D. Mohanty

D. Mohanty, F. Jijina, S. Badakere, 1996, Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

Haematuria and urolithiasis in patients with haemophilia

D. Mohanty, K. Ghosh, F. Jijina, 2003, European journal of haematology.

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.

Production of murine monoclonal anti-B.

D. Mohanty, S. Gupte, K. Vasantha, 2006, The Indian journal of medical research.

Recurrent haemoperitoneum in a female patient with type III von Willebrand’s disease responded to administration of oral contraceptive

D. Mohanty, K. Ghosh, F. Jijina, 1998, Haemophilia : the official journal of the World Federation of Hemophilia.

A novel beta+-thalassemia mutation (codon 10 GCC --> GCA) and a rare transcriptional mutation (-28A --> G) in Indians.

D. Mohanty, A. Pawar, R. Colah, 1997, Blood.

Clinical manifestations of sickle cell disease in India: misconceptions and reality

D. Mohanty, D. Jain, 2018, Current opinion in hematology.

A century after discovery of sickle cell disease: keeping hope alive!

D. Mohanty, 2014, The Indian journal of medical research.

Epidemiology of β‐thalassaemia in Western India: mapping the frequencies and mutations in sub‐regions of Maharashtra and Gujarat

D. Mohanty, K. Ghosh, A. Gorakshakar, 2010, British journal of haematology.

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.

Molecular pathogenesis and clinical variability of β‐thalassemia syndromes among Indians

D. Mohanty, K. Ghosh, R. Krishnamoorthy, 2001 .

Glucose–6–phosphate dehydrogenase deficiency in India

D. Mohanty, M. Mukherjee, R. Colah, 2004, Indian journal of pediatrics.

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

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

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.

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

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

Immunogenetic association in patients with antineutrophil cytoplasmic antibodies (ANCA) from Mumbai, Maharashtra, India.

D. Mohanty, U. Shankarkumar, K. Ghosh, 2005, Journal of autoimmunity.

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.

Microsatellite diversity among the primitive tribes of India

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

Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study

J. Mahanta, D. Mohanty, S. Sharma, 2012, Journal of Community Genetics.

Frequency of partial D in Western India

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

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.

A novel autologous stem cell procedure for the treatment of aplastic anaemia using reprogrammed mature adult cells: a pilot study

R. K. Suri, D. Mohanty, I. Abuljadayel, 2012, The Indian journal of medical research.

How Old Is Factor V Leiden Mutation?

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

Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling

D. Mohanty, A. Gorakshakar, R. Colah, 2005, Prenatal diagnosis.

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.

Haptoglobin polymorphism and serum ferritin concentration in ageing subjects

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

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.

Effect of Nitric Oxide Inhalation in Acute Pain Crisis of Sickle Cell Disease: A Preliminary Report

D. Mohanty, B. Ray, Shakti Sankar Pattanayak, 2015 .

von Willebrand disease: a laboratory approach.

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

Platelet dysfunction in nutritional vitamin b(12) deficiency.

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

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.

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

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

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.

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

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

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

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

Current concepts in platelet transfusion

D. Mohanty, 2009, Asian journal of transfusion science.

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

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

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

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

Red Cell Genetic Abnormalities, [Beta]-Globin Gene Haplotypes, and APOB Polymorphisms in the Great Andamanese, A Primitive Negrito Tribe of Andaman and Nicobar Islands, India

D. Mohanty, M. Murhekar, M. Mukherjee, 2001, Human biology.

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.

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.

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.

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.

The prevalence of proteolytic antibodies against factor VIII in hemophilia A.

S. Kaveri, S. Lacroix-Desmazes, M. Kazatchkine, 2002, The New England journal of medicine.

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 .

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.

Prevalence and spectrum of von Willebrand disease from western India.

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

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

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

Autoantibodies to factor VIII.

S. Kaveri, S. Lacroix-Desmazes, M. Kazatchkine, 2002, Autoimmunity reviews.

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.

Ophthalmic surgery in haemophilia

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

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.

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.

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.

Hb D-AGRI [β9(A6)Ser Tyr;β121(GH4)Glu Gln]: A NEW INDIAN HEMOGLOBIN VARIANT WITH TWO AMINO ACID SUBSTITUTIONS IN THE SAME β CHAIN

D. Mohanty, H. Wajcman, A. Gorakshakar, 2001 .

Molecular Characterization of FUT1(H) Gene in the Bombay Phenotypes Detected in India

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

Varied distribution of RhD epitopes in the Indian population.

S. Kulkarni, D. Mohanty, K. Vasantha, 2007, The National medical journal of India.

A bicarbonate anion-dependent anti-’N’ MoAb

D. Mohanty, K. Vasantha, M. Patwardhan, 2004, Immunohematology.

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.

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.

Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluation.

D. Mohanty, A. Gorakshakar, R. Colah, 2008, Genetic testing.

Detection of two rare β -thalassemia mutations [-90 (C ® T) and CD 26 (C ®T)] among Indians

D. Mohanty, A. Gorakshakar, R. Colah, 2005 .

Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians

D. Mohanty, A. Gorakshakar, R. Colah, 2004, Hemoglobin.

A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION

H. Takaku, D. Mohanty, R. Kiyama, 2002, Hemoglobin.

Potential of denaturing gradient gel electrophoresis for scanning of β‐thalassemia mutations in India

D. Mohanty, A. Pawar, R. Krishnamoorthy, 1999, American journal of hematology.

Evaluation of F cells in sickle cell disorders by flow cytometry – comparison with the Kleihauer–Betke's slide method

D. Mohanty, K. Y. ITALIA, R. COLAH, 2007, International journal of laboratory hematology.

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.

Sickle cell disease in India.

D. Mohanty, M. Mukherjee, R. N. Shukla, 1958, Blood.

Spectrum of Hemoglobinopathies Among the Primitive Tribes

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

Effect of α‐thalassemia on sickle‐cell anemia linked to the Arab‐Indian haplotype in India

R. Nagel, D. Mohanty, R. Gangakhedkar, 1997 .

β-Thalassemias : Expression, molecular mechanisms and mutations in Indians

D. Mohanty, R. Colah, 1998, Indian journal of pediatrics.

Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth?

D. Mohanty, R. Colah, S. Gupte, 1997, Human heredity.

EFFECT OF ASSOCIATED ALPHA -THALASSAEMIA AND ALPHA -GENE TRIPLICATION ON THE HAEMATOLOGICAL PROFILE OF BETA -THALASSAEMIA HETEROZYGOTES AND NORMAL IND IVIDUALS

D. Mohanty, A. Gorakshakar, R. Colah, 1997 .

Alpha Genotyping in a Heterogeneous Indian Population

D. Mohanty, A. Gorakshakar, R. Colah, 1996, American journal of hematology.

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.

Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India.

R. Nagel, D. Mohanty, R. Gangakhedkar, 1997, American journal of hematology.

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

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

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

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

Interaction of Iron Deficiency Anemia and Hemoglobinopathies Among College Students and Pregnant Women: A Multi Center Evaluation in India

S. Sharma, J. Mahanta, D. Mohanty, 2014, Hemoglobin.

Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of β‐thalassemia

D. Mohanty, A. Gorakshakar, A. Nadkarni, 2002, Prenatal diagnosis.

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.

Symptomatic presentation of a sickle cell heterozygote: An evaluation of genetic factors

D. Mohanty, R. Gangakhedkar, M. Mukherjee, 2001, American journal of hematology.

Prenatal diagnosis of beta-thalassemia among Indians using denaturing gradient gel electrophoresis.

D. Mohanty, A. Pawar, A. Gorakshakar, 1997, Hemoglobin.

Prenatal Diagnosis of β-Thalassemia Among Indians using Denaturing Gradient Gel Electrophoresis

D. Mohanty, A. Pawar, A. Gorakshakar, 1997 .

Origin of the codon 47 (+A) β‐thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India

D. Mohanty, A. Gorakshakar, R. Colah, 2007, British journal of haematology.

Hb D-Agri [beta9(A6)Ser --> Tyr;beta121(GH4)Glu --> Gln]: a new Indian hemoglobin variant with two amino acid substitutions in the same beta chain.

D. Mohanty, H. Wajcman, A. Gorakshakar, 2001, 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.

Evaluation of a capillary blood collection system for screening for hemoglobinopathies in remote areas

D. Mohanty, M. Mehra, P. Sawant, 2010, International journal of laboratory hematology.

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.

Molecular Characterization of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population

D. Mohanty, R. Kiyama, A. Gorakshakar, 2008, Hemoglobin.

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 .

An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia.

D. Mohanty, R. Kiyama, A. Gorakshakar, 2004, Clinical and laboratory haematology.

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.

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.

Molecular basis of G6PD deficiency in India.

D. Mohanty, M. Mukherjee, R. Colah, 2004, Blood cells, molecules & diseases.

Usefulness of prenatal detection of Usefulness of prenatal detection of

S. Kulkarni, D. Mohanty, S. Gupte, 2007 .

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.

An Improved Flow Cytometric Approach for Isolation of Fetal Cells from Maternal Blood for Non Invasive Prenatal Diagnosis of Hemoglobinopathies

Swati Kulkarni, S. Kulkarni, D. Mohanty, 2007, Hemoglobin.

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

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

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.

Autoantibodies, immunoglobulins, complement and circulating immune complexes in acute malaria.

D. Mohanty, S. Joshi, S. Badakere, 1997, The National medical journal of India.

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

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

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.

Two New β3 Integrin Mutations in Indian Patients with Glanzmann Thrombasthenia: Localization of Mutations Affecting Cysteine Residues in Integrin β3

B. Coller, D. Mohanty, D. French, 2002, Thrombosis and Haemostasis.

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.

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.

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.

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.

Frequency distribution of human platelet antigens in the Indian population

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

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

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

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.

Novel HLA Class I Alleles Associated with Indian Leprosy Patients

D. Mohanty, U. Shankarkumar, K. Ghosh, 2003, Journal of biomedicine & biotechnology.

HLA-DRB1*03 and DQB1*0302 associations in a subset of patients severely affected with systemic lupus erythematosus from western India

D. Mohanty, U. Shankarkumar, K. Ghosh, 2003, Annals of the Rheumatic Diseases.

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 .

HLA DRB1 and DQB1 Gene Diversity in Maratha Community from Mumbai India

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

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.

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

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

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

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

Frequency and potential application of HLA antibodies from pregnant women in Mumbai

D. Mohanty, U. Shankarkumar, K. Ghosh, 1998, Journal of Biosciences.

Von Willebrand Disease: An Update

D. Mohanty, 2014 .

A Patient with Congenital Dyserythropoietic Anaemia Type III Presenting with Stillbirths

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

G6PD deficiency and malaria in India

D. Mohanty, M. Mukherjee, R. Colah, 2003, American journal of hematology.

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.

Sex chromosome loss and malignancy: Does a relationship established?

D. Mohanty, 2004 .

Vascular occlusion and disseminated intravascular coagulation in falciparum malaria.

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

Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian population.

D. Mohanty, M. Mukherjee, R. Colah, 2003, Blood cells, molecules & diseases.

G6PD gene mutations in India producing drug‐induced haemolytic anaemia

D. Mohanty, R. Colah, S. Sukumar, 2002, British journal of haematology.

Red cell pyruvate kinase deficiency in neonatal jaundice cases in India

D. Mohanty, P. Warang, R. Colah, 2006, Indian journal of pediatrics.

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.

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.

Hairy Cell Leukemia – A Report of Two Cases

D. Mohanty, 2017 .

The Duffy blood groups of Jarawas – the primitive and vanishing tribe of Andaman and Nicobar Islands of India

T. Adak, D. Mohanty, S. Singh, 2005, Transfusion medicine.

Abnormal Hemoglobins (HbD and HbQ India ) and β -Thalassaemia among the Indian Sindhis

D. Mohanty, V. Rao, P. Dhas, 2013 .

Contribution of Genetic Factors in Variation of Clinical Severity Among Siblings with Homozygous β-Thalassemia in Two Indian Families

D. Mohanty, K. Ghosh, A. Gorakshakar, 2003 .

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.

HLA associations in P. falciparum malaria patients from Mumbai, western India.

D. Karnad, D. Mohanty, U. Shankarkumar, 2002, Indian journal of malariology.

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.

Leukaemia in north-west India.

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

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.

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

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

Genetic counselling in tribals in India

D. Mohanty, K. Das, 2011, The Indian journal of medical research.

Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3.

B. Coller, D. Mohanty, D. French, 2002, Thrombosis and haemostasis.

Association of HLA B*3520, B*1801, and Cw*1507 with HIV-1 infection Maharashtra, India.

D. Mohanty, M. Thakar, S. Mehendale, 2003, Journal of acquired immune deficiency syndromes.

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.

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.

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

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

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.

Antithrombin III deficiency in an Indian family.

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

Hemoglobin sickle D Punjab—a case report

D. Mohanty, R. Gangakhedkar, M. Mukherjee, 2005 .

Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study

J. Mahanta, D. Mohanty, D. Shukla, 2012, Journal of Community Genetics.

Sickle cell disease in India

D. Mohanty, M. Mukherjee, 2002, Current opinion in hematology.

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.

Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.

D. Mohanty, M. Mukherjee, R. Colah, 2005, Blood cells, molecules & diseases.

Fetal Loss Due to Anti-Hro in a Lady Having Rare Genotype of Rh (D--/D--)

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

Thrombophilia in coronary artery disease: a double jeopardy.

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

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

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

Quest for universal red cell units.

D. Mohanty, 2007, The Indian journal of medical research.

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.

Clinical heterogeneity of silent-gene B-thalassemia among Indians

D. Mohanty, A. Pawar, R. Colah, 2005, Annals of Hematology.

Relief of Acute Chest Syndrome of Sickle Cell Anaemia by Nitric Oxide Inhalation - A Report of 2 Cases

D. Mohanty, B. Ray, S. Choudhuri, 2018 .

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

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

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.

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.