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List of works by Bipin Kulkarni

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

scientific article published on 23 April 2016

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

scientific article published on 21 December 2011

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.

scientific article published on 21 August 2017

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

scientific article published on 02 October 2019

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

scientific article published on February 15, 2011

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

scientific article

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

scientific article

Association of factor VII gene polymorphisms with Budd Chiari syndrome

scientific article published on 01 April 2010

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

scientific article published in August 2007

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

scientific article published in November 2007

Diagnostic pitfalls and fallacies of measuring antiplatelet antibodies.

scientific article published in January 2006

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

scientific article published on 10 November 2009

Double mutations causing haemophilia B: a double whammy!

scientific article

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

scientific article published in July 2015

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

scientific article published on 28 February 2014

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

scientific article

Frequency distribution of antigens in the human platelet antigen-1 system in the western Indian population

scientific article published on March 2002

Frequency distribution of human platelet antigens in the Indian population.

scientific article published in April 2005

Geography too determines the causes of inherited thrombophilia.

scientific article published in February 2004

Glanzmann's thrombasthenia: updated.

scientific article

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

scientific article published in April 2009

Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease

scientific article published on 01 November 2002

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

scientific article published on 22 September 2006

Indian Bombay phenotype: it is different!

scientific article published on 24 June 2016

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

scientific article published on 16 April 2013

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

scientific article published in September 2003

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

scientific article published on 31 May 2017

JAK2 mutations across a spectrum of venous thrombosis cases

scientific article published on 01 July 2010

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

scientific article published on 01 October 2003

Molecular pathology of haemophilia A in Indian patients: Identification of 11 novel mutations ⬇️

scientific article published on August 26, 2010

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

scientific article

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

scientific article published on 23 July 2012

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

scientific article published in September 2003

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

scientific article published on 07 March 2012

Rare coagulation factor deficiencies: a countrywide screening data from India

scientific article

Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia.

scientific article

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

scientific article published on 15 April 2015

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

scientific article published on 01 September 2008

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

scientific article

The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients

scientific article

Thrombophilia: hereditary and acquired in cardiovascular disease.

scientific article

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

scientific article

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