Lack of replication of previous autism spectrum disorder GWAS hits in European populations

Analysis ofCHRNA7rare variants in autism spectrum disorder susceptibility

(2015) Elena Bacchelli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

(2015) Anne-Laure Mosca-Boidron et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

(2015) Bàrbara Torrico et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

(2015) Jinchen Li et al.   MOLECULAR PSYCHIATRY

Excess of rare, inherited truncating mutations in autism

(2015) Niklas Krumm et al.   NATURE GENETICS

From the genetic architecture to synaptic plasticity in autism spectrum disorder

(2015) Thomas Bourgeron   NATURE REVIEWS NEUROSCIENCE

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

(2015) Emma Colvert et al.   JAMA Psychiatry

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10

(2015) Lina Jonsson et al.   Molecular Autism

minimac2: faster genotype imputation

(2014) Christian Fuchsberger et al.   BIOINFORMATICS

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

(2014) Regina Waltes et al.   HUMAN GENETICS

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

Biological insights from 108 schizophrenia-associated genetic loci

(2014)   NATURE

Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations

(2014) Tong Xie et al.   NEUROBIOLOGY OF AGING

Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder

(2014) Cristina Sánchez-Mora et al.   NEUROPSYCHOPHARMACOLOGY

MACROD2 gene associated with autistic-like traits in a general population sample

(2014) Rachel M. Jones et al.   PSYCHIATRIC GENETICS

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk

(2013) Ye Cheng et al.   HUMAN MOLECULAR GENETICS

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

(2013) C Toma et al.   MOLECULAR PSYCHIATRY

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

(2013) S Hong Lee et al.   NATURE GENETICS

Genome-wide Association Study Identifies Candidate Genes for Male Fertility Traits in Humans

(2012) Gülüm Kosova et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Global Prevalence of Autism and Other Pervasive Developmental Disorders

(2012) Mayada Elsabbagh et al.   Autism Research

Genetic architecture in autism spectrum disorder

(2012) Bernie Devlin et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Evaluating the Evidence for Transmission Distortion in Human Pedigrees

(2012) W. K. Meyer et al.   GENETICS

The co-occurrence of autism spectrum disorder and attention-deficit/hyperactivity disorder symptoms in parents of children with ASD or ASD with ADHD

(2012) Daphne J. van Steijn et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Patterns and rates of exonic de novo mutations in autism spectrum disorders

(2012) Benjamin M. Neale et al.   NATURE

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

(2012) Stephan J. Sanders et al.   NATURE

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

(2012) Anna Köttgen et al.   NATURE GENETICS

Genetic architectures of psychiatric disorders: the emerging picture and its implications

(2012) Patrick F. Sullivan et al.   NATURE REVIEWS GENETICS

Novel Genetic Loci Identified for the Pathophysiology of Childhood Obesity in the Hispanic Population

(2012) Anthony G. Comuzzie et al.   PLoS One

The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families

(2012) Paola Prandini et al.   PSYCHIATRIC GENETICS

A Noncoding RNA Antisense to Moesin at 5p14.1 in Autism

(2012) T. Kerin et al.   Science Translational Medicine

Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC

(2012) Claudio Toma et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

Common genetic variants, acting additively, are a major source of risk for autism

(2012) Lambertus Klei et al.   Molecular Autism

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

(2011) Sarah Curran et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Two-marker association tests yield new disease associations for coronary artery disease and hypertension

(2011) Thomas P. Slavin et al.   HUMAN GENETICS

Genome-wide association study identifies five new schizophrenia loci

(2011)   NATURE GENETICS

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

(2011) A. C. Lionel et al.   Science Translational Medicine

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

(2011) John P Hussman et al.   Molecular Autism

Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population

(2010) Beate St. Pourcain et al.   AMERICAN JOURNAL OF PSYCHIATRY

Variants in several genomic regions associated with asperger disorder

(2010) D. Salyakina et al.   Autism Research

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

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

Hotspots of Large Rare Deletions in the Human Genome

(2010) W. Edward C. Bradley et al.   PLoS One

Genetics in psychiatry: common variant association studies

(2010) Joseph D Buxbaum et al.   Molecular Autism

A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

(2009) Deqiong Ma et al.   ANNALS OF HUMAN GENETICS

Common body mass index-associated variants confer risk of extreme obesity

(2009) Chris Cotsapas et al.   HUMAN MOLECULAR GENETICS

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Epidemiology of Pervasive Developmental Disorders

(2009) Eric Fombonne   PEDIATRIC RESEARCH

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

(2009) B. Xu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics