about
The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysisFunctional impact of global rare copy number variation in autism spectrum disordersGenome-wide association scan of the time to onset of attention deficit hyperactivity disorderGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsDoes parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scanIndividual common variants exert weak effects on the risk for autism spectrum disordersConduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics studyGenome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associationsA genome-wide scan for common alleles affecting risk for autismPolygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes dataParent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.Genome-wide association scan of attention deficit hyperactivity disorderOn genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls.Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interactionNon-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism.The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings.Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settingsGenome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region.MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants.Prospects for epigenetic research within cohort studies of psychological disorder: a pilot investigation of a peripheral cell marker of epigenetic risk for depression.Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders.Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample.A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
P50
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P50
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