Published in Cell Mol Neurobiol on March 02, 2014
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Significant association of ANKK1 and detection of a functional polymorphism with nicotine dependence in an African-American sample. Neuropsychopharmacology (2008) 1.31
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Association of multiple DRD2 polymorphisms with anorexia nervosa. Neuropsychopharmacology (2005) 1.06
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Association between DRD4 gene and performance of children with ADHD in a test of sustained attention. Biol Psychiatry (2006) 0.91
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DOPA decarboxylase gene is associated with nicotine dependence. Pharmacogenomics (2006) 0.89
Absence of the 7-repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls. Am J Med Genet B Neuropsychiatr Genet (2008) 0.89
Polymorphisms in dopamine system genes are associated with individual differences in attention in infancy. Dev Psychol (2010) 0.89
Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants. Pharmacogenomics J (2009) 0.88
ADHD candidate gene (DRD4 exon III) affects inhibitory control in a healthy sample. BMC Neurosci (2009) 0.88
Association of the dopamine D2 receptor gene with alcohol dependence: haplotypes and subgroups of alcoholics as key factors for understanding receptor function. Pharmacogenet Genomics (2009) 0.86
A dopamine D2 receptor gene-related polymorphism is associated with schizophrenia in a Spanish population isolate. Psychiatr Genet (2007) 0.86
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Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD. Am J Med Genet B Neuropsychiatr Genet (2008) 0.83
Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands. Prog Neuropsychopharmacol Biol Psychiatry (2011) 0.81
Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent. BMC Res Notes (2012) 0.81
Genetic interaction analysis for DRD4 and DAT1 genes in a group of Mexican ADHD patients. Neurosci Lett (2009) 0.80
Genetic factors of reaction time performance: DRD4 7-repeat allele associated with slower responses. Genes Brain Behav (2010) 0.80
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A case-control association study of the polymorphism at the promoter region of the DRD4 gene in Korean boys with attention deficit-hyperactivity disorder: evidence of association with the -521 C/T SNP. Prog Neuropsychopharmacol Biol Psychiatry (2007) 0.79
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Do SNPs of DRD4 gene predict adult persistence of ADHD in a Chinese sample? Psychiatry Res (2012) 0.77
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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
MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children. Am J Med Genet B Neuropsychiatr Genet (2006) 0.86
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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
Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population. J Oral Pathol Med (2011) 0.84
Correlation of plasma dopamine beta-hydroxylase activity with polymorphisms in DBH gene: a study on Eastern Indian population. Cell Mol Neurobiol (2008) 0.84
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
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
Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children. Behav Brain Funct (2005) 0.82
Risk of Down syndrome conferred by MTHFR C677T polymorphism: Ethnic variations. Indian J Hum Genet (2007) 0.82
Serotonin transporter promoter variants: Analysis in Indian autistic and control population. Brain Res (2006) 0.82
Molecular aspects of Down syndrome. Indian Pediatr (2005) 0.82
Lack of association of HOXA1 and HOXB1 variants with autism in the Indian population. Psychiatr Genet (2007) 0.81
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Dopamine receptor D4 exon 3 variable number of tandem repeat polymorphism: Distribution in eastern Indian population. Indian J Hum Genet (2007) 0.81
Screening of rural children in West Bengal for fragile-X syndrome. Indian J Med Res (2009) 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
A study of GluK1 kainate receptor polymorphisms in Down syndrome reveals allelic non-disjunction at 1173(C/T). Dis Markers (2009) 0.79
Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India. Cell Mol Neurobiol (2009) 0.79
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Down Syndrome Related Muscle Hypotonia: Association with COL6A3 Functional SNP rs2270669. Front Genet (2013) 0.78
An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal. Cell Mol Neurobiol (2010) 0.78
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Differential allelic distribution of V-ets erythroblastosis virus E26 oncogene homolog2 (ETS2) functional polymorphisms in different group of patients. Gene Expr (2010) 0.78
SNaPshot Assay in Quantitative Detection of Allelic Nondisjunction in Down Syndrome. Genet Test Mol Biomarkers (2012) 0.78
Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder. Neurosci Lett (2006) 0.78
DAT1 3'-UTR 9R allele: preferential transmission in Indian children with attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet (2007) 0.78
Role of SNAP25 explored in eastern Indian attention deficit hyperactivity disorder probands. Neurochem Res (2011) 0.78
Genetic association and gene-gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population. Prog Neuropsychopharmacol Biol Psychiatry (2013) 0.77
Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism. Am J Med Genet B Neuropsychiatr Genet (2007) 0.77
No Evidence for Mutations that Deregulate GARS-AIRS-GART Protein Levels in Children with Down Syndrome. Indian J Clin Biochem (2012) 0.77
Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal. BMC Genet (2016) 0.76
Lack of association between down syndrome and polymorphisms in dopamine receptor D4 and serotonin transporter genes. Neurochem Res (2008) 0.76
Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies. BMC Med Genet (2013) 0.76
Exploratory investigation on functional significance of ETS2 and SIM2 genes in Down syndrome. Dis Markers (2011) 0.76
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Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21. Indian J Hum Genet (2012) 0.75
Chromosomal abnormalities associated with mental retardation in female subjects. Indian J Hum Genet (2009) 0.75
MAOA exon 8 941T > G Fnu4HI polymorphism: actual rs number. Am J Med Genet B Neuropsychiatr Genet (2009) 0.75
Catecholaminergic gene variants: contribution in ADHD and associated comorbid attributes in the eastern Indian probands. Biomed Res Int (2013) 0.75
Importance of gene variants and co-factors of folate metabolic pathway in the etiology of idiopathic intellectual disability. Nutr Neurosci (2011) 0.75
Analysis of cystathionine beta-synthase 31 bp variable number tandem repeats in mentally retarded patients. Psychiatr Genet (2007) 0.75
Analysis of monoamine oxidase A promoter polymorphism in mentally retarded individuals. Psychiatr Genet (2007) 0.75
Screening for methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Indian patients with idiopathic mental retardation. Nutr Neurosci (2008) 0.75
No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with attention-deficit-hyperactivity disorder (ADHD). Neurosci Lett (2009) 0.75
Biased paternal transmission of TRH variant to female Down syndrome probands: possible correlation with low breast cancer frequency. Int J Biol Markers (2015) 0.75
Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata. Neurosci Lett (2009) 0.75
Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability. Prog Neuropsychopharmacol Biol Psychiatry (2011) 0.75
Association of monoamine oxidase A and serotonin transporter gene functional variants with intellectual disability related behavioral problems. Psychiatr Genet (2012) 0.75