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Important Announcement

Dr. Shrimati Dharmapal Shetty


Scientist-F

Email: shrimatishetty@gmail.com,
Phone: +( 91-22) 2413 8518/19
Department: Hemostasis and Thrombosis

Academic Background

  • M.Sc. Mysore University
  • Ph.D University of Mumbai

Professional Experience

  • Member of Editorial Committee NIIH Bulletin
  • Member, National Academy of Medical Sciences
  • National advisor – Indian Journal of Hematology and Blood Transfusion
  • Executive Committee Member, Indian Society of Hematology and Transfusion Medicine Member, National academy of medical Sciences
  • Executive Committee member, Mumbai hematology Group
  • Other responsible positions of International bodies: Director, International Haemophilia Training center, World Federation of Haemophilia

Research Interests

  • Haemostasis and Thrombosis, Molecular Biology, Immunology

Awards & Achievements

  • Young Scientist Award in the year 1997 Indian Society of Haematology & Blood Transfusion for the work on “ Carrier detection and antenatal diagnosis in haemophilia A and B families in Indian population”
  • L. Hiranandani Award for the Best Poster from the Mumbai Haematology Group for the paper entitled “ Comparison of the coagulation parameters with the molecular biology data in the classification of carriers and noncarriers in haemophilia A families” in the year 1998
  • BGRC Silver Jubilee Oration award from Indian Council of Medical Research (ICMR) for the year 2000 for the work on “ Genetics of Haemophilia”
  • International Society of Thrombosis & Haemostasis for the year 2003 and 2006 in their Annual Conferences held at Birmingham and Geneva.
  • Early Career Investigator award from Bayer Health Care, USA as a Principal Investigator in the project entitled “ Thrombohaemorrhagic Balance in Haemophilia – Implications for an alternative therapeutic approach” in the Annual Conference of World Haemophilia Congress held at Bangkok in 2004
  • BGRC Founders day Oration from Mumbai Haemaology group in 2011 at Seven Hills Hospital, Mumbai
  • JG Parekh Oration Award from Mumbai Haemaology group in 2015 at ITC, Mumbai

Publications

  1. Patil RK, Ghosh KK, 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. doi: 10.4103/ijmr.IJMR_1236_16. PubMedPMID: 29923523; PubMed Central PMCID: PMC6022374
  2. 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. doi: 10.1111/ijlh.12808. Epub 2018 Mar 26. PubMed PMID:29579348.
  3. 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. doi: 10.1111/hae.13307. Epub 2017 Jul 27.
  4. 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. doi: 10.1111/trf.14279. Epub 2017 Aug 21.
  5. 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. doi: 10.1016/j.placenta.2017.08.009. Epub 2017 Aug 17. PubMed PMID:28962698.
  6. 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. doi: 10.1016/j.thromres.2017.09.005. Epub 2017 Sep 6. PubMed PMID: 28910687.s
  7. 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. doi: 10.1111/jth.13757. Epub 2017 Jul 17. PubMed PMID: 28608988.
  8. 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):1709-1710. doi: 10.1111/jth.13754. Epub 2017 Jul 10. PubMed PMID:28600843.
  9. 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. doi: 10.1111/ejh.12912. Epub 2017 Jun 29. PubMed PMID:28561456.
  10. Prabhudesai A, Shetty S, Ghosh K, Kulkarni B. Dysfunctional fibrinolysis and cerebral venous thrombosis. Blood Cells Mol Dis. 2017 Jun;65:51-55. doi:10.1016/j.bcmd.2017.05.007. Epub 2017 May 13. PubMed PMID: 28552473.
  11. 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] PubMed PMID: 28049362.
  12. Patil R, Ghosh K, Shetty S. Betrixaban in Acutely Ill Medical Patients. N Engl J Med. 2016 Dec 15;375(24):e50. doi: 10.1056/NEJMc1613217. PubMed PMID: 27974030
  13. 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. doi:10.1016/j.thromres.2016.09.022. PubMed PMID: 27710856.
  14. Ali S, Shetty S, Ghosh K. Bengal macrothrombocytopenia is not totally an innocuous condition. Blood Cells Mol Dis. 2016 Sep;60:3-6. doi:10.1016/j.bcmd.2016.05.011. PubMed PMID: 27519935.
  15. 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. 2016Jun 24:1-3. doi: 10.2450/2016.0266-15. [Epub ahead of print] PubMed PMID:27416578.
  16. Shanbhag S, Ghosh K, Shetty S. First trimester prenatal diagnosis of severe FXIII deficiency. Haemophilia. 2016 Sep;22(5):e443-4. doi: 10.1111/hae.12982.PubMed PMID: 27340806.
  17. 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. doi: 10.2337/db16-0295. PubMed PMID: 27329960.
  18. Ali S, Ghosh K, Daly ME, Hampshire DJ, Makris M, Ghosh M, Mukherjee L, Bhattacharya M, Shetty S. Congenital macrothrombocytopenia is a heterogeneous disorder in India. Haemophilia. 2016 Jul;22(4):570-82. doi: 10.1111/hae.12917. PubMed PMID: 27291889.
  19. 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. doi:10.1093/trstmh/trw026. PubMed PMID: 27198213; PubMed Central PMCID: PMC4914876.
  20. 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. doi: 10.1016/j.thromres.2016.04.012. PubMed PMID: 27161325.
  21. 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. doi: 10.1111/1471-0528.13688. PubMed PMID: 27149359.
  22. Shetty S, Ghosh K. Why should hemophilia B be milder than hemophilia A? Haematologica. 2016 May;101(5):e213. doi: 10.3324/haematol.2016.144022. PubMedPMID: 27132281; PubMed Central PMCID: PMC5004364.
  23. 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. doi: 10.1002/uog.15739. PubMed PMID: 26940676.
  24. 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. 2016 Feb 25. [Epub ahead of print] PubMed PMID: 26919454.
  25. 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. doi: 10.1016/j.mrfmmm.2016.02.002.PubMed PMID: 26897466.
  26. 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. doi: 10.1016/j.ajog.2016.02.014. PubMed PMID: 26875942.
  27. 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. doi: 10.1016/j.bcmd.2016.01.002. PubMed PMID: 26852661.
  28. 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. 2016 Feb 4. [Epub ahead of print] PubMed PMID: 26849716.
  29. 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. doi: 10.4103/0971-5916.174570. PubMed PMID: 26831425; PubMed Central PMCID: PMC4774073.
  30. Jadli AS, Ghosh K, Shetty S. Preeclampsia: simplified or still miles to go? Am J Obstet Gynecol. 2016 May;214(5):668-9. doi: 10.1016/j.ajog.2016.01.005. PubMed PMID: 26772792.
  31. Patil R, Mukaddam A, Ghosh K, Shetty S. Management of pregnancy in dysfibrinogenemia cases: a dilemma. Blood Coagul Fibrinolysis. 2016 Jan 11. [Epubahead of print] PubMed PMID: 26757015.
  32. Shetty S, Sharma N, Ghosh K. Epidemiology of hepatocellular carcinoma (HCC) in hemophilia. Crit Rev Oncol Hematol. 2016 Mar;99:129-33. doi: 10.1016/j.critrevonc.2015.12.009. Review.
  33. Patil R, Ghosh K, Shetty S.Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.Ann Hematol. 2015 Nov 14. [Epub ahead of print] No abstract available.PMID:26566984
  34. Patil R, Ghosh K, Shetty S. A simple clot based assay for detection of procoagulant cell-derived microparticles.Clin Chem Lab Med. 2015 Oct 30. pii: /j/cclm.ahead-of-print/cclm-2015-0508/cclm-2015-0508.xml. doi: 10.1515/cclm-2015-0508. [Epub ahead of print]PMID:26516932
  35. 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. doi: 10.1016/j.bcmd.2015.09.005. Epub 2015 Sep 21.PMID:26460267
  36. 36. 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. 2015 Oct 1. pii: S0165-2478(15)30037-7. doi: 10.1016/j.imlet.2015.09.013. [Epub ahead of print]
  37. 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.doi: 10.7326/L15-5137. PubMed PMID: 26370018.
  38. 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. doi: 10.1002/uog.14926. PubMed PMID: 26338238.
  39. 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 Aug 17. doi: 10.1111/hae.12788. [Epub ahead of print] PubMed PMID: 26278915.
  40. 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 JMed Res. 2015 Jul;142(1):85-7. doi: 10.4103/0971-5916.162130. PubMed PMID:26261171.
  41. 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. doi: 10.1016/j.bcmd.2015.06.008. Epub 2015 Jun 23.PubMed PMID: 26227844.
  42. 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. doi:10.1111/jth.13050. Epub 2015 Jul 28. PubMed PMID: 26179190.
  43. 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. doi: 10.1016/j.thromres.2015.05.011. Epub 2015 May 20. Review. PubMed PMID: 26024824.
  44. 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. PubMed PMID:25963489; PubMed Central PMCID: PMC4442326.
  45. 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 Apr 28. doi: 10.1111/bjh.13460.[Epub ahead of print] PubMed PMID: 25921354.
  46. 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. doi: 10.1007/s00277-015-2382-3.PubMed PMID: 25911135.
  47. Mukaddam A, Patil R, Jadli A, Chandrakala S, Ghosh K, Shetty S. Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbaimutation. Am J Clin Pathol. 2015 May;143(5):755-7. doi: 10.1309/AJCPDQL7LXMY7SHW.PubMed PMID: 25873512.
  48. 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. doi:10.1007/s00277-015-2373-4. Epub 2015 Apr 15. PubMed PMID: 25869031.
  49. Shanbhag S, Pai N, Ghosh K, Shetty S. Prenatal diagnosis in a family with purfura fulminans. Blood Coagul Fibrinolysis. 2015 Apr;26(3):350. doi:10.1097/MBC.0000000000000251. PubMed PMID: 25803516.
  50. Shanbhag S, Lulla C, Ghosh K, Shetty S. Prenatal diagnosis in a haemophilia carrier with triplet pregnancy. Haemophilia. 2015 May;21(3):e228-30. doi:10.1111/hae.12630. Epub 2015 Feb 4. PubMed PMID: 25649477.
  51. Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A. Clin Appl Thromb Hemost. 2014 Dec 29. pii: 1076029614562951. [Epub ahead of print] PubMed PMID: 25550078.
  52. 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. doi:10.1016/j.bcmd.2014.11.012. Epub 2014 Nov 25. Review. PubMed PMID: 25486929.
  53. 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. doi:10.1007/s12288-014-0342-z. Epub 2014 Feb 5. PubMed PMID: 25435742; PubMed CentralPMCID: PMC4243412.
  54. 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: asystematic review. PLoS One. 2014 Oct 2;9(9):e108683. doi:10.1371/journal.pone.0108683. eCollection 2014. Review. PubMed PMID: 25275492;PubMed Central PMCID: PMC4183524.
  55. Ghosh K, Shetty S, Patil R. Is thrombophilia associated withplacenta-mediated pregnancy complications? A prospective cohort study: comment. JThromb Haemost. 2014 Aug;12(8):1377-8. doi: 10.1111/jth.12630. Epub 2014 Jul 15. PubMed PMID: 24913766.
  56. Gaikwad T, Ghosh K, Shetty S. VKORC1 and CYP2C9 genotype distribution inAsian countries. Thromb Res. 2014 Sep;134(3):537-44. doi:10.1016/j.thromres.2014.05.028. Epub 2014 May 27. PubMed PMID: 24908449.
  57. Shetty S, Ghosh K. Paternal factor V Leiden and recurrent pregnancy loss: anew concept behind fetal genetics? Comment. J Thromb Haemost. 2014Oct;12(10):1758-9. doi: 10.1111/jth.12621. Epub 2014 Sep 8. PubMed PMID:24894632.
  58. 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. 2014May 20;9(5):e97337. doi: 10.1371/journal.pone.0097337. eCollection 2014. PubMedPMID: 24845853; PubMed Central PMCID: PMC4028251.
  59. Pinto P, Ghosh K, Shetty S. Analysis of F8 inversions as risk factors forFVIII inhibitor development in Indian severe haemophilia A patients. Blood Cells Mol Dis. 2014 Sep;53(3):161-3. doi: 10.1016/j.bcmd.2014.04.007. Epub 2014 May 11.PubMed PMID: 24824129.
  60. Pinto P, Parasannanavar D, Ghosh K, Shetty S. The association of HLA-DRB1 andHLA-DQB1 alleles with the development of factor VIII inhibitors in severehaemophilia A patients in India. Tissue Antigens. 2014 Aug;84(2):235-7. doi:10.1111/tan.12364. Epub 2014 Apr 23. PubMed PMID: 24758334.
  61. Kasatkar P, Shetty S, Ghosh K. Genetic heterogeneity in a large cohort ofIndian type 3 von Willebrand disease patients. PLoS One. 2014 Mar 27;9(3):e92575.doi: 10.1371/journal.pone.0092575. eCollection 2014. PubMed PMID: 24675615;PubMed Central PMCID: PMC3967998.
  62. Gaikwad T, Ghosh K, Kulkarni B, Shetty S. Factor V Leiden mutation modulates the bleeding phenotype in warfarin sensitive patients. Thromb Res. 2014May;133(5):955-6. doi: 10.1016/j.thromres.2014.02.022. Epub 2014 Feb 28. PubMedPMID: 24630642.
  63. Shetty S, Ghosh K. Genetic thrombophilia and natural anticoagulants:importance of polymorphisms within and outside the genes. Haematologica. 2014Mar;99(3):e30. doi: 10.3324/haematol.2013.102533. PubMed PMID: 24598856; PubMedCentral PMCID: PMC3943326.
  64. Shetty S, Shelar T, Mirgal D, Nawadkar V, Pinto P, Shabhag S, Mukaddam A,Kulkarni B, Ghosh K. Rare coagulation factor deficiencies: a countrywidescreening data from India. Haemophilia. 2014 Jul;20(4):575-81. doi:10.1111/hae.12368. Epub 2014 Feb 28. PubMed PMID: 24581247.
  65. 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. doi: 10.1002/pd.4315. Epub 2014 Jan 28.PubMed PMID: 24390653.
  66. Gaikwad T, Ghosh K, Shetty S. Possible impact of factor V Leiden genotype on warfarin induced bleeding. Indian J Hum Genet. 2013 Jul;19(3):377-8. doi:10.4103/0971-6866.120807. PubMed PMID: 24339560; PubMed Central PMCID:PMC3841572.
  67. Gaikwad T, Shetty S, Ghosh K. Warfarin pharmacogenetics: How close are we toclinical practice? Indian J Hum Genet. 2013 Jul;19(3):277-8. doi:10.4103/0971-6866.120806. PubMed PMID: 24339537; PubMed Central PMCID:PMC3841549
  68. Patil R, Ghosh K, Satoskar P, Shetty S. Elevated procoagulant endothelial andtissue factor expressing microparticles in women with recurrent pregnancy loss.PLoS One. 2013 Nov 20;8(11):e81407. doi: 10.1371/journal.pone.0081407.eCollection 2013. PubMed PMID: 24278436; PubMed Central PMCID: PMC3835417.
  69. Pinto P, Ghosh K, Shetty S. A specific and sensitive activated partialthromboplastin time (APTT)-based factor VIII inhibitor screening assay. Clin ChemLab Med. 2014 Mar;52(3):e39-41. doi: 10.1515/cclm-2013-0595. PubMed PMID:24088610.
  70. Gaikwad T, Jadli A, Ghosh K, Shetty S. Delayed Vitamin K deficiency relatedbleeding: is it genetically linked? Indian J Pediatr. 2014 Mar;81(3):310-1. doi:10.1007/s12098-013-1219-0. Epub 2013 Sep 14. PubMed PMID: 24037478.
  71. Ali S, Ghosh K, Shetty S. Novel genetic abnormalities in Bernard-Souliersyndrome in India. Ann Hematol. 2014 Mar;93(3):381-4. doi:10.1007/s00277-013-1895-x. Epub 2013 Sep 1. PubMed PMID: 23995613.
  72. Patil R, Ghosh K, Shetty S. Profibrinolytic microparticles are not adequatelyproduced to compensate their prothrombotic effect. Haematologica. 2013Jul;98(7):e69. doi: 10.3324/haematol.2013.083808. PubMed PMID: 23813649; PubMedCentral PMCID: PMC3696594.
  73. Kasatkar P, Ghosh K, Shetty S. Acquired von Willebrand syndrome: a raredisorder of heterogeneous etiology. J Postgrad Med. 2013 Apr-Jun;59(2):98-101.doi: 10.4103/0022-3859.113816. PubMed PMID: 23793308.
  74. Kasatkar P, Ghosh K, Shetty S. The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: arebuttal. J Thromb Haemost. 2013 Sep;11(9):1784-5. doi: 10.1111/jth.12323. PubMedPMID: 23773799.
  75. Gaikwad T, Shetty S, Ghosh K. Polymorphisms of warfarin metabolizing enzymes in an Indian population. Blood Cells Mol Dis. 2013 Oct;51(3):203. doi:10.1016/j.bcmd.2013.05.004. Epub 2013 Jun 2. PubMed PMID: 23739742.
  76. Shetty S, Ghosh K. APTT reagents for different coagulation tests: one sizedoes not fit all. Am J Clin Pathol. 2012 Nov;138(5):757; author reply 757-8.PubMed PMID: 23667956.
  77. Kasatkar P, Ghosh K, Shetty S. An atypical manifestation of acquired vonWillebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).Ann Hematol. 2014 Jan;93(1):173-5. doi: 10.1007/s00277-013-1767-4. Epub 2013 Apr 27. PubMed PMID: 23625134.
  78. Gaikwad T, Ghosh K, Kulkarni B, Kulkarni V, Ross C, Shetty S. Influence ofCYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation andother adverse outcomes in Indian population. Eur J Pharmacol. 2013 Jun15;710(1-3):80-4. doi: 10.1016/j.ejphar.2013.04.006. Epub 2013 Apr 16. PubMedPMID: 23602689.
  79. Pai N, Ghosh K, Shetty S. Hereditary thrombophilia in cerebral venousthrombosis: a study from India. Blood Coagul Fibrinolysis. 2013 Jul;24(5):540-3. doi: 10.1097/MBC.0b013e32835fad1e. PubMed PMID: 23518830.
  80. Shetty S, Patil R, Ghosh K. Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review. Eur J Obstet Gynecol Reprod Biol. 2013Jul;169(2):123-9. doi: 10.1016/j.ejogrb.2013.02.011. Epub 2013 Mar 13. Review.PubMed PMID: 23490540
  81. Pai N, Ghosh K, Shetty S. Acquired and Heritable Thrombophilia in IndianPatients With Pediatric Deep Venous Thrombosis (DVT). Clin Appl Thromb Hemost.2014 Sep;20(6):573-6. doi: 10.1177/1076029613476339. Epub 2013 Feb 12. PubMedPMID: 23406614.
  82. Ali S, Ghosh K, Shetty S. Molecular pathology of Bernard-Soulier syndrome in Indian patients. Platelets. 2013;24(7):571-3. doi: 10.3109/09537104.2012.748186. Epub 2013 Feb 12. PubMed PMID: 23402648.
  83. 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):1147-8. doi: 10.1007/s00277-013-1680-x. Epub 2013 Jan 27. PubMedPMID: 23354996.
  84. Ghosh K, Shetty S. Malignancies in persons with haemophilia: 25-year data from India. Natl Med J India. 2012 Jul-Aug;25(4):251-2. PubMed PMID: 23278795.
  85. Pinto P, Ghosh K, Shetty S. Factor VIII haplotypes in severe hemophilia Apatients in India. Ann Hematol. 2013 Jul;92(7):999-1000. doi:10.1007/s00277-012-1658-0. Epub 2012 Dec 23. PubMed PMID: 23262994.
  86. Patil A, Poudyal BS, Kapali SM, Ghosh K, Shetty S. Prevalence of factor VG1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenouspopulation of Nepal. Ann Hematol. 2013 Jan;92(2):261-2. doi:10.1007/s00277-012-1544-9. Epub 2012 Aug 11. PubMed PMID: 22885990.
  87. Jadli A, Kulkarni B, Ghosh K, Shetty S. Non conventional mutations associatedwith myeloproliferative disorders are absent in splanchnic venous thrombosis cases. Liver Int. 2012 Nov;32(10):1596-7. doi: 10.1111/j.1478-3231.2012.02851.x. Epub 2012 Jul 23. PubMed PMID: 22816981.
  88. Nair PS, Shetty S, Ghosh K. A homozygous female hemophilia A. Indian J Hum Genet. 2012 Jan;18(1):134-6. doi: 10.4103/0971-6866.96685. PubMed PMID: 22754241;PubMed Central PMCID: PMC3385172.
  89. 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. doi:10.1007/s00228-012-1332-4. Epub 2012 Jun 17. PubMed PMID: 22706625.
  90. Pinto P, Ghosh K, Shetty S. Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indiansevere haemophilia A patients. Haemophilia. 2012 Sep;18(5):794-7. doi:10.1111/j.1365-2516.2012.02845.x. Epub 2012 May 28. PubMed PMID: 22630053.
  91. Ghosh K, Shetty S. Bone health in persons with haemophilia: a review. Eur J Haematol. 2012 Aug;89(2):95-102. doi: 10.1111/j.1600-0609.2012.01803.x. Epub 2012Jun 22. Review. PubMed PMID: 22587752.
  92. Pai N, Ghosh K, Shetty S. Hereditary protein C deficiency in Indian patients with venous thrombosis. Ann Hematol. 2012 Sep;91(9):1471-6. doi:10.1007/s00277-012-1483-5. Epub 2012 May 11. PubMed PMID: 22576310.
  93. Pai N, Ghosh K, Shetty S. Cause of deep venous thrombosis and pulmonaryembolism in young patients from India as compared with other ethnic groups. BloodCoagul Fibrinolysis. 2012 Jun;23(4):257-61. doi: 10.1097/MBC.0b013e3283502961.PubMed PMID: 22498980.
  94. Shetty S, Ghosh K. Cancers in patients with hemophilia: a retrospective studyfrom the Italian Association of Hemophilia Centers: a rebuttal. J Thromb Haemost.2012 Jun;10(6):1200-1;author reply 1201-2. doi: 10.1111/j.1538-7836.2012.04737.x.PubMed PMID: 22497975.
  95. Kulkarni B, Kanakia S, Ghosh K, Shetty S. Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation. Ann Hematol. 2012Oct;91(10):1667-8. doi: 10.1007/s00277-012-1442-1. Epub 2012 Mar 7. PubMed PMID: 22392504.
  96. 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 inindigenous Nepali population. Haemophilia. 2012 Mar;18(2):e44-5. doi:10.1111/j.1365-2516.2011.02736.x. Epub 2012 Jan 4. PubMed PMID: 22221849.
  97. Lobo V, Shetty S, Kulkarni B, Butera D, Magalhaes GS, Ghosh K. A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers. AnnHematol. 2012 Jun;91(6):917-21. doi: 10.1007/s00277-011-1390-1. Epub 2011 Dec 21.Erratum in: Ann Hematol. 2015 Jul;94(7):1259. Butera, Diego [added]; Magalhaes,Geraldo S [added]. PubMed PMID: 22183252.
  98. Ghosh K, Shetty S. Epidemiology, diagnosis, and management of von Willebrand disease in India. Semin Thromb Hemost. 2011 Jul;37(5):595-601. doi:10.1055/s-0031-1281048. Epub 2011 Nov 18. PubMed PMID: 22102205.
  99. 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. doi:10.1177/1076029611418965. Epub 2011 Sep 2. PubMed PMID: 21890571.
  100. 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. doi: 10.1111/j.1365-2516.2011.02590.x. Epub 2011 Jun 9. PubMed PMID: 21658166.
  101. Shetty S, Kasatkar P, Ghosh K. Pathophysiology of acquired von Willebrand disease: a concise review. Eur J Haematol. 2011 Aug;87(2):99-106. doi:10.1111/j.1600-0609.2011.01636.x. Review. PubMed PMID: 21535159.
  102. Ghosh K, Shetty S. Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands? Blood Coagul Fibrinolysis. 2011Apr;22(3):241-2. doi: 10.1097/MBC.0b013e32834356a3. PubMed PMID: 21455035.
  103. 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. doi: 10.1111/j.1574-695X.2011.00794.x. Epub 2011 Mar 16. PubMed PMID: 21332827.
  104. 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. doi:10.1111/j.1365-2516.2010.02456.x. Epub 2011 Feb 15. PubMed PMID: 21323796.
  105. Shetty S, Bhave M, Ghosh K. Challenges of multiple mutations in individual patients with haemophilia. Eur J Haematol. 2011 Mar;86(3):185-90. doi:10.1111/j.1600-0609.2010.01564.x. Epub 2011 Jan 11. Review. PubMed PMID:21175850.
  106. Shetty S, Bhave M, Ghosh K. Acquired hemophilia a: diagnosis, aetiology,clinical spectrum and treatment options. Autoimmun Rev. 2011 Apr;10(6):311-6.doi: 10.1016/j.autrev.2010.11.005. Epub 2010 Nov 27. Review. PubMed PMID:21115138.
  107. 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. doi:10.1016/j.thromres.2010.09.019. Epub 2010 Oct 20. Review. PubMed PMID: 20961602.
  108. 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. doi: 10.1016/j.cca.2010.08.026. Epub 2010 Aug 26.PubMed PMID: 20800587
  109. 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. 2010Jul;134(1):82-5. doi: 10.1309/AJCP7VO4HAIZYATP. PubMed PMID: 20551270.
  110. Nair PS, Shetty S, Ghosh K. Double mutations in haemophilia: muddling strangers or indifferent partners in crime? Haemophilia. 2010 Nov;16(6):970-1. doi: 10.1111/j.1365-2516.2010.02326.x. PubMed PMID: 20546034.
  111. 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 Sep;21(6):608-10. doi: 10.1097/MBC.0b013e32833b645c. PubMed PMID: 20531166.
  112. Jain A, Shetty S, Kulkarni B, Ghosh K. Association of factor VII gene polymorphisms with Budd Chiari syndrome. Blood Coagul Fibrinolysis. 2010 Apr;21(3):296-7. doi: 10.1097/MBC.0b013e328337b44d. PubMed PMID: 20351643.
  113. Mota L, Shetty S, Idicula-Thomas S, Ghosh K. Molecular basis of factor Xdeficiency cases from India. Haemophilia. 2010 Jul 1;16(4):693-7. doi:10.1111/j.1365-2516.2010.02213.x. Epub 2010 Mar 16. PubMed PMID: 20331754.
  114. 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. doi:10.1007/s00277-009-0893-5. Epub 2010 Jan 14. PubMed PMID: 20077116.
  115. Kasatkar P, Shetty S, Ghosh K. VWF pseudogene: Mimics, masks and spoils. Clin Chim Acta. 2010 Apr 2;411(7-8):607-9. doi: 10.1016/j.cca.2009.12.024. Epub 2010 Jan 7. PubMed PMID: 20060388.
  116. 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. doi:10.1177/1076029609351290. Epub 2009 Nov 10. PubMed PMID: 19903694.
  117. 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. doi: 10.1016/j.cca.2009.11.004. Epub 2009 Nov 11.PubMed PMID: 19900433.
  118. Ghosh K, Shetty S, Sahu D. Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI).Haemophilia. 2010 Jan;16(1):61-5. doi: 10.1111/j.1365-2516.2009.02097.x. Epub 2009 Sep 23. PubMed PMID: 19780846.
  119. 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. doi: 10.1016/j.cca.2009.09.007. Epub 2009 Sep 13.PubMed PMID: 19751712.
  120. Ghosh K, Shetty S, Vora S. Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss. Int J Gynaecol Obstet. 2009 Nov;107(2):159-60. doi: 10.1016/j.ijgo.2009.06.017. Epub 2009 Jul 22. PubMed PMID: 19628210.
  121. 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. PubMed PMID: 19562834.
  122. 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. doi:10.1111/j.1365-2516.2009.02034.x. Epub 2009 Jun 22. PubMed PMID: 19549166.
  123. 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. doi:10.1111/j.1600-0897.2009.00714.x. Review. PubMed PMID: 19527228.
  124. Pai N, Shetty SD, Ghosh K. Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis. Clin Appl Thromb Hemost. 2009 Apr 28. [Epub ahead ofprint] PubMed PMID: 19403521.
  125. Ghosh K, Quadros L, Shetty S. Spectrum of factor IX gene mutations causing haemophilia B from India. Blood Coagul Fibrinolysis. 2009 Jul;20(5):333-6. doi:10.1097/MBC.0b013e32832b27d1. PubMed PMID: 19357501.
  126. 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):785-7. PubMed PMID: 19350130.
  127. Vora S, Shetty S, Khare M, Ghosh K. Placental histomorphology in unexplained foetal loss with thrombophilia. Indian J Med Res. 2009 Feb;129(2):144-9. PubMedPMID: 19293440.
  128. Quadros L, Ghosh K, Shetty S. Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes. J PediatrHematol Oncol. 2009 Mar;31(3):157-60. doi: 10.1097/MPH.0b013e31818b3759. PubMedPMID: 19262239.
  129. 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. doi:10.1111/j.1365-2141.2009.07618.x. Epub 2009 Feb 19. PubMed PMID: 19236374.
  130. Vijapurkar M, Ghosh K, Shetty S. Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India. Platelets. 2009 Feb;20(1):35-40. doi:10.1080/09537100802434861. PubMed PMID: 19172520
  131. Ghosh K, Shetty S. Immune response to FVIII in hemophilia A: an overview of risk factors. Clin Rev Allergy Immunol. 2009 Oct;37(2):58-66. doi:10.1007/s12016-009-8118-1. Review. PubMed PMID: 19148784.
  132. Ghosh K, Kulkarni B, Shetty S, Nair S. Antiplatelet antibodies in cases of Glanzmann's thrombasthenia with and without a history of multiple platelettransfusion. Indian J Hum Genet. 2009 Jan;15(1):23-7. doi:10.4103/0971-6866.50866. PubMed PMID: 20407646; PubMed Central PMCID: PMC2846565.
  133. Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K. Thrombophilia and unexplained pregnancy loss in Indian patients. Natl Med J India. 2008 May-Jun;21(3):116-9.PubMed PMID: 19004141.
  134. 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. doi: 10.1111/j.1365-2516.2008.01894.x. Epub 2008 Sep 18. PubMed PMID: 18803553.
  135. Banait VS, Sandeep MS, Shetty S, Bapat MR, Rathi PM, Ghosh K, Mohanty D,Abraham P. Hypercoagulable state in idiopathic ulcerative colitis: role of hyperhomocysteinemia and hyperfibrinogenemia. Indian J Gastroenterol. 2008 May-Jun;27(3):94-8. PubMed PMID: 18787277.
  136. Mukundan P, Shetty S, Kulkarni B, Ghosh K. Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population. Prenat Diagn. 2008 Oct;28(10):920-2. doi: 10.1002/pd.2068. PubMed PMID: 18702107.
  137. Vora S, Shetty S, Ghosh K. Thrombophilic dimension of recurrent fetal loss in Indian patients. Blood Coagul Fibrinolysis. 2008 Sep;19(6):581-4. doi:10.1097/MBC.0b013e328304dffc. PubMed PMID: 18685442.
  138. Ghosh K, Mota L, Shetty S, Kulkarni B. Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulation. Blood Coagul Fibrinolysis. 2008 Sep;19(6):577-80. doi: 10.1097/MBC.0b013e328307089d. PubMedPMID: 18685441.
  139. Prabhu R, Jijina F, Shetty S, Ghosh K. Successful surgery in severe haemophilia--a two-stage replacement therapy in resource-poor countries.Haemophilia. 2008 Sep;14(5):1125-6. doi: 10.1111/j.1365-2516.2008.01793.x. Epub2008 Jul 8. PubMed PMID: 18625030.
  140. Ghosh K, Shetty S. Deep venous thrombosis associated with antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient. BloodCoagul Fibrinolysis. 2008 Jul;19(5):464-5. doi: 10.1097/MBC.0b013e328304e056.PubMed PMID: 18600102.
  141. Shetty S, Ghosh K. Reduced clinical severity in a mutationallywell-characterized cohort of severe hemophilia with associated thrombophilia. Am J Clin Pathol. 2008 Jul;130(1):84-7; quiz 146. doi: 10.1309/6A8UURH9NU2YNFBP. PubMed PMID: 18550475.
  142. Ghosh K, Shetty S, Mota L. Aspirin resistance in patients with coronaryartery disease - which test to use in routine management? Blood CoagulFibrinolysis. 2008 Jun;19(4):324-6. doi: 10.1097/MBC.0b013e3282fa1a1f. PubMed PMID: 18469557.
  143. Ghosh K, Gangodkar S, Jain P, Shetty S, Ramjee S, Poddar P, Basu A. Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy. J Electron Microsc (Tokyo). 2008 Jun;57(3):113-8. doi: 10.1093/jmicro/dfn007. Epub 2008 May 8. PubMed PMID: 18467742.
  144. Vijapurkar M, Ghosh K, Shetty S, McLane MA, Moura da Silva AM, Butera D. A simple, novel and robust test to diagnose type I Glanzmann thrombasthenia.Haematologica. 2008 May;93(5):797-8. doi: 10.3324/haematol.12288. PubMed PMID:18450741.
  145. Ghosh K, Shetty S, Mota L. Falciparum malaria selected while HIV-1 slaughtered. Indian J Hum Genet. 2008 May;14(2):70. doi: 10.4103/0971-6866.44109.PubMed PMID: 20300298; PubMed Central PMCID: PMC2840787.
  146. Ghosh K, Shetty S. A plethora of techniques to detect mutations: Which one to choose? Indian J Hum Genet. 2008 May;14(2):35-6. doi: 10.4103/0971-6866.44102.PubMed PMID: 20300291; PubMed Central PMCID: PMC2840791.
  147. 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. doi: 10.1111/j.1365-2516.2008.01704.x.Epub 2008 Apr 3. PubMed PMID: 18393981.
  148. 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 Jun;53(1):46-51. doi:10.1111/j.1574-695X.2008.00399.x. Epub 2008 Mar 25. PubMed PMID: 18371071.
  149. Ghosh K, Shetty S. Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing inhaemophilia. Haemophilia. 2008 Mar;14(2):392-3. doi:10.1111/j.1365-2516.2007.01641.x. Epub 2007 Dec 29. PubMed PMID: 18179571.
  150. 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. Epub 2007 Dec 26. PubMed PMID: 18160603.
  151. Ghosh K, Shetty S. Blood coagulation in falciparum malaria--a review. Parasitol Res. 2008 Mar;102(4):571-6. Epub 2007 Dec 8. Review. PubMed PMID:18066597.
  152. 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. Epub 2007 Nov 19. PubMed PMID: 18028421.
  153. 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. PubMed PMID: 17973850.
  154. 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. PubMed PMID: 17762534.
  155. 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.PubMed PMID: 17659055.
  156. 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. Epub 2007 Jul 17. PubMedPMID: 17644242.
  157. 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. PubMed PMID: 17610719; PubMed Central PMCID: PMC1950495.
  158. Ghosh K, Vora S, Shetty S. Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis. Br J Haematol. 2007 Aug;138(4):557. Epub2007 Jun 21. PubMed PMID: 17590183
  159. Ghosh K, Madkaikar M, Jijina F, Shetty S. Fractures of long bones in severe haemophilia. Haemophilia. 2007 May;13(3):337-9. PubMed PMID: 17498087.
  160. Ghosh K, Khare A, Shetty S. Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India. IndianHeart J. 2007 May-Jun;59(3):242-5. PubMed PMID: 19124933.
  161. 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.PubMed PMID: 17356389.
  162. 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 themajority of the Gujarati population. Ann Hematol. 2007 May;86(5):377-9. Epub 2007Feb 17. PubMed PMID: 17308903.
  163. 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. PubMed PMID: 17286770.
  164. Ghosh K, Khare A, Shetty S, Kulkarni B. Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern ofresponse to oral folic acid, vitamin B12, B6 therapy. Clin Chim Acta. 2007Feb;377(1-2):281-2. Epub 2006 Sep 22. PubMed PMID: 17069780.
  165. Shetty S, Ghosh K, Jijina F. First-trimester prenatal diagnosis inhaemophilia A and B families--10 years experience from a centre in India. Prenat Diagn. 2006 Nov;26(11):1015-7. PubMed PMID: 16941728.
  166. Kulkarni B, Nair S, Shetty S, Ghosh K. Diagnostic pitfalls and fallacies of measuring antiplatelet antibodies. Acta Haematol. 2006;116(1):75-6. PubMed PMID: 16809896.
  167. Ghosh K, Khare A, Shetty S, Nair S, Kulkarni B, Mohanty D. Flowcytometric evidence of platelet activation in patients on aspirin following myocardialinfarction. Natl Med J India. 2006 Mar-Apr;19(2):73-4. PubMed PMID: 16756193.
  168. Ghosh K, Trasi S, Shetty S, Mohanty D. Use of a new enzyme-linked immunosorbent assay for the detection of type 2N von Willebrand disease and its prevalence in an Indian population. Blood Coagul Fibrinolysis. 2006Jan;17(1):7-11. PubMed PMID: 16607072.
  169. Ghosh K, Vora S, Shetty S. Thrombophilia and pregnancy loss--picking up a needle from the haystack! Am J Obstet Gynecol. 2006 Mar;194(3):900; author reply 901. PubMed PMID: 16522434
  170. Trasi S, Mohanty D, Pathare A, Shetty S, Ghosh K. Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection invon Willebrand disease families in the Indian population. Acta Haematol.2006;115(1-2):64-7. PubMed PMID: 16424652.
  171. Trasi S, Mohanty D, Shetty S, Ghosh K. Prenatal diagnosis of von Willebrand disease in a family. Natl Med J India. 2005 Jul-Aug;18(4):187-8. PubMed PMID:16252548.
  172. Ghosh K, Khare A, Shetty S. Implications of human genome and modern cell biology research in management of cardiovascular diseases. Indian Heart J. 2005 May-Jun;57(3):270-3. Review. PubMed PMID: 16196190.
  173. Ghosh K, Nair AP, Jijina F, Madkaikar M, Shetty S, Mohanty D. Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country. Haemophilia. 2005 Sep;11(5):459-62. PubMed PMID: 16128888.
  174. Mohanty D, Ghosh K, Shetty S, Spreafico M, Garagiola I, Peyvandi F.Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indianfamilies with combined deficiency of factor V and VIII. Am J Hematol. 2005Aug;79(4):262-6. PubMed PMID: 16044454.
  175. Trasi S, Ghosh K, Shetty S, Mohanty D. von Willebrand disease: a laboratory approach. Natl Med J India. 2005 Mar-Apr;18(2):78-84. Review. PubMed PMID:15981443.
  176. Trasi S, Shetty S, Ghosh K, Mohanty D. Prevalence and spectrum of von Willebrand disease from western India. Indian J Med Res. 2005 May;121(5):653-8.PubMed PMID: 15937368.
  177. Khare A, Shetty S, Ghosh K, Mohanty D, Chatterjee S. Evaluation of markers of endothelial damage in cases of young myocardial infarction. Atherosclerosis.2005 Jun;180(2):375-80. PubMed PMID: 15910865.
  178. Ghosh K, Nair S, Shetty S, Rajapurkar M, Mohanty D. Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: a unified pathology?Platelets. 2005 Mar;16(2):85-9. PubMed PMID: 15823864.
  179. Nair S, Ghosh K, Shetty S, Mohanty D. Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients. J Thromb Haemost. 2005 Mar;3(3):482-8. PubMed PMID: 15748237.
  180. Colah RB, Shetty SD, Surve RR, Phanasgaonkar SP, Nadkarni AH, Gorakshakar AC, Ghosh K, Parekh SJ, Mohanty D. Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon association. Hemoglobin.2004;28(4):343-6. PubMed PMID: 15658191.
  181. Nair S, Ghosh K, Shetty S, Mohanty D. A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patient. Haematologica. 2004 Dec;89(12):1529-30. PubMed PMID: 15590407.
  182. Ghosh K, Shetty S. Anticoagulation in haemophilia patients with prosthetic valve replacement. Haemophilia. 2004 Nov;10(6):743. PubMed PMID: 15569172.
  183. Colah R, Shetty S, Nadkarni A, Ghosh K, Mohanty D. Masking of the clinical severity of severe haemophilia A in a patient with beta-thalassemia major—its implications in prenatal diagnosis. Prenat Diagn. 2004 Nov;24(11):925-6. PubMed PMID: 15565557.
  184. Khare A, Ghosh K, Shetty S, Kulkarni B, Mohanty D. Combination of thrombophilia markers in acute myocardial infarction of the young. Indian J Med Sci. 2004 Sep;58(9):381-8. PubMed PMID: 15470279.
  185. Ghosh K, Shetty S, Mohanty D. Inversion of intron 1 is a rare cause of severe hemophilia A in Indian population. J Thromb Haemost. 2004 Aug;2(8):1481-2.PubMed PMID: 15304066.
  186. Trasi SA, Pathare AV, Shetty SD, Ghosh K, Salvi V, Mohanty D. The spectrum of bleeding disorders in women with menorrhagia: a report from Western India. AnnHematol. 2005 May;84(5):339-42. Epub 2004 Jul 30. PubMed PMID: 15290102.
  187. Shetty S, Ghosh K, Mohanty D. Major disorganization of factor VIII gene as a cause of severe hemophilia A in Indian patients. Am J Hematol. 2004 May;76(1):96.PubMed PMID: 15114612.
  188. Ghosh K, Khare A, Kulkarni B, Shetty S, Mohanty D. Geography too determines the causes of inherited thrombophilia. J Thromb Haemost. 2004 Feb;2(2):363-4.PubMed PMID: 14996018.
  189. Shetty S, Ghosh K, Mohanty D. Genetic disorder following assisted reproductive technology - prevent if you can, but always counsel! Br J Haematol. 2004 Feb;124(4):561. PubMed PMID: 14984513.
  190. Ghosh K, Shetty S, Jijina F, Mohanty D. Role of epsilon amino caproic cid in the management of haemophilic patients with inhibitors. Haemophilia. 2004 Jan;10(1):58-62. PubMed PMID: 14962221.
  191. Mohanty D, Colah RB, Gorakshakar AC, Nadkarni AH, Phanasgaonkar SP, Shetty S, Ghosh K, Mukherjee MB. Genetic disorders in haematological practice in India. Community Genet. 2002;5(3):197-200. PubMed PMID: 14960892.
  192. Shetty S, Ghosh K, Mohanty D. Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements. J Assoc Physicians India. 2003 Sep;51:916-8. PubMed PMID: 14710984.
  193. Mohanty D, Ghosh K, Shetty S. Selection bias largely explains the differential distribution of factor V Leiden in different patient populations between the centers--a rebuttal. J Thromb Haemost. 2003 Dec;1(12):2697-8. PubMed PMID: 14675117.
  194. Ghosh K, Nair S, Kulkarni B, Khare A, Shetty S, Mohanty D. Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function. Platelets. 2003 Sep;14(6):351-4. PubMed PMID:14602548.
  195. Ghosh K, Nair S, Kulkarni B, Shetty S, Mohanty D. Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state.J Thromb Haemost. 2003 Oct;1(10):2255-6. PubMed PMID: 14521621.
  196. Ghosh K, Trasi S, Nair S, Shetty S, Mohanty D. Prevalence of inherited bleeding disorders in cases of idiopathic menorrhagia: a case of five blind men describing an elephant. J Thromb Haemost. 2003 Oct;1(10):2242-3. PubMed PMID:14521612.
  197. Ghosh K, Nair S, Kulkarni B, Khare A, Trasi S, Shetty S, Mohanty D.Inherited haemostatic disorders in idiopathic menorrhagia: do the special interest of a hemostatic laboratory make a difference? Haemophilia. 2003 Sep;9(5):660-1. PubMed PMID: 14511314.
  198. Shetty S, Ghosh K, Mohanty D. ELISA for factor VIII antibodies: does it detect antibodies much before the conventional Bethesda assay? Haemophilia. 2003 Sep;9(5):654. PubMed PMID: 14511311.
  199. Ghosh K, Nabar A, Shetty S, Soren D, Mohanty D. Is there a prethrombotic state in left atrial blood in rheumatic mitral stenosis? Am J Hematol. 2003 Oct;74(2):144. PubMed PMID: 14508805.
  200. Shetty S, Ghosh K, Mohanty D. Direct detection of factor IX gene deletions in Indian haemophiliacs by multiplex PCR. Eur J Haematol. 2003 Sep;71(3):233-4.PubMed PMID: 12930328.
  201. Shetty S, Ghosh K, Mohanty D. Comparison of four commercially available activated partial thromboplastin time reagents using a semi-automated coagulometer. Blood Coagul Fibrinolysis. 2003 Jul;14(5):493-7. PubMed PMID:12851537.
  202. Shetty S, Ghosh K, Anbhavne S, Mohanty D. Requiem to prenatal diagnosis of haemophilia A and B using coagulation activity and antigen based assays: not yet!Eur J Haematol. 2003 Apr;70(4):253-4. PubMed PMID: 12656753.
  203. Ghosh K, Shankarkumar U, Shetty S, Mohanty D. Chronic synovitis and HLA B27 in patients with severe haemophilia. Lancet. 2003 Mar 15;361(9361):933-4. PubMed PMID: 12648975.
  204. Ghosh K, Madkaikar M, Jijina F, Gandhi S, Shetty S, Mohanty D. Open heart surgery with mitral valve replacement--ordeal of an undiagnosed haemophiliapatient. Clin Lab Haematol. 2003 Apr;25(2):131-3. PubMed PMID: 12641618.
  205. Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D. Glanzmann's thrombasthenia: updated. Platelets. 2002 Nov;13(7):387-93. Review. PubMed PMID:12487785.
  206. Shetty S, Ghosh K, Mohanty D. An ELISA assay for the detection of factor VIII antibodies - comparison with the conventional Bethesda assay in a large cohort of haemophilia samples. Acta Haematol. 2003;109(1):18-22. PubMed PMID:12486318.
  207. Ghosh K, Jijina F, Shetty S, Madkaikar M, Mohanty D. First-time development of FVIII inhibitor in haemophilia patients during thepostoperative period.Haemophilia. 2002 Nov;8(6):776-80. PubMed PMID: 12410646.
  208. Ghosh K, Kulkarni B, Nair S, Shetty S, Mohanty D. Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease. Br J Haematol. 2002 Nov;119(2):348-53. PubMed PMID: 12406067.
  209. Manisha M, Ghosh K, Shetty S, Nair S, Khare A, Kulkarni B, Pathare AV,Baindur S, Mohanty D. Spectrum of inherited bleeding disorders from Western India. Haematologia (Budap). 2002;32(1):39-47. PubMed PMID: 12243554.
  210. Ghosh K, Shetty S, Jijina F, Mohanty D. Development of anti-VWF antibody in a patient with severe haemophilia A following the development of high-grade non-Hodgkin's lymphoma. Clin Lab Haematol. 2002 Jun;24(3):191-3. PubMed PMID:12067287.
  211. Ghosh K, Shetty S, Pawar A, Mohanty D. Danazol therapy in factor X deficiency: more questions than answers. Haemophilia. 2002 Jan;8(1):61-2. PubMed PMID: 11886468.
  212. Ghosh K, Shetty S, Pawar A, Mohanty D. Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges. Haemophilia. 2002Jan;8(1):51-5. PubMed PMID: 11886465.
  213. Pawar AR, Shetty S, Ghosh K, Mohanty D. How old is factor V Leiden mutation? Thromb Haemost. 2001 Dec;86(6):1591-2. PubMed PMID: 11776338.
  214. Shetty S, Ghosh K, Mohanty D. Hemophilia B in a female. Acta Haematol. 2001;106(3):115-7. PubMed PMID: 11713376.
  215. Ghosh K, Shetty S, Mohanty D. Congenital deficiency of vitamin K dependent coagulation factors--its rarity and need for an international registry. Thromb Haemost. 2001 Oct;86(4):1131. PubMed PMID: 11686345.
  216. Mohanty D, Shetty S, Ghosh K, Pawar A, Abraham P. Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India. Hepatology. 2001 Oct;34(4 Pt 1):666-70. PubMed PMID: 11584361.
  217. Ghosh K, Shetty S, Mohanty D. Haemorrhage in upper cervical cord: an unusual manifestation in moderate haemophilia patients who ride motorbikes. Haemophilia. 2001 Sep;7(5):515-6. PubMed PMID: 11554943.
  218. Shetty S, Ghosh K, Parekh S, Mohanty D. Combined factor VIII and IX deficiency in a family. Clin Lab Haematol. 2001 Jun;23(3):201-4. PubMed PMID:11553064.
  219. Shetty S, Ghosh K, Bhide A, Mohanty D. Carrier detection and prenatal diagnosis in families with haemophilia. Natl Med J India. 2001Mar-Apr;14(2):81-3. PubMed PMID: 11396323.
  220. Ghosh K, Shetty S, Kulkarni B, Nair S, Pawar A, Khare A, Baindur S, Mohanty D. Development of inhibitors in patients with haemophilia from India.Haemophilia. 2001 May;7(3):273-8. PubMed PMID: 11380631.
  221. Ghosh K, Shetty S, Madkaikar M, Pawar A, Nair S, Khare A, Pathare A, Jijina F, Mohanty D. Venous thromboembolism in young patients from western India: astudy. Clin Appl Thromb Hemost. 2001 Apr;7(2):158-65. PubMed PMID: 11292195.
  222. Tullu MS, Dixit PS, Nair SB, Kamat JR, Vaswani RK, Shetty SD, Pawar AR.Glanzmann's thrombasthenia.Indian J Pediatr. 2001 Jun;68(6):563-6
  223. Ghosh K, Shetty S, Mohanty D. Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one-stage assay.Haemophilia. 2001 Jan;7(1):9-12. PubMed PMID: 11136374.
  224. Shetty S, Ghosh K, Mohanty D. St 14 (DX S52) VNTR polymorphism in the Indianpopulation and its application in carrier detection and prenatal diagnosis ofhaemophilia A families. Haematologia (Budap). 2000;30(3):203-7. PubMed PMID:11128113.
  225. Ghosh K, Joshi SH, Shetty S, Pawar A, Chipkar S, Pujari V, Madkaikar M, Pathare AV, Jijina F, Mohanty D. Transfusion transmitted diseases in haemophilics from western India. Indian J Med Res. 2000 Aug;112:61-4. PubMed PMID: 11037680.
  226. Ghosh K, Shetty S, Mohanty D. Detection of unexpected lupus anticoagulant during preparation of normal pooled plasma (NPP) from healthy volunteers. Thromb Haemost. 2000 Sep;84(3):519-21. PubMed PMID: 11019985.
  227. Shetty S, Madkaikar M, Nair S, Pawar A, Baindur S, Pathare A, Ghosh K,Mohanty D. Combined factor V and VIII deficiency in Indian population.Haemophilia. 2000 Sep;6(5):504-7. PubMed PMID: 11012693.
  228. Shetty S, Colah R, Gorakshakar A, Bhide A, Ghosh K, Pathare A, Jijina F,Mohanty D. Prenatal diagnosis of haemophilia: a preliminary report. Natl Med J India. 1998 Sep-Oct;11(5):218-9. PubMed PMID: 10997168.
  229. Shetty S, Ghosh K, Pathare A, Mohanty D. Clinically significant inhibitors in hemophilia A patients from India tend to persist. Acta Haematol.2000;103(3):175-6. PubMed PMID: 10940659.
  230. Pawar A, Ghosh K, Shetty S, Colah R, Mohanty D. High frequency of factor V Leiden mutation in Parsis--a highly endogamous population in India. Thromb Haemost. 2000 Jun;83(6):965. PubMed PMID: 10896258.
  231. Ghosh K, Shetty S, Pathare A, Mohanty D. Epsilon-aminocaproic acid inhibits the activity of factor VIII inhibitors in patients with severe haemophilia A invivo and in vitro. Acta Haematol. 2000;103(2):67-72. PubMed PMID: 10838448.
  232. Ghosh K, Shetty S, Mohanty D. Haemophilia following successful in vitro fertilization. Haemophilia. 1999 Sep;5(5):364. PubMed PMID: 10583520.
  233. Shetty S, Ghosh K, Pathare A, Mohanty D. Carrier detection in haemophilia A families: comparison of conventional coagulation parameters with DNA polymorphism analysis - first report from India. Haemophilia. 1999 Jul;5(4):243-6. PubMed PMID: 10469177.
  234. Shetty S, Ghosh K, Pathare A, Jijina F, Mohanty D. Molecular characterization of haemophilia A & B in Indians. Haemophilia. 1998 Nov;4(6):802-5. PubMed PMID: 10028301.
  235. Shetty S, Pathare A, Ghosh K, Jijina F, Mohanty D. Intron 22 inversions in factor VIII gene in Indian hemophiliacs. Thromb Haemost. 1998 Apr;79(4):881.
  236. Mohanty D, Shetty S, Narayanan TS, Abraham P. Factor V leiden mutation and Budd-Chiari syndrome. Blood. 1998 Sep 1;92(5):1838-9.
  237. 239. Shetty S, Ghosh K, Pathare A, Colah R, Badakare S, Mohanty D. Factor VIII and IX gene polymorphisms and carrier analysis in Indian population. Am J Hematol. 1997 Apr;54(4):271-5. PubMed PMID: 9092680.
  238. Mohanty D, Ghosh K, Nandwani SK, Shetty S, Phillips C, Rizvi S, Parmar BD. Fibrinolysis, inhibitors of blood coagulation, and monocyte derived coagulant activity in acute malaria. Am J Hematol. 1997 Jan;54(1):23-9. PubMed PMID: 8980257.
  239. Ghosh K, Shetty S, Mohanty D. Inherited deficiency of multiple vitamin K-dependent coagulation factors and coagulation inhibitors presenting as hemorrhagic diathesis, mental retardation, and growth retardation. Am J Hematol. 1996 May;52(1):67. PubMed PMID: 8638624.

Projects

Projects Ongoing:

  1. A rapid nanoparticle-based lateral flow immunoassay for the detection of von Willebrand factor and alloantibodies to von Willebrand factor and procoagulant factor FVIII from human plasma samples (Funded By ICMR Medical Innovation Scheme, 2017 - 2019).
  2. Modulation of the function of activated protein C(APC) to improve the clinical phenotype of haemophilia A (Funded By ICMR, 2015 - 2018 )
  3. Phenotypic and genotypic characterization of antithrombin (AT) deficiency in Indian patients with thrombosis ( Funded By ICMR, 2015 - 2018)
  4. Increasing the hemostatic potential of recombinant factor VIII by combining it with platelet-derived microparticles / synthetic phospholipid vesicles containing phospatidylserine (Funded By SERB, 2016 - 2018)
  5. Clinical spectrum and molecular basis of thrombotic microangiopathies ( Funded By ICMR, 2016 - 2019)
  6. Assessment of diagnostic tests for monitoring bypassing agent therapy in Hemophilia patients with inhibitors ( Funded By DHR, 2016 - 2019)
  7. Defects in the fibrinolytic pathway as a cause of bleeding disorder in Indian patients (Funded By ICMR – SRF Project, 2017 - 2019)

Projects Completed:

  1. Disorders of Fibrinolysis as a cause of thrombophilia in Indian patients with Deep Vein Thrombosis (DVT) (Funded By ICMR, 2014- 2017)
  2. Assessing the role of cell – Derived microparticles in Dengue virus infection (Funded By ICMR Post Doctoral Fellowship, 2016 - 2017)

Research Staff

Haemostasis and Thrombosis

Sr. No. Name Designation
1 Mr. Aniket Prabhudesai SRF, Ph.D Student
2 Ms. Rutuja Deshpande PhD Student
3 Ms. Darshana Mirgal PhD Student
4 Ms. Puja Soni PhD Student
5 Ms. Sneha Yadav PhD Student
6 Mr. Nikesh Kawankar Ph.D Student