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Richard Anney

Institution

Trinity College Dublin

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Subjects

Psychiatry

Details
Publications 40
As first author 11
As last author 3
Unique topics 275
Collaborations 46
Sources 10
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2018

Effects of MiR‐137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls
2017

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls.
2017

MiR-137-derived polygenic risk: Effects on cognitive performance in patients with schizophrenia and controls
2016

A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.
2016

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.
2015

Detecting Allelic Expression Imbalance at Candidate Genes Using 5' Exonuclease Genotyping Technology.
2015

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
2014

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.
2014

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
2014

Synaptic, transcriptional and chromatin genes disrupted in autism.
2014

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis
2014

The phenotypic manifestations of rare CNVs in schizophrenia.
2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
2014

Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.
2013

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
2013

Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data.
2013

Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings.
2013

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis.
2012

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
2012

Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data.
2012

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
2012

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
2012

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
2011

A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.
2011

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation.
2011

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.
2011

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
2011

Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings.
2010

A genomewide scan for common alleles affecting risk for autism.
2010

Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression.
2010

Functional impact of global rare copy number variation in autism spectrum disorders
2010

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism.
2009

ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.
2009

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies.
2008

Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.
2008

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
2008

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.
2008

Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.
2008

Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.
2006

Variation in the gene coding for the M5 muscarinic receptor (CHRM5) influences cigarette dose but is not associated with dependence to drugs of addiction: evidence from a prospective population based cohort study of young adults.

These arethe10 unique sources for Richard Anney's 40 publications. A single publication may appear in multiple sources. Click on a name or publication count to see the publications for a particular source.

Source #
Ireland -> Dublin City University 1
Ireland -> Dublin City University -> PubMed 1
Ireland -> National College Ireland 5
Ireland -> National College of Ireland 3
Ireland -> National University of Ireland Galway 1
Ireland -> National University of Ireland Galway -> PubMed 1
Ireland -> Trinity College Dublin 35
Ireland -> Trinity College Dublin -> PubMed 18
Ireland -> University College Dublin 4
Ireland -> University College Dublin -> PubMed 1

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