Published in Am J Med Genet B Neuropsychiatr Genet on January 05, 2007
The involvement of Reelin in neurodevelopmental disorders. Neuropharmacology (2012) 1.32
Current developments in the genetics of autism: from phenome to genome. J Neuropathol Exp Neurol (2008) 1.26
Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder. Cell Mol Neurobiol (2007) 0.92
Mapping pathological phenotypes in reelin mutant mice. Front Pediatr (2014) 0.81
An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal. Cell Mol Neurobiol (2010) 0.78
Reelin and Neuropsychiatric Disorders. Front Cell Neurosci (2016) 0.76
Mice with Dab1 or Vldlr insufficiency exhibit abnormal neonatal vocalization patterns. Sci Rep (2016) 0.75
Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians. Diabetes (2010) 2.16
EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda. Proc Natl Acad Sci U S A (2010) 1.74
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers. Clin Chem (2007) 1.50
Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population. J Hum Genet (2012) 1.43
Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children. Indian Pediatr (2005) 1.42
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Diabetes (2012) 1.40
Role of genetic polymorphism peroxisome proliferator-activated receptor-gamma2 Pro12Ala on ethnic susceptibility to diabetes in South-Asian and Caucasian subjects: Evidence for heterogeneity. Diabetes Care (2006) 1.39
Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. Neurosci Lett (2008) 1.13
Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India. Neurosci Lett (2003) 1.12
NADPH oxidase 1-mediated oxidative stress leads to dopamine neuron death in Parkinson's disease. Antioxid Redox Signal (2012) 1.12
Mapping quantitative trait loci in humans: achievements and limitations. J Clin Invest (2005) 1.08
Polymorphisms at XPD and XRCC1 DNA repair loci and increased risk of oral leukoplakia and cancer among NAT2 slow acetylators. Int J Cancer (2007) 1.03
Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population. BMC Med Genet (2010) 1.02
Single nucleotide polymorphisms in homocysteine metabolism pathway genes: association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia. Circ Cardiovasc Genet (2009) 1.01
Genetic variations in the FTO gene are associated with type 2 diabetes and obesity in south Indians (CURES-79). Diabetes Technol Ther (2011) 1.01
Genetic association of ADIPOQ gene variants with type 2 diabetes, obesity and serum adiponectin levels in south Indian population. Gene (2013) 1.01
Mitochondrial NAD+-linked State 3 respiration and complex-I activity are compromised in the cerebral cortex of 3-nitropropionic acid-induced rat model of Huntington's disease. J Neurochem (2007) 0.99
Polymorphisms at p53, p73, and MDM2 loci modulate the risk of tobacco associated leukoplakia and oral cancer. Mol Carcinog (2009) 0.96
Common variants of FTO and the risk of obesity and type 2 diabetes in Indians. J Hum Genet (2011) 0.94
Association analysis of TNFRSF1B polymorphisms with type 2 diabetes and its related traits in North India. Genomic Med (2009) 0.93
NADPH oxidase 1 mediates α-synucleinopathy in Parkinson's disease. J Neurosci (2012) 0.93
Elevated levels of C-reactive protein as a risk factor for metabolic syndrome in Indians. Atherosclerosis (2011) 0.92
Common variants of IL6, LEPR, and PBEF1 are associated with obesity in Indian children. Diabetes (2012) 0.92
Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder. Cell Mol Neurobiol (2007) 0.92
Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians. J Hum Genet (2011) 0.91
Association between inflammatory markers and cardiovascular risk factors in women from Kolkata, W.B, India. Arq Bras Cardiol (2010) 0.91
Major dietary patterns and their associations with cardiovascular risk factors among women in West Bengal, India. Br J Nutr (2011) 0.91
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses. BMC Proc (2009) 0.91
A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Hum Genet (2008) 0.90
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc (2007) 0.89
Genetic variations at microRNA and processing genes and risk of oral cancer. Tumour Biol (2013) 0.89
Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians. Exp Diabetes Res (2011) 0.87
Association of calpain 10 gene polymorphisms with type 2 diabetes mellitus in Southern Indians. Metabolism (2010) 0.87
Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13. Genet Epidemiol (2003) 0.86
Vitamin B12 deficiency is associated with coronary artery disease in an Indian population. Clin Chem Lab Med (2009) 0.86
A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet (2006) 0.86
Potential contribution of dopaminergic gene variants in ADHD core traits and co-morbidity: a study on eastern Indian probands. Cell Mol Neurobiol (2014) 0.86
MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children. Am J Med Genet B Neuropsychiatr Genet (2006) 0.86
Common variants of FTO are associated with childhood obesity in a cross-sectional study of 3,126 urban Indian children. PLoS One (2012) 0.85
Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis. Cell Mol Neurobiol (2007) 0.84
Uncoupling protein 2 and 3 gene polymorphisms and their association with type 2 diabetes in asian indians. Diabetes Technol Ther (2011) 0.84
Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal. Brain Res (2008) 0.84
Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer. PLoS One (2013) 0.84
Serotonergic candidate genes and puerperal psychosis: an association study. Psychiatr Genet (2007) 0.84
Selective maternal inheritance of risk alleles and genetic interaction between serotonin receptor-1B (5-HTR1B) and serotonin transporter (SLC6A4) in ADHD. Psychiatry Res (2012) 0.83
Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population. Am J Med Genet B Neuropsychiatr Genet (2006) 0.83
Genetic variant of AMD1 is associated with obesity in urban Indian children. PLoS One (2012) 0.83
Power comparison between population-based case-control studies and family-based transmission-disequilibrium tests: An empirical study. Indian J Hum Genet (2011) 0.82
Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children. Behav Brain Funct (2005) 0.82
Serotonin transporter promoter variants: Analysis in Indian autistic and control population. Brain Res (2006) 0.82
Evidence for an association with type 2 diabetes mellitus at the PPARG locus in a South Indian population. Metabolism (2009) 0.81
Effect of population stratification on false positive rates of population-based association analyses of quantitative traits. Ann Hum Genet (2012) 0.81
Purification and characterization of a serine protease (CESP) from mature coconut endosperm. BMC Res Notes (2009) 0.81
Strong influence of variants near MC4R on adiposity in children and adults: a cross-sectional study in Indian population. J Hum Genet (2012) 0.81
Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. Prog Neuropsychopharmacol Biol Psychiatry (2011) 0.81
Evaluating epistatic interaction signals in complex traits using quantitative traits. BMC Proc (2009) 0.81
Common variants in CRP and LEPR influence high sensitivity C-reactive protein levels in North Indians. PLoS One (2011) 0.81
Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population. Psychiatr Genet (2007) 0.81
Conformation and activity dependent interaction of glucose oxidase with CdTe quantum dots: towards developing a nanoparticle based enzymatic assay. Photochem Photobiol Sci (2009) 0.81
Screening of rural children in West Bengal for fragile-X syndrome. Indian J Med Res (2009) 0.80
Statistical equivalent of the classical TDT for quantitative traits and multivariate phenotypes. J Genet (2015) 0.80
Risk factors for hypertension in a population-based sample of postmenopausal women in Kolkata, West Bengal, India. Asia Pac J Public Health (2013) 0.80
Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes. Neurochem Int (2009) 0.80
Size dependent interaction of biofunctionalized CdS nanoparticles with tyrosine at different pH. Chem Commun (Camb) (2005) 0.80
Mitochondrial functional alterations in relation to pathophysiology of Huntington's disease. J Bioenerg Biomembr (2010) 0.80
Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India. Cell Mol Neurobiol (2009) 0.79
Graphene as a reversible spin manipulator of molecular magnets. Phys Rev Lett (2011) 0.79