Published in Thromb Haemost on April 01, 2009
Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. Br J Haematol (2010) 2.12
CAMP: a useful resource for research on antimicrobial peptides. Nucleic Acids Res (2009) 2.02
Acquired hemophilia a: diagnosis, aetiology, clinical spectrum and treatment options. Autoimmun Rev (2010) 1.90
Hereditary thrombophilia in cerebral venous thrombosis: a study from India. Blood Coagul Fibrinolysis (2013) 1.66
Combination of thrombophilia markers in acute myocardial infarction of the young. Indian J Med Sci (2004) 1.52
Bone health in persons with haemophilia: a review. Eur J Haematol (2012) 1.44
Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: a single centre experience. Indian Pediatr (2013) 1.44
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype. Blood Cells Mol Dis (2008) 1.43
Prevalence and spectrum of von Willebrand disease from western India. Indian J Med Res (2005) 1.43
Antihistone and other autoantibodies in beta-thalassemia major patients receiving iron chelators. Acta Haematol (2003) 1.40
Mitochondrial DNA variations in myelodysplastic syndrome. Ann Hematol (2013) 1.39
CAMP: Collection of sequences and structures of antimicrobial peptides. Nucleic Acids Res (2013) 1.24
Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: an overview. Mutat Res (2013) 1.17
Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians. Genet Test (2008) 1.16
Tuberculosis and immune thrombocytopenia. Haematologica (2002) 1.15
Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review. Thromb Res (2010) 1.10
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India. Clin Chim Acta (2009) 1.09
Immune response to FVIII in hemophilia A: an overview of risk factors. Clin Rev Allergy Immunol (2009) 1.08
Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India. Indian Heart J (2009) 1.08
Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population. Blood Cells Mol Dis (2009) 1.08
Potential of commercial anti-D reagents in the identification of partial D variants in Indian population. Indian J Med Res (2007) 1.07
Newborn screening shows a high incidence of sickle cell anemia in Central India. Hemoglobin (2012) 1.04
First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India. Prenat Diagn (2006) 1.03
Glanzmann's thrombasthenia: updated. Platelets (2002) 1.03
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India. Indian J Hum Genet (2010) 1.03
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. J Clin Pathol (2012) 0.99
Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss. Ann Intern Med (2015) 0.98
Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases. Trans R Soc Trop Med Hyg (2007) 0.98
Blood coagulation in falciparum malaria--a review. Parasitol Res (2007) 0.98
Osteoporosis in young haemophiliacs from western India. Am J Hematol (2007) 0.96
A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population. Blood Transfus (2012) 0.95
Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients. Br J Haematol (2007) 0.95
Novel homozygous mutations in Desert hedgehog gene in patients with 46,XY complete gonadal dysgenesis and prediction of its structural and functional implications by computational methods. Eur J Med Genet (2011) 0.94
Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from India. PLoS One (2012) 0.94
Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation and other adverse outcomes in Indian population. Eur J Pharmacol (2013) 0.94
Beta-globin gene cluster haplotypes linked to the betaS gene in western India. Hemoglobin (2004) 0.93
Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups. Blood Coagul Fibrinolysis (2012) 0.92
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII. Am J Hematol (2005) 0.92
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family. Am J Hematol (2005) 0.92
Anti-phospholipid antibodies and other immunological causes of recurrent foetal loss--a review of literature of various therapeutic protocols. Am J Reprod Immunol (2009) 0.91
Hereditary protein C deficiency in Indian patients with venous thrombosis. Ann Hematol (2012) 0.91
Mannose binding lectin (MBL) in autoimmunity and its role in systemic lupus erythematosus (SLE). J Assoc Physicians India (2010) 0.91
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. J Clin Pathol (2010) 0.90
Immune-mediated thrombocytopenia following dactinomycin therapy in a child with alveolar rhabdomyosarcoma: the unresolved issues. J Pediatr Hematol Oncol (2004) 0.89
Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India. Thromb J (2007) 0.89
Molecular diversity of hemoglobin H disease in India. Am J Clin Pathol (2010) 0.89
HLA A*02 allele frequencies and B haplotype associations in Western Indians. Hum Immunol (2003) 0.89
Human platelet specific antigens and their importance. Indian Pediatr (2004) 0.88
Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations. Eur J Haematol (2009) 0.88
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. Clin Appl Thromb Hemost (2007) 0.88
Advances in autoimmune lymphoproliferative syndromes. Eur J Haematol (2011) 0.87
Sickle cell disease in India. Curr Opin Hematol (2014) 0.87
JAK2 mutations across a spectrum of venous thrombosis cases. Am J Clin Pathol (2010) 0.87
Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population. J Pediatr Hematol Oncol (2010) 0.85
A chemical proteomics approach to profiling the ATP-binding proteome of Mycobacterium tuberculosis. Mol Cell Proteomics (2013) 0.85
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches. Hemoglobin (2010) 0.85
An unusual presentation of pediatric acute lymphoblastic leukemia. Indian J Hematol Blood Transfus (2008) 0.85
Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype. Br J Haematol (2014) 0.85
Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and alpha-thalassemia trait. Pediatr Hematol Oncol (2002) 0.85
Pathophysiology of acquired von Willebrand disease: a concise review. Eur J Haematol (2011) 0.85
Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario. Indian J Med Res (2015) 0.85
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation. J Allergy Clin Immunol (2012) 0.84
Letter: HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India. Epilepsia (2009) 0.84
Chronic synovitis and HLA B27 in patients with severe haemophilia. Lancet (2003) 0.84
Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy. J Electron Microsc (Tokyo) (2008) 0.84
Sickle cell disease in tribal populations in India. Indian J Med Res (2015) 0.84
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India. Indian J Hum Genet (2013) 0.84
Elevated procoagulant endothelial and tissue factor expressing microparticles in women with recurrent pregnancy loss. PLoS One (2013) 0.83
Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature. Gene (2013) 0.83
Thrombophilic dimension of recurrent fetal loss in Indian patients. Blood Coagul Fibrinolysis (2008) 0.83
Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation. Eur J Haematol (2009) 0.83
Recent developments in drug resistance mechanism in chronic myeloid leukemia: a review. Eur J Haematol (2011) 0.83
Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India. Platelets (2009) 0.82
Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3). Indian J Hum Genet (2007) 0.82
ClassAMP: a prediction tool for classification of antimicrobial peptides. IEEE/ACM Trans Comput Biol Bioinform (2012) 0.82
A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families. Ann Hematol (2013) 0.82
Defining the allelic variants of HLA A19 in the western Indian population. Hum Immunol (2002) 0.82
The spectrum of bleeding disorders in women with menorrhagia: a report from Western India. Ann Hematol (2004) 0.82
Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells. FEMS Immunol Med Microbiol (2008) 0.81