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  • Shankarkumar U, Ghosh K.
    MHC non -HLA gene polymorphisms in transplantation.
    Indian J Pathol Microbiol. 2007 Oct;50(4):881-5. [18306597] (IF: 0.57)

  • 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;64(4):160-3. [18236737]. (IF: 0.590)

  • Madkaikar M, 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;64(4):157-9. [18236736] (IF: 0.590)

  • Kulkarni SS, Gupte SC, Vasantha K, Mohanty D, Ghosh K.
    Varied distribution of RhD epitopes in the Indian population.
    Natl Med J India. 2007 Jul-Aug ;20(4):169-71 (IF: 0.911)

  • Rao VB, Korgaonkar S, Kerketta L, Ghosh K.
    Differentiation of Nijmegen breakage syndrome from Fanconi anemia.
    Genet Mol Res. 2007 Sept 30;6(3):622-6. (IF: 1.013)

  • 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 Nov;13(6):734-9. [17973850] (IF:2.394)

  • 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 Jun 30;6(2):470-5. (IF: 1.013)

  • Madkaikar M, 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;118(3):153-9. Epub 2007 Sep 20. (IF: 1.316)

  • Ghosh K, Ghosh K.
    Pathogenesis of anemia in malaria: a concise review
    Parasitol Res. 2007 Nov;10 (6):1463-9. [17874326]. (IF: 3.938)

  • Vora S, Shetty S, Ghosh K.
    Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
    Blood Coagul Fibrinolysis. 2007 Sep;18(6):571-4. (IF: 1.506)

  • 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)

  • Ghosh K, Ghosh K.
    Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of threcases.
    Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26. (IF: 2.615)

  • 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)

  • 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)

  • 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)

  • Ghosh K, Vora S, Shetty S.
    Varied distribution of RhD epitopes in the Indian population.
    Natl Med J India. 2007 Jul-Aug ;20(4):169-71 (IF: 0.911)

  • Ghosh K, Madkaikar M, Jijina F, Shetty S.
    Fractures of long bones in severe haemophilia.
    Haemophilia. 2007 May;13(3):337-9. (IF: 2.394).

  • 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)

  • Ghosh K, Ghosh K.
    Microarray genetic screening: the other side of the coin.
    Lancet. 2007 Mar 24;369(9566):992. [17382825] (IF: 33.63)

  • 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)

  • 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)

  • Quadros L, Ghosh K, Shetty S.
    A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population.
    Ann Hematol. 2007 May;86(5):377-9. [17308903] (IF: 2.688)

  • 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)

  • Nair AP, Jijina F, Ghosh K, Madkaikar M, Shrikhande M, Nema M.
    Osteoporosis in young haemophiliacs from western India.
    Am J Hematol. 2007 Jun;82(6):453-7. [17278114] (IF: 3.576)

  • 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)

  • 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)

  • 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. (IF: 0.37)

  • Ernest Beutler, Duparc S, Doumbo O, Ghosh K, Vinicious M, de Lacerda G, 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)

  • 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)

  • Shankarkumar U, Pawar A, and Ghosh K.
    Human leukocyte antigen polymorphism and association: a review.
    Anthropologist 2007; Special Vol. No.3: 367-72.

  • Rao VB, Kerketta L, Korgaonkar S, Ghosh K. Dandy
    Varied distribution of RhD epitopes in the Indian population.
    Natl Med J India. 2007 Jul-Aug ;20(4):169-71 (IF: 0.911)

  • Rao VB, Kerketta L, Korgaonkar S, Ghosh K. Dandy
    Walker malformation in a case of partial trisomy 9p (p12.1pter) due to maternal translocationt(9;12) (p12.1; p13.3)
    Indian J Hum Genet 2007;13(1): 33-5. (IF: 0.11)

  • 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)

  • 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)

  • 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. (IF: --)

  • Ghosh K.
    Coagulation disorders seen through the window of molecular biology.
    Indian J Hum Genet 2007; 13(3) 79-85. (IF: 0.11)

  • Italia KY, Colah R, Mohanty D
    Evaluation of F cells in sickle cell disorders by flow cytometry – comparison with the Kleihouer- Betke’s slide method.
    Int J Lab Hematol 2007 Dec: 29 (6): 409-14. (IF: 1.304)

  • 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)

  • 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)

  • D’Souza E, Kulkarni S, 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)

  • Gupta N, Bianchi P, Fermo E, Kabra M. Warang P, Kedar P, Gupta N, Colah R
    Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family.
    41.Prenat Diagn. 2007 Feb; 27(2): 117-8. (IF: 2.152)

  • Ghosh K, Shetty S, Tulsiani M.
    Evolution of prenatal 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. (IF: 1.286)

  • Dhurandhar PS, Shankarkumar U
    43.HLA association in seronegative spondyloarthritis patients from Mumbai, India.
    Int. J Hum Genet. 2007; 7(3): 235-9. (IF: 0.238)
 
  • 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)

  • Ghosh K, Pradhan V, Ghosh K.
    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)

  • 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)

  • Ghosh K, Madkaikar M, Jijina F.
    Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage.
    Acta Haematol. 2008 Feb 20;119(2):69-72 (IF: 1.316)

  • 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)

  • Ghosh K, Shetty S.
    Blood coagulation in falciparum malaria-a review.
    Parasitol Res. 2008 Mar;102(4):571-6. [18066597] (IF: 3.938)

  • 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)

  • 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)

  • 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)

  • 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. (IF: --)

  • Ghosh K, Shetty S and Ghosh K. Hemophilia
    A high cost low volume disease: suitable preventive strategies for developing and developed countries.
    The Open Hematol J 2008; 2: 20-4. (IF: --)

  • Ghosh K, Gangodkar S, Jain P, Shetty S, Ramjee S, Poddar P and 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)

  • 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)

  • Ghosh K, Pradhan V, Patwardhan M and Gupta M.
    Antiendothelial cell antibodies in systemic lupus erytematosus.
    Intl J Rheumatol Dis 2008; 11:121-6. (IF: 0.205)

  • 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)

  • Ghosh K, Shetty S
    Deep venous thrombosis associated with antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
    Blood Coagul Fibrinolysis 2008 Jul;19(5):464-65.[18600102] (IF: 1.506)

  • 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)

  • Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Sawant P, Surve R, Mohanty D, Ghosh K.
    Hb Showa Yakushi [beta 110(612) LeuPro ] in three families from Western India: First report on homozygous Hb showa Yakushiji.
    Blood Cells Mol Dis. 2008 May 19. (IF: 2.549)

  • 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)

  • Vundinti BR, Kerketta L, Madkaikar M, Jijina F, Ghosh K.
    Three way translocation in a new variant of +(8;21) acute myeloid leukemia involving Xp22.
    Indian J Cancer. 2008 Jan-Mar; 45(1):30-2. (IF: 0.91)

  • Vijapurkar M, Ghosh K, Shetty S, McLane MA, Moura da Silva AM,
    A simple, novel and robust test to diagnose type I glanzmann thrombasthenia.
    Haematologica. 2008 May; 93 (5) :797-8. (IF: 6.416)

  • 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)

  • Meera V, Jijina F, Shrikande M, Madkaikar M, 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)

  • Kulkarni S, 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)

  • 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)

  • 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).

  • 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. (IF: )

  • 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)

  • Edna D’Souza, Pratibha M. Sawant, Anita H. Nadkarni, Ajit Gorakshakar,Dipika Mohanty, Kanjaksha Ghosh, and Roshan B. Colah
    Evaluation of the Use of Monoclonal Antibodies and Nested PCR for Noninvasive Prenatal Diagnosis of Hemoglobinopathies in India.
    AJCP Aug2008; 130(2):202-209.(IF: 2.89)

  • Anita Nadkarni, Marukh Wadia, Ajit Gorakshakar, Ryoiti Kiyama, Roshan B. Colah, Dipika Mohanty
    Molecular Characterization of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population
    Hemoglobin Sep-Oct 2008, Vol. 32, No. 5: 425–433.(IF: 1.00)

  • Prabhakar Kedar, Kazuyuki Shimizu, Kanjaksha Ghosh, Hisaichi Fujji, Roshan Colah and Hitoshi Kanno.
    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)

  • 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. (IF: 0.696)

  • Malay Mukherjee.
    Laboratory diagnosis of sickle cell syndrome.
    J Community Med 2008 Jan; 4(1): 11-14. (IF: 0.10)

  • 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. (IF: --)

  • Konkankar S, Shankarkumar U.
    HLA DRB1 alleles in chronic hepatitis B infected patients.
    Intl J Hum Genet 2008; 72: 275. (IF: --)

 
  • 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)

  • 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)

  • Nadkarni A, Gorakshakar A, Surve R, Sawant P, Phanasgaonkar S, Nair S, Ghosh K, Colah RB.
    Novel mutations in GP IIb gene in Glanzmann’s thrombasthenia from India.
    Platelets. 2009 Feb;20(1):35-40.(IF: 2.271)

  • Ghosh K, Shetty S.
    Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors.
    Clin Rev Allergy Immunol. 2009 Jan 17. [Epub ahead of print] (IF: 2.080)

  • 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)

  • 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)

  • Kedar P, 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)

  • 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)

  • 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) (IF: --)

  • 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)

  • Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K.
    Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First report from India.
    Thromb Haemost 2009 Apr;101(4):785-87.(IF:3.413)

  • 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)

  • Shankarkumar U, Pradhan VD, 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • Kanjaksha Ghosh, Manisha Patwardhan, Vandana Pradhan
    Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas.
    Rheumatol Int 2009 Jul;29(9):1047-50.(IF:1.327)

  • Umapathy Shankarkumar, Krishnakumar 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)

  • 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)

  • Ghosh K.
    Challenges of haemophilia care in India: lest we forget.
    Indian J Med Res. 2009 Jul;130(1):87-8. (IF: 1.883)

  • Shetty S, Ghosh K.
    Anti-phospholipid antibodies and other immunological causes of recurrent foetal loss--a review of literature of various therapeutic protocols.
    Am J Reprod Immunol. 2009 Jul;62(1):9-24. Review.(IF: 2.172)

  • 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)

  • 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)

  • Madkaikar M, 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).

  • 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)

  • 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)

  • 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)

  • Ghosh K, Ghosh K.
    Private practice in India.
    Natl Med J India. 2008 Nov-Dec;21(6):328-9.(IF:0.911)

  • Vaswani RK, Dharaskar PG, Kulkarni S, Ghosh K.
    Iron Deficiency as a Risk Factor for First Febrile Seizure.
    Indian Pediatr. 2009 Sep 3. [Epub ahead of print] (IF:0.956)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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).

  • 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)

  • 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)

  • Kanjaksha Ghosh.
    Molecular evolution of Globin Gene Pathology-Its Driver, Challenges and Solution.
    Journal of the Asiatic Society 2009 Vol. 51(20):73-8.(IF:--)

  • Roshan Colah.
    Antenatal Diagnosis of Thalasssemias-Diagnostic technology suitable for the country.
    Journal of the Asiatic Society 2009 Vol 51 (2):69-72(IF:--)

  • Tripathy AS, Shankarkumar U, Chadha MS, Ghosh K, Arankalle VA.
    Association of HLA alleles with hepatitis C infection in Maharashtra, Western India.
    ndian J Med Res. 2009 Nov;130(5):550-5. (IF: 1.883)

  • Vandana D Pradhan, 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)

  • Mamta Muranjan, Tejasvi Choudhary and Baburao Vundinti.
    Phenotypic heterogencity and parental origin of extra chromosome 21 in down syndrome.
    Indian Pediat. 2009 July 1; [Epub ahead of print] (IF:0.956)

  • Ajit Gorakshakar, Colah RB.
    Cascade screening for β-thalassemia; A practical approach for identifying and counseling carriers in India.
    Indian J. Comm. Med. 2009; Oct 34(4) :354-56. (IF: 0.25)

  • 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)

  • 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)

  • Pradhan VD, Ghosh K.
    Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
    Indian J Dermatol. 2009 Jul;54(3):258-62. (IF: 0.19)

  • Singh R, Pradhan V, 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. (IF: 0.35)

  • 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. (IF: 0.35)

 
  • 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)

  • Pradhan VD, Deshpande NR, Ghosh K.
    Proteomic approach to autoimmune disorders : A review.
    Indian J Biotechnol 2010 Jan;9 : 13-7. (IF:--)

  • 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:--) .

  • 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)

  • Ghosh K.
    Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
    Indian J Hum Genet. 2010 Jan;16(1):6-7. (IF: 0.27)

  • 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)

  • 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)

  • Swaminathan S, Madkaikar M, 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)

  • 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)

  • 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)

  • Pradhan V, 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. (IF: 6.46)

  • Kanjaksha Ghosh
    βThalassemia- What is it ?
    Physician’ s Digest 2010; Pg: 63-69. (IF: 0.68)

  • Colah R, Gorakshakar A, and Nadkarni A
    Global burden, distribution and prevention of β-Thalassemia and hemoglobin E disorders.
    Expert Rev. Hematol 2010 Mar, 3(1):103-117.(IF:1.161)

  • Italia K, Jijina F, Chandrakala S, Nadkarni A, Sawant P, Ghosh K, Colah R.
    Exposure to hydroxyurea during pregnancy in sickle β-thalassemia - A report of 2 cases.
    J.Clin. Pharmacol 50; 231-4; 2010. (IF:3.59)

  • Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, Bellgard M, Bittles AH.
    Profiling β-Thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counseling programmes.
    Hugo J. 2009 Dec; 3(1-4): 51–62. (IF: )

  • Pradhan VD, 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)

  • 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)

  • ain 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)

  • 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. (IF: 0.27)

  • Kanjaksha Ghosh, Kinjalka Ghosh.
    Advances in Haematological Pharmacotherapy in 21st Century.
    Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40. (IF: --)

  • Pradhan V, Deshpande N, Nadkarni A, Patwardhan M, Surve P, Ghosh K.
    Fc gamma R IIIB polymorphisms: 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)

  • Vaswani RK, Dharaskar PG, Kulkarni S, Ghosh K.
    Iron deficiency as a risk factor for first febrile seizure.
    Indian Pediatr. 2010 May;47(5):437-9. (IF: 0.9)

  • 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. (IF: 0.27)

  • 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)

  • 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)

  • Gangodkar S, Jain P, Dixit N, Ghosh K, Basu A.
    Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure imaged by electron tomography and whole-mount grid-cell culture techniques.
    J Electron Microsc (Tokyo). 2010 Jun;59(6):503-11. (IF 1.77)

  • 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)

  • 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)

  • 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)

  • 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)

  • Pradhan V, 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)

  • 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)

  • 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)

  • Mukherjee MB, Nadkarni AH, Gorakshakar AC, Ghosh K, Mohanty D, Colah RB.
    Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India.
    Indian J Hum Genet. 2010 Sep;16(3):154-8. (IF: 0.27)

  • 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)

  • Shankarkumar U.
    Complexities and similarities of HLA antigen distribution in Asian subcontinent.
    Indian J Hum Genet. 2010 Sep;16(3):108-10. (IF: 0.27)

  • 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)

  • Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar M, 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)

  • 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)

  • Chandrakala S, Jijina F and Ghosh K.
    Diffuse alveolar haemorrhage with severe haemophilia.
    Haemophilia 2010 Nov;16(6): 962-4. (IF 2.394)

  • 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)

  • 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)

  • Pradhan V, 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. (IF: 0.68)

  • 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)

  • 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)

  • Pai N, Shetty S, Kulkarni B, Ghosh K.
    Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from India.
    Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700.(IF:1.476)

  • Shankarkumar U, Pawar A, Devraj JP, Bhupali K, Ghosh K.
    The HLA system- A review.
    Anthopologist, 2010;Special Vol.6:183-97. (IF: 0.24)

 
  • 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)

  • Kanjaksha Ghosh, Roshan Colah.
    Phenotypic diversity of sickle cell disorders: a rebuttal.
    Curr Sci 2011 Jan; 100(2):149. (IF:0.897)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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).

  • 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)

  • 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)

  • 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)

  • Pradhan V, Patwardhan M, Nadkarni A, Ghosh K.
    Fc γ R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients.
    Indian J Med Res. 2011 Aug;134(2):181-5.(IF: 1.837)

  • 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. (IF: 0.69)

  • 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)

  • 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. (IF: 7.06)

  • 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: 1.17)

  • 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: 1.17)

  • Shankarkumar U, Shankarkumar A, Ghosh K.
    Human immunodeficiency virus therapeutics and pharmacogenomics.
    Indian J Hum Genet. 2011 May;17 Suppl 1:S22-6. (IF: 0.69)

  • 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)

  • 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)

  • 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)

  • 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).

  • 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)

  • A Shankarkumar and U Shankarkumar
    Third national science symposium on HIV/AIDS: HIV Science 2010.
    Indian J Hum Genet. 2011 Jan-Apr; 17(1):35-36. (IF: 0.69)

  • Shankarkumar U, Shankarkumar A, Ghosh K
    HIV and Malaria co-infection in Mumbai Western India.
    J Vector Borne Dis. 2011 Sep; 48(3):155-58.(IF: 1.177)

  • 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. (IF: 1.15)

  • 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. (IF: --)

  • Shankarkumar U, Shankarkumar A, Ghosh K.
    HIV and Malaria co-infection in India.
    Intl J Immunol Res. 2011; 2(1): 13-16.(IF ICV:4.85)

  • 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. (IF: 0.31)

  • 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. (IF: --)

  • 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)

  • 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)

  • 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)

  • 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. (IF: 0.69)

  • 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. (IF: 0.69)

  • 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)

  • 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)

  • 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)

  • 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. (IF: 0.69)

  • Desai –Gorakshakar K, Padwal V, Ghosh K.
    Women scientists in India are marching ahead.
    Curr Sci 2011 Aug; 101: 3. (IF: 0.935)

  • Ghosh K.
    Haematology research in India: past, present and future.
    Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)

  • 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)

  • 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: 1.17)

  • Vundinti BR, Ghosh K/strong>
    Incidence of down syndrome: Hypotheses and reality.
    Indian J Hum Genet. 2011 Sep;17(3):117-9. (IF: 0.69)

  • 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)

  • Ghosh K, Ghosh K, Chowdhury JR.
    Tuberculosis and female reproductive health.
    J Postgrad Med. 2011 Oct-Dec;57(4):307-13.(IF: 1.389)

  • 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)

  • 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)

 
  • 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)

  • 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)

  • 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, Roos D.
    Hematologically important mutations: Leukocyte adhesion deficiency (first update)
    Blood Cells Mol Dis 2012 Jan 15; 48(1):53-61.(IF: 2.351)

  • Pradhan V, Patwardhan M, Athavale A, Taushid S, Ghosh K.
    Mycobacterium tuberculosis triggers autoimmunity?
    Indian J Tuberc. 2012 Jan;59(1):49-51. (IF: 0.94)

  • 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)

  • 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 β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?
    Hemoglobin. 2012 Feb; 36(2):114-23. (IF: 1.304)

  • 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)

  • 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)

  • Shukla P, Ghosh K and Vundinti BR
    Current and emerging therapeutic strategies for Fanconi anemia.
    The Hugo J 2012 Mar; 6:1.(IF: 0.40)

  • 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)

  • 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. (IF: 0.85)

  • 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. (IF: 0.85)

  • Nair PS, Shetty S, Ghosh K
    A homozygous female hemophilia A.
    Indian J Hum Genet 2012 Jan-Apr; 18(1): 134-6. (IF: 0.85)

  • 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. (IF: 0.79)

  • 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)

  • Gorakshakar A, Sathe P, Colah R, Nadkarni A, Ghosh K.
    Hemoglobin Showa-Yakushiji: A Common β Thalassemia Mutation Among the Agri Community from Western India.
    Genet Test Mol Biomarkers. 2012 Apr;16(4): 302-5. (IF: 1.110)

  • 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)

  • 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)

  • 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)

  • 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)

  • Italia K, Sheth J, Sawant P, Nadkarni A, Ghosh K, Colah R.
    Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at risk.
    Prenat Diagn. 2012 Jul;32(7):703-7.(IF: 2.106)

  • 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.(IF: 2.472)

  • 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)

  • 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)

  • 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)

  • Ghosh K.
    Haematology research in India: past, present and future.
    Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)

  • 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)

  • 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)

  • 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)

  • Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB.
    First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
    J Clin Pathol. 2012 Jul;65(7):654-9.(IF: 2.306)

  • 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. (IF: 0.85)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R.
    Variable haematological and clinical presentation of β-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)

  • 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)

  • 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. (IF: --)

  • 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)

  • 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: --)

  • 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: --)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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. (IF: --)

  • 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, Iliodromitis EK, Lang IM, Lee TI, Marz W, Nair SB, Pascual G, Peteiro J, Sakamoto C, Satomura A, Schiza SE, Starkel P, Stojakovic T, Vesely DL, Walters DL, Yilmaz Y.
    Research update for articles published in EJCI in 2010
    Eur J Clin Invest 2012 Nov; 42(11):1149-64. (IF: 3.365)

  • 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)

  • 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)

  • 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. (IF: --)

 
  • 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)

  • 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 23 bp insertion polymorphisms in indigenous population of Nepal.
    Ann Hematol. 2013 Jan;92(2):261-2. (IF: 2.615)

  • 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).

  • 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 β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study.
    J Community Genet. 2013 Jan;4(1):33-42. (IF: 2.20)

  • .D'Souza E, Sawant PM, Nadkarni AH, Gorakshakar A, Ghosh K, Colah RB.
    Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma.
    J Postgrad Med. 2013 Jan-Mar;59(1):15-20. (IF: 1.389)

  • 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)

  • Pooja Dabke, Roshan Colah, Kanjaksha Ghosh, Anita Nadkarni
    Effect of Cis Acting Potential Regulators in the β 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: --)

  • 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)

  • 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)

  • Nair S, Ghosh K.
    The myriad effects of cigarette smoke.
    J Thromb Haemost. 2013 Feb;11(2):387-8. (IF: 5.731)

  • 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).

  • 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. (IF: 2.48)

  • Dabke P, Colah RB, Ghosh K, Nadkarni A.
    Effect of a group of genetic markers around the 5' regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia.
    Blood Cells Mol Dis. 2013 Mar;50(3):156-60.(IF:2.361)

  • Pradhan V, Ghosh K
    Immunological disturbances associated with malarial infection.
    J Parasitic Dis 2013 Apr;37(1):11-15. Review. (IF: 0.98)

  • 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)

  • 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)

  • Parasannanavar DJ, Yeola A, Pradhan V, Rajyadhaksha A, Ghosh K.
    HLA-DRβ1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients.
    Rheumatol Int. 2013 Apr; 33(4): 867-70.(IF: 2.200)

  • Shukla P, Rao A, Ghosh K, Vundinti BR.
    Identification of a novel large intragenic deletion in a family with Fanconi Anemia: First molecular report from India and review of literature.
    Gene. 2013 Apr 15; 518(2): 470-5. (IF:2.443)

  • 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 γ-mRNA expression by hydroxyurea in Hemoglobinopathies.
    Indian J Hum Genet. 2013 Apr;19(2):251-8. (IF: 0.66)

  • Bhukhanvala DS, Sorathiya SM, Sawant P, Colah R, Ghosh K, Gupte SC.
    Antenatal screening for identification of couples for prenatal diagnosis of severe hemoglobinopathies in surat, South Gujarat.
    J Obstet Gynaecol India. 2013 Apr;63(2):123-7. (IF: --)

  • 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)

  • 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)

  • Ghosh K.
    Multifactorial aetiology for bone disease in patients with haemophilia.
    Eur J Haematol. 2013 May;90(5):435. (IF:2.066)

  • Ghosh S, Ghosh K.
    Maternal and neonatal outcomes in gestational diabetes mellitus.
    J Indian Med Assoc. 2013 May;111(5):330-1, 336. (IF: 0.28)

  • Ankolkar M, Salvi V, Warke H, Vundinti BR, Balasinor NH.
    Methylation status of imprinted genes DLK1-GTL2, MEST (PEG1), ZAC (PLAGL1), and LINE-1 elements in spermatozoa of normozoospermic men, unlike H19 imprinting control regions, is not associated with idiopathic recurrent spontaneous miscarriages.
    Fertil Steril. 2013 May;99(6):1668-73.(IF: 3.55)

  • 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)

  • 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)

  • 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 Indian systemic lupus erythematosus patients.
    Rheumatol Int 2013 Jun; 33(6): 1533-9.(IF: 1.885)

  • .Gaikwad T, Ghosh K, Kulkarni B, Kulkarni V, Ross C, Shetty S.
    Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation and other adverse outcomes in Indian population.
    Eur J Pharmacol. 2013 Jun 15;710(1-3):80-4.(IF:2.684)

  • Madkaikar M, Mishra A, Ghosh K.
    Diagnostic approach to primary immunodeficiency disorders.
    Indian Pediatr. 2013 Jun 8;50(6):579-86. (IF:1.044)

  • 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)

  • Gupta M, Madkaikar M, 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)

  • Patil R, Ghosh K, Shetty S.
    Profibrinolytic microparticles are not adequately produced to compensate their prothrombotic effect.
    Haematologica. 2013 Jul;98(7):e69. (IF:5.868)

  • 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. (IF: )

  • 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)

  • 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)

  • 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)

  • 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 )

  • 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)

  • 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)

  • Gorakshakar AC, Ghosh K.
    Transfusion transmitted infections in Indian thalassemics: a perspective.
    Indian J Hematol Blood Transfus. 2013 Sep;29(3):189-90. (IF: 0.69)

  • Gorakshakar AC, Ghosh K.
    Transfusion Transmitted Infections in Indian Thalassemics: a perspective.
    Indian J Hematol Blood Transf. 2013 Sep;29(3):189-90.(IF:0.056)

  • 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)

  • 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)

  • 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)

  • 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 leukemia.
    Hum Pathol. 2013 Oct; 44(10):2365-9.(IF: 3.077)

  • 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. 2013 Oct 2:1-3. (2.955)

  • 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 Single Centre Experience.
    Indian Pediatr.2013 Oct;50(10):929-33 (IF : 0.77)

  • Garg S, Madkaikar M, Ghosh K.
    Investigating cell surface markers on normal hematopoietic stem cells in three different niche conditions.
    Int J Stem Cells. 2013 Nov;6(2):129-33. (IF:0.625)

  • 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)

  • 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. (IF: 0.28)

  • Shukla P, Solanki A, Ghosh K, Vundinti BR.
    DNA interstrand cross-link repair: understanding role of Fanconi anemia pathway and therapeutic implications.
    Eur J Haematol. 2013 Nov;91(5):381-93 (IF:2.066)

  • Bhukhanvala DS, Italia K, Sawant P, Colah R, Ghosh K, Gupte SC.
    Molecular characterization of β-thalassemia in four communities in South Gujarat-codon 30 (G → A) a predominant mutation in the Kachhiya Patel community.
    Ann Hematol.2013 Nov;92(11):1473-6. (IF:2.615)

  • Ghosh K, Madkaikar M, Gupta M, Jijina F.
    Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination for paroxysmal nocturnal hemoglobinuria.
    Turk J Haematol. 2013 Dec;30(4):366-70.(IF:0.34)

  • 55.Ghosh K, Ghosh K.
    Pulmonary hydatidosis, strongyloidiasis and paragonimiasis in India.
    J Assoc Physicians India. 2013 Dec;61(12):954-5 (IF: 0.76)

  • 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. (IF: --)

 
  • 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)

  • 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)

  • 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)

  • 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:--)

  • Ghosh K.
    Familial Mediterranean fever: An unusal disease enlightening the inflammation biology.
    Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • Shetty S, Ghosh K.
    Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within and outside the genes.
    Haematologica. 2014 Mar;99(3):e30. (IF:5.868)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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:--)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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. (IF: 0.76)

  • 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 India.
    Indian J Hum Genet. 2014 Apr;20(2):160-5. (IF: 0.76)

  • Vundinti BR.
    Methylenetetrahydrofolatereductase C677T polymorphism and folate metabolism in human health.
    Indian J Hum Genet. 2014 Apr;20(2):99-100. (IF: 0.76)

  • 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)

  • Colah R, Mukherjee M, Ghosh K.
    Sickle cell disease in India.
    Curr Opin Hematol. 2014 May;21(3):215-23.(IF:4.053)

  • 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)

  • Prasannavar DJ, Yeola A, Pradhan V, Patwardhan M, Rajadhyaksha A, Ghosh K.
    Distribution of HLA-DRβ1 alleles among well-characterized rheumatoid arthritis patients from Western India
    Rheumatol Int. 2014 May;34(5):705-8.(IF:1.516)

  • 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)

  • Warang P, Nair S, Nadkarni A, Kedar P, Bhave A, Ghosh K, Colah R.
    Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from India.
    Hematology. 2014 Jun;19(4):199-201.(IF:1.393)

  • Solanki A, Vundinti BR.
    Prenatal detection of Fanconi anemia.
    Indian Pediatr. 2014 Jun;51(6):501. (IF: 0.72)

  • hetty 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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. (IF: 0.68)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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 (IF: 4.17)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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: --)

  • 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)

  • Pinto P, Shelar T, Nawadkar V, Mirgal D, Mukaddam A, Nair P, Kasatkar P, Gaikwad T, Ali S, Jadli A, Patil R, Parihar A, Shanbhag S, Kulkarni B, Ghosh K, Shetty S.
    The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients.
    Indian J Hematol Blood Transfus. 2014 Dec;30(4):356-63. (IF:0.250)

  • Upadhye DS, Jain DL, Trivedi YL, Nadkarni AH, Ghosh K, Colah RB.
    Newborn screening for haemoglobinopathies by high performance liquid chromatography (HPLC): diagnostic utility of different approaches in resource-poor settings.
    Clin Chem Lab Med. 2014 Dec; 52(12):1791-6.(IF:2.955)

  • 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:2.398)

  • Nair PS, Shetty S, Ghosh K.
    Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
    Clin Appl Thromb Hemost.2016 May;22(4):381-5. (IF: 2.392)

  • Umare V, Pradhan V, Nadkar M, Rajadhyaksha A, Patwardhan M, Ghosh K, Nadkarni AH.
    Effect of proinflammatory cytokines (IL-6, TNF-α, and IL-1β) on clinical manifestations in Indian SLE patients.
    Mediators Inflamm. 2014;2014:385297.Epub 2014 Dec 7. (IF: 3.236)

 
  • 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)

  • 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)

  • 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:4.411)

  • 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)

  • 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 )

  • 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: 1.826)

  • 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 Mutations in Sickle Cell Disease in Western India.
    Clin Appl Thromb Hemost. 2015 Mar;21(2):186-9.(IF: 1.973)

  • 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)

  • 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)

  • 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 )

  • Shetty S, Ghosh K.
    Novel therapeutic approaches for haemophilia.
    Haemophilia2015 Mar;21(2):152-61. (IF: 2.673 )

  • 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)

  • 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: 1.826)

  • 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)

  • 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 )

  • Koduri PR, Kedar PS, Warang P.
    Erythrocytosis, methemoglobinemia, and the saturation gap.
    Ann Hematol. 2015 Mar;94(3):509-10.(IF: 3.022)

  • 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: 1.722)

  • 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)

  • 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 )

  • 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)

  • 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: --)

  • 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: 1.826)

  • 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: 1.826 )

  • Ghosh K, Colah RB, Mukherjee MB.
    Haemoglobinopathies in tribal populations of India.
    Indian J Med Res. 2015 May;141(5):505-8. (IF: 1.826)

  • 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 )

  • 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)

  • 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 )

  • Korgaonkar S, Vundinti BR.
    Tetrasomy X in a Child with Upper Limb Deformity.
    Indian Pediatr. 2015 May;52(5):439. (IF: 0.972 )

  • 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)

  • Ghosh K.
    Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH).
    Indian J Hematol Blood Transfus. 2015 Jun;31(2):314-6. (IF: 0.232)

  • 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: 1.826)

  • 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)

  • Merchant R, Italia K, Ahmed J, Ghosh K, Colah RB.
    A successful twin pregnancy in a patient with HbE-β-thalassemia in western India.
    J Postgrad Med. 2015 Jul-Sep;61(3):203-5. (IF: 0.87)

  • 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 )

  • 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: 2.731)

  • 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)

  • 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)

  • Dalal K., Shankarkumar A.
    Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma.

  • 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)

  • 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)

  • 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)

  • Korgaonkar S, Vundinti BR.
    Trisomy 8 Mosaicism in a Boy with Dysmorphic Features.
    Indian Pediatr. 2015 Sep;52(9):812-3. (IF: 0.972)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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 β-thalassemias with triplicated α-globin genes.
    Ann Hematol. 2015 Dec;94(12):1953-8. (IF: 3.022)

  • Dalal B, Shankarkumar A, Ghosh K. Individualization of antiretroviral therapy
    Pharmacogenomic aspect.
    Indian J Med Res. 2015 Dec;142(6):663-74. (IF: 1.826)

  • 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)

  • 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)

  • 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:  1.826)

  • 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)

 
  • 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)

  • 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)

  • 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)

  • 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)

  • Gorakshakar AC, Ghosh K.
    Use of lectins in immunohematology.
    Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF: 1.06)

  • 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)

  • 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)

  • Garg S, Shanmukhaiah C, Marathe S, Mishra P, Babu Rao V, Ghosh K, Madkaikar M.
    Differential antigen expression and aberrant signaling via PI3/AKT, MAP/ERK, JAK/STAT, and Wnt/β catenin pathways in Lin-/CD38-/CD34+ cells in acute myeloid leukemia.
    Eur J Haematol. 2016 Mar;96(3):309-17.(IF: 2.653)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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: --)

  • 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 )

  • 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)

  • 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;17(4):439-48.(IF: 3.294)

  • 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)

  • 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 influencing fetal growth.
    BJOG. 2016 Apr;123(5):844.(IF: 5.051)

  • 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)

  • Garg S, Ghosh K, Madkaikar M.
    Antigen expression on a putative leukemic stem cell population and AML blast.
    Int J Hematol. 2016 May;103(5):567-71.(IF: 1.61)

  • Nair PS, Shetty S, Ghosh K.
    Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
    Clin Appl Thromb Hemost. 2016 May;22(4):381-5.(IF: 2.096)

  • 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)

  • 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: --)

  • Shetty S, Ghosh K.
    Why should hemophilia B be milder than hemophilia A?
    Haematologica. 2016 May;101(5):e213. (IF: 7.702)

  • 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)

  • Madkaikar M, 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)

  • Fleisher TA, Madkaikar M, Rosenzweig SD.
    Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies.
    Indian J Pediatr. 2016 May;83(5):444-9.(IF: 0.945)

  • Madkaikar M, 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)

  • Disha S Parchure, Swati S Kulkarni
    Noninvasive fetal RHD genotyping from maternal plasma
    Global Journal of Transfusion Science 2016 Jan-Jun;1(1): 21-28.(IF:--)

  • 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)

  • 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)

  • Gogri H, Kulkarni S, 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)

  • 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)

  • 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)

  • Colah RB, Nadkarni A, Gorakshakar A, Sawant P, Gorivale M, Mehta P, Sawant M, Ghosh K.
    Five Rare β Globin Chain Hemoglobin Variants in India.
    Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):282-6.(IF: 0.403)

  • 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)

  • 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)

  • Shabrish S, Gupta M, Madkaikar M
    A Modified NK Cell Degranulation Assay Applicable for Routine Evaluation of NK Cell Function.
    J Immunol Res. 2016;2016:3769590.(IF: 4.856) 

  • 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)

  • 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)

  • 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)

  • Italia K, Chandrakala S, Ghosh K, Colah R.
    Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?
    Free Radic Res. 2016 Jul; 27:1-7.(IF: 3.188)

  • Ali S, Ghosh K, Daly ME, Hampshire DJ, Makris M, Ghosh M, Mukherjee L, Bhattacharya M, Shetty S.w
    Congenital macrothrombocytopenia is a heterogeneous disorder in India.
    Haemophilia. 2016 Jul; 22(4):570-82.(IF: 3.569)

  • 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)

  • Kulkarni S, 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)

  • Gupta M, Aluri J, Terrance A, Madkaikar M.
    Adenosine Deaminase Deficiency with a Novel Gene Mutation.
    Indian J Pediatr. 2016 Aug;83(8):875-6. (IF: 0.945)

  • Ghosh K, 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)

  • Garg S, Shanmukhaiah C, Ghosh K, Madkaikar M.
    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) 

  • Shanbhag S, Ghosh K, Shetty S.
    First trimester prenatal diagnosis of severe FXIII deficiency.
    Haemophilia. 2016 Sep;22(5):e443-4. (IF: 3.569)

  • 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)

  • Italia K, Dabke P, Sawant P, Nadkarni A, Ghosh K, Colah RB.
    Hb E-β-Thalassemia in Five Indian States.
    Hemoglobin. 2016 Sep;40(5):310-315.(IF: 0.77)

  • 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)

  • 52.Kulkarni M, Desai M, Gupta M, Dalvi A, Taur P, Terrance A, Bhat S, Manglani M, Raj R, 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)

  • 53.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)

  • P Hariharan, S Colaco, R Colah, K Ghosh A Nadkarni.
    Do Beta-globin gene variants contribute in substantial reduction in HbA2 levels?
    Int. J. Lab Hematol 2016 Dec;38(6):610-615.(IF: 2.03)

 
  • 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)

  • 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)

  • 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)

  • 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. 2017 Jan 1:1076029616683046. doi: 10.1177/1076029616683046. [Epub ahead of print] (IF: 2.096)

  • 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)

  • 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) 

  • 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)

  • Umare VD, Pradhan VD, Rajadhyaksha AG, Patwardhan MM, Ghosh K, Nadkarni AH.
    Impact of TNF-α and LTα gene polymorphisms on genetic susceptibility in Indian SLE patients.
    Hum Immunol. 2017 Feb;78(2):201-208. (IF: 2.311)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • 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.
    Int J Lab Hematol. 2017 Apr;39(2):e51-e54. (IF: 2.03)

  • Prashant Warang, Roshan Colah and Prabhakar Kedar.
    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)

  • 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)

  • 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: )

  • 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)

  • Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K.
    Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers.
    J Clin Lab Anal. 2017 May;31(3).(IF: 1.521)

  • 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)

  • 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)

  • 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)

  • 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)

  • Kulkarni S, Parchure DS, Gopalkrishnan V, Madkaikar M.
    Screening for DEL phenotype in RhD negative Indians.
    J Clin Lab Anal. 2017 Jun 23. doi: 10.1002/jcla.22288. [Epub ahead of print] (IF: 1.521)

  • 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)

  • 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)

  • 25.Warang P, Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M.
    Does novel P5'N-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)

  • 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: 4.686)

  • 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)

  • 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)

  • Kedar P.
    Next-generation sequencing: emerging technology in the area of hematology and blood disorder.
    Hematol Blood Disord 2017 Sep;1(1):1-2. (IF: )

  • Roshan Colah, Anita Nadkarni, Ajit Gorakshakar, Pratibha Sawant, Khusnooma Italia, Dipti Upadhye, Harshali Gaikwad, Kanjaksha Ghosh.
    Prenatal Diagnosis of HBE-halassemia: experience of a center in Western India.

  • 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)

  • 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)

  • 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)

  • 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)

  • 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)

  • Pranatharthiharan S, Patel MD, Malshe VC, Pujari V, Gorakshakar A, Madkaikar M, 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)

  • 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)

  • Kedar P, Parmar V, Devendra R, Gupta V, Warang P, Madkaikar M
    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)

  • Kulkarni M, Gupta M, Madkaikar M
    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: 2.256)

  • Zaidi AU, Kedar P, 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) 

 
  • 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: 1.29)

  • 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)

  • Umare V, Pradhan V, Rajadhyaksha A, Ghosh K, Nadkarni A.
    Predisposition of IL-1β (-511 C/T) polymorphism to renal and hematologic disorders in Indian SLE patients.
    Gene  2018 Jan 30;641:41-45.(IF: 1.74)

  • 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: 1.84)

  • 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: 1.826)

  • 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)

  • 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)

  • 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: 1.724)

  • Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar M
    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 Feb 27:1-7. (IF: 1.42)

  • Aluri J, Gupta M, Dalvi A, Mhatre S, Kulkarni M, Hule G, Desai M, Shah N, Taur P, Vedam R, Madkaikar M.
    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: 3.35)

  • 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: 1.935)

  • 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)

  • 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 Mar 26. (IF: 0.02)

  • 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: 1.29)

  • 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 Apr 30;62:205-210. (IF: 2.885)

  • 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. 2018 Apr 17. doi: 10.1097/MPH.0000000000001164. [Epub ahead of print] (IF: 1.08)

  • Patil R, Bajpai S, Ghosh K, Shetty S.
    Microparticles as prognostic biomarkers in dengue virus infection.
    Acta Trop. 2018 May;181:21-24. (IF: 1.84)

  • Kulkarni SS, Gogri H, Parchure D, Mishra G, Ghosh K, Rajadhyaksha S, Madkaikar M, Férec C, Fichou Y.
    RHD-Positive Alleles among D- C/E+ Individuals from India.
    Transfus Med Hemother. 2018 May;45(3):173-177. (IF: 1.76)

  • 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: 0.02)

  • Gogri H, Pitale P, Madkaikar M, Kulkarni S.
    Molecular genotyping of Indian blood group system antigens in Indian blood donors.
    Transfus Apher Sci. 2018 Jun;57(3):388-390. (IF: 1.3)

  • Fichou Y, Parchure D, Gogri H, Gopalkrishnan V, Le Maréchal C, Chen JM, Férec C, Madkaikar M, 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: 0.18)

  • Gupta M, Aluri J, Desai M, Lokeshwar M, Taur P, Lenardo M, Bergerson J, Dalvi A, Mhatre S, Kulkarni M, Kambli P, Madkaikar M.
    Clinical, Immunological, and Molecular Findings in Four Cases of B Cell Expansion With NF-κB and T Cell Anergy Disease for the First Time From India.
    Front Immunol. 2018 Jun 14;9:1049. doi: 10.3389/fimmu.2018.01049. eCollection 2018. (IF: 3.35)

  • Warang P, Homma T, Pandya R, Sawant A, Shinde N, Pandey D, Fujii J, Madkaikar M, Mukherjee MB.
    Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
    Br J Haematol. 2018 Jul 5. doi: 10.1111/bjh.15437. [Epub ahead of print] (IF: 5.67)

  • 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 Jul 23. doi: 10.4103/ijdvl.IJDVL_182_17. [Epub ahead of print]\ (IF: 0.61)

  • Blood Group Reference Centre: A handbook published by Indian Council of Medical Research, New Delhi, 1975.
  • 20 years of Research in Immunohaematology, published by Blood Group Reference Centre ; Bombay, 1977.
  • 'Recent Trends in Immunohaematology' Eds Bhatia HM, Contractor NM. Proceedings of an International Symposium, Bombay. Published by Institute of Immunohaematology (ICMR) Bombay, 1984.
  • Techniques in Blood Banking, Ed. Bhatia HM. Published by Institute of Immunohaematology (ICMR), Mumbai, 1985.
  • 'Genetic Atlas of Indian Tribes' Eds Bhatia HM, Rao VR. Published by Institute of Immunohaematology (ICMR), Mumbai, 1986.
  • 'Hemoglobinopathies in India: Bibliography'. Rao VR, Naik SR, Mukherjee P. Published by Indian Society of Human Genetics 1988.
  • 'Collaborative study on thalassemia : An ICMR task force study' Eds Sood SK, Madan N, Colah R,Sharma S, Apte SV. Published by Indian Council of Medical Research, New Delhi, 1993.
  • 'Biotechnology in health care : Popular lecture series. Organized by Institute of Immunohaematology (ICMR) Mumbai Sponsored by Dept. of Biotechnology, New Delhi, 1994.
  • Proceedings of first National Symposium on Venoms and Toxins. Eds. Mohanty D., Ghosh K. Published by Indian Council of Medical Research, New delhi, 1996.
  • 'Emerging Trends in Haematology and Immunohaematology ' Eds. Colah R, Vasantha K, Shetty S. Proceeding of International Conference, Mumbai. Published by Institute of Immunohaematology, Mumbai 2007.
  • 'Golden Collection of Institute of Immunohaematology- commemorative volume 2007'. Eds.Ghosh K , Colah R, Vasantha K, Iyer YS, Gorakshakar A, Shankarkumar U, Babu Rao V, Mukherjee MB, Shetty SD, Nadkarni AH, Pawar AR. Golden Jubilee Publications. Compiled by : Padwal VG, Nair SB, Kulkarni BP and Ghavnalkar R. Publisher: Institute of Immunohaematology, Mumbai 2007.
  • 'Bibliotheca IIHica' (1957-2007). Eds. Padwal VG, Nair SB and Ghavnalkar RR. Golden Jubilee Publications. Published by Institute of Immunohaematology, Mumbai 2007.
  • Project Report
    Mohanty D, Colah R, Gorakshakar A Eds. Jai Vigyan S and T Mission Project on Community Control of Thalassemia Syndromes – Awareness, Screening, Genetic Counseling and Prevention. Final Report (2000-2005), Institute of Immunohaematology, (ICMR), Mumbai, 2007.
  • Laboratory Manual for screening, diagnosis and molecular analysis of hemoglobinopathies and red cell enzymopathies. Eds Mohanty D, Colah R. Published by Bhalani Publishing House, Mumbai 2008.
  • Book
    Gorakshakar AC: Contributor, Laboratory manual for screening, Diagnosis and Molecular Analysis of Hemoglobinopathies and Red cell Enzymopathies. Eds. Mohanty D. and Colah R. Bhalani Publishing House, Mumbai, 2008.
  • '2nd International Conference on Primary Immunodeficiency Diseases 2nd -4th February 2013'. Eds. Madkaikar M. Scientific Proceedings. Published by Indian Society for Primary Immune Deficiency (ISPID), Mohali, Foundation for Primary Immunodeficiency Diseases (FPID), National Insitute of Immunohaematology (ICMR) Mumbai, Bai Jerbai Wadia Hospital for Children, Mumbai and Division of Basic &Clinical Immunology, University of California, USA 2013.