
2011 | |
| 624 |
Shetty S, Bhave M, Ghosh K. Challenges of multiple mutations in individual patients with haemophilia.
Eur J Haematol. 2011 Mar; 86(3): 185-90. (IF 2.785)
|
2011 | |
| 625 |
Madkaikar MR, Mhatre S, Gupta M, Ghosh K. Advances in Autoimmune Lymphoproliferative Syndromes (ALPS).
Eur J Haematol. 2011 Jul; 87(1): 1-9. Review (IF 2.785)
|
2011 | |
| 626 |
Vundinti BR, Korgaonkar S, Kerketta L, Ghosh K. A rare case of B-cell chronic lymphocytic leukemia with t(2;14)(p13;q32), +X, +11, +12, +13,+der(1p) karyotype.
Indian J Cancer. 2011 Jul-Sep;48(3):387-8.(IF: 0.961)
|
2011 | |
| 627 |
Vandana VP, Patwardhan M, Nadkarni A, Ghosh K. Fc ? R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients.
Indian J Med Res. 2011 Aug;134(2):181-5.(IF: 1.837)
|
2011 | |
| 628 |
Ghosh K, Gorakshakar A. Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?
Indian J Hum Genet. 2011 Jan;17(1):1-2.
|
2011 | |
| 629 |
Shetty S, Ghosh K. Response to the letter of Casserta et al. Acquired hemophilia a following influenza vaccination.
Autoimmun Rev. 2011 Jul 23. [Epub ahead of print](IF: 6.624)
|
2011 | |
| 630 |
Umapathy S, Pawar A, Bajpai S, Pazare AR, Ghosh K HLA involvement in nevirapine-induced dermatological reaction in antiretroviral-treated HIV-1 patients.
J Pharmacol Pharmacother. 2011 Apr;2(2):114-5.
|
2011 | |
| 631 |
Korgaonkar S, Ghosh K, Vundinti BR. A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotype.
J Hum Reprod Sci. 2011 Jan;4(1):53-5. (IF )
|
2011 | |
| 632 |
Umapathy S, Shankarkumar A, Ramrakhiyani V, Ghosh K. Role of anti-human lymphocyte culture cytotoxic antibodies in recurrent spontaneous pregnancy loss women.
J Hum Reprod Sci. 2011 Jan;4(1):17-9. (IF)
|
2011 | |
| 633 |
Shankarkumar U, Shankarkumar A, Ghosh K. Human immunodeficiency virus therapeutics and pharmacogenomics.
Indian J Hum Genet. 2011 May;17 Suppl 1:S22-6.
|
2011 | |
| 634 |
Saravanan S, Madhavan B, Murugavel KG, Balakrishnan P, Solomon SS, Umapathy S, Kantor R, Kumarasamy N, Yepthomi T, Smith DM, Mayer KH, Solomon S The association between HIV-1 subtype C antiretroviral resistance and HLA prevalence in southern India.
J Acquir Immune Defic Syndr. 2011 May;57(1):e17-19. (IF: 4.570)
|
2011 | |
| 635 |
Shankarkumar A, Shankarkumar U, Ghosh K CCR5 chemokine receptor polymorphism in patients with HIV-1 from Western India.
J Acquir Immune Defic Syndr. 2011 Jun 1;57(2):e21. (IF: 4.570)
|
2011 | |
| 636 |
Shanbhag S, Shetty S, Ghosh K Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5. (IF 2.597)
|
2011 | |
| 637 |
Shetty S, Kasatkar P, Ghosh K. Pathophysiology of acquired von Willebrand disease: a concise review
Eur J Haematol. 2011 Aug;87(2):99-106. Review. (IF 2.785).
|
2011 | |
| 638 |
Ghosh K, Shetty S Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands?
Blood Coagul Fibrinolysis. 2011 Apr;22(3):241-2. (IF 1.549)
|
2011 | |
| 639 |
A Shankarkumar and U Shankarkumar HIV and Malaria co-infection in Mumbai Western India.
J Vector Borne Dis. 2011 Sep; 48(3):155-58.(IF: 1.177)
|
2011 | |
| 640 |
Shankarkumar U, Shankarkumar A, Ghosh K. Involvement of HLA in serum BETA-2 Microglobin levels among Mumbai HIV-1 patients
J Adv Lab Res Biol 2011; I(III):133-35.
|
2011 | |
| 641 |
Shankarkumar U, Sridharan B. Glioma Indian Scenario: Is there a Human Leukocyte Antigen association?
J Nat Sci Biol Med 2011 Jul; 2(2):205-8.
|
2011 | |
| 642 |
Shankarkumar U, Vandana VPD, Patwardhan M, Pawar A, Ghosh K. Autoantibody profile and immunological parameters in Recurrent Spontaneous Abortion patients.
Nigerian Med J 2011 Jul; 52(3):163-66.
|
2011 | |
| 643 |
Shankarkumar U, Devraj JP, Ghosh K. Molecular characterization of HLA B*07 alleles in HLA B27 negative seronegative spondarthritis patients from India
IUP J Genet Evolution 2011; IV(3):1-8.
|
2011 | |
| 644 |
Shankarkumar U, Pawar A, Mitra R, Khuperkar D, Devaraj JP, Ghosh K, Khopkar U HLA-A and HLA-B alleles associated in psoriasis patient’s from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct; 56(5): 510-13.(IF: 0.979)
|
2011 | |
| 645 |
Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Glader B, Rivera A, Brugnara C, Alper SL Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Am J Physiol Cell Physiol 2011 May; 300(5):C1034-C1046.(IF: 3.817)
|
2011 | |
| 646 |
Shetty S, Bhave M, Ghosh K Acquired hemophilia A: diagnosis, aetiology, clinical spectrum and treatment options.
Autoimmun Rev. 2011 Apr;10(6):311-6. Review.(IF: 6.624)
|
2011 | |
| 647 |
Vaidya S, Madkaikar MR, Ghosh K, Vundinti BR. Deletion of ABL/BCR on der(9) associated with severe basophilia.
Indian J Hum Genet. 2011 May;17(2):100-3.
|
2011 | |
| 648 |
Vundinti BR, Ghosh K. Chromosomal aberrations in hematological malignancies: A guide to the identification of novel oncogenes.
Indian J Hum Genet. 2011 May;17(2):43-4
|
2011 | |
| 649 |
Shetty S, Ghosh K Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review.
Thromb Res. 2011 Jun;127(6):505-12. Epub 2010 Oct 20. Review.(IF: 2.44)
|
2011 | |
| 650 |
Ghosh K, Shetty S Epidemiology, diagnosis, and management of von Willebrand disease in India.
Semin Thromb Hemost. 2011 Jul;37(5):595-601. (IF: 4.524)
|
2011 | |
| 651 |
Kawankar N, Jijina F, Ghosh K, Vundinti BR Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.
Cancer Epidemiol. 2011 Aug;35(4):e1-5.(IF: 2.010)
|
2011 | |
| 652 |
Vandana VP, Gorakshakar A Are mannose-binding lectin gene 2 (MBL2) polymorphisms and MBL deficiency associated with infections?
Indian J Hum Genet 2011 May; 17(2):45-47.
|
2011 | |
| 653 |
Desai –Gorakshakar K, Padwal V, Ghosh K. Women scientists in India are marching ahead.
Curr Sci 2011 Aug; 101: 3. (IF: 0.935)
|
2011 | |
| 654 |
Ghosh K. Haematology research in India: past, present and future
Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)
|
2011 | |
| 655 |
Shanbhag S, Shetty S, Ghosh K Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5.(IF: 2.597)
|
2011 | |
| 656 |
Shankarkumar U, Shankarkumar A, Chedda Z, Ghosh K Role of 14-bp deletion/insertion polymorphism in exon 8 of the HLA-G gene in recurrent spontaneous abortion patients.
J Hum Reprod Sci. 2011 Sep;4(3):143-6. (IF:)
|
2011 | |
| 657 |
Vundinti BR, Ghosh K Incidence of down syndrome: Hypotheses and reality
Indian J Hum Genet. 2011 Sep;17(3):117-9.
|
2011 | |
| 658 |
Umapathy S, Pawar A, Mitra R, Khuperkar D, Devaraj JP, Ghosh K, Khopkar U. Hla-a and hla-B alleles associated in psoriasis patients from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct;56(5):497-500.(IF: 0.979)
|
2011 | |
| 659 |
Ghosh K, Ghosh K, Chowdhury JR. Tuberculosis and female reproductive health.
J Postgrad Med. 2011 Oct-Dec;57(4):307-13.(IF: 1.389)
|
2011 | |
| 660 |
Colah RB, Gorakshakar AC & Nadkarni AH Invasive and non-invasive approaches for prenatal diagnosis of haemoglobinopathies: Experiences from India.
Ind. J. Med. Res. 2011 Oct; 134(4): 552-60.(IF: 1.837)
|
2011 | |
| 661 |
Vaidya S, Ghosh K, Vundinti BR. Recent developments in drug resistance mechanism in chronic myeloid leukemia: A review.
Eur J Haematol. 2011 Nov; 87(5):381-93. (IF 2.785)
|
2011 | |
| 662 |
Pai N, Shetty S, Ghosh K. Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Jan 14. [Epub ahead of print](IF: 1.496)
|
2010 | |
| 663 |
Vandana VPD, Deshpande NR, Ghosh K. Proteomic approach to autoimmune disorders : A review
Indian J Biotechnol 2010 Jan;9 : 13-7.(IF:--)
|
2010 | |
| 664 |
Korgaonkar S, Ghosh K and Babu Rao V. Clinical, Genetic and Cytogenetic study of Fanconi anemia in an Indian population
Hematology 2010 Jan;15(1):58-62. (IF:--) .
|
2010 | |
| 665 |
Warang P, Nair S, Nadkarni A, Ghosh K, Colah RB Hb H disease due to homozygosity for a rare alpha2-Globin Variant, Hb Sallanches
Hemoglobin 2010 Jan; 34(1): 45-48.(IF:1.106)
|
2010 | |
| 666 |
Ghosh K Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
Indian J Hum Genet. 2010 Jan;16(1):6-7.
|
2010 | |
| 667 |
Nair S, Nadkarni A, Warang P, Bhave A, Ghosh K, Colah R. Five alpha globin chain variants identified during screening for haemoglobinopathies.
Eur J Clin Invest. 2010 Mar; 40(3):226-32. (IF:2.784)
|
2010 | |
| 668 |
Shetty S, Mota L, Ghosh K. Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency
Clin Chim Acta. 2010 Feb;411(3-4):291. (IF:2.960)
|
2010 | |
| 669 |
Swaminathan S, Madkaikar MR, Ghosh K, Vundinti BR, Kerketta L, Gupta M. Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation.
Eur J Haematol. 2010 Feb 1;84(2):180-2.(IF:1.478)
|
2010 | |
| 670 |
Nadkarni AH, Nair SB, Italia KY, Warang P, Dalvi M, Ghosh K, Colah RB. Molecular diversity of hemoglobin H disease in India.
Am J Clin Pathol. 2010 Mar;133(3):491-4. (IF 3.576)
|
2010 | |
| 671 |
Italia KY, Jijina FF, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study
J Clin Pathol. 2010 Feb;63(2):147-50. (IF 1.78)
|
2010 | |
| 672 |
Vandana VP, Patwardhan M, Nadkarni A, Ghosh K Fc ? RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India
Autoimmune Dis 2010 Feb 9;2010.
|
2010 | |
| 673 |
Kanjaksha Ghosh ??Thalassemia- What is it ?
Physician’ s Digest 2010; Pg: 63-69.
|
2010 | |
| 674 |
Colah R, Gorakshakar A, and Nadkarni A Global burden, distribution and prevention of ?-Thalassemia and hemoglobin E disorders.
Expert Rev. Hematol 2010 Mar, 3(1):103-117.(IF:1.161)
|
2010 | |
| 675 |
Italia K, Jijina F, Chandrakala S, Nadkarni A, Sawant P, Ghosh K, Colah R. Exposure to hydroxyurea during pregnancy in sickle ?-thalassemia - A report of 2 cases.
J.Clin. Pharmacol 50; 231-4; 2010.(IF:3.59)
|
2010 | |
| 676 |
Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, Bellgard M, Bittles AH. Profiling ?-Thalassaemia mutations in India at state and regional levels: implications genetic education, screening and counseling programmes.
Hugo J. 2009 Dec; 3(1-4): 51–62.
|
2010 | |
| 677 |
Vandana VPD, Patwardhan MM, Ghosh K Anti-nucleosome antibodies as a disease marker in systemic lupus erythematosus and its correlation with disease activity and other autoantibodies
Indian J Dermatol Venereol Leprol. 2010 Mar-Apr;76(2):145-9.(IF: 0.976)
|
2010 | |
| 678 |
Kasatkar P. Shetty S, Ghosh K. VWF pseudogene; Mimics, masks and spoils.
Clin Chim Acta. 2010 Apr 2;411(7-8):607-9.(IF: 2.661)
|
2010 | |
| 679 |
Jain A, Shetty S, Kulkarni B, Ghosh K. Association of factor VII gene polymorphisms with Budd Chiari syndrome
Blood Coagul Fibrinolysis. 2010 Apr; 21(3):296-7. (IF 1.506)
|
2010 | |
| 680 |
Madan N, Sharma S, Sood SK, Colah R, Bhatia HM Frequency of B-thalassemia trait and other hemoglobinopathies in northern and western India.
Indian J Hum Genet. Jan-Apr 2010; 16(1): 16-25.
|
2010 | |
| 681 |
Kanjaksha Ghosh, Kinjalka Ghosh Advances in Haematological Pharmacotherapy in 21st Century.,
Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40.
|
2010 | |
| 682 |
Vandana VP, Deshpande N, Nadkarni A, Patwardhan M, Surve P, Ghosh K. Fc gamma R IIIBpolymorphisms:their association with clinical manifestation and autoantibodies in SLE patients from western India
Int J Rheum Dis. 2010 May; 13 (2): 138-43.(IF:0.205)
|
2010 | |
| 683 |
Vaswani RK, Dharaskar PG, Kulkarni SS, Ghosh K. \ Iron deficiency as a risk factor for first febrile seizure.
Indian Pediatr. 2010 May;47(5):437-9. (IF: 0.9)
|
2010 | |
| 684 |
Ghosh K, Gorakshakar A Integration of modern genetic knowledge and technology into public health in India.
Indian J Hum Genet. 2010 May;16(2):45-6.
|
2010 | |
| 685 |
Muranjan M, Chaudhari T and Babu Rao V. Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down Syndrome.
Indian Pediatrics 2010 May 17; 47(5): 429-432. (IF: 0.9)
|
2010 | |
| 686 |
Shankarkumar U, Pawar A, Ghosh K, Bajpai S and Pazare A. Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus-infected patients of Mumbai, India
Intl J Immunogenet 2010 Jun; 37(3): 199-204.(IF: 1.62)
|
2010 | |
| 687 |
Gangodkar S, Jain P, Dixit N, Ghosh K, Basu A Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure
J Electron Microsc (Tokyo). 2010 Jun;59(6):503-11. (IF 1.77)
|
2010 | |
| 688 |
Colah R, Gorakshakar A, Phanasgaonkar S, D Souza E, Nadkarni A, Surve R, Sawant P, Master D, Patel R, Ghosh K, Mohanty D. Epidemiology of beta – thalassemia in Western India:mapping the frequencies and mutations in sub – regions of Maharashtra and Gujarat
Br J Haematol. 2010. Jun; 149(5): 739-47.(IF 4.942)
|
2010 | |
| 689 |
Mota L, Shetty S, Idicula-Thomas S, Ghosh K. Molecular basis of factor X deficiency cases from India
Haemophilia 2010 Jul 1; 16(4): 693-7. ( IF 2.394)
|
2010 | |
| 690 |
Shetty S, Kulkarni B, Pai N, Mukundan P, Kasatkar P, Ghosh K. JAK2 mutations across a spectrum of venous thrombosis cases.
Am. J. Clin. Pathol 2010 Jul; 134(1):82-5. (IF 2.47)
|
2010 | |
| 691 |
Ghosh K Bachelor of rural health care: cutting the root and watering the stem!
Natl Med J India. 2010 Jul-Aug;23(4):250. (IF 0.541)
|
2010 | |
| 692 |
Vandana VP, Borse V, Ghosh K. PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.
J Postgrad Med. 2010 Jul-Sep;56(3):239-42. Review. (IF:1.389)
|
2010 | |
| 693 |
Ghosh K, Ghosh K Sequential serologic testing for common viral markers in blood units in India is probably not cost effective.
Transfusion 2010 Aug;50(8): 1854-55. (IF 3.3)
|
2010 | |
| 694 |
Pai N, Shetty S, Ghosh K Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Aug; 89(8): 835-6. (IF: 2.688)
|
2010 | |
| 695 |
Mukherjee MB, Nadkarni AH, Gorakshakar AC, Ghosh K, Mohanty D, Colah RB. Clinical, hematologic and molecular variability of sickle cell-? thalassemia in western India
Indian J Hum Genet. 2010 Sep;16(3):154-8.
|
2010 | |
| 696 |
Kasatkar P, Shetty S, Ghosh K. Delayed vitamin K deficiency as a cause of bleeding : still a concern in the 21st century!
Blood Coagul Fibrinolysis. 2010 Sept; 21(6):608-10. (IF 1.506)
|
2010 | |
| 697 |
Shankarkumar U. Complexities and similarities of HLA antigen distribution in Asian subcontinent.
Indian J Hum Genet. 2010 Sep;16(3):108-10.
|
2010 | |
| 698 |
Burdrukkar A, Shahid T, Murthy V, Hussain T, Mulherkar R, Babu Rao V, Deshpande M, Sengar M, Ghosh Laskar S, Agarwal JP: Squamous cell carcinoma of tongue in a patient with fanconi’s anemia treated with radiation therapy: Case Report and review of literature.
Head & Neck 2010 Oct;32(10):1422-27.(IF: 2.4)
|
2010 | |
| 699 |
Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar MR, Ghosh K, Colah RB, Alper SL. Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
Am J Hematol 2010 Oct;85(10):824-8.(IF 3.576)
|
2010 | |
| 700 |
Black ML, Sinha S, Agarwal S, Colah R, Das R, Bellgard M, Bittles AH. A descriptive profile of ?-Thalassaemia mutations in India, Pakistan and Sri Lanka
J Community Genet. 2010 Oct 10.
|
2010 | |
| 701 |
Korgaonkar S, Ghosh K, Jijina F and Vundinti BR. Chromosomal breakage study in children suspected with fanconi anemia in the Indian population.
J Pediatr Hematol Oncol 2010 Nov;32(8):606-10.(IF: 0.998)
|
2010 | |
| 702 |
Chandrakala S, Jijina F and Ghosh K Diffuse alveolar haemorrhage with severe haemophilia.
Haemophilia 2010 Nov;16(6): 962-4. (IF 2.394)
|
2010 | |
| 703 |
Nair PS, Shetty S and Ghosh K. Double mutations in haemophilia: muddling strangers or indifferent partners in crime?
Haemophilia 2010 Nov;16(6):970-1. (IF 2.394)
|
2010 | |
| 704 |
Italia KY, Jijina FF, Jain D, Merchant R, Nadkarni AH, Mukherjee M, Kanjaksha G, Colah RB The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies
Clin Biochem 2010 Nov;43(16-17):1329-1332.(IF: 2.079)
|
2010 | |
| 705 |
Vandana VP, Surve P, Ghosh K. Mannose Binding Lectin (MBL) in Autoimmunity and its role in systemic lupus erythematosus (SLE).
J Assoc Physicians India 2010 Nov; 58(11):688-90.
|
2010 | |
| 706 |
Nair PS, Shetty S, Kulkarni B, Ghosh K. Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.
Clin Chim Acta 2010 Dec 14; 411(23-24):2004-8.(IF:2.661)
|
2010 | |
| 707 |
Vundinti BR, Korgaonkar S, Ghosh K. Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.
Indian J Cancer. 2010 Oct-Dec;47(4):397-9. (IF: 0.961)
|
2010 | |
| 708 |
Pai N, Shetty S, Kulkarni B, Ghosh K. Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700.(IF:1.476)
|
2010 | |
| 709 |
Shankarkumar U, Pawar A, Devraj JP, Bhupali K, Ghosh K. The HLA system- A review.
Anthopologist, 2010;Special Vol.6:183-97.
|
2010 | |
| 710 |
Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R. Hydroxyurea in sickle cell disease - A study of clinico-pharmacological efficacy in the Indian haplotype
Blood Cells Mol Dis. 2009 Jan-Feb; 42(1): 25-31.(IF: 2.549)
|
2009 | |
| 711 |
Iyer YS, Vasantha K, Pujari V, Jadhav S, Ghosh K Murine monoclonal anti-H as typing reagent.
Indian J Med Res 2009 Jan; 129(1): 72-74. (IF: 1.883)
|
2009 | |
| 712 |
Nadkarni A, Gorakshakar A, Surve R, Sawant P, Phanasgaonkar S, Nair S, Ghosh K, Colah RB Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009 Jan-Mar; 33(1):59-65.(IF: 1.106)
|
2009 | |
| 713 |
Vijapurkar M, Ghosh K, Shetty S. Novel mutations in GP IIb gene in Glanzmann’s thrombasthenia from India.
Platelets. 2009 Feb;20(1):35-40.(IF: 2.271)
|
2009 | |
| 714 |
Ghosh K, Shetty S Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors.
Clin Rev Allergy Immunol. 2009 Oct;37(2):58-66. (IF: 2.080)
|
2009 | |
| 715 |
Vijapurkar M, Mota L, Shetty S, Ghosh K. Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
Haemophilia. 2009 Jan;15(1):199-202. (IF: 2.394)
|
2009 | |
| 716 |
Shankarkumar U, Pawar A, Ghosh K HIV-1 evolution drug resistance, and host genetics: The Indian scenario.
Virus Adaption and Treatment 2009; 1:1-4.(IF: open access)
|
2009 | |
| 717 |
Kedar PS, Hamada T, Warang P, Nadkarni A, Shimizu K, Fujji H, Ghosh K,Kanno H, Colah R. Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes
Clin Genet. 2009 Feb;75(2):157-62.(IF: 3.18)
|
2009 | |
| 718 |
Vora S, Shetty S, Khare M, Ghosh K Placental histomorphology in unexplained foetal loss with thrombophilia.
Indian J Med Res 2009 Feb; 129(2): 144-49.(1.883) (IF 1.826)
|
2009 | |
| 719 |
Devraj JP, Shankarkumar U, Ghosh K. Increased frequency of HLA-B7 among B27 – negative, seronegative spondarthritis patients from Mumbai, Western India.
Br J Biomed Sci 2009 Jan-Mar; 66(1): 25-27.(0.590)
|
2009 | |
| 720 |
Quadros L, Ghosh K, Shetty S Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes
J Pediatr Hematol Oncol. 2009 Mar;31(3):157-60.(IF:1.176)
|
2009 | |
| 721 |
Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K. Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First
Thromb Haemost 2009 Apr;101(4):785-87.(IF:3.413)
|
2009 | |
| 722 |
Pai N, Shetty SD, Ghosh K Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis.
Clin Appl Thromb Hemost. 2009 Apr 28. [Epub ahead of print] (IF: 1.286)
|
2009 | |
| 723 |
Ghosh K, Quadros L, Shetty S Spectrum of factor IX gene mutations causing haemophilia B from India.
Blood Coagul Fibrinolysis. 2009 Jul; 20(5):333-336.(IF:1.506)
|
2009 | |
| 724 |
Shankarkumar U, Vandana VPD, Patwardhan M, Pawar A, Almeida A and Ghosh K HLA alleles in anti-endothelial cell antibody positive Indian SLE patients
Int J Hum Genet 2009 Apr-Jun; 9(2): 127-30. (IF: Nil)
|
2009 | |
| 725 |
Ghosh K, Shetty S, Quadros L, Kulkarni B. Double mutations causing haemophilia B: a double whammy!
Br J Haematol. 2009 May;145(3):433-5. (IF: 3.195)
|
2009 | |
| 726 |
D Souza E, Ghosh K, Colah R A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies
Cytometry B Clin Cytom. 2009 May 76(B)(3): 175-80. (IF:1.439)
|
2009 | |
| 727 |
Ghosh K, Shetty S, Tulsiani M Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia.
Clin Appl Thromb Hemost. 2009 May-Jun;15(3):277-82. Review. (IF: 1.286)
|
2009 | |
| 728 |
Colah R, Gorakshakar A, Nadkarni A, Phanasgaonkar S, Surve R, Sawant P, Mohanty D, Ghosh K. Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
Blood Cells Mol Dis. 2009 May-Jun;42(3):241-6.(IF: 2.549)
|
2009 | |
| 729 |
Kanjaksha Ghosh, Manisha Patwardhan, Vandana VP Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas
Rheumatol Int 2009 Jul;29(9):1047-50.(IF:1.327)
|
2009 | |
| 730 |
Umapathy Shankar kumar, Krishna kumar N Shah, Kanjaksha Ghosh HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India.
Epilepsia 2009 Jul; 50(7): 1837-38.(IF:3.733)
|
2009 | |
| 731 |
Ghosh K, Shetty S, Vora S Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss.
Int J Gynaecol Obstet. 2009 Jul 21. [Epub ahead of print] (IF: 1.228)
|
2009 | |
| 732 |
Ghosh K Challenges of haemophilia care in India: lest we forget.
Indian J Med Res. 2009 Jul;130(1):87-8. (IF 1.883)
|
2009 | |
| 733 |
Shetty S, Ghosh K Anti-phospholipid antibodies and other immunological causes of recurrent foetalloss--areview of literature of various therapeutic protocols.
Am J Reprod Immunol. 2009 Jul;62(1):9-24. Review.(IF 2.172)
|
2009 | |
| 734 |
Prabu G, Iyer YS, Shankarkumar U, Ghosh K, Nachiappan V Monoclonal antibody produced against calf thymus histone.
Hybridoma (Larchmt). 2009 Aug;28(4):277-80.(IF 0.559)
|
2009 | |
| 735 |
Shankarkumar U, Pawar A, Prabu G, Ghosh K. Role of HLA class I (HLA-A, B) and HLA class II (HLA-DRB, DQB) in HIV-1 patients with and without pulmonary tuberculosis.
J Acquir Immune Defic Syndr. 2009 Aug 15;51(5):640-1.(IF 4.570)
|
2009 | |
| 736 |
Madkaikar MR, Gupta M, Jijina F, Ghosh K. Paroxysmal Nocturnal Haemoglobinuria (PNH): diagnostic tests, advantages & limitations.
Eur J Haematol. 2009 Aug ; 83:503-511.(IF 1.478).
|
2009 | |
| 737 |
Shetty S, Vora S, Kulkarni B, Mota L, Ghosh K Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency cause, consequence or a consequential cause?
Haemophilia. 2009 Sep;15(5):1104-8. (IF 2.394)
|
2009 | |
| 738 |
Italia KY, Jijina FJ, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB. Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India
Clin Chim Acta. 2009 Sep;407(1-2):10-5. (IF:2.960)
|
2009 | |
| 739 |
Chalvam R, Colah RB, Mohanty D, Ghosh K, Mukherjee MB. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Blood Cells Mol Dis. 2009 Sep-Oct;43(2):156-7.(IF: 2.549)
|
2009 | |
| 740 |
Ghosh K, Ghosh K. Private practice in India.
Natl Med J India. 2008 Nov-Dec;21(6):328-9.(IF:0.911)
|
2009 | |
| 741 |
Vaswani RK, Dharaskar PG, Kulkarni SS, Ghosh K. Iron Deficiency as a Risk Factor for First Febrile Seizure
Indian Pediatr. 2009 Sep 3. [Epub ahead of print](IF:0.956)
|
2009 | |
| 742 |
Mota L, Shetty S, Idicula-Thomas S, Ghosh K Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
Clin Chim Acta. 2009 Nov;409(1-2):106-11.Epub 2009 Sep 13. (IF:2.960)
|
2009 | |
| 743 |
Ghosh K, Ross C The teacher and the taught: medical education in India at the crossroads.
Natl Med J India. 2009 May-Jun:22(3):147-9.(IF:0.911)
|
2009 | |
| 744 |
Ghosh K, Shetty S, Sahu D. Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI).
Haemophilia. 2009 Sep 23. [Epub ahead of print] (IF: 2.394)
|
2009 | |
| 745 |
Vundinti BR, Kerketta L, Jijina F, Ghosh K. Cytogenetic study of myelodysplastic syndrome from India.
Indian J Med Res. 2009 Aug;130(2):155-9. (IF: 1.883)
|
2009 | |
| 746 |
Pai N, Shetty S, Kulkarni B, Ghosh K. Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2009 Nov 10. [Epub ahead of print] (IF: 1.286).
|
2009 | |
| 747 |
Vundinti BR, Korgaonkar S, Ghosh K. Familial small supernumerary marker chromosome (sSMC) (14)(:P(11)-q(11):) In a child with translocation down syndrome
Indian J Pediatr. 2009 Dec; 76(12):1265-7. (IF:0.646)
|
2009 | |
| 748 |
Misri R, Khopkar U, Shankarkumar U, Ghosh K. Comparative case control study of clinical features and human leukocyte antigen susceptibility between familial and nonfamilial vitiligo
Indian J Dermatol Venereol Leprol. 2009 Nov-Dec;75(6):583-7.(IF:0.588)
|
2009 | |
| 749 |
Kanjaksha Ghosh. Molecular evolution of Globin Gene Pathology-Its Driver, Challenges and
Journal of the Asiatic Society 2009 Vol. 51(20):73-8.(IF:--)
|
2009 | |
| 750 |
Roshan Colah. Antenatal Diagnosis of Thalasssemias-Diagnostic technology suitable for the country
Journal of the Asiatic Society 2009 Vol 51 (2):69-72(IF:--)
|
2009 | |
| 751 |
Tripathy AS, Shankarkumar U, Chadha MS, Ghosh K, Arankalle VA. Association of HLA alleles with hepatitis C infection in Maharashtra, Western India
Indian J Med Res. 2009 Nov;130(5):550-5. (IF: 1.883)
|
2009 | |
| 752 |
Vandana VP, Ghosh K. Development of Anti-neutrophil Cytoplasmic antibodies (ANCA) and Vasculitis in BALB/c Mice: A Prototype of human ANCA associated disease.
J. Appl. Anim. Res. 2009 Dec;36:297-302.(IF:0.178)
|
2009 | |
| 753 |
Mamta Muranjan, Tejasvi Choudhary and Baburao Vundinti. Phenotypic heterogencity and parental origin of extrachromosome 21 in down syndrome.
Indian Pediat. 2009 July 1; [Epub ahead of print] (IF:0.956)
|
2009 | |
| 754 |
Ajit Gorakshakar, Colah RB. Cascade screening for ?-thalassemia; A practical approach for identifying and counseling carriers in India.
Indian J. Comm. Med. 2009;Oct 34(4) :354-56.
|
2009 | |
| 755 |
Budrukkar A, Shahid T, Murthy V, Hussain T, Mulherkar R, Babu Rao V, Deshpande M, Sengar M, Ghosh-Laskar S, Agarwal JP Squamous cell carcinoma of base of tongue in a patient with Fanconi’s anemia treated with radiation therapy: case report and review of literature.
Head & Neck 2009; Aug 11 (E-pub ahead of print)(IF: 2.01).
|
2009 | |
| 756 |
Ghosh K. Geographical heterogeneity of immigration and career paths of medical graduates in India.
Natl Med J India. 2009 Jul-Aug;22(4):218.(IF:0.911)
|
2009 | |
| 757 |
Vandana VPD, Ghosh K. Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
Indian J Dermatol. 2009 Jul;54(3):258-62.
|
2009 | |
| 758 |
Singh R, Vandana VP, Patwardhan M, Ghosh K APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases.
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 98-102.
|
2009 | |
| 759 |
Mukherjee MB, Tripathy V, Colah RB, Solanki PK, Ghosh K, Reddy BM, Mohanty D Microsatellite diversity among the primitive tribes of India
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 114-120.
|
2009 | |
| 760 |
Basu A, Jain P, Gangodkar SV, Shetty S, Ghosh K. Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.
FEMS Immunol Med Microbiol. 2008 June ; 53 (1):46-51 (IF 2.494)
|
2008 | |
| 761 |
Ghosh K, Vandana VP Background noise of infection for using ANCA as a diagnostic tool for vasculitis in tropical and developing countries.
Parasitol Res. 2008 Apr;102(5):1093-5. Epub 2008 Feb 24. (IF 3.938)
|
2008 | |
| 762 |
Shankarkumar U, Pawar A, Ghosh K. Implications of HLA sequence-based typing in transplantation.
J PostGrad Med. 2008 Jan-Mar;54(1):41-4. (IF 1.589)
|
2008 | |
| 763 |
Ghosh K, Madkaikar MR, Jijina F Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage
Acta Haematol. 2008 Feb 20;119(2):69-72 (IF 1.316)
|
2008 | |
| 764 |
Ghosh K, Shetty S Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia.
Haemophilia. 2008 Mar;14(2):392-3. [18179571](IF 2.394)
|
2008 | |
| 765 |
Ghosh K, Shetty S, Vora S, Salvi V. Successful pregnancy outcome in women with bad obstetric history and recurrent fetal loss due to thrombophilia: effect of unfractionated heparin and low--molecular weight heparin.
Clin Appl Thromb Hemost. 2008 Apr;14(2):174-9. [18160603] (IF 1.286)
|
2008 | |
| 766 |
Ghosh K, Shetty S. Blood coagulation in falciparum malaria-a review.
Parasitol Res. 2008 Mar;102(4):571-6. [18066597] (IF 3.938)
|
2008 | |
| 767 |
Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
J Hum Genet. 2008;53(2):181-4. [18043863] (IF: 2.431)
|
2008 | |
| 768 |
Shetty S, Ghosh K, Quadros L. Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
Eur J Haematol. 2008 Jan;80(1):87-9. [18028421] (IF 1.478)
|
2008 | |
| 769 |
Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K. A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss.
Eur J Obstet Gynecol Reprod Biol 2008 Apr;137(2):136-40. (IF 1.736)
|
2008 | |
| 770 |
Shankarkumar U, Pawar A, Gaonkar P, Parsannawar D, Salvi V, Ghosh K. HLA allele associations in idiopathic recurrent spontaneous abortion patients from India.
J. Hum Reprod. Sci, 2008 Jan-Jun;1(1):19-24.
|
2008 | |
| 771 |
Ghosh K, Shetty S and Ghosh K A high cost low volume disease: suitable preventive strategies for developing and developed countries.
The Open Hematol J 2008; 2: 20-4.
|
2008 | |
| 772 |
Ghosh K, Gangodkar S, Jain P, Shetty S, Ramjee S, Poddar P,Basu A Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy
J Electron Microsc(Tokyo) 2008 Jun; 57(3):113-8. (IF 1.05)
|
2008 | |
| 773 |
Mohanty D, Mukherjee MB, Colah RB, Wadia M, Ghosh K, Chottray GP, Jain D, Italia Y, Ashokan K, Kaul R, Shukla DK & Muthuswamy V Iron deficiency anaemia in sickle cell disorders in India.
Indian J Med Res 2008 Apr; 127(4):366-9. [18577791](IF 1.826)
|
2008 | |
| 774 |
Ghosh K, Vandana VP, Patwardhan M and Gupta M. Antiendothelial cell antibodies in systemic lupus erytematosus.
Intl J Rheumatol Dis 2008; 11:121-6.(IF 0.205)
|
2008 | |
| 775 |
Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K. A novel G143D mutation in the NADH-cytochrome b(5) reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood Cells Mol Dis 2008 May-Jun; 40(3):323-7. [17964195] (IF 2.549)
|
2008 | |
| 776 |
Ghosh K, Shetty S antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
Blood Coagul Fibrinolysis 2008 Jul;19(5):464-65.[18600102] (IF 1.506)
|
2008 | |
| 777 |
Shetty S, Ghosh K Reduced clinical severity in a mutationally well – characterized cohort of severe hemophilia with associated thrombophilia
Am. J. Clin Pathol 2008 Jul; 130(1) 84-7. (IF 2.18)
|
2008 | |
| 778 |
Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Sawant P, Surve R, Mohanty D, Ghosh K Hb Showa Yakushi [beta 110(612) Leu?Pro ] in three families from Western India:First report on homozygous Hb showa Yakushiji.
Blood Cells Mol Dis. 2008 May 19. (IF 2.549)
|
2008 | |
| 779 |
Ghosh K, Shetty S, Mota L Aspirin resistance in patients with coronary artery disease- which test to use in routine management?
Blood Coagul Fibrinolysis .2008 Jun: 19(4) : 324-6. (IF 1.506)
|
2008 | |
| 780 |
Vundinti BR, Kerketta L, Madkaikar MR, Jijina F, Ghosh K translocation in a new variant of +(8;21) acute myeloid leukemia involving Xp22.
Indian J Cancer. 2008 Jan-Mar; 45(1):30-2.
|
2008 | |
| 781 |
Vijapurkar M, Ghosh K, Shetty S, McLane MA, Moura da Silva AM,Butera D. A simple, novel and robust test to diagnose type I glanzmann thrombasthenia
Haematologica. 2008 May; 93 (5) :797-8. (IF 6.416)
|
2008 | |
| 782 |
Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K. Prevalence and molecular characterization of alpha thalassemia syndromes among Indians
Genet Test. 2008 Jun; 12(2) : 177-80. (IF 1.7)
|
2008 | |
| 783 |
Meera V, Jijina F, Shrikande M, Madkaikar MR, Ghosh K Twin pregnancy in a patient of chronic myeloid leukemia on imatinib therapy
Leuk Res 2008 Oct; 32(10) : 1620-2. (IF 2.555)
|
2008 | |
| 784 |
Kulkarni SS, Colah R, Gorakshakar A, Gupte S, Vasantha K, Mohanty D,Ghosh K. Frequency of Partial D in Western India.
Transf Med 2008 Apr; 18(2):91-6.(IF 2.155)
|
2008 | |
| 785 |
Quadros L, Ghosh K, Shetty S Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India.
Haemophilia. 2008 May; 14 (3) : 628-9. (IF 2.394)
|
2008 | |
| 786 |
Colah R, Surve R. Wadia M, Solanki P, Mayekar P, Thomas M, Gorakshakar A, Dastur A, Mohanty D. Carrier screening for ?-thalassemia during pregnancy in India: a 7 year evaluation.
Genet Test. 2008 Jun : 12(2): 181-5. (IF 1.7).
|
2008 | |
| 787 |
Sadawarte S, Jijina F, Nair CK, Seth S, Ghosh K. An unusual presentation of pediatric acute leukemia
Ind J Hematol Blood Transf 2008; 24:16-22.
|
2008 | |
| 788 |
Prabhu R, Jijina F, Shetty S, Ghosh K Successful surgery in severe haemophilia – a two stage replacement therapy in resource poor countries.
Haemophilia 2008 Jul 3. (IF 2.394)
|
2008 | |
| 789 |
Edna DSouza, Pratibha M. Sawant, Anita H. Nadkarni, Ajit Gorakshakar, Dipika Mohanty, Kanjaksha Ghosh, Roshan B. Colah Evaluation of the Use of Monoclonal Antibodies and Nested PCR for Noninvasive Prenatal Diagnosis of Hemoglobinopathies in India
AJCP Aug 2008; 130(2):202-209.(If: 2.89)
|
2008 | |
| 790 |
Anita Nadkarni, Marukh Wadia, Ajit Gorakshakar, Ryoiti Kiyama, Roshan B.Colah, Dipika Mohanty Molecular Characterization of ??-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population
Hemoglobin Sep-Oct 2008, Vol. 32, No. 5: 425–433.(IF: 1.00)
|
2008 | |
| 791 |
Kedar PS, Kazuyuki Shimizu, Kanjaksha Ghosh, Hisaichi Fujji, Roshan A proteomic analysis of CBA-Pk-1slc/Pk-1slc mice with Red Blood Cell Type Pyruvate Kinase deficiency using 2DE together with MALDI-TOF-MF analysis
FASEB J 2008;22:1025. (IF 6.721)
|
2008 | |
| 792 |
Shadaan Abid, Anurupa Maitra, Pervin Meherji, Zareen Patel, Seema Kadam, Jatin Shah, Rupin Shah, Vijay Kulkarni, V BabuRao and Jyotsna Gokral. Clinical and Laboratory evaluation of idiopathic Male infertility in a secondary referral center in India.
J Clin Lab Analysis 2008; 22: 29-38.
|
2008 | |
| 793 |
Malay Mukherjee. Laboratory diagnosis of sickle cell syndrome.
J Community Med 2008 Jan; 4(1): 11-14.
|
2008 | |
| 794 |
Kanjaksha Ghosh, Shrimati Shetty and Kinjalka Ghosh Hemophilia: A High Cost Low Volume Disease:Suitable preventive strategies for developing and developed countries.
The Open Hematology Journal, 2008; 2:20-24.
|
2008 | |
| 795 |
Konkankar S, Shankarkumar U HLA DRB1 alleles in chronic hepatitis B infected patients
Intl J Hum Genet 2008; 72: 275.
|
2008 | |
| 796 |
Shankarkumar U, Ghosh K MHC non-HLA gene polymorphisms in transplantation
Indian J Pathol Microbiol
|
2007 | |
| 797 |
Phanasgaonkar S, Colah R, Ghosh K, Mohanty D, Gupte S Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India
Br J Biomed Sci
|
2007 | |
| 798 |
Madkaikar MR, Gupta M, Ghosh K, Swaminathan S, Sonawane L, Mohanty D Optimizing methods of red cell sedimentation from cord blood to maximize nucleated cell recovery prior to cryopreservation
Br J Biomed Sci
|
2007 | |
| 799 |
Kulkarni SS, Gupte SC, Vasantha K, Mohanty D, Ghosh K Varied distribution of RhD epitopes in the Indian population
Natl Med J India
|
2007 | |
| 800 |
Rao VB, Korgaonkar S, Kerketta L, Ghosh K Differentiation of Nijmegen breakage syndrome from Fanconi anemia
Genet Mol Res
|
2007 | |
| 801 |
Ghosh K, Shetty S, Kulkarni B Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients
Haemophilia
|
2007 | |
| 802 |
Kedar PS, Nampoothiri S, Sreedhar S, Ghosh K, Shimizu K, Kanno H, Colah RB First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation
Genet Mol Res
|
2007 | |
| 803 |
Madkaikar MR, Ghosh K, Gupta M, Swaminathan S, Mohanty D Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells
Acta Haematol
|
2007 | |
| 804 |
Ghosh K, Ghosh K Pathogenesis of anemia in malaria: a concise review
Parasitol Res
|
2007 | |
| 805 |
Vora S, Shetty S, Ghosh K Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
Blood Coagul Fibrinolysis
|
2007 | |
| 806 |
Nadkarni A, Surve R, Colah R, Ghosh K, Holay M, Dani A, Shrikhande A, Bharti V, Suryawanshi S. Thalassemia intermedia due to homozygosity for an Asian Indian(Agammadeltabeta) degrees deletional inversion.
Clin Chim Acta. 2007 Oct;385(1-2):81-3. Epub 2007 Jul 19. (IF 2.960)
|
2007 | |
| 807 |
Ghosh K, Ghosh K. Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia:report of three cases.
Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26.(IF 2.615)
|
2007 | |
| 808 |
Shetty S, Vora S, Kulkarni B, Mota L, Vijapurkar M, Quadros L, Ghosh K Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.
Br J Haematol. 2007 Aug;138(4):541-4.(IF 3.195)
|
2007 | |
| 809 |
Kulkarni SS, Vasantha K, Gupte SC, Mohanty D, Ghosh K. Potential of commercial anti-D reagents in the identification of partial D variants in Indian population.
Indian J Med Res. 2007 May;125(5):641-4. [17642499] (IF 1.823)
|
2007 | |
| 810 |
Vora S, Ghosh K, Shetty S, Salvi V, Satoskar P. Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
Thromb J. 2007 Jul 4;5:9. (IF 1.0)
|
2007 | |
| 811 |
Ghosh K, Vora S, Shetty S. Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis.
Br J Haematol. 2007 Aug;138(4):555-7. [17590183] (IF 3.195)
|
2007 | |
| 812 |
Ghosh K, Madkaikar MR, Jijina F, Shetty S Fractures of long bones in severe haemophilia.
Haemophilia. 2007 May;13(3):337-9. (IF 2.394).
|
2007 | |
| 813 |
Varla-Leftherioti M, Keramitsoglou T, Spyropoulou-Vlachou M,Papadimitropoulos M, Kontopoulou-Antonopoulou V, Tsekoura C, Sankarkumar U, Paparistidis N, Ghosh K, Pawar A, Vrani V, Daniilidis M, Parapanissiou E, Diler AS, Carin M, Stavropoulos-Giokas C 14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component.
Tissue Antigens. 2007 Apr; 69 Suppl 1:297-303. (IF 3.024)
|
2007 | |
| 814 |
Ghosh K, Ghosh K. Microarray genetic screening: the other side of the coin.
Lancet. 2007 Mar 24;369(9566):992. [17382825] (IF 33.63)
|
2007 | |
| 815 |
Mota L, Ghosh K, Shetty S Second trimester antenatal diagnosis in rare coagulation factor deficiencies.
J Pediatr Hematol Oncol. 2007 Mar;29(3):137-9. [17356389] (IF 1.176)
|
2007 | |
| 816 |
Umapathy S, Pawar A, Ghosh K. Specific human leukocyte antigen alleles associated with HIV-1 infection in an Indian population.
J Acquir Immune Defic Syndr. 2007 Apr 1;44(4):489-90. [17353719]. (IF 4.262)
|
2007 | |
| 817 |
Quadros L, Ghosh K, Shetty S. A common G10430A mutation (Gly 60 Ser) in the factor IX gene presence of moderate and mild hemophilia B in the majority describes the presence of moderate and mild hemophilia B in the majority of the Gujarat population.
Ann Hematol. 2007 May;86(5):377-9. [17308903] (IF 2.688)
|
2007 | |
| 818 |
Shetty S, Ghosh K. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
Haemophilia. 2007 Mar;13(2):172-7. [17286770] (IF 2.394)
|
2007 | |
| 819 |
Ghosh K, Madkaikar MR, Shrikhande M Osteoporosis in young haemophiliacs from western India.
Am J Hematol. 2007 Jun;82(6):453-7. [17278114] (IF 3.576)
|
2007 | |
| 820 |
Chalvam R, Mukherjee MB, Colah RB, Mohanty D, Ghosh K G6PD Namoru (208 T C) is the major polymorphic variant in the tribal populations in southern India.
Br J Haematol. 2007 Feb;136(3):512-3. No abstract available. (IF 3.195)
|
2007 | |
| 821 |
Ghosh K, Khare A, Shetty S, Kulkarni B. Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern of response to oral folic acid, vitamin B12, B6 therapy
Clin Chim Acta. 2007 Feb;377(1-2):281-2. Epub 2006 Sep 22. (IF 2.960)
|
2007 | |
| 822 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Ind. J. of Hum Genet. 2007 Sep –Dec; 13(3):79-85. (IF 0.11 )3
|
2007 | |
| 823 |
Ghosh K,Khare A, Shetty S Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India.
Indian Heart J 2007: 59(3):242-5.
|
2007 | |
| 824 |
Ernest Beutler, Duparc S, Doumbo O, Ghosh K, Vinicious M, de Lacerda G, Lapierre D, Looareesuwan S, Premji Z,Vulliamy T, Vhitty C. Lapierre D, Looareesuwan S, Premji Z,Vulliamy T, Vhitty C. Glucose-6- phosphate dehydrogenase deficiency and antimalarial drug development.
Am J Trop Med Hyg 2007 Oct;77(4):779-89. Rev. [17978087]. (IF 2.8)
|
2007 | |
| 825 |
Korgaonkar Seema, Babu Rao V, Kerketta L, Ghosh K. Chromosomal breakage in myelodysplatic syndrome.
Asian Pacific J Cancer Preview 2007; 8:151-4. (IF: 1.11)
|
2007 | |
| 826 |
Shankarkumar U, Pawar A, and Ghosh K Human leukocyte antigenpolymorphism and association: a review
Anthropologist 2007;Special Vol. No.3: 367-72.
|
2007 | |
| 827 |
Rao VB, Kerketta L, Korgaonkar S, Ghosh K. Dandy – Walker malformation in a case of partial trisomy 9p (p12.1àpter) due to maternal translocation
Indian J Hum Genet 2007;13(1): 33-5.
|
2007 | |
| 828 |
Gorakshakar AC, Das MK, Phanasgaonkar SP, Nadkarni AH, Colah RB,Mohanty D Origin of the Codon 47(+A) ?-thalassemia mutation among the Nicobarese of the Andaman & Nicobar islands in India.
Br J Haematol 2007 Oct;139 (2):345-6. [17897314]. (IF 3.195)
|
2007 | |
| 829 |
Colah R, Thomas M, Mayekar P Assessing the impact of screening and counseling high school children for b-thalassemia in India.
J Med Screen 2007; 14(3): 158. [17925089]. (IF 1.493)
|
2007 | |
| 830 |
Nadkarni A, Gorakshakar A, Colah R, Mohanty D, Ghosh K Evaluation of the clinical severity of ?-thalassemia homozygous patients using a phenotypic scoring system
J Chinese Clin Med 2007; 2(8): 439-447
|
2007 | |
| 831 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Indian J Hum Genet 2007; 13(3) 79-85.
|
2007 | |
| 832 |
Italia KY, Colah R, Mohanty D Evaluation of F cells in sickle cell disorders by flow cytometry – comparison with theKleihouer- Betke’s slide method
Int J Lab Hematol 2007 Dec: 29 (6): 409-14. (IF 1.304)
|
2007 | |
| 833 |
Colah RB, Surve R, Sawant P, D’Souza E, Italia K, Phanasgaonkar S, Nadkarni AH,Gorakshakar AC HPLC studies in hemoglobinopathies
Indian J Pediatr. 2007 Jul:74(7):657-62 Review. (IF 0.9)
|
2007 | |
| 834 |
Kulkarni SS, Gorakshakar AC, Colah RB, Gupte SC, Mohanty D Usefulness of prenatal detection of Rh D typing by molecular analysis in Indians
J PostGrad Med. 2007 Apr-Jun; 53(2): 149. (IF 1.589)
|
2007 | |
| 835 |
D”Souza E, Kulkarni SS, Colah RB, Mohanty D An improved flowcytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathies
Hemoglobin, 2007; 31(1): 39-48. (IF 1.106)
|
2007 | |
| 836 |
Gupta N, Bianchi P, Fermo E, Kabra M. Warang P, Kedar PS, Gupta N, Colah R Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family
Prenat Diagn. 2007 Feb; 27(2): 117-8. (IF 2.152)
|
2007 | |
| 837 |
Ghosh K, Shetty S, Tulsiani M Evolution ofprenatal diagnosis techniques from phenotypic diagnosis to gene arrays : Its likely impact on prenatal diagnosis of hemophilia
Clin Appl Thromb Hemost first published on December 26
|
2007 | |
| 838 |
Dhurandhar PS, Shankarkumar U HLA association in seronegative spondyloarthritis patients from Mumbai, India.
Int. J Hum Genet. 2007; 7(3): 235-9. (IF 0.238)
|
2007 |
