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List of works by Shrimati Shetty

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

scientific article published on 17 February 2007

A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families

scientific article published on 27 January 2013

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

scientific article published on 23 April 2016

A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss

scientific article published on 17 July 2007

A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.

scientific article published on 27 July 2017

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

scientific article published on 21 December 2011

A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patient

scientific article published in December 2004

A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia

scientific article

A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.

scientific article published on 26 March 2018

A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non-pathogenic gene variants

scientific article published on 27 November 2019

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

scientific article published on 02 October 2019

A simple clot based assay for detection of procoagulant cell-derived microparticles

scientific article published on 01 May 2016

A simple, novel and robust test to diagnose type I Glanzmann thrombasthenia

scientific article published on 01 May 2008

A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII inhibitor screening assay

scientific article published on 01 March 2014

Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT)

scientific article published on 12 February 2013

Acquired hemophilia a: diagnosis, aetiology, clinical spectrum and treatment options

scientific article

Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands? ⬇️

scientific article published on 01 April 2011

Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population

scientific article published on December 2015

Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia

scientific article published on 19 November 2007

An ELISA assay for the detection of factor VIII antibodies - comparison with the conventional Bethesda assay in a large cohort of haemophilia samples

scientific article published in January 2003

An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).

scientific article published on 27 April 2013

Analysis of F8 inversions as risk factors for FVIII inhibitor development in Indian severe haemophilia A patients

scientific article published on 11 May 2014

Anti-phospholipid antibodies and other immunological causes of recurrent foetal loss--a review of literature of various therapeutic protocols

scientific article published on July 2009

Antibody profile in Indian severe haemophilia A patients with and without FVIII inhibitors

scientific article published on 30 September 2015

Aspirin resistance in patients with coronary artery disease - which test to use in routine management?

scientific article published in June 2008

Association of factor VII gene polymorphisms with Budd Chiari syndrome

scientific article published on 01 April 2010

Bengal macrothrombocytopenia is not totally an innocuous condition

scientific article

Bone health in persons with haemophilia: a review ⬇️

scientific article published on June 22, 2012

Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups ⬇️

scientific article published on June 1, 2012

Challenges of multiple mutations in individual patients with haemophilia ⬇️

scientific article published on January 11, 2011

Chronic synovitis and HLA B27 in patients with severe haemophilia

scientific article published in March 2003

Clinical and molecular epidemiology of factor XI deficiency in India

scientific article published on 21 September 2016

Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!

scientific article published in September 2007

Combination of copeptin, placental growth factor and total annexin V microparticles for prediction of preeclampsia at 10-14 weeks of gestation

scientific article published on 17 August 2017

Combination of thrombophilia markers in acute myocardial infarction of the young

scientific article published in September 2004

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

scientific article published on 01 July 2016

Comparison of four commercially available activated partial thromboplastin time reagents using a semi-automated coagulometer

scientific article published on 01 July 2003

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

scientific article published in August 2007

Could procoagulant cell-derived microparticles have a more crucial role in pregnancy complications rather than exosomes?

scientific article

Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective

scientific article published on 14 November 2015

Deep venous thrombosis associated with antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient

scientific article published on 01 July 2008

Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India

scientific article

Delayed Vitamin K deficiency related bleeding: is it genetically linked?

scientific article published on 14 September 2013

Delayed vitamin K deficiency as a cause of bleeding: still a concern in the 21st century!

scientific article published on 01 September 2010

Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy ⬇️

scientific article published on June 17, 2012

Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells

scientific article

Dengue virus infection of SK Hep1 cells: inhibition ofin vitroangiogenesis and altered cytomorphology by expressed viral envelope glycoprotein ⬇️

scientific article published on March 16, 2011

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

Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP).

scientific article

Direct detection of factor IX gene deletions in Indian haemophiliacs by multiplex PCR.

scientific article published in September 2003

Does consumption of platelet-derived microparticles in the fibrin clot explain the decrease in their percentage during pregnancy?

scientific article published on 21 December 2015

Dysfunctional fibrinolysis and cerebral venous thrombosis.

scientific article published on 13 May 2017

Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss

scientific article published on 28 April 2015

Elevated procoagulant endothelial and tissue factor expressing microparticles in women with recurrent pregnancy loss

scientific article

Epidemiology of hepatocellular carcinoma (HCC) in hemophilia

scientific article

Epidemiology, Diagnosis, and Management ofvon Willebrand Disease in India ⬇️

scientific article published on November 18, 2011

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

scientific article published in July 2015

Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia

scientific article published on May 2009

F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association

scientific article

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

scientific article published on 28 February 2014

Factor VIII Antigen, Activity, and Mutations in Hemophilia A.

scientific article published on 29 December 2014

Factor VIII haplotypes in severe hemophilia A patients in India

scientific article

Falciparum malaria selected while HIV-1 slaughtered

scientific article

Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India.

scientific article

First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India

scientific article published in November 2006

Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.

scientific article

Genetic disorder following assisted reproductive technology - prevent if you can, but always counsel!

scientific article published in February 2004

Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients

scientific article

Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within and outside the genes

scientific article published on March 2014

Hemostasis research in India: past, present, and future

scientific article published on 2 September 2011

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

scientific article published in April 2009

Hereditary protein C deficiency in Indian patients with venous thrombosis

scientific article

Hereditary thrombophilia in cerebral venous thrombosis: a study from India

scientific article

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

scientific article published in July 2015

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

scientific article published on 01 November 2002

Hypercoagulable state in idiopathic ulcerative colitis: role of hyperhomocysteinemia and hyperfibrinogenemia.

scientific article

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

Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy

scientific article

Immune response to FVIII in hemophilia A: an overview of risk factors

scientific article published on October 2009

Implications of human genome and modern cell biology research in management of cardiovascular diseases

scientific article

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 and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss

scientific article published on 23 June 2015

JAK2 mutations across a spectrum of venous thrombosis cases

scientific article published on 01 July 2010

Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss

scientific article published on 01 September 2015

Major disorganization of factor VIII gene as a cause of severe hemophilia A in Indian patients

scientific article published in May 2004

Malignancies in persons with haemophilia: 25-year data from India.

scientific article

Management of pregnancy in dysfibrinogenemia cases: a dilemma

scientific article

Masking of the clinical severity of severe haemophilia A in a patient with beta-thalassemia major--its implications in prenatal diagnosis

scientific article

Microparticles as prognostic biomarkers in dengue virus infection

scientific article published on 26 January 2018

Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency.

scientific article

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

scientific article published on August 26, 2010

Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein Occlusion

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.

scientific article

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

scientific article published on 23 July 2012

Novel Deleterious Sequence Change in the NLRP12 Gene in a Child with the Autoinflammatory Syndrome, Joint Hypermobility and Cutis Laxa from India

scholarly article by Kanjaksha Ghosh et al published 2019 in Mediterranean journal of hematology and infectious diseases

Novel genetic abnormalities in Bernard-Soulier syndrome in India

scientific article published on 01 September 2013

Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes

scientific article

Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation

scientific article published on 01 May 2015

Pathophysiology of acquired von Willebrand disease: a concise review ⬇️

scientific article published on August 1, 2011

Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India

scientific article published on 13 September 2009

Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss

scientific article published on 22 July 2009

Polymorphisms of warfarin metabolizing enzymes in an Indian population

scientific article published on 2 June 2013

Possible impact of factor V Leiden genotype on warfarin induced bleeding

scientific article published on July 2013

Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India

scientific article published on May 2016

Prediction of preeclampsia using combination of biomarkers at 18-23 weeks of gestation: A nested case-control study

scientific article published on 03 May 2019

Preeclampsia: simplified or still miles to go?

scientific article published on 06 January 2016

Prenatal diagnosis in a family with purfura fulminans.

scientific article published in April 2015

Prenatal diagnosis in a haemophilia A family by both factor VIII activity and antigen measurements

scientific article published in September 2003

Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays

scientific article published on 28 January 2014

Prenatal diagnosis of von Willebrand disease in a family

scientific article published in July 2005

Prevalence and spectrum of von Willebrand disease from western India

scientific article published in May 2005

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 ⬇️

scientific article published on August 11, 2012

Profibrinolytic microparticles are not adequately produced to compensate their prothrombotic effect

scientific article published on July 2013

Promising prognostic markers of preeclampsia: new avenues in waiting

scientific article published on 20 May 2015

Protein C (PROC) gene mutations in two Indian families with purpura fulminans

scientific article published on 14 January 2010

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 result

scientific article published in April 2016

Reduced clinical severity in a mutationally well-characterized cohort of severe hemophilia with associated thrombophilia

scientific article

Requiem to prenatal diagnosis of haemophilia A and B using coagulation activity and antigen based assays: not yet!

scientific article published in April 2003

Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review

scientific article published on 13 March 2013

Second trimester antenatal diagnosis in rare coagulation factor deficiencies

scientific article published in March 2007

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 factor IX gene mutations causing haemophilia B from India

scientific article

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

scientific article

Synergistic effect of factor VII gene polymorphisms causing mild factor VII deficiency in a case of severe factor X deficiency

scientific article published on 25 February 2016

The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients

scientific article

Thrombophilia and pregnancy loss--picking up a needle from the haystack!

scientific article published on 01 March 2006

Thrombophilia and unexplained pregnancy loss in Indian patients

scientific article published on 01 May 2008

Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis – A concise review ⬇️

scientific article published on October 20, 2010

Thrombophilic dimension of recurrent fetal loss in Indian patients

scientific article published in September 2008

Use of a new enzyme-linked immunosorbent assay for the detection of type 2N von Willebrand disease and its prevalence in an Indian population

scientific article published in January 2006

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

scientific article

VKORC1 and CYP2C9 genotype distribution in Asian countries

scientific article (publication date: September 2014)

VWF pseudogene: Mimics, masks and spoils

scientific article published on 07 January 2010

Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection in von Willebrand disease families in the Indian population.

scientific article

Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.

scientific article published on January 2017

Warfarin pharmacogenetics: How close are we to clinical practice?

scientific article published on July 2013

Why should hemophilia B be milder than hemophilia A?

scientific article published on May 2016

von Willebrand disease: a laboratory approach

scientific article

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