S. Shetty

发表

The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients

K. Ghosh, P. Pinto, T. Shelar, 2014, Indian Journal of Hematology and Blood Transfusion.

Development of inhibitors in patients with haemophilia from India

D. Mohanty, K. Ghosh, B. Kulkarni, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

Nanoimaging in cardiovascular diseases: Current state of the art

K. Ghosh, S. Shetty, S. Deb, 2015, The Indian journal of medical research.

Statins for Primary Prevention in Adults Aged 75 Years or Older

K. Ghosh, R. Patil, S. Shetty, 2015 .

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

A. Basu, K. Ghosh, S. Shetty, 2008, FEMS immunology and medical microbiology.

Cardiovascular and Electrocardiography Changes in Obese Individuals at Rest and During Stress Test

S. Shetty, S. Varun, H. Jain, 2017 .

Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges

D. Mohanty, K. Ghosh, S. Shetty, 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

Hereditary protein C deficiency in Indian patients with venous thrombosis

K. Ghosh, S. Shetty, Navin Pai, 2012, Annals of Hematology.

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

K. Ghosh, A. Jadli, S. Shetty, 2019, Pregnancy hypertension.

Magnesium Levels in Diabetes Mellitus: A Prospective Study

V. Shetty, S. Shetty, H. Jain, 2017 .

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

K. Ghosh, S. Shetty, Navin Pai, 2012, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review.

K. Ghosh, S. Shetty, 2011, Thrombosis research.

JAK2 mutations across a spectrum of venous thrombosis cases.

K. Ghosh, P. Kasatkar, B. Kulkarni, 2010, American journal of clinical pathology.

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

K. Ghosh, S. Shetty, L. Mota, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Blood coagulation in falciparum malaria—a review

K. Ghosh, S. Shetty, 2008, Parasitology Research.

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

J. Mahanta, K. Ghosh, D. Mirgal, 2016, Transactions of the Royal Society of Tropical Medicine and Hygiene.

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

D. Mohanty, K. Ghosh, S. Shetty, 2003, European journal of haematology.

C-peptide Levels in Diagnosis of Diabetes Mellitus : A Case-control Study

V. Shetty, S. Shetty, H. Jain, 2017 .

Cell-Derived Microparticles (MPs) and their Role in Unexplained Recurrent Pregnancy Loss

R. Patil, S. Shetty, 2018, Proceedings of the Indian National Science Academy.

Elevated Procoagulant Endothelial and Tissue Factor Expressing Microparticles in Women with Recurrent Pregnancy Loss

K. Ghosh, R. Patil, S. Shetty, 2013, PloS one.

Polymorphisms of warfarin metabolizing enzymes in an Indian population.

K. Ghosh, T. Gaikwad, S. Shetty, 2013, Blood cells, molecules & diseases.

Novel therapeutic approaches for haemophilia

K. Ghosh, S. Shetty, Kanjaksha Ghosh, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Challenges and open issues in the management of acquired hemophilia A (AHA).

K. Ghosh, S. Shetty, 2015, Blood cells, molecules & diseases.

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

K. Ghosh, S. Ali, S. Shetty, 2017, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Novel genetic abnormalities in Bernard-Soulier syndrome in India

K. Ghosh, S. Ali, S. Shetty, 2014, Annals of Hematology.

Molecular pathology of Bernard–Soulier syndrome in Indian patients

K. Ghosh, S. Ali, S. Shetty, 2013, Platelets.

Serum Uric Acid Level as an Independent Mortality Marker in Patients with Acute Myocardial Infarction

V. Shetty, S. Shetty, H. Jain, 2016 .

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

D. Mohanty, K. Ghosh, S. Shetty, 2004, Haematologica.

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

K. Ghosh, R. Patil, S. Shetty, 2013, European journal of obstetrics, gynecology, and reproductive biology.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2007, British journal of haematology.

Epidemiology, Diagnosis, and Management of von Willebrand Disease in India

K. Ghosh, S. Shetty, Kanjaksha Ghosh1, 2011, Seminars in thrombosis and hemostasis.

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

K. Ghosh, S. Shetty, 2011, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

D. Mohanty, K. Ghosh, S. Shetty, 2003, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

K. Ghosh, C. Ross, T. Gaikwad, 2013, European journal of pharmacology.

Association of factor VII gene polymorphisms with Budd Chiari syndrome.

K. Ghosh, B. Kulkarni, S. Shetty, 2010, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Warfarin pharmacogenetics: How close are we to clinical practice?

K. Ghosh, T. Gaikwad, S. Shetty, 2013, Indian journal of human genetics.

Novel Mutations in Factor IX Gene From Western India With Reference to Their Phenotypic and Haplotypic Attributes

K. Ghosh, S. Shetty, L. Quadros, 2009, Journal of pediatric hematology/oncology.

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

K. Ghosh, S. Shetty, L. Quadros, 2007, Annals of Hematology.

Dysfunctional fibrinolysis and cerebral venous thrombosis.

K. Ghosh, B. Kulkarni, S. Shetty, 2017, Blood cells, molecules & diseases.

Hereditary thrombophilia as a cause of Budd‐Chiari syndrome: A study from Western India

D. Mohanty, K. Ghosh, S. Shetty, 2001, Hepatology.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2003, Platelets.

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

K. Ghosh, S. Shetty, V. Salvi, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

REVIEW ARTICLE: Anti‐phospholipid Antibodies and Other Immunological Causes of Recurrent Foetal Loss – A Review of Literature of Various Therapeutic Protocols

K. Ghosh, S. Shetty, 2009, American journal of reproductive immunology.

Clinical and molecular epidemiology of factor XI deficiency in India.

K. Ghosh, S. Shetty, N. Kawankar, 2016, Thrombosis research.

Association of Thrombophilic Factors in Pathogenesis of Osteonecrosis of Femoral Head in Indian Population

S. Shetty, A. Sathe, M. Tayade, 2020, Indian Journal of Orthopaedics.

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

K. Ghosh, A. Jadli, B. Kulkarni, 2012, Liver international : official journal of the International Association for the Study of the Liver.

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

K. Ghosh, S. Shetty, S. Vora, 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country

D. Mohanty, K. Ghosh, M. Madkaikar, 2005, Haemophilia : the official journal of the World Federation of Hemophilia.

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

K. Ghosh, S. Shetty, Purnima Satoskar, 2007, Thrombosis journal.

Prenatal diagnosis in a family with purfura fulminans.

K. Ghosh, S. Shanbhag, S. Shetty, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

K. Ghosh, R. Patil, S. Shetty, 2016, Clinical chemistry and laboratory medicine.

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

K. Ghosh, S. Shetty, Navin Pai, 2014, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

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

K. Ghosh, S. Shetty, Navin Pai, 2010, Annals of Hematology.

Haptoglobin polymorphism and serum ferritin concentration in ageing subjects

D. Mohanty, K. Ghosh, S. Shetty, 2004 .

Bone health in persons with haemophilia: a review

K. Ghosh, S. Shetty, 2012, European journal of haematology.

Differential response to FEIBA is strongly associated with the prothrombotic microparticles.

R. Patil, S. Shetty, C. Shanmukhaiah, 2020, Blood cells, molecules & diseases.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2012, Annals of Hematology.

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

K. Ghosh, S. Shetty, D. Butera, 2008, Haematologica.

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

K. Ghosh, A. Jadli, S. Shetty, 2017, Placenta.

Promising prognostic markers of preeclampsia: new avenues in waiting.

K. Ghosh, A. Jadli, S. Shetty, 2015, Thrombosis research.

An ELISA Assay for the Detection of Factor VIII Antibodies – Comparison with the Conventional Bethesda Assay in a Large Cohort of Haemophilia Samples

D. Mohanty, K. Ghosh, S. Shetty, 2002, Acta Haematologica.

Differences in Etiological and Clinical Manifestations in Upper Extremity and Lower Limb Deep Venous Thrombosis Patients From India

K. Ghosh, B. Kulkarni, S. Shetty, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients

K. Ghosh, P. Pinto, S. Shetty, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

von Willebrand disease: a laboratory approach.

D. Mohanty, K. Ghosh, S. Shetty, 2005, The National medical journal of India.

Biological: Full-length Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy

P. Poddar, A. Basu, K. Ghosh, 2008 .

Microparticles as prognostic biomarkers in dengue virus infection.

K. Ghosh, R. Patil, S. Shetty, 2018, Acta tropica.

ANTIPLATELET AGGREGATION ASSAY OF HOMOGENATE OF EUTYPHOEUS GAMMIEI- A NATIVE EARTHWORM OF TRIPURA, NORTH-EAST, INDIA

S. Shetty, Debnath Madhusudan, Sil Samir Kumar, 2017 .

Indian Society of Hematology and Blood Transfusion (ISHBT) Consensus Document on Hematological Practice During COVID-19 Pandemic

S. Shetty, A. Srivastava, H. Pati, 2021, Indian Journal of Hematology and Blood Transfusion.

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

K. Ghosh, R. Patil, S. Shetty, 2016, Blood cells, molecules & diseases.

FACTOR V LEIDEN GENE MUTATION IN YOUNG INDIAN PATIENTS WITH MYOCARDIAL INFARCTION

M. Yeolekar, D. Mohanty, K. Ghosh, 1998 .

Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors

K. Ghosh, S. Shetty, 2009, Clinical reviews in allergy & immunology.

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

P. Poddar, A. Basu, K. Ghosh, 2008, Journal of electron microscopy.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2017, European journal of haematology.

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

K. Ghosh, S. Shetty, Manali A. Bhave, 2011, Autoimmunity reviews.

Epsilon-Aminocaproic Acid Inhibits the Activity of Factor VIII Inhibitors in Patients with Severe Haemophilia A in vivo and in vitro

D. Mohanty, K. Ghosh, S. Shetty, 2000, Acta Haematologica.

Why should hemophilia B be milder than hemophilia A?

K. Ghosh, S. Shetty, 2016, Haematologica.

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

K. Ghosh, A. Mukaddam, A. Jadli, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Chronic synovitis and HLA B27 in patients with severe haemophilia

D. Mohanty, K. Ghosh, S. Shetty, 2003, The Lancet.

Milder clinical presentation of haemophilia A with severe deficiency of factor VIII as measured by one‐stage assay

D. Mohanty, K. Ghosh, S. Shetty, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

First‐time development of FVIII inhibitor in haemophilia patients during the postoperative period

D. Mohanty, K. Ghosh, M. Madkaikar, 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

Glanzmann's thrombasthenia: updated

D. Mohanty, K. Ghosh, B. Kulkarni, 2002, Platelets.

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

B. Kulkarni, S. Shetty, M. Bhattacharyya, 2019, Haemophilia.

Role of epsilon amino caproic acid in the management of haemophilic patients with inhibitors

D. Mohanty, K. Ghosh, S. Shetty, 2004, Haemophilia.

Pathophysiology of acquired von Willebrand disease: a concise review

K. Ghosh, P. Kasatkar, S. Shetty, 2011, European journal of haematology.

Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI)

K. Ghosh, S. Shetty, D. Sahu, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Hemophilia: A High Cost Low Volume Disease: Suitable Preventive Strategies for Developing and Developed Countries

K. Ghosh, S. Shetty, Kinjalka Ghosh, 2008 .

Haemorrhage in upper cervical cord: an unusual manifestation in moderate haemophilia patients who ride motorbikes

D. Mohanty, K. Ghosh, S. Shetty, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

Transfusion transmitted diseases in haemophilics from western India.

D. Mohanty, K. Ghosh, M. Madkaikar, 2000, The Indian journal of medical research.

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

D. Mirgal, S. Shanbhag, S. Shetty, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Mutations in Intron 1 and Intron 22 Inversion Negative Haemophilia A Patients from Western India

K. Ghosh, P. Nair, S. Shetty, 2014, PloS one.

Low‐dose prophylaxis and its impact on the health of haemophilia patients

S. Bansal, S. Rangarajan, S. Shetty, 2022, Vox sanguinis.

A homozygous female hemophilia A

K. Ghosh, P. Nair, S. Shetty, 2012, Indian journal of human genetics.

Challenges of multiple mutations in individual patients with haemophilia

K. Ghosh, S. Shetty, Manali A. Bhave, 2011, European journal of haematology.

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

S. Idicula-Thomas, K. Ghosh, S. Shetty, 2009, Clinica chimica acta; international journal of clinical chemistry.

Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected

K. Ghosh, S. Shanbhag, S. Shetty, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Spectrum of inherited bleeding disorders from Western India.

D. Mohanty, K. Ghosh, B. Kulkarni, 2002, Haematologia.

Review Article Alternate strategies for carrier detection and antenatal diagnosis in haemophilias in developing countries

D. Mohanty, K. Ghosh, S. Shetty, 2003 .

Clinically Significant Inhibitors in Hemophilia A Patients from India Tend to Persist

D. Mohanty, K. Ghosh, S. Shetty, 2000, Acta Haematologica.

Factor VIII and IX gene polymorphisms and carrier analysis in Indian population

D. Mohanty, K. Ghosh, S. Shetty, 1997, American journal of hematology.

Evolution of Prenatal Diagnostic Techniques From Phenotypic Diagnosis to Gene Arrays: Its Likely Impact on Prenatal Diagnosis of Hemophilia

K. Ghosh, S. Shetty, Mukesh Tulsiani, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Hemostasis Research in India

K. Ghosh, S. Shetty, Kinjalka Ghosh, 2012, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

Prevalence and spectrum of von Willebrand disease from western India.

D. Mohanty, K. Ghosh, S. Shetty, 2005, The Indian journal of medical research.

Molecular Pathology of Rare Bleeding Disorders (RBDs) in India: A Systematic Review

K. Ghosh, S. Shanbhag, B. Kulkarni, 2014, PloS one.

Haemophilia - diagnosis and management challenges

S. Shetty, 2014, Molecular Cytogenetics.

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

K. Ghosh, S. Shetty, 2012, The National medical journal of India.

Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders

K. Ghosh, S. Shetty, 2007, Haemophilia : the official journal of the World Federation of Hemophilia.

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

K. Ghosh, S. Shetty, F. Jijina, 2006, Prenatal diagnosis.

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

K. Ghosh, P. Pinto, S. Shetty, 2016, Mutation research.

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

S. Kaveri, S. Lacroix-Desmazes, K. Ghosh, 2016, Immunology letters.

Glanzmann’s thrombasthenia – newer treatment options

K. Ghosh, S. Shetty, 2014 .

Rare Occurrence of Inhibitors in Von Willebrand Disease: A Case Report

B. Kulkarni, S. Shetty, C. Shanmukhaiah, 2022, Frontiers in Medicine.

Combined factor VIII and IX deficiency in a family.

D. Mohanty, K. Ghosh, S. Shetty, 2001, Clinical and laboratory haematology.

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

D. Mohanty, K. Ghosh, F. Peyvandi, 2005, American journal of hematology.

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

K. Ghosh, P. Nair, B. Kulkarni, 2010, Clinica chimica acta; international journal of clinical chemistry.

Second Trimester Antenatal Diagnosis in Rare Coagulation Factor Deficiencies

K. Ghosh, S. Shetty, L. Mota, 2007, Journal of pediatric hematology/oncology.

Carrier detection and prenatal diagnosis in families with haemophilia.

D. Mohanty, A. Bhide, K. Ghosh, 2001, The National medical journal of India.

Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.

K. Ghosh, S. Shetty, N. Sharma, 2016, Critical reviews in oncology/hematology.

Rare coagulation factor deficiencies: a countrywide screening data from India

S. Shabhag, K. Ghosh, P. Pinto, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Prenatal Diagnosis in a Family at Risk for β‐Thalassemia and Hemophilia A: An Uncommon Association

D. Mohanty, K. Ghosh, S. Shetty, 2004, Hemoglobin.

Hemophilia B in a Female

D. Mohanty, K. Ghosh, S. Shetty, 2001, Acta Haematologica.

Prenatal diagnosis of haemophilia: a preliminary report.

D. Mohanty, A. Bhide, K. Ghosh, 1998, The National medical journal of India.

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

K. Ghosh, P. Kasatkar, S. Shetty, 2010, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Bengal macrothrombocytopenia is not totally an innocuous condition.

K. Ghosh, S. Ali, S. Shetty, 2016, Blood cells, molecules & diseases.

Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent

K. Ghosh, S. Shetty, L. Mota, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients

K. Ghosh, P. Kasatkar, S. Shetty, 2014, PloS one.

Inherited and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss.

K. Ghosh, R. Patil, S. Shetty, 2015, Blood cells, molecules & diseases.

Thrombophilia and unexplained pregnancy loss in Indian patients.

K. Ghosh, S. Shetty, Purnima Satoskar, 2008, The National medical journal of India.

Hereditary thrombophilia in cerebral venous thrombosis: a study from India

K. Ghosh, S. Shetty, Navin Pai, 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2004, Indian journal of medical sciences.

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

K. Ghosh, S. Shetty, B. Poudyal, 2012, Annals of Hematology.

Venous Thromboembolism in Young Patients From Western India: A Study

D. Mohanty, K. Ghosh, M. Madkaikar, 2001, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

ROLE OF THROMPHOPHILIC MUTATIONS IN THE DEVELOPMENT OF AVN IN INDIAN POPULATION

S. Shetty, A. Jogani, Pratap Jadhav, 2020 .

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

K. Ghosh, B. Kulkarni, S. Shetty, 2018, The Journal of the Association of Physicians of India.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2016, Thrombosis research.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2002, British journal of haematology.

Triple jeopardy: A case of Glanzmann's thrombasthenia with anti-GPIIb-IIIa antibodies and HPA incompatibility resulting in stillbirth.

R. Patil, S. Shetty, C. Shanmukhaiah, 2019, Thrombosis research.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2009, Indian journal of human genetics.

Diagnostic Pitfalls and Fallacies of Measuring Antiplatelet Antibodies

K. Ghosh, B. Kulkarni, S. Shetty, 2006, Acta Haematologica.

The spectrum of bleeding disorders in women with menorrhagia: a report from Western India

D. Mohanty, K. Ghosh, S. Shetty, 2005, Annals of Hematology.

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

K. Ghosh, A. Jadli, B. Kulkarni, 2015, The Indian journal of medical research.

Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients

D. Mohanty, K. Ghosh, S. Shetty, 2005, Journal of thrombosis and haemostasis : JTH.

Delayed Vitamin K Deficiency Related Bleeding: Is it Genetically Linked?

K. Ghosh, T. Gaikwad, A. Jadli, 2014, The Indian Journal of Pediatrics.

An improved, semi quantitative clot based assay for factor XIII

K. Ghosh, S. Shanbhag, B. Kulkarni, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic Disorders in Haematological Practice in India

D. Mohanty, K. Ghosh, S. Shetty, 2002, Public Health Genomics.

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

D. Mohanty, K. Ghosh, P. Rathi, 2008, Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology.

Novel RASGRP2 variants in platelet function defects: Indian study

B. Kulkarni, S. Shetty, N. Kawankar, 2022, British journal of haematology.

Ankle Brachial Pressure Index Correlation with Diastolic Blood Pressure , Dyslipidemia and Anthropometric Measurement in Patients of Essential Hypertension

V. Shetty, S. Shetty, H. Jain, 2017 .

Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India

K. Ghosh, S. Shetty, M. Vijapurkar, 2009, Platelets.

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

K. Ghosh, P. Kasatkar, S. Shetty, 2015, The Indian journal of medical research.

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

S. Idicula-Thomas, K. Ghosh, B. Kulkarni, 2009, Thrombosis and Haemostasis.

Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients.

R. Patil, Anita Parihar, S. Shetty, 2018, Thrombosis research.

COVID‐19 and preeclampsia: The unique and the mutually nonexclusive clinical manifestations

S. Bansal, S. Rangarajan, S. Shetty, 2023, American journal of reproductive immunology.

Preeclampsia: simplified or still miles to go?

K. Ghosh, A. Jadli, S. Shetty, 2016, American journal of obstetrics and gynecology.

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

P. Patel, K. Ghosh, K. Mishra, 2019, Mediterranean journal of hematology and infectious diseases.

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

K. Ghosh, S. Shetty, Purnima Satoskar, 2008, European journal of obstetrics, gynecology, and reproductive biology.

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

K. Ghosh, S. Shetty, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein.

A. Basu, K. Ghosh, S. Shetty, 2011, FEMS immunology and medical microbiology.

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

F. Kamali, K. Ghosh, T. Gaikwad, 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

VKORC1 and CYP2C9 genotype distribution in Asian countries.

K. Ghosh, T. Gaikwad, S. Shetty, 2014, Thrombosis research.

Management of pregnancy in dysfibrinogenemia cases: a dilemma.

K. Ghosh, A. Mukaddam, R. Patil, 2017, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

K. Ghosh, A. Mukaddam, A. Jadli, 2015, American journal of clinical pathology.

Evaluation of light emitting diode-based fluorescence microscopy for the detection of mycobacteria in a tuberculosis-endemic region.

M. Pai, S. Shenai, S. Shetty, 2011, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

Thrombophilic dimension of recurrent fetal loss in Indian patients

K. Ghosh, S. Shetty, S. Vora, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

D. Mohanty, K. Ghosh, S. Shetty, 2006, Acta Haematologica.

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

K. Ghosh, P. Kasatkar, S. Shetty, 2014, Prenatal Diagnosis.

Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia

K. Ghosh, B. Kulkarni, S. Shetty, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

VWF pseudogene: Mimics, masks and spoils.

K. Ghosh, P. Kasatkar, S. Shetty, 2010, Clinica chimica acta; international journal of clinical chemistry.

Double mutations causing haemophilia B: a double whammy!

K. Ghosh, B. Kulkarni, S. Shetty, 2009, British journal of haematology.

St 14 (DX S52) VNTR polymorphism in the Indian population and its application in carrier detection and prenatal diagnosis of haemophilia A families.

D. Mohanty, K. Ghosh, S. Shetty, 2000, Haematologia.

Genetics and classification of hemophilia

K. Ghosh, S. Shetty, 2014 .

Is peripheral blood corin level clinically relevant for prediction of pre‐eclampsia?

K. Ghosh, A. Jadli, S. Shetty, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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

K. Ghosh, S. Ali, S. Shetty, 2015, Blood cells, molecules & diseases.

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

K. Ghosh, S. Shetty, 2014, Haematologica.

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

K. Ghosh, S. Shetty, A. Khare, 2007, Indian Heart Journal.

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

K. Ghosh, P. Kasatkar, S. Shetty, 2013, Annals of Hematology.

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

K. Ghosh, R. Patil, S. Shetty, 2016, Annals of Hematology.

A possible need for routine screening for Strongyloides stercoralis infection in Indian haemophilia patients

K. Ghosh, R. Patil, S. Shetty, 2018, The Indian journal of medical research.

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

K. Ghosh, S. Shetty, 2008, American journal of clinical pathology.

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

K. Ghosh, S. Shetty, L. Quadros, 2007, European Journal of Haematology.

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

D. Mohanty, K. Ghosh, S. Shetty, 2004, American journal of hematology.

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

K. Ghosh, P. Pinto, S. Shetty, 2013, Clinical chemistry and laboratory medicine.

Factor VIII haplotypes in severe hemophilia A patients in India

K. Ghosh, P. Pinto, S. Shetty, 2013, Annals of Hematology.

Mortality caused by intracranial bleeding in non‐severe hemophilia A patients: comment

K. Ghosh, R. Patil, S. Shetty, 2017, Journal of thrombosis and haemostasis : JTH.

Spectrum of factor IX gene mutations causing haemophilia B from India

K. Ghosh, S. Shetty, L. Quadros, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population

K. Ghosh, S. Shetty, B. Poudyal, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Factor VIII Antigen, Activity, and Mutations in Hemophilia A

K. Ghosh, P. Nair, S. Shetty, 2016, Clinical and applied thrombosis/hemostasis.

Double mutations in haemophilia: muddling strangers or indifferent partners in crime?

K. Ghosh, P. Nair, S. Shetty, 2010, Haemophilia.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2008, Prenatal diagnosis.

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

K. Ghosh, B. Kulkarni, S. Shetty, 2008, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

K. Ghosh, S. Shanbhag, S. Shetty, 2016, Blood cells, molecules & diseases.

Fibrinolysis, inhibitors of blood coagulation, and monocyte derived coagulant activity in acute malaria

D. Mohanty, S. Rizvi, K. Ghosh, 1997, American journal of hematology.

Inherited deficiency of multiple vitamin K‐dependent coagulation factors and coagulation inhibitors presenting as hemorrhagic diathesis, mental retardation, and growth retardation

D. Mohanty, K. Ghosh, S. Shetty, 1996, American journal of hematology.

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

A. Jadli, S. Shanbhag, S. Shetty, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

A Study of Lipid Profile in Diabetes Mellitus

V. Shetty, S. Shetty, H. Jain, 2017 .

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.

K. Ghosh, B. Kulkarni, S. Shetty, 2007, Clinica chimica acta; international journal of clinical chemistry.

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

J. Mahanta, K. Ghosh, D. Mirgal, 2016, Transactions of the Royal Society of Tropical Medicine and Hygiene.

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

K. Ghosh, R. Patil, S. Shetty, 2015, British journal of haematology.

Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: A unified pathology?

D. Mohanty, K. Ghosh, S. Shetty, 2005, Platelets.

Combined factor V and VIII deficiency in Indian population

Shetty, Pathare, M. Madkaikar, 2000, Haemophilia : the official journal of the World Federation of Hemophilia.

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

K. Ghosh, P. Kasatkar, S. Shetty, 2013, Annals of Hematology.

Dysfunctional fibrinolysis and cerebral venous thrombosis.

K. Ghosh, B. Kulkarni, S. Shetty, 2017, Blood cells, molecules & diseases.

Low dose emicizumab prophylaxis in haemophilia a patients: A pilot study from India

K. Fischer, S. Rangarajan, S. Shetty, 2023, Haemophilia : the official journal of the World Federation of Hemophilia.

Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia

S. Shetty, Kanjaksha Ghosh, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.

K. Ghosh, S. Shetty, N. Sharma, 2016, Critical reviews in oncology/hematology.

Annexin A5 levels or circulating microparticles: what we see depends mainly on what we look for

R. Patil, S. Shetty, K. Ghosh, 2016, Journal of internal medicine.