Important Announcement Annual Training Program in Immnohaematology... Read More

2016

  • 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.(IF:2.673)
  • 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:0.963)
  • 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)
  • 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:2.514)
  • 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:0.31)
  • 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:2.320)
  • 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:--)
  • 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:2.544)
  • 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:1.846)
  • 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:3.093)
  • 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:0.963)
  • Gorakshakar AC, Ghosh K. Use of lectins in immunohematology. Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF:1.06)
  • 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:0.31)
  • 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:0.747)
  • 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:2.921)
  • 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.(IF3.853)
  • Jadli AS, Ghosh K, Shetty S. Preeclampsia: simplified or still miles to go? Am J Obstet Gynecol. 2016 May;214(5):668-9.(IF:4.681)
  • 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:3.022)
  • 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:2.320)
  • 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:2.372)
  • 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:0.963)
  • 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:2.09)
  • 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:1.631)
  • 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:2.646)
  • 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:2.822)
  • 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. 2016 Aug 26. doi: 10.1002/jcla.22054. [Epub ahead of print](IF:1.549)
  • 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:1.973)
  • P Hariharan, S Colaco, R Colah, K Ghosh A Nadkarni. Do -globin gene variants contribute in substantial reduction in HbA2 levels? Int. J. Lab Hematol 2016 Dec;38(6):610-615.(IF:2.401)
  • 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)
  • 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:3.022)
  • 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:3.022)
  • 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:2.646)
  • 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:3.017)
  • 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.(IF3.448)
  • 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:4.681)
  • 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:7.803)
  • 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: 8.784)
  • Patil R, Ghosh K, Shetty S. Betrixaban in Acutely Ill Medical Patients. N Engl J Med. 2016 Dec 15;375(24):e50.(IF:59.558)
  • 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:2.512)
  • 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:2.93)
  • 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)
  • 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:4.843)
  • 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:5.812)
  • 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:2.646)
  • Shanbhag S, Ghosh K, Shetty S. First trimester prenatal diagnosis of severe FXIII deficiency. Haemophilia. 2016 Sep;22(5):e443-4. (IF:2.673)
  • Shetty S, Sharma N, Ghosh K. Epidemiology of hepatocellular carcinoma (HCC) in hemophilia. Crit Rev Oncol Hematol. 2016 Mar;99:129-33.(IF:5.98)
  • Shetty S, Ghosh K. Why should hemophilia B be milder than hemophilia A? Haematologica. 2016 May;101(5):e213. (IF:6.671)
  • 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:3.54)
  • 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. 2016 Aug 17. doi: 10.4103/0022-3859.188550. [Epub ahead of print] (IF:0.87)
  • 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:3.54)
  • 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:3.022)

2015

  • 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)
  • 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)
  • Adams SP, Wilson M, Harb E, Fairbanks L, Xu-Bayford J, Brown L, Kearney L, Madkaikar M, Bobby Gaspar H. Spectrum of mutations in a cohort of UK patients with ADA deficient SCID: Segregation of genotypes with specific ethnicities. Clin Immunol. 2015 Dec;161(2):174-9. (IF:2.44)
  • 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:2.646)
  • Colah RB, Mukherjee MB, Martin S, Ghosh K. Sickle cell disease in tribal populations in India. Indian J Med Res. 2015 May;141(5):509-15.(IF:1.446)
  • Dalal B, Shankarkumar A, Ghosh K. Individualization of antiretroviral therapy Pharmacogenomic aspect. Indian J Med Res. 2015 Dec;142(6):663-74.(IF1.446)
  • Dalal K., Shankarkumar A. Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma. Intl J Res Engg Applied Sci 2015Aug; 5(8): 76-89.(IF:6.573)
  • Deb S, Ghosh K, Shetty SD. Nanoimaging in cardiovascular diseases: Current state of the art. Indian J Med Res. 2015 Mar;141(3):285-98.(IF:1.446)
  • 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:--)
  • 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:1.31)
  • Ghosh K. Sickle cell anaemia: The need for new approaches in management. Natl Med J India. 2015 Mar-Apr;28(2):90-3.(IF:0.33)
  • Ghosh K, Colah RB, Mukherjee MB. Haemoglobinopathies in tribal populations of India. Indian J Med Res. 2015 May;141(5):505-8.(IF:1.446)
  • 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:0.31)
  • 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:4.959)
  • Italia Y, 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:3.099)
  • 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:2.646)
  • 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:2.320)
  • 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:3.853)
  • 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:1.575)
  • 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)
  • Kasatkar P, Ghosh K, Shetty S. Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population. Indian J Med Res. 2015 Dec;142(6):759-62.(IF:1.446)
  • Koduri PR, Kedar PS, Warang P. Erythrocytosis, methemoglobinemia, and the saturation gap. Ann Hematol. 2015 Mar;94(3):509-10.(IF:2.866)
  • Korgaonkar S, Vundinti BR. Tetrasomy X in a Child with Upper Limb Deformity. Indian Pediatr. 2015 May;52(5):439.(IF:1.040)
  • Korgaonkar S, Vundinti BR. Trisomy 8 Mosaicism in a Boy with Dysmorphic Features. Indian Pediatr. 2015 Sep;52(9):812-3(IF:1.040)
  • 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)
  • 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)
  • 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)
  • 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.(IF3.094)
  • 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)
  • 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)
  • 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)
  • 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)
  • Mishra A, Italia K, Gupta M, Desai M, Madkaikar M. Syndrome due to CD40 Deficiency: Possibly the first case from India. J Postgrad Med. 2015 Jan-Mar; 61:41-48.(IF:0.77)
  • 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 Pacific J Public Health. 2015 Mar;27(2):NP562-71. (IF:1.056)
  • 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):755-7.(IF:2.278)
  • 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)
  • Mukherjee MB, Colah RB, Martin S, Ghosh K. Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario. Indian J Med Res. 2015 May;141(5):516-20.(IF:1.446)
  • 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)
  • 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:2.646)
  • 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 = 5.114)
  • 41. 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:--)
  • 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:4.71)
  • 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)
  • 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:2.646)
  • 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)
  • Pradhan V, Surve P, Rajadhyaksha A, Rajendran V, Patwardhan M, Umare V, Ghosh K, Nadkarni A. Mannose binding lectin (MBL) 2 gene polymorphism & its association with clinical manifestations in systemic lupus erythematosus (SLE) patients from western India. Indian J Med Res. 2015 Feb;141(2):199-204.(IF:1.446)
  • 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:1.516)
  • 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)
  • 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)
  • 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:0.233)
  • 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:6.226)
  • 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)
  • 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)
  • Shetty S, Ghosh K. Novel therapeutic approaches for haemophilia. Haemophilia. 2015 Mar;21(2):152-61. (IF:3.170)
  • 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)
  • 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:1.870)
  • 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.(IF:3.234)
  • 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:2.54)
  • 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:3.652)
  • 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:2.866)
  • 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:2.955)
  • A.Sonawane Patil, A Shankarkumar Pawar. 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 = 5.121)

2014

  • 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).
  • Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ 100(G2)Pro - Ser; HBD: C.301C>T] in Cis. Hemoglobin 2014 Jan-Feb; 38(1):24-7. .(IF:0.955)
  • 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.
  • 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).
  • Colah R, Mukherjee M, Ghosh K. Sickle cell disease in India. Curr Opin Hematol. 2014 May; 21(3):215-23.
  • 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.
  • 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:1.385).
  • 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.
  • 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).
  • 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.
  • Gaikwad T, Ghosh K, Shetty S. VKORC1 and CYP2C9 genotype distribution in Asian countries. Thromb Res. 2014 Sep; 134(3):537-44.
  • Ghosh K. Familial Mediterranean fever: An unusal disease enlightening the inflammation biology. Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--).
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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).
  • 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.
  • 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.
  • 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:--).
  • 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).
  • 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.
  • 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.
  • 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.
  • 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).
  • 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.
  • 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.
  • 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.
  • Mohanty D, Gorakshakar AC, Colah RB, 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. Interaction of iron deficiency anemia and hemoglobinopathies among college students and pregnant women: a multi center evaluation in India. Hemoglobin. 2014;38(4):252-7.
  • 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 Dec 17. [Epub ahead of print].
  • Nadkarni A, Dabke P, Colah RB, Ghosh K. Fetal hemoglobin in sickle cell anemia. Blood Cells Mol Dis. 2014 Apr;52(4):175.
  • 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.
  • Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A. Clin Appl Thromb Hemost. 2014 Dec 29. [Epub ahead of print].
  • Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A. Clin Appl Thromb Hemost. 2014 Dec 29. [Epub ahead of print].
  • 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:--).
  • Parasannanavar 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.
  • 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).
  • 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.
  • 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.
  • 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.
  • 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.
  • Purohit A, Aggarwal M, Colah RB, Nadkarni AH, Pati HP. A Case of Iron Deficiency Anemia with Co-existing Hb Fontainebleau. J Hematol Infect Dis. 2014 Jul 1;6(1):e2014051.
  • 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).
  • 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).
  • 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).
  • 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).
  • Shetty S, Shelar T, Mirgal D, Nawadkar V, Pinto P, Shabhag S, Mukaddam A, Kulkarni B, Ghosh K. Rare coagulation factor deficiencies: a countrywide screening data from India. Haemophilia. 2014 Jul; 20(4):575-81.
  • 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.
  • 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.
  • Umare V, Pradhan V, Nadkar M, Rajadhyaksha A, Patwardhan M, Ghosh KK, 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.
  • 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 1; 52(12):1791-6.
  • 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).
  • 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.
  • 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.

2013

  • 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)
  • 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 Jan; 50(1): 156-60.(IF:2.361)
  • 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)
  • 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)
  • 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 Jan 27. [Epub ahead of print] (IF: 2.615)
  • 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 Jan 28. [Epub ahead of print] (IF:2.443)
  • Chaudhary AK, Pandya S, Ghosh K, Nadkarni A. Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: An overview. Mutat Res Rev. 2013 Jan 28. [Epub ahead of print](IF: 3.133)
  • 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)
  • Pai N, Ghosh K, Shetty S. Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT). Clin Appl Thromb Hemost. 2013 Feb 12. [Epub ahead of print](IF: 1.332)
  • Ali S, Ghosh K, Shetty S. Molecular pathology of Bernard-Soulier syndrome in Indian patients. Platelets. 2013 Feb 12. [Epub ahead of print](IF: 1.827)
  • Gupta M, Madkaikar M, Rao VB, Mishra A, Govindaraj P, Thangaraj K, Ghosh K Mitochondrial DNA variations in myelodysplastic syndrome. Ann Hematol. 2013 Mar 9. [Epub ahead of print] (IF: 2.615)
  • 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 Mar 9. [Epub ahead of print](IF:1.974)
  • 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. 2013 Mar 19. [Epub ahead of print](IF: 1.056 )
  • Nair SB, Nadkarni AH, Ghosh K, Colah RB. Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal a T Indian (AATAAA>AATA- -) Mutation in Four Indian Families. Hemoglobin. 2013 Mar 21. [Epub ahead of print] (IF: 1.304)
  • Pai N, Ghosh K, Shetty S. Hereditary thrombophilia in cerebral venous thrombosis: a study from India. Blood Coagul Fibrinolysis . 2013 Mar 20. [Epub ahead of print](IF:1.238)
  • 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. 2013:33(4): 867-870. (IF: 2.214)
  • Parasannanavar DJ , Yeola A, Pradhan V, Manisha P, Rajadhyaksha.A, Ghosh K. Distribution of HLA-DRβ1alleles among well characterized Rheumatoid Arthritis patients from Western India. Rheumatology International.( 2013) DOI: 10.1007/s00296-013-2758-4. (IF: 2.214)
  • Devraj J. Parasannanavar, Anjali Rajadhyaksha, and Kanjaksha Ghosh . Application of a Simple In-House PCR-SSP Technique for HLA-B* 27 Typing in Spondyloarthritis Patients. Arthritis (2013), Article ID 504109, 4 pages

2012

  • 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)
  • Madkaikar MR, Gupta M, Rao M, Ghosh K. Prenatal Diagnosis of LAD-I on Cord Blood by Flowcytometry. Indian J Pediatr. 2012 Apr 4.(IF: 0.521)
  • 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. 2012Jul;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.(2.472)
  • Pai N, Ghosh K, Shetty S. Hereditary protein C deficiency in Indian patients with venous thrombosis. Ann Hematol. 2012Sep;91(9):1471-6.(IF: 2.615)
  • 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. 2012 May 24. [Epub ahead of print](IF: 1.885)
  • 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)
  • Gorakshakar AC, Ghosh K. Transfusion Transmitted Infections in Indian Thalassemics: a perspective. Indian J Hematol Blood Transf. 2012 Jun.(IF:0.056)
  • Abuljadayel IS, Mohanty D, Suri RK A novel autologous stem cell procedure for the treatment of aplastic anaemia using reprogrammed mature adult cells: a pilot study. Indian J Med Res. 2012 Jun; 135(6):853-72.(IF: 1.837)
  • Jain D, Italia K, Sarathi V, Ghosh K, Colah R. Sickle Cell Disease from Central India: A Retrospective Analysis. Indian Pediatr. 2012 Jun 10. [Epub ahead of print](IF:1.048)
  • 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.
  • 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)
  • Pradhan V,Patwardhan M, Rajadhyaksha A and Ghosh K. Clinical and Immunological profile of systemic lupus erythematosus. Indian Pediatr 2012 Aug 05. [Epub ahead of print](IF: 1.048)
  • 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 Aug 16.[Epub ahead of print](IF: 2.795)
  • 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.
  • 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 V, Ghosh K Immunological disturbances associated with malarial infection. J Parasitic Dis Sep 27; 2012 (published online).
  • 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: )
  • Nair SB, Colah R. Five a-globin chain variants identified during screening for haemoglobinopathies. Eur J Clin Invest. 2012 Sep 7 [Epub ahead of print](IF:3.018)
  • 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)
  • 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. 2012 Oct 31. [Epub ahead of print] (IF:3.077)
  • 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. 2012 Nov 9. [Epub ahead of print] (IF: 2.615)
  • 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.
  • 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, 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. 2012 Dec 19. [Epub ahead of print](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 2012 Dec 20. [Epub ahead of print](IF: 1.885)
  • Nair S, Ghosh K. The myriad effects of cigarette smoke. J Thromb Haemost. 2012 Dec 22.[Epub ahead of print](IF: 5.731)
  • Pinto P, Ghosh K, Shetty S Factor VIII haplotypes in severe hemophilia A patients in India. Ann Hematol. 2012 Dec 23. [Epub ahead of print] (IF: 2.615)

2011

  • 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.
  • Kanjaksha Ghosh, Roshan Colah. Phenotypic diversity of sickle cell disorders: a rebuttal. Curr Sci 2011 Jan; 100(2):149.
  • 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.
  • 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 Jan 3. [Epub ahead of print] PubMed PMID: 21198350.
  • 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 Cytometry). 2011 Feb; 80B:186-190.
  • 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 Feb 19. doi: 10.1111/j.1574-695X.2011.00794.x. [Epub ahead of print] PubMed PMID: 21332827.
  • Shanbhag S, Shetty S, Kulkarni B, Ghosh K. An improved, semi quantitative clot based assay for factor XIII. Haemophilia. 2011 Feb 15. doi: 10.1111/j.1365-2516.2010.02456.x. [Epub ahead of print] PubMed PMID: 21323796.
  • 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. doi: 10.1002/ajh.21956. Epub 2011 Feb 15. PubMed PMID: 21328435.
  • Shetty S, Bhave M, Ghosh K. Challenges of multiple mutations in individual patients with haemophilia. Eur J Haematol. 2011 Mar; 86(3): 185-90.
  • Madkaikar M, Mhatre S, Gupta M, Ghosh K. Advances in Autoimmune Lymphoproliferative Syndromes (ALPS). Eur J Haematol .

2010

  • 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.
  • Kasatkar P. Shetty S, Ghosh K . VWF pseudogene; Mimics, masks and spoils. Clin Chim Acta. 2010 Apr 2;411(7-8):607-9.
  • 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.
  • 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.
  • Kanjaksha Ghosh, Kinjalka Ghosh. Advances in Haematological Pharmacotherapy in 21 st Century. Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • Ghosh K. Bachelor of rural health care: cutting the root and watering the stem! Natl Med J India. 2010 Jul-Aug;23(4):250.
  • 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.
  • 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.
  • 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.
  • 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.
  • Kasatkar P, Shetty S, Ghosh K. Delayed vitamin K deficiency as a cause of bleeding: still a concern in the 21 st century! Blood Coagul Fibrinolysis. 2010 Sept; 21(6):608-10.
  • Shankarkumar U. Complexities and similarities of HLA antigen distribution in Asian subcontinent. Indian J Hum Genet . 2010 Sep;16(3):108-10.
  • 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.
  • 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.
  • Shetty S, Ghosh K. Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis - A concise review. Thromb Res. 2010 Oct 19. [Epub ahead of print] PubMed PMID: 20961602.
  • Black ML, Sinha S, Agarwal S, Colah R, Das R, Bellgard M, Bittles AH. A descriptive profile of b -Thalassaemia mutations in India, Pakistan and Sri Lanka. J Community Genet.
  • 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.
  • Chandrakala S, Jijina F and Ghosh K. Diffuse alveolar haemorrhage with severe haemophilia. Haemophilia 2010 Nov;16(6): 962-4.
  • 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.
  • 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.
  • Pradhan V, Surve P, Ghosh K. Mannose Binding Lectin (MBL) in Autoimmunity and its role in systemic lupus erythematosus (SLE). J Asso Physicians India 2010 Nov; 58(11):688-90.
  • Shetty S, Bhave M, Ghosh K. Acquired hemophilia A: Diagnosis, aetiology, clinical spectrum and treatment options. Autoimmun Rev. 2010 Nov 27. [Epub ahead of print] PubMed PMID: 21115138.
  • 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.
  • 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.
  • 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.
  • Kawankar N, Jijina F, Ghosh K, Vundinti BR. Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.Cancer Epidemiol. 2010 Dec 28. [Epub ahead of print]

2009

  • 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)
  • Vijapurkar M, Ghosh K, Shetty S. Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India . Platelets . 2009 Feb;20(1):35-40.(IF: 2.271)
  • 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)
  • 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)
  • 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)
  • Pai N, Shetty SD , Ghosh K. Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis. Clin Appl Thromb Hemost. 2009 Apr 28. [Epub ahead of print] (IF: 1.286)
  • 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. (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 . Indian 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.
  • 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.
  • 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.
  • 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.

2008

  • 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. Epub 2008 Mar 25
  • 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.
  • Shankarkumar U, Pawar A, Ghosh K. Implications of HLA sequence-based typing in transplantation. J PostGrad Med. 2008 Jan-Mar;54(1):41-4.
  • Ghosh K, Madkaikar M, Jijina F. Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage. Acta Haematol. 2008 Feb 20;119(2):69-72 [Epub ahead of print]
  • Ghosh K, Shetty S. Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia. Haemophilia. 2008 Mar;14(2):392-3. [18179571]
  • 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]
  • Ghosh K, Shetty S. Blood coagulation in falciparum malaria-a review. Parasitol Res. 2008 Mar;102(4):571-6. [18066597]
  • 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]
  • 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]
  • 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.
  • Shankarkumar U, Pawar U, 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.
  • 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.
  • 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.
  • 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.
  • Ghosh K, Pradhan V, Patwardhan M and Gupta M. Antiendothelial cell antibodies in systemic lupus erytematosus. Intl J Rheumatol Dis 2008; 11:121-6.
  • 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]
  • 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]
  • 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.
  • Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Sawant P, Surve R, Mohanty D, Ghosh K. Hb Showa Yakushiji [beta 110 (G12) Leu-->Pro] in 3 families from Western India: first report on homozygous Hb Showa Yakushiji. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):166-8
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • Colah R, Surve R. Wadia M, Solanki P, Mayekar P, Thomas M, Gorakshakar A, Dastur A, Mohanty D. Carrier screening for beta-thalassemia during pregnancy in India: a 7 year evaluation. Genet Test. 2008 Jun : 12(2): 181-5.
  • 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.
  • 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.
  • 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.
  • 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.
  • Malay Mukherjee. Laboratory diagnosis of sickle cell syndrome. J Community Med 2008 Jan; 4(1): 11-14.
  • Kanjaksha Ghosh, Shreimati Shetty and Kinjalka Ghosh Hmophilia: A High Cost Low Volume Disease: Suitable preventive strategies for developing and developed countries. The Open Hematology Journal, 2008, 2, 20-24 .
  • Kanjaksha Ghosh, Vandana Pradhan, Manisha M Patwardhan and Maya Gupta Antiendothelial cell antibodies in systemic lupus erythematosus. International Journal of Rheumatic Diseases 2008; 11;121-126.
  • Sonal Vora, Shrimati Shetty and Kanjaksha Ghosh: Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring. Blood Coagul Fibrinolysis 18: 571-574.
  • Edna D'Souza, Pratibha M. Sawant, Anita H Nadkarni, Ajit Gorakshakar, Dipika Mohanty, Kanjaksha Ghosh, Roshan Colah Evaluation of the use of monoclonal antibodies and nested PCR for noninvasive prenatal diagnosis of hemoglobinopathies in India. Am. J Clin Pathol 2008; 130:202-209.

2007

  • Shankarkumar U, Ghosh K. MHC non -HLA gene polymorphisms in transplantation. Indian J Pathol Microbiol. 2007 Oct;50(4):881-5. [18306597]
  • 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].
  • 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]
  • 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.
  • 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.
  • 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]
  • 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.
  • 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.
  • Ghosh K, Ghosh K. Pathogenesis of anemia in malaria: a concise review. Parasitol Res. 2007 Nov;10 (6):1463-9. [17874326].
  • 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.
  • 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.
  • Ghosh K, Ghosh K. Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases. Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26.
  • 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.
  • Kulkarni SS, Vasantha K, Gupte SC, Mohanty D, Ghosh K. Potential of commercial anti-D reagents in the identification of partial D ariants in Indian population. Indian J Med Res. 2007 May;125(5):641-4. [17642499]
  • 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.
  • Ghosh K, Vora S, Shetty S. Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis. Br J Haematol. 2007 Aug;138(4):555-7. [17590183]
  • Ghosh K, Madkaikar M, Jijina F, Shetty S. Fractures of long bones in severe haemophilia. Haemophilia. 2007 May;13(3):337-9.
  • 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.
  • Ghosh K, Ghosh K. Microarray genetic screening: the other side of the coin. Lancet. 2007 Mar 24;369(9566):992. [17382825]
  • 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]
  • 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].
  • 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]
  • 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]
  • Ghosh Kanjaksha. Coagulation disorders seen through the window of molecular biology. Ind. J. of Hum Genet. 2007 Sep –Dec; 13(3):79-85.
  • 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.
  • 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]
  • Korgaonkar Seema, Babu Rao V, Kerketta L, Ghosh K. Chromosomal breakage in myelodysplatic syndrome. Asian Pacific J Cancer Preview 2007; 9:151-4.
  • 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 – Walker malformation in a case of partial trisomy 9p (p12.1 à pter) due to maternal translocation t(9;12) (p12.1; p13.3) Indian J Hum Genet 2007;13(1): 33-5.
  • 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].
  • 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].
  • Nadkarni A, Gorakshakar A, Colah R, Mohanty D, Ghosh K Evaluation of the clinical severity of β-thalassemia homozygous patients using a phenotypic scoring system J Chinese Clin Med 2007; 2(8): 439-447.
  • Ghosh K. Coagulation disorders seen through the window of molecular biology. Indian J Hum Genet 2007; 13(3) 81-87
  • 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.
  • 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.
  • 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.
  • 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.
  • Gupta N, Bianchi P, Fermo E, Kabra M. Warana P, Kedar P, Gupta N, Colah R Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family. Prenat Diagn. 2007 Feb; 27(2): 117-8.
  • 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.
  • Dhurandhar PS, Shankarkumar U HLA association in seronegative spondyloarthritis patients from Mumbai, India. Int. J Hum Genet. 2007; 7(3): 235-9.

1967

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