Published in Indian J Hum Genet on January 01, 2012
An update on conformation sensitive gel electrophoresis. Hum Mutat (2002) 1.32
Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions. Haemophilia (2005) 1.05
Female hemophilia A heterozygous for a de novo frameshift and a novel missense mutation of factor VIII. J Thromb Haemost (2006) 0.96
Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene. Haemophilia (2008) 0.86
Molecular mechanisms underlying hemophilia A phenotype in seven females. J Thromb Haemost (2009) 0.86
Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser. Thromb Haemost (2010) 0.85
Female haemophilia A caused by skewed X inactivation. Haemophilia (2008) 0.85
Analysis of 18 novel mutations in the factor VIII gene. Br J Haematol (2003) 0.84
Hemophilia B in a female. Acta Haematol (2001) 0.82
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
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
A method to reduce nasopharyngeal trauma from nasogastric tube placement. Anesth Analg (1994) 1.57
Combination of thrombophilia markers in acute myocardial infarction of the young. Indian J Med Sci (2004) 1.52
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
Is non-woven fabric a useful method of packaging instruments for operation theatres in resource constrained settings? Indian J Med Microbiol (2015) 1.39
Human hepatic sinusoidal endothelial cells can be distinguished by expression of phenotypic markers related to their specialised functions in vivo. World J Gastroenterol (2006) 1.39
Placental histomorphology in unexplained foetal loss with thrombophilia. Indian J Med Res (2009) 1.39
Mitochondrial DNA variations in myelodysplastic syndrome. Ann Hematol (2013) 1.39
How safe is sugarcane juice? Indian J Med Microbiol (2007) 1.38
Sex from W to Z: evolution of vertebrate sex chromosomes and sex determining genes. J Exp Zool (2001) 1.36
Antiplatelet antibodies in cases of Glanzmann's thrombasthenia with and without a history of multiple platelet transfusion. Indian J Hum Genet (2009) 1.28
DNA structure and flexibility in the sequence-specific binding of papillomavirus E2 proteins. J Mol Biol (1998) 1.27
Beneficial effects of yoga lifestyle on reversibility of ischaemic heart disease: caring heart project of International Board of Yoga. J Assoc Physicians India (2004) 1.23
Cysticercosis of the masseter: MRI and sonographic correlation. Dentomaxillofac Radiol (2015) 1.22
P53 mutation and MDM2 amplification frequency in pediatric rhabdomyosarcoma tumors and cell lines. Med Pediatr Oncol (2000) 1.22
Orofacial pain - a presenting symptom of bisphosphonate associated osteonecrosis of the jaws. Br Dent J (2007) 1.19
Exenatide and acute pancreatitis. J Assoc Physicians India (2008) 1.18
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
Fibrinolysis, inhibitors of blood coagulation, and monocyte derived coagulant activity in acute malaria. Am J Hematol (1997) 1.13
Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India. Hepatology (2001) 1.11
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
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
Effects of sex chromosome aneuploidy on male sexual behavior. Genes Brain Behav (2008) 1.05
Supporting new vaccine introduction decisions: lessons learned from the Hib Initiative experience. Vaccine (2010) 1.04
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
Development of inhibitors in patients with haemophilia from India. Haemophilia (2001) 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
Evaluation of light emitting diode-based fluorescence microscopy for the detection of mycobacteria in a tuberculosis-endemic region. Int J Tuberc Lung Dis (2011) 1.01
Marfan syndrome: report of two cases with review of literature. Niger J Clin Pract (2012) 1.00
A comparative study of oral health knowledge, attitude and behaviour of first and final year dental students of Udaipur city, Rajasthan, India. Int J Dent Hyg (2008) 0.99
Acute adult supraglottitis: current management and treatment. South Med J (2010) 0.99
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
Transfusion transmitted diseases in haemophilics from western India. Indian J Med Res (2000) 0.99
Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss. Ann Intern Med (2015) 0.98
Is assessment of popliteal artery diameter in patients undergoing screening for abdominal aortic aneurysms a worthwhile procedure. Eur J Vasc Endovasc Surg (2005) 0.98
Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases. Trans R Soc Trop Med Hyg (2007) 0.98
Intracranial haemorrhage in severe haemophilia: prevalence and outcome in a developing country. Haemophilia (2005) 0.98
Long-term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia. Prenat Diagn (2000) 0.97
Awareness of Consumer Protection Act among Doctors in Udaipur City, India. J Dent (Tehran) (2010) 0.97
Osteoporosis in young haemophiliacs from western India. Am J Hematol (2007) 0.96
CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy. Clin Genet (2010) 0.95
Unicystic plexiform ameloblastoma: an insight for pediatric dentists. J Indian Soc Pedod Prev Dent (2009) 0.95
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
Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study: comment. J Thromb Haemost (2014) 0.95
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
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family. Am J Hematol (2005) 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
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
A comparative study of oral health knowledge, attitude and behaviour of non-medical, para-medical and medical students in Udaipur city, Rajasthan, India. Int J Dent Hyg (2010) 0.90
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
First-time development of FVIII inhibitor in haemophilia patients during the postoperative period. Haemophilia (2002) 0.90
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
Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India. Thromb J (2007) 0.89
Immune-mediated thrombocytopenia following dactinomycin therapy in a child with alveolar rhabdomyosarcoma: the unresolved issues. J Pediatr Hematol Oncol (2004) 0.89
Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost (2001) 0.88
Recurrent ameloblastoma of the infratemporal fossa: diagnostic implications and a review of the literature. Dentomaxillofac Radiol (2007) 0.88
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
A minimal murine Msx-1 gene promoter. Organization of its cis-regulatory motifs and their role in transcriptional activation in cells in culture and in transgenic mice. J Biol Chem (1997) 0.88
Advances in autoimmune lymphoproliferative syndromes. Eur J Haematol (2011) 0.87
The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal. J Thromb Haemost (2013) 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
Evaluation of oral hygiene status, salivary characteristics and dental caries experience in acute lymphoblastic leukemic (ALL) children. J Clin Pediatr Dent (2011) 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
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches. Hemoglobin (2010) 0.85
Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI). Haemophilia (2009) 0.85
When and how to evaluate a patient with nephrolithiasis. Urol Clin North Am (2000) 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
Rapid neural Fos responses to oestradiol in oestrogen receptor alphabeta double knockout mice. J Neuroendocrinol (2006) 0.85
Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population. J Pediatr Hematol Oncol (2010) 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
Anticoagulation in haemophilia patients with prosthetic valve replacement. Haemophilia (2004) 0.84
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation. J Allergy Clin Immunol (2012) 0.84
Phenotype, activation and lymphokine secretion by gamma/delta T lymphocytes from schistosomiasis and carcinoma of the urinary bladder. Eur J Immunol (1992) 0.84
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India. Indian J Hum Genet (2013) 0.84
Spectrum of inherited bleeding disorders from Western India. Haematologia (Budap) (2002) 0.84
Fractures of long bones in severe haemophilia. Haemophilia (2007) 0.84
Pseudomonas aeruginosa elastase stimulates ERK signaling pathway and enhances IL-8 production by alveolar epithelial cells in culture. Inflamm Res (2002) 0.84
Genetic disorders in haematological practice in India. Community Genet (2002) 0.84