Browsing Psychiatry by Author "ANNEY, RICHARD"
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Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
CORVIN, AIDEN; HERON, ELIZABETH; GILL, MICHAEL; DONOHOE, GARY; ANNEY, RICHARD; GALLAGHER, LOUISE; MORRIS, DEREK; TROPEA, DANIELA; KENNY, ELAINE (2014) -
A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.
ANNEY, RICHARD; GILL, MICHAEL (2011)BACKGROUND: Impulsive drive for immediate reward (IDIR) and delay aversion are dissociable elements of the preference for immediate over delayed rewards seen in attention-deficit/hyperactivity disorder (ADHD). We ... -
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
GILL, MICHAEL; GALLAGHER, LOUISE; ANNEY, RICHARD; KENNY, ELAINE (2011)Recent genome-wide association studies (GWAS) have implicated a range of genes from discrete biological pathways in the aetiology of autism. However, despite the strong influence of genetic factors, association studies ... -
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
ANNEY, RICHARD; GILL, MICHAEL; HAWI, ZIARIH (2012) -
A genomewide scan for common alleles affecting risk for autism.
ANNEY, RICHARD; GALLAGHER, LOUISE; GILL, MICHAEL; BOLSHAKOVA, NADIA; SEGURADO, RICARDO; HERON, ELIZABETH; MCGRATH, JANE; TANSEY, KATHERINE; BRENNAN, SEAN; MERIKANGAS, ALISON; MERIKANGAS, ALISON KATHLEEN (2010)Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the ... -
Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings
GILL, MICHAEL; ANNEY, RICHARD (2011) -
Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings.
ANNEY, RICHARD (2013)We wished to ascertain if there is an association between symptoms of attention-deficit/hyperactivity disorder (ADHD) and home environment in children with ADHD and non-ADHD siblings, controlling for other environmental ... -
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
ANNEY, RICHARD; MERIKANGAS, ALISON; HERON, ELIZABETH; GILL, MICHAEL; GALLAGHER, LOUISE (2012)While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To ... -
Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.
ANNEY, RICHARD; GILL, MICHAEL (2008) -
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
ANNEY, RICHARD; MERIKANGAS, ALISON; MCGRATH, JANE; GALLAGHER, LOUISE (2012)Autism spectrum disorder (ASD) is a highly heritable disorder of complex and heterogeneous aetiology. It is primarily characterized by altered cognitive ability including impaired language and communication skills and ... -
The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis
HARGREAVES, APRIL; GILL, MICHAEL; MORRIS, DEREK; ANNEY, RICHARD; CORVIN, AIDEN; DONOHOE, GARY (2013) -
The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
HERON, ELIZABETH; GILL, MICHAEL; ANNEY, RICHARD; CORVIN, AIDEN; GALLAGHER, LOUISE (2014)Significant evidence exists for the association between copy number variants (CNVs) and Autism Spectrum Disorder (ASD); however, most of this work has focused solely on the diagnosis of ASD. There is limited understanding ... -
The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
ANNEY, RICHARD; CORVIN, AIDEN; GILL, MICHAEL; GALLAGHER, LOUISE (2015) -
Synaptic, transcriptional and chromatin genes disrupted in autism.
GALLAGHER, LOUISE; ANNEY, RICHARD; GILL, MICHAEL (2014) -
Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.
ANNEY, RICHARD; GILL, MICHAEL; DONOHOE, GARY (2014)IMPORTANCE We investigated the variation in neuropsychological function explained by risk alleles at the psychosis susceptibility gene ZNF804A and its interacting partners using single nucleotide polymorphisms (SNPs), ...