K. Ghosh

K. Ghosh, M. Mukherjee, R. Colah, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

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.

Major Blood Group Antigens - A Determinant of Factor VIII Levels in Blood?

A. P. Chauhan, D. Mohanty, K. Ghosh, 1984, Thrombosis and Haemostasis.

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

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

Cancers in patients with hemophilia: a retrospective study from the Italian Association of Hemophilia Centers: a rebuttal

K. Ghosh, S. Shetty, 2012, Journal of thrombosis and haemostasis : JTH.

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.

Iron deficiency anaemia in sickle cell disorders in India.

D. Mohanty, K. Ghosh, M. Mukherjee, 2008, The Indian journal of medical research.

Innate immune gene polymorphisms and their association with neonatal sepsis.

K. Ghosh, M. Mukherjee, R. Colah, 2018, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

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.

Human platelet specific antigens and their importance.

K. Ghosh, D. Mohanty, B. Kulkarni, 2004, Indian pediatrics.

Evaluation of markers of endothelial damage in cases of young myocardial infarction.

D. Mohanty, K. Ghosh, A. Khare, 2005, Atherosclerosis.

Unusual Clinical Presentations of Familial Hemophagocytic Lymphohistiocytosis Type-2

K. Ghosh, M. Madkaikar, F. Jijina, 2014, Journal of pediatric hematology/oncology.

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.

Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas

K. Ghosh, M. Patwardhan, V. Pradhan, 2009, Rheumatology International.

Experimental animal model to study iron overload and iron chelation and review of other such models.

K. Ghosh, R. Colah, K. Italia, 2015, Blood cells, molecules & diseases.

Warfarin pharmacogenetics: How close are we to clinical practice?

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

Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus‐infected patients of Mumbai, India

K. Ghosh, A. Pawar, A. Pazare, 2010, International journal of immunogenetics.

Hydroxyurea Could Be a Good Clinically Relevant Iron Chelator

K. Ghosh, R. Colah, K. Italia, 2013, PloS one.

New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia

K. Ghosh, P. Warang, R. Colah, 2013, Annals of Hematology.

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.

Changes in platelet glycoprotein receptors after smoking – a flow cytometric study

S. Kulkarni, D. Mohanty, K. Ghosh, 2001, 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.

Microsatellite diversity among the primitive tribes of India

D. Mohanty, K. Ghosh, V. Tripathy, 2009, Indian journal of human genetics.

Frequency of partial D in Western India

S. Kulkarni, D. Mohanty, K. Vasantha, 2008, Transfusion medicine.

Clinical and molecular epidemiology of factor XI deficiency in India.

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

Pancytopenia in nutritional megaloblastic anaemia. A study from north-west India.

K. Ghosh, N. Marwaha, R. Marwaha, 1989, Tropical and geographical medicine.

Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.

K. Ghosh, B. Vundinti, Purvi Mohanty, 2016, Blood cells, molecules & diseases.

Impact of Autoantibodies to Complement Components on the Disease Activity in SLE.

S. Kaveri, K. Ghosh, J. Bayry, 2021, The Journal of the Association of Physicians of India.

Placental histomorphology in unexplained foetal loss with thrombophilia.

K. Ghosh, S. Shetty, M. Khare, 2009, The Indian journal of medical research.

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.

Common human leucocyte antigen haplotypes in Indians – its implications in finding unrelated compatible bone marrow donors

D. Mohanty, K. Ghosh, U. Shankarkumar, 2002, Transfusion medicine.

Incidence of down syndrome: Hypotheses and reality

K. Ghosh, B. Vundinti, 2011, Indian journal of human genetics.

Red Cell Distribution Width (RDW): Normative Data in Indian Neonates

K. Ghosh, N. Kabra, M. Mukherjee, 2019, Journal of pediatric hematology/oncology.

Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario

K. Ghosh, M. Mukherjee, R. Colah, 2015, The Indian journal of medical research.

Dengue Virus NS1 Exposure Affects von Willebrand Factor Profile and Platelet Adhesion Properties of Cultured Vascular Endothelial Cells

A. Basu, K. Ghosh, S. Gangodkar, 2018, Indian Journal of Hematology and Blood Transfusion.

Chromosomal breakage in myelodysplatic syndrome.

K. Ghosh, L. Kerketta, S. Korgaonkar, 2008, Asian Pacific journal of cancer prevention : APJCP.

Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation

S. Swaminathan, K. Ghosh, B. Vundinti, 2010, European journal of haematology.

Twin pregnancy in a patient of chronic myeloid leukemia on imatinib therapy.

K. Ghosh, M. Madkaikar, F. Jijina, 2008, Leukemia research.

Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases

K. Ghosh, L. Kerketta, S. Korgaonkar, 2006 .

First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders

K. Ghosh, R. Colah, A. Nadkarni, 2012, Journal of Clinical Pathology.

How Old Is Factor V Leiden Mutation?

D. Mohanty, K. Ghosh, A. Pawar, 2001, Thrombosis and Haemostasis.

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.

A new simple approach for the determination of pyrimidine 5′‐nucleotidase activity in human erythrocytes using an ELISA reader

K. Ghosh, P. Warang, R. Colah, 2012, International journal of laboratory hematology.

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.

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

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

Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.

K. Ghosh, R. Colah, A. Nadkarni, 2012, Clinica chimica acta; international journal of clinical chemistry.

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.

Osteoporosis in young haemophiliacs from western India

K. Ghosh, M. Madkaikar, M. Shrikhande, 2007, American journal of hematology.

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.

Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?

K. Ghosh, R. Colah, K. Italia, 2016, Free radical research.

Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adults.

K. Ghosh, M. Mukherjee, R. Colah, 2011, Genetic testing and molecular biomarkers.

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.

Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories.

K. Ghosh, S. Shanbhag, S. Shetty, 2017, Thrombosis research.

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.

Platelet dysfunction in nutritional vitamin b(12) deficiency.

D. Mohanty, K. Ghosh, V. Krishna, 1991, Platelets.

Evolution and selection of human leukocyte antigen alleles by Plasmodium falciparum infection.

K. Ghosh, 2008, Human immunology.

Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.

D. Mohanty, K. Ghosh, A. Gorakshakar, 2004, Blood cells, molecules & diseases.

Erratum to: Familial small supernumerary marker chromosome (sSMC) (14) (:p11-q11:) in a child with translocation down syndrome

K. Ghosh, B. Vundinti, Seema Korgoankar, 2010 .

Defining the allelic variants of HLA A19 in the western Indian population.

D. Mohanty, K. Ghosh, U. Shankarkumar, 2002, Human immunology.

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.

Hb M Hyde Park and Hb M Boston in two Indian families – a rare cause of methaemoglobinemia

K. Ghosh, P. Warang, R. Colah, 2015, International journal of laboratory hematology.

HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association

K. Ghosh, R. Colah, A. Nadkarni, 2014, Mediterranean journal of hematology and infectious diseases.

Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India

K. Ghosh, R. Colah, S. Nair, 2013, Indian journal of human genetics.

Five α globin chain variants identified during screening for haemoglobinopathies

K. Ghosh, P. Warang, R. Colah, 2010, European journal of clinical investigation.

Centrosome Aberration Frequency and Disease Association in B-Acute Lymphoblastic Leukemia.

K. Ghosh, B. Vundinti, M. Madkaikar, 2017, In vivo.

A novel 5-way translocation t(9;11;13;19;22) in a case of chronic-phase chronic myeloid leukemia.

K. Ghosh, B. Vundinti, Prantar Chakrabarti, 2013, Human pathology.

Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.

K. Ghosh, R. Colah, R. Merchant, 2009, Clinica chimica acta; international journal of clinical chemistry.

Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.

D. Mohanty, K. Ghosh, R. Colah, 2009, Blood cells, molecules & diseases.

Development of Anti-neutrophil Cytoplasmic Antibodies (ANCA) and Vasculitis in BALB/c Mice: A Prototype of Human ANCA Associated Disease

K. Ghosh, V. Pradhan, K. Ghosh, 2009 .

Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH‐cytochrome b5 reductase gene mutations

K. Ghosh, P. Warang, R. Colah, 2011, American journal of hematology.

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

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

Comprehensive Report of Primary Immunodeficiency Disorders from a Tertiary Care Center in India

K. Ghosh, M. Madkaikar, M. Desai, 2012, Journal of Clinical Immunology.

HLA A*02 allele frequencies and B haplotype associations in Western Indians.

D. Mohanty, K. Ghosh, U. Shankarkumar, 2003, Human immunology.

SPLENIC FUNCTION IN OMANI CHILDREN WITH SICKLE CELL DISEASE: Correlation with Severity Index, Hemoglobin Phenotype, Iron Status, and α -Thalassemia Trait

K. Ghosh, Y. Wali, Z. al-Lamki, 2002, Pediatric hematology and oncology.

Haematology Research in India: Past, Present and Future

K. Ghosh, 2011, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

HLA Antigen Distribution in Selected Caste Groups from Mumbai, Maharastra, India

D. Mohanty, K. Ghosh, U. Shankarkumar, 2002 .

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

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

Ex vivo Expansion of Umbilical Cord Blood Stem Cells Using Different Combinations of Cytokines and Stromal Cells

D. Mohanty, S. Swaminathan, K. Ghosh, 2007, Acta Haematologica.

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

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

Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.

K. Ghosh, R. Colah, A. Nadkarni, 2019, Genomics.

Chimeric fusion karyotypes in childhood B-cell acute lymphoblastic leukemia.

K. Ghosh, L. Kerketta, V. B. Rao, 2014, Indian pediatrics.

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.

Mannose binding lectin (MBL) in autoimmunity and its role in systemic lupus erythematosus (SLE).

K. Ghosh, V. Pradhan, P. Surve, 2010, The Journal of the Association of Physicians of India.

Feasibility of a Newborn Screening and Follow-up Programme for Sickle Cell Disease among South Gujarat (India) Tribal Populations

L. Krishnamurti, K. Ghosh, R. Colah, 2015, Journal of medical screening.

Sickle cell disease in India

K. Ghosh, M. Mukherjee, R. Colah, 2014, Current opinion in hematology.

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

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

Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH)

K. Ghosh, 2015, Indian Journal of Hematology and Blood Transfusion.

Familial small supernumerary marker chromosome (sSMC) (14)(:P11–q11:)In a child with translocation down syndrome

K. Ghosh, B. Vundinti, S. Korgaonkar, 2009, Indian journal of pediatrics.

Pulmonary hypertension in patients with hematological disorders following splenectomy

K. Ghosh, F. Jijina, V. Meera, 2009, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

Differentiation of Nijmegen breakage syndrome from Fanconi anemia.

K. Ghosh, L. Kerketta, S. Korgaonkar, 2007, Genetics and molecular research : GMR.

Management of haemophilia and its complications in developing countries.

K. Ghosh, 2004, Clinical and laboratory haematology.

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.

Fractures of long bones in severe haemophilia

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

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.

Studies on the mechanism of synthesis and release of the procoagulant activity from leukaemic cells

D. Mohanty, K. Ghosh, K. C. Das, 1991, Medical Oncology and Tumor Pharmacotherapy.

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.

Open heart surgery with mitral valve replacement--ordeal of an undiagnosed haemophilia patient.

D. Mohanty, K. Ghosh, M. Madkaikar, 2003, Clinical and laboratory haematology.

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.

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

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

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.

Successful surgery in severe haemophilia – a two‐stage replacement therapy in resource‐poor countries

K. Ghosh, R. Prabhu, F. Jijina, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

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

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

Development of anti-VWF antibody in a patient with severe haemophilia A following the development of high-grade non-Hodgkin's lymphoma.

D. Mohanty, K. Ghosh, F. Jijina, 2002, Clinical and laboratory haematology.

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.

Anticoagulation in haemophilia patients with prosthetic valve replacement

K. Ghosh, S. Shetty, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.

K. Ghosh, P. Warang, R. Colah, 2008, Blood cells, molecules & diseases.

Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.

D. Mohanty, K. Ghosh, R. Colah, 2002, Haematologia.

Acquired inhibitor to factor VIII: report of two unusual cases

D. Mohanty, K. Ghosh, S. Ghamande, 1997, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

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.

Ophthalmic surgery in haemophilia

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

Glanzmann’s thrombasthenia – newer treatment options

K. Ghosh, S. Shetty, 2014 .

Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.

S. Duga, K. Ghosh, F. Peyvandi, 2006, Haematologica.

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.

Intron 22 Inversions in Factor VIII Gene in Indian Hemophiliacs

D. Mohanty, K. Ghosh, F. Jijina, 1998, Thrombosis and Haemostasis.

Coagulation disorders seen through the window of molecular biology

K. Ghosh, 2007, Indian journal of human genetics.

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.

Seronegative spondarthritis and human leucocyte antigen association

D. Mohanty, K. Ghosh, U. Shankarkumar, 2002, British journal of biomedical science.

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.

Predisposition of IL-1β (-511 C/T) polymorphism to renal and hematologic disorders in Indian SLE patients.

K. Ghosh, A. Nadkarni, A. Rajadhyaksha, 2018, Gene.

Leukocyte Adhesion Deficiency-I with a Novel Intronic Mutation Presenting with Pyoderma Gangrenosum- Like Lesions

S. Dogra, K. Ghosh, M. Madkaikar, 2015, Journal of Clinical Immunology.

A study of prevalence of autoantibodies in patients with lichen planus from Mumbai, India

K. Ghosh, V. Kharkar, M. Patwardhan, 2018, Indian journal of dermatology, venereology and leprology.

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.

Sickle cell disease in tribal populations in India

K. Ghosh, M. Mukherjee, R. Colah, 2015, The Indian journal of medical research.

Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-β-thalassaemia: a genotypic and phenotypic study

K. Ghosh, R. Colah, R. Merchant, 2010, Journal of Clinical Pathology.

Rapid flow cytometry based cytotoxicity assay for evaluation of NK cell function.

K. Ghosh, M. Madkaikar, M. Desai, 2014, Indian journal of experimental biology.

Iron deficiency in healthy blood donors exposes vulnerability of the nation to iron deficiency.

K. Ghosh, 2006, The Indian journal of medical research.

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 *

K. Ghosh, S. Shetty, L. Quadros, 2008, Haemophilia : the official journal of the World Federation of Hemophilia.

The angiotensin‐converting enzyme gene insertion/deletion polymorphism in Indian patients with vitiligo: a case–control study and meta‐analysis

M. Teare, D. Gawkrodger, K. Ghosh, 2013, The British journal of dermatology.

PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.

K. Ghosh, V. Pradhan, V. Borse, 2010, Journal of postgraduate medicine.

Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.

D. Mohanty, K. Ghosh, A. Gorakshakar, 2009, Blood cells, molecules & diseases.

Guidelines for screening, diagnosis and management of hemoglobinopathies

D. Mohanty, R. Saxena, K. Ghosh, 2014, Indian journal of human genetics.

Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians.

D. Mohanty, K. Ghosh, R. Colah, 2008, Genetic testing.

β‐Globin Gene Cluster Haplotypes Linked to the βS Gene in Western India

D. Mohanty, K. Ghosh, R. Gangakhedkar, 2004, Hemoglobin.

Prenatal Diagnosis of HbE-β-Thalassemia: Experience of a Center in Western India

K. Ghosh, Harsha S Gaikwad, A. Gorakshakar, 2018, Indian Journal of Hematology and Blood Transfusion.

Fetal hemoglobin in sickle cell anemia.

Anita Nadkarni, K. Ghosh, K Ghosh, 2014, Blood cells, molecules & diseases.

Does HbF induction by hydroxycarbamide work through MIR210 in sickle cell anaemia patients?

K. Ghosh, R. Colah, A. Nadkarni, 2016, British journal of haematology.

The Fc Receptor Polymorphisms and Expression of Neutrophil Activation Markers in Patients with Sickle Cell Disease from Western India

K. Ghosh, R. Colah, F. Jijina, 2013, BioMed Research International.

The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades

D. Mohanty, K. Ghosh, A. Gorakshakar, 2021, Hemoglobin.

Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India

K. Ghosh, A. Gorakshakar, R. Colah, 2018, Hemoglobin.

Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partner

K. Ghosh, R. Colah, A. Nadkarni, 2015, Prenatal Diagnosis.

Molecular characterization of β-thalassemia in four communities in South Gujarat—codon 30 (G → A) a predominant mutation in the Kachhiya Patel community

S. Gupte, K. Ghosh, R. Colah, 2013, Annals of Hematology.

Variable haematological and clinical presentation of β‐thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population

K. Ghosh, R. Colah, K. Italia, 2012, European journal of haematology.

Hemoglobin Showa-Yakushiji: a common β thalassemia mutation among the Agri community from western India.

K. Ghosh, A. Gorakshakar, R. Colah, 2012, Genetic testing and molecular biomarkers.

Effect of Cis Acting Potential Regulators in the β Globin Gene Cluster on the Production of HbF in Thalassemia Patients

K. Ghosh, R. Colah, A. Nadkarni, 2013, Mediterranean journal of hematology and infectious diseases.

Variable clinical severity of Hb E beta-thalassemia among Indians.

D. Mohanty, K. Ghosh, A. Gorakshakar, 1999, The Journal of the Association of Physicians of India.

Newborn screening for haemoglobinopathies by high performance liquid chromatography (HPLC): diagnostic utility of different approaches in resource-poor settings

K. Ghosh, R. Colah, A. Nadkarni, 2014, Clinical chemistry and laboratory medicine.

Asialoglycoprotein receptor targeted delivery of doxorubicin nanoparticles for hepatocellular carcinoma

V. C. Malshe, P. Devarajan, Sandhya Pranatharthiharan, 2017, Drug delivery.

Role of HLA class I (HLA-A, B) and HLA class II (HLA-DRB, DQB) in HIV-1 patients with and without pulmonary tuberculosis.

K. Ghosh, A. Pawar, U. Shankarkumar, 2009, Journal of acquired immune deficiency syndromes.

Spectrum of Hemoglobinopathies Among the Primitive Tribes

D. Mohanty, K. Ghosh, D. Shukla, 2015, Asia-Pacific journal of public health.

Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?

K. Ghosh, R. Colah, K. Italia, 2012, Hemoglobin.

Thalassemia intermedia due to homozygosity for an Asian Indian (Aγδβ)° deletional inversion

K. Ghosh, R. Colah, M. Holay, 2007 .

Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: A single centre experience

K. Ghosh, R. Colah, V. Sarathi, 2013, Indian Pediatrics.

Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India

K. Ghosh, R. Colah, A. Nadkarni, 2018, Indian Journal of Hematology and Blood Transfusion.

Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A TIndian (AATAAA>AATA– –) Mutation in Four Indian Families

K. Ghosh, R. Colah, A. Nadkarni, 2013, Hemoglobin.

Molecular diversity of hemoglobin H disease in India.

K. Ghosh, P. Warang, R. Colah, 2010, American journal of clinical pathology.

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

D. Mohanty, K. Ghosh, M. Mukherjee, 2010, Indian journal of human genetics.

Clinical and hematological presentation among Indian patients with common hemoglobin variants.

K. Ghosh, A. Gorakshakar, R. Colah, 2014, Clinica chimica acta; international journal of clinical chemistry.

Clinical Diversity of Sickle Cell Disease in Western India – Influence of Genetic Factors

D. Mohanty, K. Ghosh, M. Mukherjee, 2000, Acta Haematologica.

Hb E-β-Thalassemia in Five Indian States

K. Ghosh, R. Colah, K. Italia, 2016, Hemoglobin.

Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India

K. Ghosh, M. Mukherjee, R. Colah, 2018, Hemoglobin.

Antenatal Screening for Identification of Couples for Prenatal Diagnosis of Severe Hemoglobinopathies in Surat, South Gujarat

S. Gupte, K. Ghosh, R. Colah, 2013, The Journal of Obstetrics and Gynecology of India.

Sickle cell disease in India: A perspective

K. Ghosh, G. Serjeant, Jyotish G. Patel, 2016, The Indian journal of medical research.

Haemoglobinopathies in tribal populations of India

K. Ghosh, M. Mukherjee, R. Colah, 2015, The Indian journal of medical research.

Feasibility of Antenatal Screening of β-Thalassemia in Mumbai, India

D. Mohanty, K. Ghosh, A. Gorakshakar, 2001, Acta Haematologica.

Prenatal diagnosis of HbE‐Lepore and Hb Lepore‐β‐thalassemia: the importance of accurate genotyping of the couple at risk

K. Ghosh, J. Sheth, R. Colah, 2012, Prenatal diagnosis.

Masking of a β-Thalassemia Determinant by a Novel δ-Globin Gene Defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis

K. Ghosh, R. Colah, A. Nadkarni, 2014, Hemoglobin.

Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.

K. Ghosh, P. Warang, R. Colah, 2013, Blood cells, molecules & diseases.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

Fc γ R IIIB polymorphisms: their association with clinical manifestations and autoantibodies in SLE patients from Western India

K. Ghosh, M. Patwardhan, A. Nadkarni, 2010, International journal of rheumatic diseases.

Prenatal Diagnosis of LAD-I on Cord Blood by Flowcytometry

K. Ghosh, M. Madkaikar, Maya Gupta, 2012, The Indian Journal of Pediatrics.

Delta globin gene variations leading to reduction in HbA2 levels

K. Ghosh, R. Colah, A. Nadkarni, 2016, International journal of laboratory hematology.

Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population

K. Ghosh, A. Gorakshakar, R. Colah, 2009, Hemoglobin.

Hb Showa Yakushiji [beta 110 (G12) Leu-->Pro] in 3 families from Western India: first report on homozygous Hb Showa Yakushiji.

D. Mohanty, K. Ghosh, A. Gorakshakar, 2008, Blood cells, molecules & diseases.

Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID) Disorders

K. Ghosh, M. Madkaikar, Maya Gupta, 2014, Journal of Clinical Immunology.

Evaluation of the use of monoclonal antibodies and nested PCR for noninvasive prenatal diagnosis of hemoglobinopathies in India.

D. Mohanty, K. Ghosh, A. Gorakshakar, 2008, American journal of clinical pathology.

Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes

K. Ghosh, R. Colah, A. Nadkarni, 2015, Annals of Hematology.

The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India.

D. Mohanty, K. Ghosh, R. Gangakhedkar, 1998, The Indian journal of medical research.

β‐Thalassemia gene flow from India to Mauritius

D. Mohanty, K. Ghosh, A. Gorakshakar, 2000 .

Impact of h globin gene mutations on the clinical phenotype of h thalassemia in India

D. Mohanty, K. Ghosh, A. Gorakshakar, 2004 .

Detection of the beta s gene: an evaluation of the solubility test against automated chromatography and haemoglobin electrophoresis.

D. Mohanty, K. Ghosh, M. Mukherjee, 2000, British journal of biomedical science.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2006, National Medical Journal of India.

MicroRNA profile in understanding pathogenesis of systemic lupus erythematosus

K. Ghosh, V. Pradhan, Harshada Hire, 2012 .

A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotype

K. Ghosh, B. Vundinti, S. Korgaonkar, 2011, Journal of human reproductive sciences.

18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype.

D. Mohanty, K. Ghosh, L. Kerketta, 2001, Annales de genetique.

Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India

K. Ghosh, M. Mukherjee, R. Colah, 2018, Molecular Biology Reports.

Bengal macrothrombocytopenia is not totally an innocuous condition.

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

FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India

S. Swaminathan, K. Ghosh, M. Madkaikar, 2014, Indian journal of human genetics.

Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patient.

K. Ghosh, V. B. Rao, M. Dipika, 2003, Annales de genetique.

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.

Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family

K. Ghosh, P. Warang, R. Colah, 2012, Annals of Hematology.

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

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

A 46, XY, dup (1) (q21q32), add(11) (q23) karyotype in a case of Fanconi anemia.

D. Mohanty, K. Ghosh, V. Babu Rao, 2001, Leukemia research.

Tuberculosis and female reproductive health.

K. Ghosh, K. Ghosh, J. Chowdhury, 2011, Journal of postgraduate medicine.

Thrombophilia and unexplained pregnancy loss in Indian patients.

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

Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India

K. Ghosh, M. Madkaikar, M. Desai, 2011, BMJ Case Reports.

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

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

Circulating microfilariae in haematological malignancies: do they have a role in pathogenesis?

K. Ghosh, L. Kerketta, 2017, Journal of Helminthology.

Functional and ultrastructural changes of platelets in malarial infection.

D. Mohanty, K. Ghosh, N. Marwaha, 1988, Transactions of the Royal Society of Tropical Medicine and Hygiene.

Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection

K. Ghosh, V. B. Rao, Lily S. Kerketta, 2012, Tropical medicine & international health : TM & IH.

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.

The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India

K. Ghosh, R. Colah, F. Jijina, 2015, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

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.

Geography too determines the causes of inherited thrombophilia

D. Mohanty, K. Ghosh, B. Kulkarni, 2004, Journal of thrombosis and haemostasis : JTH.

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.

Evolution of BCR/ABL Gene Mutation in CML Is Time Dependent and Dependent on the Pressure Exerted by Tyrosine Kinase Inhibitor

K. Ghosh, B. Vundinti, Prantar Chakrabarti, 2015, PloS one.

FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India

S. Swaminathan, K. Ghosh, B. Vundinti, 2012, Annals of Hematology.

High Frequency of Factor V Leiden Mutation in Parsis – a Highly Endogamous Population in India

D. Mohanty, K. Ghosh, A. Pawar, 2000, Thrombosis and Haemostasis.

Thrombophilia in coronary artery disease: a double jeopardy.

D. Mohanty, K. Ghosh, D. Mohanty, 2004, The Indian journal of medical research.

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.

Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population

K. Ghosh, B. Vundinti, S. Korgaonkar, 2010, Hematology.

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.

Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India

K. Ghosh, R. Colah, A. Nadkarni, 2016, PloS one.

Antihistone and Other Autoantibodies in β-Thalassemia major Patients Receiving Iron Chelators

K. Ghosh, V. Pradhan, S. Badakere, 2002, Acta Haematologica.

Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.

K. Ghosh, M. Madkaikar, M. Manglani, 2015, Blood cells, molecules & diseases.

Deferiprone (L1) as an adjuvant therapy for Plasmodium falciparum malaria.

D. Karnad, D. Mohanty, K. Ghosh, 2002, The Indian journal of medical research.

Optimising methods of red cell sedimentation from cord blood to maximise nucleated cell recovery prior to cryopreservation

D. Mohanty, S. Swaminathan, K. Ghosh, 2007, British journal of biomedical science.

Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: The first report from India

K. Ghosh, P. Warang, R. Colah, 2014, Hematology.

HIV-1 evolution, drug resistance, and host genetics: The Indian scenario

K. Ghosh, A. Pawar, U. Shankarkumar, 2009 .

Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations

K. Ghosh, M. Madkaikar, Maya Gupta, 2009, European journal of haematology.

Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage

K. Ghosh, M. Madkaikar, F. Jijina, 2008, Acta Haematologica.

Immunotherapy in benzene-induced aplastic anemia using a biotherapeutic approach--is it durable?

K. Ghosh, M. Madkaikar, 2004, Stem cells and development.

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.

Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.

S. Kulkarni, D. Mohanty, K. Ghosh, 2003, Clinical and laboratory haematology.

Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure imaged by electron tomography and whole-mount grid-cell culture techniques

A. Basu, K. Ghosh, P. Jain, 2010, Journal of electron microscopy.

CMV seropositivity and mycosis fungoides--the Indian perspectives.

K. Ghosh, 2003, Blood.

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.

Frequency distribution of human platelet antigens in the Indian population

D. Mohanty, K. Ghosh, B. Kulkarni, 2005, Transfusion medicine.

Variable phenotypes of sickle cell disease in India with the Arab‐Indian haplotype

K. Ghosh, R. Colah, K. Italia, 2015, British journal of haematology.

Influence of auto-antibody specificities on the clinical course in patients with chronic and acute ITP.

D. Mohanty, K. Ghosh, S. Badakere, 2000, Platelets.

X-linked hyper IgM syndrome: clinical, immunological and molecular features in patients from India.

N. Radhakrishnan, K. Ghosh, M. Madkaikar, 2014, Blood cells, molecules & diseases.

Diagnostic approach to primary immunodeficiency disorders

K. Ghosh, M. Madkaikar, K. Ghosh, 2013, Indian Pediatrics.

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.

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

D. Mohanty, K. Ghosh, B. Kulkarni, 2003, Journal of thrombosis and haemostasis : JTH.

Functional and fibrinogen receptor studies in platelets in pre-eclamptic toxaemia of pregnancy.

S. Kulkarni, D. Mohanty, K. Ghosh, 1999, Platelets.

Evaluation of Danazol, Cyclosporine, and Prednisolone as Single Agent or in Combination for Paroxysmal Nocturnal Hemoglobinuria

K. Ghosh, M. Madkaikar, Maya Gupta, 2013, Turkish journal of haematology : official journal of Turkish Society of Haematology.

HLA allele associations in idiopathic recurrent spontaneous abortion patients from India.

K. Ghosh, A. Pawar, U. Shankarkumar, 2008 .

HLA Class I Antigen Profile Among Brahmins And Related Caste Groups From Mumbai, Maharashtra, India

D. Mohanty, K. Ghosh, U. Shankarkumar, 2000 .

HLA Antigen Distribution in Marathi Speaking Hindu Population from Mumbai, Maharastra, India

D. Mohanty, S. Gupte, K. Ghosh, 1999 .

Distribution of HLA Antigens in Bhils and Pawars of Dhadgaon, Maharashtra, India

D. Mohanty, S. Gupte, K. Ghosh, 1999 .

Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: an overview.

K. Ghosh, A. Chaudhary, A. Nadkarni, 2013, Mutation research.

HLA DRB 1 and DQB 1 Gene Diversity in Maratha Community from Mumbai India

D. Mohanty, K. Ghosh, U. Shankarkumar, 2003 .

Role of HLA antigens in Rh (D) alloimmunized pregnant women from Mumbai, Maharashtra, India

D. Mohanty, S. Gupte, K. Ghosh, 2002, Journal of Biosciences.

Association of Human Leucocyte Antigen (HLA) class II with systemic lupus erythematosis (SLE) patients from western India

K. Ghosh, M. Nadkar, S. Parekh, 2018, Meta Gene.

14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component.

K. Ghosh, A. Pawar, M. Spyropoulou-Vlachou, 2007, Tissue antigens.

HLA-DRβ1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients

K. Ghosh, V. Pradhan, D. Parasannanavar, 2013, Rheumatology International.

Role of HLA-B Alleles and Clinical Presentation of B27 Negative Spondyloarthritis Patients from Mumbai, Western India

K. Ghosh, A. Rajadhyaksha, D. Parasannanavar, 2014, Autoimmune diseases.

HLA involvement in nevirapine-induced dermatological reaction in antiretroviral-treated HIV-1 patients

K. Ghosh, A. Pawar, A. Pazare, 2011, Journal of pharmacology & pharmacotherapeutics.

A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India

K. Ghosh, M. Mukherjee, R. Colah, 2008, Journal of Human Genetics.

Milder clinical course of sickle cell disease in patients with alpha thalassemia in the Indian subcontinent.

D. Mohanty, K. Ghosh, R. Krishnamoorthy, 1997, Blood.

Combined protein- and nucleic acid-level effects of rs1143679 (R77H), a lupus-predisposing variant within ITGAM.

L. Looger, K. Chua, J. Harley, 2014, Human molecular genetics.

Non haematological effects of iron deficiency - a perspective.

K. Ghosh, 2006, Indian journal of medical sciences.

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

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

Evaluation of the clinical severity of β唱thalassemia homozygous patients using a phenotypic scoring system

D. Mohanty, K. Ghosh, A. Gorakshakar, 2007 .

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.

Congenital dyserythropoietic anaemia (CDA) type I--a case report with ultrastructural study.

K. Ghosh, D. Mohanty, K. C. Das, 1985, Folia haematologica.

A Patient with Congenital Dyserythropoietic Anaemia Type III Presenting with Stillbirths

D. Yavagal, D. Mohanty, K. Ghosh, 1998, Acta Haematologica.

Leukocyte Adhesion Deficiency-I with a Novel Intronic Mutation Presenting with Pyoderma Gangrenosum- Like Lesions

S. Dogra, K. Ghosh, M. Madkaikar, 2015, Journal of Clinical Immunology.

Clinical and serological features of male Systemic Lupus Erythematosus patients from Western India

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2012 .

Catalytic antibodies in patients with systemic lupus erythematosus.

S. Kaveri, S. Lacroix-Desmazes, M. Lecerf, 2018, European journal of rheumatology.

Low cost autologous peripheral blood stem cell transplantation performed in a municipal hospital for a patient with plasma cell leukaemia.

D. Mohanty, K. Ghosh, M. Madkaikar, 2002, Clinical and laboratory haematology.

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients

K. Ghosh, R. Colah, A. Nadkarni, 2014, Hematology.

Mitochondrial DNA variations in myelodysplastic syndrome

K. Thangaraj, P. Govindaraj, K. Ghosh, 2013, Annals of Hematology.

Vascular occlusion and disseminated intravascular coagulation in falciparum malaria.

A. P. Chauhan, D. Mohanty, K. Ghosh, 1985, British medical journal.

Differential antigen expression and aberrant signaling via PI3/AKT, MAP/ERK, JAK/STAT, and Wnt/β catenin pathways in Lin−/CD38−/CD34+ cells in acute myeloid leukemia

K. Ghosh, M. Madkaikar, S. Marathe, 2016, European journal of haematology.

Deletion of ABL/BCR on der(9) associated with severe basophilia

K. Ghosh, B. Vundinti, M. Madkaikar, 2011, Indian journal of human genetics.

Spectrum of anti-neutrophil cytoplasmic antibodies in patients with pulmonary tuberculosis overlaps with that of Wegener's granulomatosis.

K. Ghosh, Kanjaksha Ghosh, Vandana D Pradhan, 2004, Indian journal of medical sciences.

Familial Mediterranean fever: An unusual disease enlightening the inflammation biology

K. Ghosh, 2014, Indian journal of human genetics.

Mannose binding lectin (MBL) 2 gene polymorphism & its association with clinical manifestations in systemic lupus erythematosus (SLE) patients from western India

K. Ghosh, M. Patwardhan, A. Nadkarni, 2015, The Indian journal of medical research.

Spectrum of novel mutations in the human PKLR gene in pyruvate kinase‐deficient Indian patients with heterogeneous clinical phenotypes

K. Ghosh, H. Kanno, P. Warang, 2009, Clinical genetics.

First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.

S. Nampoothiri, K. Ghosh, H. Kanno, 2007, Genetics and molecular research : GMR.

Genetic Disorders in Haematological Practice in India

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

Tuberculosis and immune thrombocytopenia.

D. Mohanty, K. Ghosh, M. Madkaikar, 2002, Haematologica.

False-positive serological tests in acute malaria.

D. Mohanty, K. Ghosh, S. Joshi, 2001, British journal of biomedical science.

Clinical and immunological profile of systemic lupus erythematosus

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2013, Indian Pediatrics.

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.

Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case.

D. Mohanty, K. Ghosh, R. Colah, 2004, Clinica chimica acta; international journal of clinical chemistry.

Flow cytometric osmotic fragility—An effective screening approach for red cell membranopathies

K. Ghosh, P. Warang, R. Colah, 2011, Cytometry. Part B, Clinical cytometry.

Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

K. Ghosh, P. Warang, M. Mukherjee, 2014, Annals of Hematology.

Pulmonary hypertension in patients with hematological disorders following splenectomy

K. Ghosh, F. Jijina, V. Meera, 2010, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele

C. Férec, Y. Fichou, S. Kulkarni, 2018, Transfusion.

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

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

Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years

K. Ghosh, M. Mukherjee, K. Dave, 2022, Frontiers in Medicine.

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.

RHD-Positive Alleles among D- C/E+ Individuals from India

C. Férec, G. Mishra, Y. Fichou, 2018, Transfusion Medicine and Hemotherapy.

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.

Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India

K. Ghosh, P. Warang, R. Colah, 2015, Clinical genetics.

Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.

K. Ghosh, S. Sanyal, P. Warang, 2014, Clinica chimica acta; international journal of clinical chemistry.

Prevalence of inherited bleeding disorders in cases of idiopathic menorrhagia: a case of five blind men describing an elephant

D. Mohanty, K. Ghosh, S. Nair, 2003, Journal of Thrombosis and Haemostasis.

Tissue factor expressed by circulating cancer cell‐derived microparticles drastically increases the incidence of deep vein thrombosis in mice: comment

K. Ghosh, R. Patil, S. Shetty, 2015, Journal of thrombosis and haemostasis : JTH.

Preeclampsia: simplified or still miles to go?

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

Chromosomal instability and cancer: An insight into the rhythm of life

K. Ghosh, B. Vundinti, 2009, Indian journal of human genetics.

Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma.

K. Ghosh, A. Gorakshakar, R. Colah, 2013, Journal of postgraduate medicine.

An unusual presentation of pediatric acute lymphoblastic leukemia

C. Nair, K. Ghosh, S. Seth, 2008, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

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.

Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.

K. Ghosh, B. Vundinti, C. Shanmukhaiah, 2015, European journal of pharmacology.

Down-regulation of miR-199b associated with imatinib drug resistance in 9q34.1 deleted BCR/ABL positive CML patients.

K. Ghosh, B. Vundinti, S. Korgaonkar, 2014, Gene.

Cytogenetic study of myelodysplastic syndrome from India.

K. Ghosh, B. Vundinti, L. Kerketta, 2009, The Indian journal of medical research.

Clonal non random Cytogenetic study of myelodysplastic syndrome from India

K. Ghosh, B. Vundinti, L. Kerketta, 2009 .

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.

Investigating cell surface markers on normal hematopoietic stem cells in three different niche conditions.

K. Ghosh, M. Madkaikar, S. Garg, 2013, International journal of stem cells.

Neuropsychiatric manifestations and associated autoantibodies in systemic lupus erythematosus patients from Western India

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2015, Rheumatology International.

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.

Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D

S. Alper, K. Ghosh, M. Madkaikar, 2010, American journal of hematology.

High sensitivity C-reactive protein (hsCRP): Association with clinical subsets in systemic lupus erythematosus (SLE) patients from Western India

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2013 .

UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.

K. Ghosh, M. Mukherjee, R. Colah, 2013, Gene.

Tyrosine kinase inhibitors: New class of antimalarials on the horizon?

K. Ghosh, R. Colah, V. Pathak, 2015, Blood cells, molecules & diseases.

Association of clinical and serological parameters of systemic lupus erythematosus patients with Epstein‐Barr virus antibody profile

S. Kaveri, K. Ghosh, M. Nadkar, 2018, Journal of medical virology.

Prevalence of Anti-Cardiolipin and Anti-β2 Glycoprotein Antibodies in Indian Systemic Lupus Erythematosus Patients

Pranaya V. Joshi, K. Ghosh, M. Patwardhan, 2011 .

Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients

S. Nath, K. Ghosh, A. Rajadhyaksha, 2019, Lupus.

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.

Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience

K. Ghosh, P. Warang, R. Colah, 2015, Clinical chemistry and laboratory medicine.

Is thrombophilia associated with placenta‐mediated pregnancy complications? A prospective cohort study: comment

K. Ghosh, R. Patil, S. Shetty, 2014, Journal of thrombosis and haemostasis : JTH.

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.

Leukaemia in north-west India.

D. Shome, D. Mohanty, K. Ghosh, 1985, Acta haematologica.

Exposure to Hydroxyurea During Pregnancy in Sickle‐β Thalassemia: A Report of 2 Cases

K. Ghosh, R. Colah, K. Italia, 2010, Journal of clinical pharmacology.

Report of proceedings of the national meeting on "Guidelines for Immunophenotyping of Hematolymphoid Neoplasms by Flow Cytometry".

K. Ghosh, M. Madkaikar, S. Gujral, 2008, Indian journal of pathology & microbiology.

The association of HLA-DRB1 and HLA-DQB1 alleles with the development of factor VIII inhibitors in severe haemophilia A patients in India.

K. Ghosh, P. Pinto, S. Shetty, 2014, Tissue antigens.

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 .

Anti-C1q antibodies and their association with complement components in Indian systemic lupus erythematosus patients

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2012, Indian journal of nephrology.

Fc γ RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India

K. Ghosh, M. Patwardhan, A. Nadkarni, 2010, Autoimmune diseases.

Immunological disturbances associated with malarial infection

K. Ghosh, V. Pradhan, 2012, Journal of Parasitic Diseases.

Pleiotropic Roles of Metalloproteinases in Hematological Malignancies: an Update.

K. Ghosh, A. Chaudhary, A. Nadkarni, 2016, Asian Pacific journal of cancer prevention : APJCP.

Comprehensive Report of Primary Immunodeficiency Disorders from a Tertiary Care Center in India

K. Ghosh, M. Madkaikar, M. Desai, 2013, Journal of Clinical Immunology.

Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease

K. Ghosh, M. Madkaikar, P. Warang, 2022, Hemoglobin.

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.

Biphenotypic expression in a case of acute leukemia with pericentric inv(6)(p12q24).

D. Mohanty, K. Ghosh, L. Kerketta, 2005, Cancer genetics and cytogenetics.

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene

K. Ghosh, P. Warang, R. Colah, 2012, International Journal of Hematology.

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

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

De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.

K. Ghosh, B. Vundinti, S. Korgaonkar, 2012, Gene.

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.

Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India

K. Ghosh, M. Mukherjee, R. Colah, 2018, Molecular Biology Reports.

Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.

K. Ghosh, B. Vundinti, S. Korgaonkar, 2010, Indian journal of cancer.

A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies

K. Ghosh, R. Colah, E. D'Souza, 2009, Cytometry. Part B, Clinical cytometry.

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.

Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymhoblastic leukemia cases from India

K. Ghosh, L. Kerketta, V. Baburao, 2014, Indian journal of human genetics.

Cell signaling in putative leukemic stem cells and blast population in acute myeloid leukemia

K. Ghosh, M. Madkaikar, S. Garg, 2016, Leukemia & lymphoma.

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.

Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype

K. Ghosh, R. Colah, A. Nadkarni, 2017, Molecular Biology Reports.

Five Rare β Globin Chain Hemoglobin Variants in India

K. Ghosh, A. Gorakshakar, R. Colah, 2016, Indian Journal of Hematology and Blood Transfusion.

Hemoglobin Lepore Hollandia in India

K. Ghosh, R. Colah, K. Italia, 2012, International journal of laboratory hematology.

Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches

K. Ghosh, P. Warang, R. Colah, 2010, Hemoglobin.

Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus

K. Ghosh, V. Pradhan, P. Surve, 2012, Indian journal of human genetics.

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.

D. Mohanty, K. Ghosh, M. Mukherjee, 2009, Blood cells, molecules & diseases.

Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in India

D. Mohanty, K. Ghosh, M. Mukherjee, 2011, Annals of human biology.

G6PD Namoru (208 T→ C) is the major polymorphic variant in the tribal populations in southern India

D. Mohanty, K. Ghosh, M. Mukherjee, 2007, British journal of haematology.

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.

Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.

K. Ghosh, B. Vundinti, F. Jijina, 2011, Cancer epidemiology.

Inversion of intron is a rare cause of severe hemophilia A in Indian population

D. Mohanty, K. Ghosh, S. Shetty, 2004, Journal of thrombosis and haemostasis : JTH.

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.

The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles: a rebuttal

K. Ghosh, P. Kasatkar, S. Shetty, 2013, Journal of thrombosis and haemostasis : JTH.

FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients

K. Ghosh, B. Vundinti, P. Shukla, 2016, PloS one.

Anti-haemophilic globulin and salivary secretor status in healthy Indians.

D. Mohanty, K. Ghosh, N. Marwaha, 1987, Medical laboratory sciences.

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.

Systemic Capillary Leak Syndrome Preceding Plasma Cell Leukaemia

D. Mohanty, K. Ghosh, M. Madkaikar, 2001, Acta Haematologica.

The Human Leukocyte Antigen (HLA) System

D. Mohanty, K. Ghosh, U. Shankarkumar, 2002, The Journal of the Association of Physicians of India.

Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?

K. Ghosh, R. Colah, A. Nadkarni, 2017, Annals of human genetics.

Plasma transcobalamins in chronic granulocytic leukaemia--changing pattern from chronic phase to blast crisis.

K. Ghosh, G. Garewal, D. Mohanty, 1987, Indian journal of cancer.

Antithrombin III deficiency in an Indian family.

D. Mohanty, K. Ghosh, G. Garewal, 1982, Thrombosis research.

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.

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.

Cytogenetics in paediatric aplastic anaemia: Does it give an insight on the evolution of the disease?

K. Ghosh, 2013, The Indian journal of medical research.

Role of antiidiotypic antibodies on the clinical course of idiopathic thrombocytopenic purpura.

D. Mohanty, K. Ghosh, S. Badakere, 2003, The Journal of laboratory and clinical medicine.

Study of PTPN22 1858C/T polymorphism in rheumatoid arthritis patients from Western India

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2012 .

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.

Previous fetal loss significantly increases the risk of pre‐partal deep‐vein thrombosis

K. Ghosh, S. Shetty, S. Vora, 2007, British Journal of Haematology.

Factor XIII Deficiency Managed With Individualized Homoeopathic Medicine In Intellectually Disabled Child: An Evidence Based Case Report

K. Ghosh, Afroz Shaikh, O. Kumat, 2022, Homoeopathic Links.

Molecular Cytogenetic Evaluation of Xq Deletion Mosaicism in a Case of Primary Amenorrhea

D. Mohanty, K. Ghosh, B. Vundinti, 2004 .

Anti-C reactive protein antibodies in Indian patients with systemic lupus erythematosus

K. Ghosh, M. Patwardhan, A. Rajadhyaksha, 2013, Indian journal of nephrology.

Cytokine genes multi-locus analysis reveals synergistic influence on genetic susceptibility in Indian SLE - A multifactor-dimensionality reduction approach.

K. Ghosh, A. Nadkarni, A. Rajadhyaksha, 2020, Cytokine.

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.

HLA Antigen Distribution in Maratha Community from Mumbai, Maharastra, India

D. Mohanty, K. Ghosh, U. Shankarkumar, 2001 .

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.

The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.

K. Ghosh, M. Mukherjee, R. Colah, 2010, Clinical Biochemistry.

Antigen expression on a putative leukemic stem cell population and AML blast

K. Ghosh, M. Madkaikar, S. Garg, 2016, International Journal of Hematology.

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.

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.

Congenital Deficiency of Vitamin K Dependent Coagulation Factors – Its Rarity and Need for an International Registry

D. Mohanty, K. Ghosh, S. Shetty, 2001, Thrombosis and Haemostasis.

Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adults.

K. Ghosh, M. Mukherjee, R. Colah, 2011, Genetic testing and molecular biomarkers.

Thrombohaemorrhagic balance in diabetes mellitus.

K. Ghosh, 2002, Journal of the Indian Medical Association.

Fc γ R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients

K. Ghosh, M. Patwardhan, A. Nadkarni, 2011, The Indian journal of medical research.

Feasibility of a Newborn Screening and Follow-up Programme for Sickle Cell Disease among South Gujarat (India) Tribal Populations

L. Krishnamurti, K. Ghosh, R. Colah, 2015, Journal of medical screening.

Sickle cell disease in tribal populations in India

K. Ghosh, M. Mukherjee, R. Colah, 2015, The Indian journal of medical research.

Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.

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

Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism

K. Ghosh, S. Parekh, V. Pradhan, 2018, Meta Gene.

HLA and KIR Gene Polymorphism in LupusNephritis Patients from Western India

K. Ghosh, M. Nadkar, S. Parekh, 2018 .

Association of Serum Ferritin Levels with Hematological Manifestations in Systemic Lupus Erythematosus Patients from Western India.

S. Kaveri, M. Lecerf, K. Ghosh, 2016, The Journal of the Association of Physicians of India.

Hemoglobin variants in Muslim community in South Gujarat, Western India

K. Ghosh, K. Italia, R. Surve, 2014, International journal of laboratory hematology.

Molecular characterization of haemophilia A & B in Indians

Shetty, Pathare, D. Mohanty, 1998, Haemophilia : the official journal of the World Federation of Hemophilia.

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

D. Mohanty, K. Ghosh, S. Shetty, 2003, The Journal of the Association of Physicians of India.