| 1 |
Pai N, Shetty S, Ghosh K. Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Jan 14. [Epub ahead of print](IF: 1.496) |
| 2 |
Pradhan VD, Deshpande NR, Ghosh K. Proteomic approach to autoimmune disorders : A review
Indian J Biotechnol 2010 Jan;9 : 13-7.(IF:--) |
| 3 |
Korgaonkar S, Ghosh K and Babu Rao V. Clinical, Genetic and Cytogenetic study of Fanconi anemia in an Indian population
Hematology 2010 Jan;15(1):58-62. (IF:--) . |
| 4 |
Warang P, Nair S, Nadkarni A, Ghosh K, Colah RB Hb H disease due to homozygosity for a rare alpha2-Globin Variant, Hb Sallanches
Hemoglobin 2010 Jan; 34(1): 45-48.(IF:1.106) |
| 5 |
Ghosh K Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
Indian J Hum Genet. 2010 Jan;16(1):6-7. |
| 6 |
Kanjaksha Ghosh ??Thalassemia- What is it ?
Physician s Digest 2010; Pg: 63-69. |
| 7 |
Italia K, Jijina F, Chandrakala S, Nadkarni A, Sawant P, Ghosh K, Colah R. Exposure to hydroxyurea during pregnancy in sickle ?-thalassemia - A report of 2 cases.
J.Clin. Pharmacol 50; 231-4; 2010.(IF:3.59) |
| 8 |
Shankarkumar U, Pawar A, Devraj JP, Bhupali K, Ghosh K. The HLA system- A review.
Anthopologist, 2010;Special Vol.6:183-97. |
| 9 |
Shetty S, Mota L, Ghosh K. Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency
Clin Chim Acta. 2010 Feb;411(3-4):291. (IF:2.960) |
| 10 |
Swaminathan S, Madkaikar M, Ghosh K, Vundinti BR, Kerketta L, Gupta M. Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation.
Eur J Haematol. 2010 Feb 1;84(2):180-2.(IF:1.478) |
| 11 |
Italia KY, Jijina FF, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study
J Clin Pathol. 2010 Feb;63(2):147-50. (IF 1.78) |
| 12 |
Pradhan V, Patwardhan M, Nadkarni A, Ghosh K Fc ? RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India
Autoimmune Dis 2010 Feb 9;2010. |
| 13 |
Nair S, Nadkarni A, Warang P, Bhave A, Ghosh K, Colah R. Five alpha globin chain variants identified during screening for haemoglobinopathies.
Eur J Clin Invest. 2010 Mar; 40(3):226-32. (IF:2.784) |
| 14 |
Nadkarni AH, Nair SB, Italia KY, Warang P, Dalvi M, Ghosh K, Colah RB. Molecular diversity of hemoglobin H disease in India.
Am J Clin Pathol. 2010 Mar;133(3):491-4. (IF 3.576) |
| 15 |
Colah R, Gorakshakar A, and Nadkarni A Global burden, distribution and prevention of ?-Thalassemia and hemoglobin E disorders.
Expert Rev. Hematol 2010 Mar, 3(1):103-117.(IF:1.161) |
| 16 |
Pradhan VD, Patwardhan MM, Ghosh K Anti-nucleosome antibodies as a disease marker in systemic lupus erythematosus and its correlation with disease activity and other autoantibodies
Indian J Dermatol Venereol Leprol. 2010 Mar-Apr;76(2):145-9.(IF: 0.976) |
| 17 |
Kasatkar P. Shetty S, Ghosh K. VWF pseudogene; Mimics, masks and spoils.
Clin Chim Acta. 2010 Apr 2;411(7-8):607-9.(IF: 2.661) |
| 18 |
Jain A, Shetty S, Kulkarni B, Ghosh K. Association of factor VII gene polymorphisms with Budd Chiari syndrome
Blood Coagul Fibrinolysis. 2010 Apr; 21(3):296-7. (IF 1.506) |
| 19 |
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. |
| 20 |
Pradhan V, Deshpande N, Nadkarni A, Patwardhan M, Surve P, Ghosh K. Fc gamma R IIIB polymorphisms: their association with clinical manifestation and autoantibodies in SLE patients from western India
Int J Rheum Dis. 2010 May; 13 (2): 138-43.(IF:0.205) |
| 21 |
Vaswani RK, Dharaskar PG, Kulkarni S, Ghosh K. \ Iron deficiency as a risk factor for first febrile seizure.
Indian Pediatr. 2010 May;47(5):437-9. (IF: 0.9) |
| 22 |
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. |
| 23 |
Muranjan M, Chaudhari T and Babu Rao V. Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down Syndrome.
Indian Pediatrics 2010 May 17; 47(5): 429-432. (IF: 0.9) |
| 24 |
Kanjaksha Ghosh, Kinjalka Ghosh Advances in Haematological Pharmacotherapy in 21st Century.
Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40. |
| 25 |
Shankarkumar U, Pawar A, Ghosh K, Bajpai S and Pazare A. Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus-infected patients of Mumbai, India
Intl J Immunogenet 2010 Jun; 37(3): 199-204.(IF: 1.62) |
| 26 |
Gangodkar S, Jain P, Dixit N, Ghosh K, Basu A Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure
J Electron Microsc (Tokyo). 2010 Jun;59(6):503-11. (IF 1.77) |
| 27 |
Colah R, Gorakshakar A, Phanasgaonkar S, D'Souza E, Nadkarni A, Surve R, Sawant P, Master D, Patel R, Ghosh K, Mohanty D. Epidemiology of beta thalassemia in Western India:mapping the frequencies and mutations in sub regions of Maharashtra and Gujarat
Br J Haematol. 2010. Jun; 149(5): 739-47. (IF 4.942) |
| 28 |
Mota L, Shetty S, Idicula-Thomas S, Ghosh K. Molecular basis of factor X deficiency cases from India
Haemophilia 2010 Jul 1; 16(4): 693-7. ( IF 2.394) |
| 29 |
Shetty S, Kulkarni B, Pai N, Mukundan P, Kasatkar P, Ghosh K. JAK2 mutations across a spectrum of venous thrombosis cases.
Am. J. Clin. Pathol 2010 Jul; 134(1):82-5. (IF 2.47) |
| 30 |
Ghosh K Bachelor of rural health care: cutting the root and watering the stem!
Natl Med J India. 2010 Jul-Aug;23(4):250. (IF 0.541) |
| 31 |
Ghosh K, Ghosh K Sequential serologic testing for common viral markers in blood units in India is probably not cost effective.
Transfusion 2010 Aug;50(8): 1854-55. (IF 3.3) |
| 32 |
Pai N, Shetty S, Ghosh K Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Aug; 89(8): 835-6. (IF: 2.688) |
| 33 |
Pradhan V, Borse V, Ghosh K. PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.
J Postgrad Med. 2010 Jul-Sep;56(3):239-42. Review. (IF:1.389) |
| 34 |
Mukherjee MB, Nadkarni AH, Gorakshakar AC, Ghosh K, Mohanty D, Colah RB. Clinical, hematologic and molecular variability of sickle cell-? thalassemia in western India
Indian J Hum Genet. 2010 Sep;16(3):154-8. |
| 35 |
Kasatkar P, Shetty S, Ghosh K. Delayed vitamin K deficiency as a cause of bleeding : still a concern in the 21st century!
Blood Coagul Fibrinolysis. 2010 Sept; 21(6):608-10. (IF 1.506) |
| 36 |
Shankarkumar U. Complexities and similarities of HLA antigen distribution in Asian subcontinent.
Indian J Hum Genet. 2010 Sep;16(3):108-10. |
| 37 |
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 fanconis anemia treated with radiation therapy: Case Report and review of literature.
Head & Neck 2010 Oct;32(10):1422-27.(IF: 2.4) |
| 38 |
Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar M, Ghosh K, Colah RB, Alper SL. Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
Am J Hematol 2010 Oct;85(10):824-8.(IF 3.576) |
| 39 |
Black ML, Sinha S, Agarwal S, Colah R, Das R, Bellgard M, Bittles AH. A descriptive profile of ?-Thalassaemia mutations in India, Pakistan and Sri Lanka
J Community Genet. 2010 Oct 10. |
| 40 |
Korgaonkar S, Ghosh K, Jijina F and Vundinti BR. Chromosomal breakage study in children suspected with fanconi anemia in the Indian population.
J Pediatr Hematol Oncol 2010 Nov;32(8):606-10.(IF: 0.998) |
| 41 |
Chandrakala S, Jijina F and Ghosh K Diffuse alveolar haemorrhage with severe haemophilia.
Haemophilia 2010 Nov;16(6): 962-4. (IF 2.394) |
| 42 |
Nair PS, Shetty S and Ghosh K. Double mutations in haemophilia: muddling strangers or indifferent partners in crime?
Haemophilia 2010 Nov;16(6):970-1. (IF 2.394) |
| 43 |
Italia KY, Jijina FF, Jain D, Merchant R, Nadkarni AH, Mukherjee M, Kanjaksha G, Colah RB The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies
Clin Biochem 2010 Nov;43(16-17):1329-1332.(IF: 2.079) |
| 44 |
Pradhan V, Surve P, Ghosh K. Mannose Binding Lectin (MBL) in Autoimmunity and its role in systemic lupus erythematosus (SLE).
J Assoc Physicians India 2010 Nov; 58(11):688-90. |
| 45 |
Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, Bellgard M, Bittles AH. Profiling ?-Thalassaemia mutations in India at state and regional levels: implications genetic education, screening and counseling programmes.
Hugo J. 2009 Dec; 3(1-4): 5162. |
| 46 |
Nair PS, Shetty S, Kulkarni B, Ghosh K. Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.
Clin Chim Acta 2010 Dec 14; 411(23-24):2004-8.(IF:2.661) |
| 47 |
Vundinti BR, Korgaonkar S, Ghosh K. Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.
Indian J Cancer. 2010 Oct-Dec;47(4):397-9. (IF: 0.961) |
| 48 |
Pai N, Shetty S, Kulkarni B, Ghosh K. Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700.(IF:1.476) |
| 49 |
Iyer YS, Vasantha K, Pujari V, Jadhav S, Ghosh K Murine monoclonal anti-H as typing reagent.
Indian J Med Res 2009 Jan; 129(1): 72-74. (IF: 1.883) |
| 50 |
Ghosh K, Shetty S Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors.
Clin Rev Allergy Immunol. 2009 Oct;37(2):58-66. (IF: 2.080) |
| 51 |
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) |
| 52 |
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) |
| 53 |
Kanjaksha Ghosh. Molecular evolution of Globin Gene Pathology-Its Driver, Challenges and
Journal of the Asiatic Society 2009 Vol. 51(20):73-8.(IF:--) |
| 54 |
Roshan Colah. Antenatal Diagnosis of Thalasssemias-Diagnostic technology suitable for the country
Journal of the Asiatic Society 2009 Vol 51 (2):69-72(IF:--) |
| 55 |
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) |
| 56 |
Vijapurkar M, Ghosh K, Shetty S. Novel mutations in GP IIb gene in Glanzmanns thrombasthenia from India.
Platelets. 2009 Feb;20(1):35-40.(IF: 2.271) |
| 57 |
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) |
| 58 |
Vora S, Shetty S, Khare M, Ghosh K Placental histomorphology in unexplained foetal loss with thrombophilia.
Indian J Med Res 2009 Feb; 129(2): 144-49.(1.883) (IF 1.826) |
| 59 |
Nadkarni A, Gorakshakar A, Surve R, Sawant P, Phanasgaonkar S, Nair S, Ghosh K, Colah RB Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009 Jan-Mar; 33(1):59-65.(IF: 1.106) |
| 60 |
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) |
| 61 |
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) |
| 62 |
Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K. Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First
Thromb Haemost 2009 Apr;101(4):785-87.(IF:3.413) |
| 63 |
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) |
| 64 |
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) |
| 65 |
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) |
| 66 |
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 |
| 67 |
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) |
| 68 |
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) |
| 69 |
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) |
| 70 |
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) |
| 71 |
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) |
| 72 |
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) |
| 73 |
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 |
| 74 |
Ghosh K Challenges of haemophilia care in India: lest we forget.
Indian J Med Res. 2009 Jul;130(1):87-8. (IF 1.883) |
| 75 |
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) |
| 76 |
Mamta Muranjan, Tejasvi Choudhary and Baburao Vundinti. Phenotypic heterogencity and parental origin of extrachromosome 21 in down syndrome.
Indian Pediat. 2009 July 1; [Epub ahead of print] (IF:0.956) |
| 77 |
Pradhan VD, Ghosh K. Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
Indian J Dermatol. 2009 Jul;54(3):258-62. |
| 78 |
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) |
| 79 |
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) |
| 80 |
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). |
| 81 |
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) |
| 82 |
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 Fanconis anemia treated with radiation therapy: case report and review of literature.
Head & Neck 2009; Aug 11 (E-pub ahead of print)(IF: 2.01). |
| 83 |
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) |
| 84 |
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) |
| 85 |
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) |
| 86 |
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) |
| 87 |
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) |
| 88 |
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) |
| 89 |
Ajit Gorakshakar, Colah RB. Cascade screening for ?-thalassemia; A practical approach for identifying and counseling carriers in India.
Indian J. Comm. Med. 2009;Oct 34(4) :354-56. |
| 90 |
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) |
| 91 |
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). |
| 92 |
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) |
| 93 |
Ghosh K, Ghosh K. Private practice in India.
Natl Med J India. 2008 Nov-Dec;21(6):328-9.(IF:0.911) |
| 94 |
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) |
| 95 |
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) |
| 96 |
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) |
| 97 |
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. |
| 98 |
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. |
| 99 |
Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
J Hum Genet. 2008;53(2):181-4. [18043863] (IF: 2.431) |
| 100 |
Shetty S, Ghosh K, Quadros L. Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
Eur J Haematol. 2008 Jan;80(1):87-9. [18028421] (IF 1.478) |
| 101 |
Ghosh K, Shetty S and Ghosh K A high cost low volume disease: suitable preventive strategies for developing and developed countries.
The Open Hematol J 2008; 2: 20-4. |
| 102 |
Ghosh K, Pradhan V, Patwardhan M and Gupta M. Antiendothelial cell antibodies in systemic lupus erytematosus.
Intl J Rheumatol Dis 2008; 11:121-6. (IF 0.205) |
| 103 |
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. |
| 104 |
Prabhakar Kedar, Kazuyuki Shimizu, Kanjaksha Ghosh, Hisaichi Fujji, Roshan A proteomic analysis of CBA-Pk-1slc/Pk-1slc mice with Red Blood Cell Type Pyruvate Kinase deficiency using 2DE together with MALDI-TOF-MF analysis
FASEB J 2008;22:1025. (IF 6.721) |
| 105 |
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. |
| 106 |
Malay Mukherjee. Laboratory diagnosis of sickle cell syndrome.
J Community Med 2008 Jan; 4(1): 11-14. |
| 107 |
Kanjaksha Ghosh, Shrimati Shetty and Kinjalka Ghosh Hemophilia: A High Cost Low Volume Disease: Suitable preventive strategies for developing and developed countries.
The Open Hematology Journal, 2008; 2:20-24. |
| 108 |
Konkankar S, Shankarkumar U HLA DRB1 alleles in chronic hepatitis B infected patients
Intl J Hum Genet 2008; 72: 275. |
| 109 |
Ghosh K, Pradhan V Background noise of infection for using ANCA as a diagnostic tool for vasculitis in tropical and developing countries.
Parasitol Res. 2008 Apr;102(5):1093-5. Epub 2008 Feb 24. (IF 3.938) |
| 110 |
Ghosh K, Madkaikar M, Jijina F Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage
Acta Haematol. 2008 Feb 20;119(2):69-72 (IF 1.316) |
| 111 |
Shankarkumar U, Pawar A, Ghosh K. Implications of HLA sequence-based typing in transplantation.
J PostGrad Med. 2008 Jan-Mar;54(1):41-4. (IF 1.589) |
| 112 |
Ghosh K, Shetty S Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia.
Haemophilia. 2008 Mar;14(2):392-3. [18179571] (IF 2.394) |
| 113 |
Ghosh K, Shetty S. Blood coagulation in falciparum malaria-a review.
Parasitol Res. 2008 Mar;102(4):571-6. [18066597] (IF 3.938) |
| 114 |
Vundinti BR, Kerketta L, Madkaikar M, Jijina F, Ghosh K translocation in a new variant of +(8;21) acute myeloid leukemia involving Xp22.
Indian J Cancer. 2008 Jan-Mar; 45(1):30-2. |
| 115 |
Ghosh K, Shetty S, Vora S, Salvi V. Successful pregnancy outcome in women with bad obstetric history and recurrent fetal loss due to thrombophilia: effect of unfractionated heparin and low--molecular weight heparin.
Clin Appl Thromb Hemost. 2008 Apr;14(2):174-9. [18160603] (IF 1.286) |
| 116 |
Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K. A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss.
Eur J Obstet Gynecol Reprod Biol. 2008 Apr;137(2):136-40. (IF 1.736) |
| 117 |
Mohanty D, Mukherjee MB, Colah RB, Wadia M, Ghosh K, Chottray GP, Jain D, Italia Y, Ashokan K, Kaul R, Shukla DK & Muthuswamy V Iron deficiency anaemia in sickle cell disorders in India.
Indian J Med Res 2008 Apr; 127(4):366-9. [18577791] (IF 1.826) |
| 118 |
Kulkarni S, Colah R, Gorakshakar A, Gupte S, Vasantha K, Mohanty D,Ghosh K. Frequency of Partial D in Western India.
Transf Med. 2008 Apr; 18(2):91-6. (IF 2.155) |
| 119 |
Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Sawant P, Surve R, Mohanty D, Ghosh K Hb Showa Yakushi [beta 110(612) Leu?Pro ] in three families from Western India: First report on homozygous Hb showa Yakushiji.
Blood Cells Mol Dis. 2008 May 19. (IF 2.549) |
| 120 |
Vijapurkar M, Ghosh K, Shetty S, McLane MA, Moura da Silva AM,Butera D. A simple, novel and robust test to diagnose type I glanzmann thrombasthenia
Haematologica. 2008 May; 93 (5) :797-8. (IF 6.416) |
| 121 |
Quadros L, Ghosh K, Shetty S Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India.
Haemophilia. 2008 May; 14 (3) : 628-9. (IF 2.394) |
| 122 |
Basu A, Jain P, Gangodkar SV, Shetty S, Ghosh K. Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.
FEMS Immunol Med Microbiol. 2008 June ; 53 (1):46-51 (IF 2.494) |
| 123 |
Shankarkumar U, Pawar A, Gaonkar P, Parsannawar D, Salvi V, Ghosh K. HLA allele associations in idiopathic recurrent spontaneous abortion patients from India.
J. Hum Reprod. Sci, 2008 Jan-Jun;1(1):19-24. |
| 124 |
Ghosh K, Gangodkar S, Jain P, Shetty S, Ramjee S, Poddar P,Basu A Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy
J Electron Microsc(Tokyo) 2008 Jun; 57(3):113-8. (IF 1.05) |
| 125 |
Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K. A novel G143D mutation in the NADH-cytochrome b(5) reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood Cells Mol Dis 2008 May-Jun; 40(3):323-7. [17964195] (IF 2.549) |
| 126 |
Ghosh K, Shetty S, Mota L Aspirin resistance in patients with coronary artery disease- which test to use in routine management?
Blood Coagul Fibrinolysis .2008 Jun: 19(4) : 324-6. (IF 1.506) |
| 127 |
Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K. Prevalence and molecular characterization of alpha thalassemia syndromes among Indians
Genet Test. 2008 Jun; 12(2) : 177-80. (IF 1.7) |
| 128 |
Colah R, Surve R. Wadia M, Solanki P, Mayekar P, Thomas M, Gorakshakar A, Dastur A, Mohanty D. Carrier screening for ?-thalassemia during pregnancy in India: a 7 year evaluation.
Genet Test. 2008 Jun : 12(2): 181-5. (IF 1.7). |
| 129 |
Ghosh K, Shetty S antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
Blood Coagul Fibrinolysis 2008 Jul;19(5):464-65.[18600102] (IF 1.506) |
| 130 |
Shetty S, Ghosh K Reduced clinical severity in a mutationally well characterized cohort of severe hemophilia with associated thrombophilia
Am. J Clin Pathol 2008 Jul; 130(1) 84-7. (IF 2.18) |
| 131 |
Prabhu R, Jijina F, Shetty S, Ghosh K Successful surgery in severe haemophilia a two stage replacement therapy in resource poor countries.
Haemophilia 2008 Jul 3. (IF 2.394) |
| 132 |
Edna DSouza,Pratibha M. Sawant,Anita H. Nadkarni,Ajit Gorakshakar,Dipika Mohanty, Kanjaksha Ghosh, and Roshan B. Colah Evaluation of the Use of Monoclonal Antibodies and Nested PCR for Noninvasive Prenatal Diagnosis of Hemoglobinopathies in India
AJCPAug2008; 130(2):202-209.(If: 2.89) |
| 133 |
Meera V, Jijina F, Shrikande M, Madkaikar M, Ghosh K Twin pregnancy in a patient of chronic myeloid leukemia on imatinib therapy
Leuk Res. 2008 Oct; 32(10) : 1620-2. (IF 2.555) |
| 134 |
Anita Nadkarni,Marukh Wadia,Ajit Gorakshakar,Ryoiti Kiyama,Roshan B. Colah, Dipika Mohanty Molecular Characterization of ??-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population
Hemoglobin Sep-Oct 2008, Vol. 32, No. 5: 425433.(IF: 1.00) |
| 135 |
Phanasgaonkar S, Colah R, Ghosh K, Mohanty D, Gupte S Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India
Br J Biomed Sci. 2007;64(4):160-3. [18236737]. (IF 0.590) |
| 136 |
Madkaikar M, Gupta M, Ghosh K, Swaminathan S, Sonawane L, Mohanty D. Optimizing methods of red cell sedimentation from cord blood to maximize nucleated cell recovery prior to cryopreservation
Br J Biomed Sci. 2007;64(4):157-9. [18236736] (IF 0.590) |
| 137 |
Madkaikar M, Ghosh K, Gupta M, Swaminathan S, Mohanty D Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells
Acta Haematol. 2007;118(3):153-9. Epub 2007 Sep 20. (IF 1.316) |
| 138 |
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. |
| 139 |
Korgaonkar Seema, Babu Rao V, Kerketta L, Ghosh K. Chromosomal breakage in myelodysplatic syndrome.
Asian Pacific J Cancer Preview 2007; 8:151-4. (IF: 1.11) |
| 140 |
Shankarkumar U, Pawar A, and Ghosh K Human leukocyte antigenpolymorphism and association: a review
Anthropologist 2007;Special Vol. No.3: 367-72. |
| 141 |
Rao VB, Kerketta L, Korgaonkar S, Ghosh K. Dandy Walker malformation in a case of partial trisomy 9p (p12.1pter) due to maternal translocation
Indian J Hum Genet 2007;13(1): 33-5. |
| 142 |
Colah R, Thomas M, Mayekar P Assessing the impact of screening and counseling high school children for b-thalassemia in India.
J Med Screen 2007; 14(3): 158. [17925089]. (IF 1.493) |
| 143 |
Nadkarni A, Gorakshakar A, Colah R, Mohanty D, Ghosh K Evaluation of the clinical severity of ?-thalassemia homozygous patients using a phenotypic scoring system
J Chinese Clin Med 2007; 2(8): 439-447 |
| 144 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Indian J Hum Genet 2007; 13(3) 79-85. |
| 145 |
DSouza E, Kulkarni S, Colah RB, Mohanty D An improved flowcytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathies
Hemoglobin, 2007; 31(1): 39-48. (IF 1.106) |
| 146 |
Dhurandhar PS, Shankarkumar U HLA association in seronegative spondyloarthritis patients from Mumbai, India.
Int. J Hum Genet. 2007; 7(3): 235-9. (IF 0.238) |
| 147 |
Chalvam R, Mukherjee MB, Colah RB, Mohanty D, Ghosh K G6PD Namoru (208 T--> C) is the major polymorphic variant in the tribal populations in southern India.
Br J Haematol. 2007 Feb;136(3):512-3. No abstract available. (IF 3.195) |
| 148 |
Ghosh K, Khare A, Shetty S, Kulkarni B. Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern of response to oral folic acid, vitamin B12, B6 therapy
Clin Chim Acta. 2007 Feb;377(1-2):281-2. Epub 2006 Sep 22. (IF 2.960) |
| 149 |
Gupta N, Bianchi P, Fermo E, Kabra M. Warang P, Kedar P, Gupta N, Colah R Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family
Prenat Diagn. 2007 Feb; 27(2): 117-8. (IF 2.152) |
| 150 |
Ghosh K, Ghosh K. Microarray genetic screening: the other side of the coin.
Lancet. 2007 Mar 24;369(9566):992. [17382825] (IF 33.63) |
| 151 |
Mota L, Ghosh K, Shetty S Second trimester antenatal diagnosis in rare coagulation factor deficiencies.
J Pediatr Hematol Oncol. 2007 Mar;29(3):137-9. [17356389] (IF 1.176) |
| 152 |
Shetty S, Ghosh K. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
Haemophilia. 2007 Mar;13(2):172-7. [17286770] (IF 2.394) |
| 153 |
Varla-Leftherioti M, Keramitsoglou T, Spyropoulou-Vlachou M, Papadimitropoulos M, Kontopoulou-Antonopoulou V, Tsekoura C, Sankarkumar U, Paparistidis N, Ghosh K, Pawar A, Vrani V, Daniilidis M, Parapanissiou E, Diler AS, Carin M, Stavropoulos-Giokas C 14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component.
Tissue Antigens. 2007 Apr; 69 Suppl 1:297-303. (IF 3.024) |
| 154 |
Umapathy S, Pawar A, Ghosh K. Specific human leukocyte antigen alleles associated with HIV-1 infection in an Indian population.
J Acquir Immune Defic Syndr. 2007 Apr 1;44(4):489-90. [17353719]. (IF 4.262) |
| 155 |
Kulkarni SS, Vasantha K, Gupte SC, Mohanty D, Ghosh K. Potential of commercial anti-D reagents in the identification of partial D variants in Indian population.
Indian J Med Res. 2007 May;125(5):641-4. [17642499] (IF 1.823) |
| 156 |
Ghosh K, Madkaikar M, Jijina F, Shetty S Fractures of long bones in severe haemophilia.
Haemophilia. 2007 May;13(3):337-9. (IF 2.394). |
| 157 |
Quadros L, Ghosh K, Shetty S. A common G10430A mutation (Gly 60 Ser) in the factor IX gene presence of moderate and mild hemophilia B in the majority describes the presence of moderate and mild hemophilia B in the majority of the Gujarat population.
Ann Hematol. 2007 May;86(5):377-9. [17308903] (IF 2.688) |
| 158 |
Kedar PS, Nampoothiri S, Sreedhar S, Ghosh K, Shimizu K, Kanno H, Colah RB First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation
Genet Mol Res. 2007 Jun 30;6(2):470-5. (IF 1.013) |
| 159 |
Ghosh K, Madkaikar M, Shrikhande M Osteoporosis in young haemophiliacs from western India.
Am J Hematol. 2007 Jun;82(6):453-7. [17278114] (IF 3.576) |
| 160 |
Kulkarni SS, Gorakshakar AC, Colah RB, Gupte SC, Mohanty D Usefulness of prenatal detection of Rh D typing by molecular analysis in Indians
J PostGrad Med. 2007 Apr-Jun; 53(2): 149. (IF 1.589) |
| 161 |
Vora S, Ghosh K, Shetty S, Salvi V, Satoskar P. Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
Thromb J. 2007 Jul 4;5:9. (IF 1.0) |
| 162 |
Colah RB, Surve R, Sawant P, DSouza E, Italia K, Phanasgaonkar S, Nadkarni AH, Gorakshakar AC HPLC studies in hemoglobinopathies
Indian J Pediatr. 2007 Jul:74(7):657-62 Review. (IF 0.9) |
| 163 |
Kulkarni SS, Gupte SC, Vasantha K, Mohanty D, Ghosh K Varied distribution of RhD epitopes in the Indian population
Natl Med J India. 2007 Jul-Aug ;20(4):169-71 (IF 0.911) |
| 164 |
Shetty S, Vora S, Kulkarni B, Mota L, Vijapurkar M, Quadros L, Ghosh K Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.
Br J Haematol. 2007 Aug;138(4):541-4.(IF 3.195) |
| 165 |
Ghosh K, Vora S, Shetty S. Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis.
Br J Haematol. 2007 Aug;138(4):555-7. [17590183] (IF 3.195) |
| 166 |
Rao VB, Korgaonkar S, Kerketta L, Ghosh K. Differentiation of Nijmegen breakage syndrome from Fanconi anemia.
Genet Mol Res. 2007 Sept 30;6(3):622-6. (IF 1.013) |
| 167 |
Vora S, Shetty S, Ghosh K. Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
Blood Coagul Fibrinolysis. 2007 Sep;18(6):571-4. (IF 1.506) |
| 168 |
Shankarkumar U, Ghosh K MHC non -HLA gene polymorphisms in transplantation
Indian J Pathol Microbiol. 2007 Oct;50(4):881-5. [18306597] (IF 0.57) |
| 169 |
Nadkarni A, Surve R, Colah R, Ghosh K, Holay M, Dani A, Shrikhande A, Bharti V, Suryawanshi S. Thalassemia intermedia due to homozygosity for an Asian Indian (Agammadeltabeta) degrees deletional inversion.
Clin Chim Acta. 2007 Oct;385(1-2):81-3. Epub 2007 Jul 19. (IF 2.960) |
| 170 |
Ernest Beutler, Duparc S, Doumbo O, Ghosh K, Vinicious M, de Lacerda G, Lapierre D, Looareesuwan S, Premji Z, Vulliamy T, Vhitty C. Lapierre D, Looareesuwan S, Premji Z, Vulliamy T, Vhitty C. Glucose-6- phosphate dehydrogenase deficiency and antimalarial drug development.
Am J Trop Med Hyg 2007 Oct;77(4):779-89. Rev. [17978087]. (IF 2.8) |
| 171 |
Gorakshakar AC, Das MK, Phanasgaonkar SP, Nadkarni AH, Colah RB,Mohanty D Origin of the Codon 47(+A) ?-thalassemia mutation among the Nicobarese of the Andaman & Nicobar islands in India.
Br J Haematol 2007 Oct;139 (2):345-6. [17897314]. (IF 3.195) |
| 172 |
Ghosh K, Shetty S, Kulkarni B Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients
Haemophilia. 2007 Nov;13(6):734-9. [17973850] (IF 2.394) |
| 173 |
Ghosh K, Ghosh K. Pathogenesis of anemia in malaria: a concise review
Parasitol Res. 2007 Nov;10 (6):1463-9. [17874326]. (IF 3.938) |
| 174 |
Ghosh K, Ghosh K. Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases.
Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26.(IF 2.615) |
| 175 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Ind. J. of Hum Genet. 2007 Sep Dec; 13(3):79-85. (IF 0.11 )3 |
| 176 |
Italia KY, Colah R, Mohanty D Evaluation of F cells in sickle cell disorders by flow cytometry comparison with the Kleihouer- Betkes slide method
Int J Lab Hematol 2007 Dec: 29 (6): 409-14. (IF 1.304) |
| 177 |
Ghosh K, Shetty S, Tulsiani M Evolution of prenatal diagnosis techniques from phenotypic diagnosis to gene arrays : Its likely impact on prenatal diagnosis of hemophilia
Clin Appl Thromb Hemost first published on December 26, 2007. ( IF 1.286) |
