Published in Indian J Ophthalmol on December 01, 2002
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Primary role of CYP1B1 in Indian juvenile-onset POAG patients. Mol Vis (2006) 1.26
Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India. Mol Vis (2005) 1.06
Distribution of p53 codon 72 polymorphism in Indian primary open angle glaucoma patients. Mol Vis (2002) 1.04
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Comparison of health effects between individuals with and without skin lesions in the population exposed to arsenic through drinking water in West Bengal, India. J Expo Sci Environ Epidemiol (2006) 1.03
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Toxicogenomics of arsenic: classical ideas and recent advances. Mutat Res (2008) 1.01
Mutations in MYOC gene of Indian primary open angle glaucoma patients. Mol Vis (2002) 0.98
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis (2008) 0.97
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water. Int J Cancer (2006) 0.95
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma. Mol Vis (2005) 0.91
Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders. Mol Vis (2004) 0.90
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification. Hum Mutat (2005) 0.89
A Line 1 insertion in the Factor IX gene segregates with mild hemophilia B in dogs. Mamm Genome (2003) 0.88
Myocilin variants in Indian patients with open-angle glaucoma. Arch Ophthalmol (2007) 0.88
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change. BMC Mol Biol (2007) 0.88
Evaluation of genetic markers linked to hemophilia A locus: an Indian experience. Haematologica (2007) 0.86
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase gene. Mol Vis (2005) 0.86
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Mitochondrial genome analysis of primary open angle glaucoma patients. PLoS One (2013) 0.84
Association of IL1A and IL1B loci with primary open angle glaucoma. BMC Med Genet (2010) 0.84
SLC45A2 variations in Indian oculocutaneous albinism patients. Mol Vis (2007) 0.83
Comprehensive analysis of myocilin variants in east Indian POAG patients. Mol Vis (2012) 0.83
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Did myocilin evolve from two different primordial proteins? Mol Vis (2002) 0.82
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient. Behav Brain Funct (2010) 0.80
Cloning and characterization of opticin cDNA: evaluation as a candidate for canine oculo-skeletal dysplasia. Gene (2002) 0.80
DNA linkage based diagnosis of Wilson disease in asymptomatic siblings. Indian J Med Res (2003) 0.80
Role of tau kinases (CDK5R1 and GSK3B) in Parkinson's disease: a study from India. Neurobiol Aging (2010) 0.79
Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians. Neurosci Lett (2009) 0.79
Evaluation of PINK1 variants in Indian Parkinson's disease patients. Parkinsonism Relat Disord (2009) 0.79
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients. J Invest Dermatol (2010) 0.79
Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos. J Genet (2013) 0.79
Complex genetics of glaucoma: defects in CYP1B1, and not MYOC, cause pathogenesis in an early-onset POAG patient with double variants at both loci. J Genet (2008) 0.79
Upregulation of human mitochondrial NADH dehydrogenase subunit 5 in intestinal epithelial cells is modulated by Vibrio cholerae pathogenesis. FEBS Lett (2005) 0.78
Indian genetic disease database. Nucleic Acids Res (2010) 0.78
Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohort. Dis Markers (2012) 0.78
Genetic study on frontotemporal lobar degeneration in India. Parkinsonism Relat Disord (2013) 0.78
SNPs in genes with copy number variation: a question of specificity. J Genet (2008) 0.78
Cosegregation of a factor VIII microsatellite marker with mild hemophilia A in Golden Retriever dogs. J Vet Intern Med (2005) 0.78
Genetic association and gene-gene interaction of HAS2, HABP1 and HYAL3 implicate hyaluronan metabolic genes in glaucomatous neurodegeneration. Dis Markers (2012) 0.77
Simple and effective strategies for detection of allele dropout in PCR-based diagnosis of Wilson disease. Clin Chem (2006) 0.77
WDR36 variants in East Indian primary open-angle glaucoma patients. Mol Vis (2011) 0.76
Analysis of COCH and TNFA variants in East Indian primary open-angle glaucoma patients. Biomed Res Int (2013) 0.75
TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian origin. J Genet (2016) 0.75
Movement disorders: Indian scenario: a clinico-genetic review. Neurol India (2013) 0.75
Mitochondrial genome variations among arsenic exposed individuals and potential correlation with apoptotic parameters. Environ Mol Mutagen (2013) 0.75
Ligand and Structure Based Models for the Identification of Beta 2 Adrenergic Receptor Antagonists. Curr Comput Aided Drug Des (2015) 0.75
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of India. J Genet (2010) 0.75
Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucoma. Indian J Ophthalmol (2003) 0.75
Genetics of eye diseases: preface. J Genet (2009) 0.75