Personal information

Activities

Employment (1)

ICMR- National Institute of Immunohaematology: Mumbai, Maharashtra, IN

2001-11 to present | Scientist (Department of Haemostasis and Thrombosis)
Employment
Source: Self-asserted source
Bipin Kulkarni

Education and qualifications (2)

Emory University: Atlanta, GA, US

2007 to 2008 | Post Doctorate (Department of Human Genetics)
Education
Source: Self-asserted source
Bipin Kulkarni

ICMR- National Institute of Immunohaematology/ University of Mumbai: Mumbai, IN

1999 to 2004 | Ph.D. (Applied Biology) (Hemostasis and Thrombosis)
Education
Source: Self-asserted source
Bipin Kulkarni

Works (50 of 57)

Items per page:
Page 1 of 2

Congenital PAI-1 deficiency results in psoas hematoma in an Indian patient.

Thrombosis research
2020-04 | Journal article
Contributors: Prabhudesai A; Sharma R; Shetty S; Phadnis A; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

A rare cause of bleeding in two Indian families with congenital alpha-2-antiplasmin deficiency.

Haemophilia : the official journal of the World Federation of Hemophilia
2019-10 | Journal article
Contributors: Prabhudesai A; Shetty S; Shanmukhaiah C; Kalantri S; Bhattacharyya M; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Multiple heritable and acquired risk factors in a case of recurrent retinal vein occlusion.

Journal of Association of Physicians of India
2018-03 | Journal article
Source: Self-asserted source
Bipin Kulkarni

A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.

Transfusion
2017-08 | Journal article
Contributors: Yadav S; Shetty S; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.

European journal of haematology
2017-06 | Journal article
Contributors: Prabhudesai A; Shetty S; Ghosh K; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Dysfunctional fibrinolysis and cerebral venous thrombosis.

Blood cells, molecules & diseases
2017-05 | Journal article
Contributors: Prabhudesai A; Shetty S; Ghosh K; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Standardization of microparticle enumeration across different flow cytometry platforms: results of a multicenter collaborative workshop.

J Thromb Haemost.
2017-01 | Journal article
Source: Self-asserted source
Bipin Kulkarni

Indian Bombay phenotype: it is different!

Blood transfusion = Trasfusione del sangue
2016-06 | Journal article
Contributors: Kulkarni B; Gorakshakar A; Singh V; Parihar A; Donta A; Gogri H; Jadhav S; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis.

Thrombosis research
2016-04 | Journal article
Contributors: Deshpande R; Kulkarni B; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia.

Haemophilia : the official journal of the World Federation of Hemophilia
2015-12 | Journal article
Contributors: Kulkarni B; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families.

Haemophilia : the official journal of the World Federation of Hemophilia
2015-08 | Journal article
Contributors: Mukaddam A; Kulkarni B; Jadli A; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Erratum to: A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.

Annals of hematology
2015-07 | Journal article
Contributors: Lobo V; Shetty S; Kulkarni B; Butera D; Magalhaes GS; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.

The Indian journal of medical research
2015-07 | Journal article
Contributors: Jadli A; Kulkarni B; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.

Annals of hematology
2015-04 | Journal article
Contributors: Kasatkar P; Kulkarni B; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.

PloS one
2014-10 | Journal article
Contributors: Kulkarni BP; Nair SB; Vijapurkar M; Mota L; Shanbhag S; Ali S; Shetty SD; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Factor V Leiden mutation modulates the bleeding phenotype in warfarin sensitive patients.

Thrombosis research
2014-02 | Journal article
Contributors: Gaikwad T; Ghosh K; Kulkarni B; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Rare coagulation factor deficiencies: a countrywide screening data from India.

Haemophilia : the official journal of the World Federation of Hemophilia
2014-02 | Journal article
Contributors: Shetty S; Shelar T; Mirgal D; Nawadkar V; Pinto P; Shabhag S; Mukaddam A; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients.

Indian Journal of Hematology & Blood Transfusion
2014-02 | Journal article
Contributors: Pinto P; Shelar T; Nawadkar V; Mirgal D; Mukaddam A; Nair P; Kasatkar P; Gaikwad T; Ali S; Jadli A et al.
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Abstracts of the Lectures During Haematocon 2013.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
2013-10 | Journal article
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Haematacon 2013 (54th Annual Conference of Indian Society of Haematology & Blood Transfusion).

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
2013-10 | Journal article
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation and other adverse outcomes in Indian population.

European journal of pharmacology
2013-04 | Journal article
Contributors: Gaikwad T; Ghosh K; Kulkarni B; Kulkarni V; Ross C; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

53rd National Conference of Indian Society of Hematology & Blood Transfusion (ISHBT) 2012, 9–11 November 2012, Puri, India.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
2012-10 | Journal article
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases.

Liver international : official journal of the International Association for the Study of the Liver
2012-07 | Journal article
Contributors: Jadli A; Kulkarni B; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.

Annals of hematology
2012-03 | Journal article
Contributors: Kulkarni B; Kanakia S; Ghosh K; Shetty S
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.

Annals of hematology
2011-12 | Journal article
Contributors: Lobo V; Shetty S; Kulkarni B; Butera D; Magalhaes GS; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

An improved, semi quantitative clot based assay for factor XIII.

Haemophilia : the official journal of the World Federation of Hemophilia
2011-02 | Journal article
Contributors: Shanbhag S; Shetty S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.

Clinica chimica acta; international journal of clinical chemistry
2010-08 | Journal article
Contributors: Nair PS; Shetty S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

JAK2 mutations across a spectrum of venous thrombosis cases.

American journal of clinical pathology
2010-07 | Journal article
Contributors: Shetty S; Kulkarni B; Pai N; Mukundan P; Kasatkar P; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Association of factor VII gene polymorphisms with Budd Chiari syndrome.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
2010-04 | Journal article
Contributors: Jain A; Shetty S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Differences in etiological and clinical manifestations in upper extremity and lower limb deep venous thrombosis patients from India.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
2009-11 | Journal article
Contributors: Pai N; Shetty S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency: cause, consequence or a consequential cause?

Haemophilia : the official journal of the World Federation of Hemophilia
2009-06 | Journal article
Contributors: Shetty S; Vora S; Kulkarni B; Mota L; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.

Thrombosis and haemostasis
2009-04 | Journal article
Contributors: Pai N; Shetty S; Idicula-Thomas S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Double mutations causing haemophilia B: a double whammy!

British journal of haematology
2009-02 | Journal article
Contributors: Ghosh K; Shetty S; Quadros L; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Antiplatelet antibodies in cases of Glanzmann's thrombasthenia with and without a history of multiple platelet transfusion.

Indian J Hum Genet.
2009-01 | Journal article
Source: Self-asserted source
Bipin Kulkarni
grade
Preferred source (of 2)‎

Utility of an exon 14 BslI polymorphism for improved genetic diagnosis of hemophilia A in Indian population.

Prenatal diagnosis
2008-10 | Journal article
Contributors: Mukundan P; Shetty S; Kulkarni B; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Spectrum of changes in endogenous thrombin potential due to heritable disorders of coagulation.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
2008-09 | Journal article
Contributors: Ghosh K; Mota L; Shetty S; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients.

Haemophilia : the official journal of the World Federation of Hemophilia
2007-11 | Journal article
Contributors: Ghosh K; Shetty S; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.

British journal of haematology
2007-08 | Journal article
Contributors: Shetty S; Vora S; Kulkarni B; Mota L; Vijapurkar M; Quadros L; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

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.

Clinica chimica acta; international journal of clinical chemistry
2006-09 | Journal article
Contributors: Ghosh K; Khare A; Shetty S; Kulkarni B
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Flowcytometric evidence of platelet activation in patients on aspirin following myocardial infarction.

Natl Med J India.
2006-03 | Journal article
Source: Self-asserted source
Bipin Kulkarni
grade
Preferred source (of 2)‎

Diagnostic pitfalls and fallacies of measuring antiplatelet antibodies.

Acta haematologica
2006-01 | Journal article
Contributors: Kulkarni B; Nair S; Shetty S; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Frequency distribution of human platelet antigens in the Indian population.

Transfusion medicine (Oxford, England)
2005-04 | Journal article
Contributors: Kulkarni B; Mohanty D; Ghosh K
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Combination of thrombophilia markers in acute myocardial infarction of the young.

Indian J Med Sci.
2004-09 | Journal article
Source: Self-asserted source
Bipin Kulkarni
grade
Preferred source (of 2)‎

Human platelet specific antigens and their importance.

Indian Pediatr.
2004-08 | Journal article
Source: Self-asserted source
Bipin Kulkarni
grade
Preferred source (of 2)‎

Thrombophilia in coronary artery disease: a double jeopardy.

Indian J Med Res.
2004-07 | Journal article
Source: Self-asserted source
Bipin Kulkarni
grade
Preferred source (of 2)‎

Geography too determines the causes of inherited thrombophilia.

Journal of thrombosis and haemostasis : JTH
2004-02 | Journal article
Contributors: Ghosh K; Khare A; Kulkarni B; Shetty S; Mohanty D
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Milder bleeding tendency in Glanzmann's thrombasthenia patients inheriting HPA-1b in the homozygous state.

Journal of thrombosis and haemostasis : JTH
2003-10 | Journal article
Contributors: Ghosh K; Nair S; Kulkarni B; Shetty S; Mohanty D
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Inherited haemostatic disorders in idiopathic menorrhagia: do the special interest of a hemostatic laboratory make a difference?

Haemophilia : the official journal of the World Federation of Hemophilia
2003-09 | Journal article
Contributors: Ghosh K; Nair S; Kulkarni B; Khare A; Trasi S; Shetty S; Mohanty D
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.

Platelets
2003-09 | Journal article
Contributors: Ghosh K; Nair S; Kulkarni B; Khare A; Shetty S; Mohanty D
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central

Glanzmann's thrombasthenia: updated.

Platelets
2002-11 | Journal article
Contributors: Nair S; Ghosh K; Kulkarni B; Shetty S; Mohanty D
Source: Self-asserted source
Bipin Kulkarni via Europe PubMed Central
Items per page:
Page 1 of 2

Peer review (5 reviews for 3 publications/grants)

Review activity for Indian journal of pediatrics. (3)
Review activity for Pediatric hematology oncology journal. (1)
Review activity for PloS one. (1)