आय सी एम आर - राष्ट्रीय प्रतिरक्षा रुधिर विज्ञान संस्थान

ICMR-National Institute of Immunohaematology

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2021-Till Date




Publications 2011-2015
1 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)
2 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)
3 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)
4 Warang P, Devendra R, D'Silva S, Chiddarwar A, Kedar P,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)
5 Pradhan V, 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)
6 Mishra A, Italia K, Gupta M, Desai M, Madkaikar M Syndrome due to CD40 Deficiency: Possibly the first case from India.
Journal of Postgraduate Medicine. 2015 Jan-Mar; 61:41-48. (IF: 0.87 )
7 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)
8 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)
9 Pradhan V, 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)
10 Warang P, Kedar P, 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 )
11 Shetty S,Ghosh K Novel therapeutic approaches for haemophilia.
Haemophilia 2015 Mar;21(2):152-61. (IF: 2.673 )
12 Shetty SD,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)
13 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 )
14 Madkaikar M, 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)
15 Mhatre S, Madkaikar M, 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 )
16 Koduri PR, Kedar PS, Warang P. Erythrocytosis, methemoglobinemia, and the saturation gap.
Ann Hematol. 2015 Mar;94(3):509-10.(IF: 3.022)
17 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)
18 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)
19 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 )
20 Upadhye D, Koduri P, Tarakeshwari S, Mehta P, Surve R, Warang P, Kedar P, 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)
21 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: )
22 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)
23 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 )
24 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)
25 Madkaikar M, 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;35(4):431-4. (IF: 3.094 )
26 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)
27 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 )
28 Korgaonkar S,Vundinti BR. Tetrasomy X in a Child with Upper Limb Deformity.
Indian Pediatr. 2015 May;52(5):439. (IF: 0.972 )
29 Ghosh K, Ghosh K Factors Modulating Blood HbA1C Level and Diabetic Retinopathy.
J Assoc Physicians India. 2015 May;63(5):95-6. (IF: 0.37)
30 Ghosh K. Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Indian J Hematol Blood Transfus. 2015 Jun;31(2):314-6.(IF: 0.232)
31 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)
32 Lobo V, Shetty S, Kulkarni B, Butera D, Magalhaes GS,Ghosh K Erratum to: A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
Ann Hematol. 2015 Jul;94(7):1259. (IF: 3.022)
33 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)
34 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 )
35 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)
36 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)
37 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)
38 Dalal K., Shankarkumar A. Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma.
Intl J Res Engg Applied Sci 2015Aug; 5(8): 76-89. (IF:)
39 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)
40 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)
41 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)
42 Korgaonkar S,Vundinti BR. Trisomy 8 Mosaicism in a Boy with Dysmorphic Features.
Indian Pediatr. 2015 Sep;52(9):812-3. (IF: 0.972)
43 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)
44 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)
45 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)
46 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)
47 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; 6(4): (B) 981-987. (IF: 0.36)
48 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)
49 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. 2015Nov;21(6):e519-23. (IF: 2.673)
50 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)
51 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)
52 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)
53 Gorivale M, Sawant P, Mehta P, Nadkarni A,Ghosh K, Colah R. Challenges in Prenatal Diagnosis of Beta Thalassaemia: Couples with Normal HbA2in One Partner.
Prenat Diagn. 2015 Dec;35(13):1353-7. (IF: 3.043)
54 Ali S,Ghosh K, Shetty S. Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP).
Blood Cells Mol Dis. 2015 Dec;55(4):410-4. (IF: 2.731)
55 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)
56 Dalal B, Shankarkumar A, Ghosh K. Individualization of antiretroviral therapy Pharmacogenomic aspect.
Indian J Med Res. 2015 Dec;142(6):663-74. (IF: )
57 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)
58 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)
59 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)
60 Kulkarni B,Ghosh K, Shetty S. Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia.
Haemophilia. 2015 Dec 28. [Epub ahead of print] (IF: 2.673)
61 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)
62 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)
63 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:--)
64 Ghosh K. Familial Mediterranean fever: An unusal disease enlightening the inflammation biology
Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--)
65 Merchant RH, Parekh D, Ahmed N, Madkaikar M, Ahmed J X linked agammaglobulinemia: a single centre experience from India
Indian J Pediatr 2014 Jan; 81(1):92-4. (IF:0.919)
66 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)
67 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)
68 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)
69 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:--)
70 Ghosh K, Gorakshakar A. Dr. Bhatia's legacy in the development of immunohematology research in the country
Asian J Transfus Sci. 2014;8(Suppl 1):S1-2.
71 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)ProSer; HBD: C.301C>T] in Cis
Hemoglobin 2014 Jan-Feb; 38(1):24-7. .(IF:0.955)
72 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)
73 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)
74 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)
75 Shetty S,Ghosh K. Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within
Haematologica. 2014 Mar;99(3):e30. (IF:5.868)
76 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)
77 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)
78 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)
79 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)
80 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)
81 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)
82 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)
83 Mishra A, Gupta M, Dalvi A, Ghosh K, Madkaikar M Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID
J Clin Immunol 2014 Apr; 34(3):316-22.(IF:3.184)
84 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.
85 Swaminathan S, Garg S, Madkaikar M, 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.
86 Vundinti BR. Methylenetetrahydrofolatereductase C677T polymorphism and folate metabolism in
Indian J Hum Genet. 2014 Apr;20(2):99-100
87 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)
88 Colah R, Mukherjee M, Ghosh K Sickle cell disease in India.
Curr Opin Hematol. 2014 May;21(3):215-23.(IF:4.053)
89 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)
90 Prasannavar DJ, Yeola A, Pradhan V, 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)
91 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.
92 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)
93 Warang P, Nair S, Nadkarni A, Kedar P, 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)
94 Solanki A,Vundinti BR. Prenatal detection of Fanconi anemia.
Indian Pediatr. 2014 Jun;51(6):501
95 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)
96 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)
97 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)
98 Maiti AK, Kim-Howard X, Motghare P, Pradhan V, 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)
99 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)
100 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)
101 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)
102 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)
103 Madkaikar M, 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)
104 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)
105 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)
106 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)
107 Kulkarni BP, 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
108 Mhatre S, Madkaikar M, 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)
109 Pradhan V, 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)
110 Mhatre S, Madkaikar M, 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)
111 Kedar P, 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)
112 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:-)
113 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)
114 Umare V, Pradhan V, 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.
115 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)
116 Patil A, Poudyal BS, Kapali SM, Ghosh K, Shetty S Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reaductase C677T and endothelial protein C receptor 23bp insertion polymorphisms in indigenous population of Nepal.
Ann Hematol. 2013 Jan;92(2):261-2. (IF: 2.615)
117 Kulkarni S, 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).
118 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.
119 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)
120 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: )
121 Magerus-Chatinet A, Stolzenberg MC, Lanzarotti N, Neven B, Daussy C, Picard C, Neveux N, Desai M, Rao M, Ghosh K, Madkaikar M, 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)
122 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)
123 Nair S, Ghosh K. The myriad effects of cigarette smoke.
J Thromb Haemost. 2013 Feb;11(2):387-8.(IF: 5.731)
124 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)
125 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).
126 Pradhan V, 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.
127 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)
128 Pradhan V, Ghosh K Immunological disturbances associated with malarial infection
J Parasitic Dis 2013 Apr;37(1):11-15. Review.
129 Madkaikar M, 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)
130 Pradhan V,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)
131 Parasannanavar DJ, Yeola A, Pradhan V, 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)
132 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)
133 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.
134 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.
135 Warang P, Kedar P, 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)
136 Ghosh S,Ghosh K Maternal and neonatal outcomes in gestational diabetes mellitus
J Indian Med Assoc. 2013 May;111(5):330-1, 336.
137 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.
138 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)
139 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)
140 Patwardhan M, Pradhan V, 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)
141 Pradhan V, 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)
142 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)
143 Madkaikar M, Mishra A,Ghosh K. Diagnostic approach to primary immunodeficiency disorders.
Indian Pediatr. 2013 Jun 8;50(6):579-86.(IF:1.044)
144 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)
145 Gupta M, Madkaikar M, Rao VB, Mishra A, Govindaraj P, ThangarajK, Ghosh K Mitochondrial DNA variations in myelodysplastic syndrome
Ann Hematol. 2013 Jul;92(7): 871-6. (IF: 2.615)
146 Patil R,Ghosh K, Shetty S. Profibrinolytic microparticles are not adequately produced to compensate their
Haematologica. 2013 Jul;98(7):e69.(IF:5.868)
147 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.
148 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)
149 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)
150 DSilva 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 )
151 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)
152 Ghosh K Multifactorial aetiology for bone disease in patients with haemophilia.
Eur J Haematol. 2013 May;90(5):435(IF:2.066)
153 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)
154 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)
155 Gorakshakar AC,Ghosh K. Transfusion transmitted infections in Indian thalassemics: a perspective
Indian J Hematol Blood Transfus. 2013 Sep;29(3):189-90.
156 Lugade AA, Bharali DJ, Pradhan V, 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)
157 Warang P, Kedar P,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)
158 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)
159 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)
160 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)
161 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 : )
162 Garg S, Madkaikar M,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)
163 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)
164 Pradhan V, 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.
165 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)
166 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)
167 Ghosh K, Madkaikar M, 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)
168 Ghosh K, Ghosh K. Pulmonary hydatidosis, strongyloidiasis and paragonimiasis in India.
J Assoc Physicians India. 2013 Dec;61(12):954-5
169 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.
170 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)
171 Vijver Edith van de, Maddelena A, Sanal O, Holland SM, Uzel G, Madkaikar M, 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)
172 Pradhan V, Patwardhan M, Athavale A, Taushid S,Ghosh K. Mycobacterium tuberculosis triggers autoimmunity?
Indian J Tuberc. 2012 Jan;59(1):49-51.
173 Madkaikar M, 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)
174 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)
175 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)
176 Gupta S, Madkaikar M, Singh S, Sehgal S. Primary immunodeficiencies in India: a perspective.
Ann N Y Acad Sci. 2012 Feb;1250:73-9.(IF: 3.155)
177 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)
178 Shukla P, Ghosh K and Vundinti BR Current and emerging therapeutic strategies for Fanconi anemia.
The Hugo J 2012 Mar; 6:1.(IF: )
179 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)
180 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.
181 DSouza 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.
182 Nair PS, Shetty S, Ghosh K A homozygous female hemophilia A.
Indian J Hum Genet 2012 Jan-Apr; 18(1): 134-6.
183 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)
184 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)
185 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)
186 Pradhan V, 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)
187 Kawankar N, Korgaonkar S, Kerketta L, Madkaikar M, 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)
188 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)
189 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)
190 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.
191 Warang P, Kedar P, 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)
192 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)
193 Ghosh K. Haematology research in India: past, present and future.
Indian J Hematol Blood Transfus. 2012 Jun;27(2):55-64. (IF: 0.056)
194 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)
195 Lobo V, Shetty S, Kulkarni B,Ghosh K. A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
Ann Hematol. 2012 Jun; 91(6):917-21.(IF: 2.615)
196 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)
197 Kulkarni S, 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)
198 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)
199 Pradhan VD, 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.
200 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)
201 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)
202 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)
203 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)
204 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)
205 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)
206 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)
207 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)
208 Pradhan V, 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.
209 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)
210 Pradhan VD 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:)
211 Pradhan VD, 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: )
212 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)
213 Kundu T, Shaikh A, Kutty A, Nalvade A, Kulkarni S, 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)
214 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)
215 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)
216 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)
217 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)
218 Ghosh K, Swaminathan S, Madkaikar M, 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)
219 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.
220 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)
221 Kedar P, 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)
222 Madkaikar MR, 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)
223 Patwardhan M, Pradhan V, 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.
224 Chalvam R, Colah RB, Mohanty D, Ghosh K, Mukherjee MB Restriction fragment length 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)
225 Kanjaksha Ghosh, Roshan Colah. Phenotypic diversity of sickle cell disorders: a rebuttal
Curr Sci 2011 Jan; 100(2):149.(IF:0.897)
226 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)
227 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.
228 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 )
229 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)
230 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.
231 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.
232 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).
233 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)
234 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)
235 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.
236 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)
237 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)
238 Warang P, Gupta M, Kedar P, 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)
239 Shankarkumar U, Shankarkumar A, Ghosh K. Human immunodeficiency virus therapeutics and pharmacogenomics.
Indian J Hum Genet. 2011 May;17 Suppl 1:S22-6.
240 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)
241 Vaidya S, Madkaikar M, 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.
242 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
243 Pradhan V, 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.
244 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)
245 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)
246 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)
247 Ghosh K. Haematology research in India: past, present and future
Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)
248 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)
249 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)
250 Madkaikar M, 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)
251 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)
252 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.
253 Shankarkumar U, Pradhan VD, 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.
254 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)
255 Pradhan V, 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)
256 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).
257 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)
258 Desai Gorakshakar K, Padwal V, Ghosh K. Women scientists in India are marching ahead.
Curr Sci 2011 Aug; 101: 3. (IF: 0.935)
259 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)
260 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)
261 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)
262 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)
263 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:)
264 Vundinti BR,Ghosh K Incidence of down syndrome: Hypotheses and reality
Indian J Hum Genet. 2011 Sep;17(3):117-9.
265 Shankarkumar U, 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): 510-13.(IF: 0.979)
266 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)
267 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)
268 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)
269 Ghosh K, Ghosh K, Chowdhury JR. Tuberculosis and female reproductive health.
J Postgrad Med. 2011 Oct-Dec;57(4):307-13.(IF: 1.389)

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