Lista de obras - Richard Anney - Dominio Público Uruguay

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

artículo científico publicado en 2011

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

artículo científico publicado en 2016

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.

artículo científico publicado en 2008

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

artículo científico publicado en 2011

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

artículo científico publicado en 2010

ASD Diagnosis in Adults: Phenotype and Genotype Findings from a Clinically-derived Cohort

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

scientific article published on 03 January 2017

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

artículo científico publicado en 2011

Association between 5-HTTLPR genotypes and persisting patterns of anxiety and alcohol use: results from a 10-year longitudinal study of adolescent mental health

artículo científico publicado en 2005

Association between dependent smoking and a polymorphism in the tyrosine hydroxylase gene in a prospective population-based study of adolescent health

artículo científico publicado en 2004

Association between dopamine D3 receptor gene polymorphisms and schizophrenia in an isolate population

artículo científico publicado en 2005

Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health

artículo científico publicado en 2005

Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity

artículo científico publicado en 2008

Autism Symptoms in Attention-Deficit/Hyperactivity Disorder: A Familial Trait which Correlates with Conduct, Oppositional Defiant, Language and Motor Disorders

article

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders

artículo científico publicado en 2008

COMT Val(158)Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study.

artículo científico publicado en 2007

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder ⬇️

artículo científico publicado el 5 de agosto de 2010

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.

artículo científico publicado en 2002

Common Genetic Variants in Autism Spectrum Disorders

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

artículo científico publicado en 2015

Common risk variants identified in autism spectrum disorder

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

artículo científico publicado en 2014

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

scientific journal article

Conservation of CNS1 and exclusion of its role in atopic eczema susceptibility

artículo científico publicado en 2002

Contributors

article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan

scientific journal article

Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder.

artículo científico publicado en 2009

Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence

artículo científico publicado en 2010

Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

article

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

artículo científico publicado en 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Genome-wide association scan of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

scientific journal article

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

artículo científico publicado en 2011

High loading of polygenic risk for ADHD in children with comorbid aggression

artículo científico publicado en 2013

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

artículo científico publicado en 2011

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach

artículo científico publicado en 2010

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder

artículo científico publicado en 2008

Intelligence in DSM‐IV combined type attention‐deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention‐deficit/hyperactivity disorder

article

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample

artículo científico publicado en 2010

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

artículo científico publicado en 2008

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

artículo científico publicado el 1 de agosto de 2010

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

artículo científico publicado en 2017

Nicotine dependence in a prospective population-based study of adolescents: the protective role of a functional tyrosine hydroxylase polymorphism

artículo científico publicado en 2004

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

artículo científico publicado en 2008

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

scholarly article by X. Xu et al published 5 March 2009 in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

scholarly article by X. Xu et al published 5 January 2009 in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

No evidence that common genetic risk variation is shared between schizophrenia and autism

artículo científico publicado en 2012

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

artículo científico publicado en 2008

Novel Insight into the Aetiology of Autism Spectrum Disorder Gained by Integrating Expression Data with Genome-wide Association Statistics

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls

artículo científico publicado en 2010

Overlap between ADHD and Autism – Clinical and Genetic Evidence

article

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

artículo científico publicado en 2010

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

artículo científico publicado en 2008

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants ⬇️

artículo científico publicado en 2013

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

article

Poster #112 NO EVIDENCE THAT COMMON GENETIC RISK VARIANTS ARE SHARED BETWEEN SCHIZOPHRENIA AND AUTISM

Prospects for epigenetic research within cohort studies of psychological disorder: a pilot investigation of a peripheral cell marker of epigenetic risk for depression.

artículo científico publicado en 2009

Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region

artículo científico publicado en 2015

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.

artículo científico publicado en 2008

S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations

article

Sex differences in gene expression in the human fetal brain

article

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant

artículo científico publicado en 2003

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

artículo científico publicado en 2010

The Genetic Architecture of Autism and Related Conditions

scholarly article published 6 March 2013

The Social Communication Questionnaire in a sample of the general population of school-going children

artículo científico publicado en 2008

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

artículo científico publicado en 2006

The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction

artículo científico publicado en 2008

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) analysis

artículo científico publicado en 2008

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

artículo científico publicado en 2013

The phenotypic manifestations of rare CNVs in schizophrenia

artículo científico publicado en 2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Lista de obras de Richard Anney

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

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

A genome-wide scan for common alleles affecting risk for autism

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.

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

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

ASD Diagnosis in Adults: Phenotype and Genotype Findings from a Clinically-derived Cohort

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

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

Association between 5-HTTLPR genotypes and persisting patterns of anxiety and alcohol use: results from a 10-year longitudinal study of adolescent mental health

Association between dependent smoking and a polymorphism in the tyrosine hydroxylase gene in a prospective population-based study of adolescent health

Association between dopamine D3 receptor gene polymorphisms and schizophrenia in an isolate population

Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health

Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity

Autism Symptoms in Attention-Deficit/Hyperactivity Disorder: A Familial Trait which Correlates with Conduct, Oppositional Defiant, Language and Motor Disorders

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders

COMT Val(158)Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study.

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder ⬇️

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.

Common Genetic Variants in Autism Spectrum Disorders

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

Common risk variants identified in autism spectrum disorder

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

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

Conservation of CNS1 and exclusion of its role in atopic eczema susceptibility

Contributors

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

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

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

Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan

Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder.

Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence

Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

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

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

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

Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants

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

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

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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

Genome-wide association scan of attention deficit hyperactivity disorder

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

High loading of polygenic risk for ADHD in children with comorbid aggression

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

Identification of common genetic risk variants for autism spectrum disorder

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach

Individual common variants exert weak effects on the risk for autism spectrum disorders

Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder

Intelligence in DSM‐IV combined type attention‐deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention‐deficit/hyperactivity disorder

Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample

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

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

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

Nicotine dependence in a prospective population-based study of adolescents: the protective role of a functional tyrosine hydroxylase polymorphism

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

No evidence that common genetic risk variation is shared between schizophrenia and autism

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

Novel Insight into the Aetiology of Autism Spectrum Disorder Gained by Integrating Expression Data with Genome-wide Association Statistics

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls

Overlap between ADHD and Autism – Clinical and Genetic Evidence

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

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

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants ⬇️

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Poster #112 NO EVIDENCE THAT COMMON GENETIC RISK VARIANTS ARE SHARED BETWEEN SCHIZOPHRENIA AND AUTISM

Prospects for epigenetic research within cohort studies of psychological disorder: a pilot investigation of a peripheral cell marker of epigenetic risk for depression.

Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.

S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations

Sex differences in gene expression in the human fetal brain

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

The Genetic Architecture of Autism and Related Conditions