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

Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation

(2015) Richard Howey et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

(2015) Pauline Chaste et al.   BIOLOGICAL PSYCHIATRY

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

(2015) Stephan J. Sanders et al.   NEURON

Investigation of Maternal Genotype Effects in Autism by Genome-Wide Association

(2014) Han Yuan et al.   Autism Research

Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits

(2014) S. Connolly et al.   BRIEFINGS IN BIOINFORMATICS

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

(2014) R. Nudel et al.   GENES BRAIN AND BEHAVIOR

The Familial Risk of Autism

(2014) Sven Sandin et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

Detecting signals in pharmacogenomic genome-wide association studies

(2014) J Wakefield et al.   PHARMACOGENOMICS JOURNAL

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

(2014) Claire S. Leblond et al.   PLoS Genetics

Genomic imprinting and parent-of-origin effects on complex traits

(2013) Heather A. Lawson et al.   NATURE REVIEWS GENETICS

A Genome-Wide Survey of Transgenerational Genetic Effects in Autism

(2013) Kathryn M. Tsang et al.   PLoS One

PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling

(2012) Richard Howey et al.   BMC BIOINFORMATICS

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

(2012) Richard Anney et al.   HUMAN MOLECULAR GENETICS

Commentary: Genome-wide significance thresholds via Bayes factors

(2012) Jon Wakefield   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Autism recurrence in half siblings: strong support for genetic mechanisms of transmission in ASD

(2012) J N Constantino et al.   MOLECULAR 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

De Novo Gene Disruptions in Children on the Autistic Spectrum

(2012) Ivan Iossifov et al.   NEURON

Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype

(2012) Sylvie Tordjman et al.   PLoS One

Chapter 11: Genome-Wide Association Studies

(2012) William S. Bush et al.   PLoS Computational Biology

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

(2012) Lambertus Klei et al.   Molecular Autism

Evidence for involvement of GNB1L in autism

(2011) Ying-Zhang Chen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

(2011) Joachim Hallmayer   ARCHIVES OF GENERAL PSYCHIATRY

Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families

(2011) Raphael Bernier et al.   Autism Research

Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia

(2011) Christopher T. Johansen et al.   Circulation-Cardiovascular Genetics

Parent of origin effects

(2011) A Guilmatre et al.   CLINICAL GENETICS

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

(2011) João Peça et al.   NATURE

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring

(2010) Holly F. Ainsworth et al.   GENETIC EPIDEMIOLOGY

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

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

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

(2010) Dalila Pinto et al.   NATURE

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

(2010) Gerald D. Fischbach et al.   NEURON

Replication in Genome-Wide Association Studies

(2010) Peter Kraft et al.   STATISTICAL SCIENCE

HLA-DR4 as a Risk Allele for Autism Acting in Mothers of Probands Possibly During Pregnancy

(2009) William G. Johnson et al.   ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE

Overlap With the Autism Spectrum in Young Children With Williams Syndrome

(2009) Bonita P. Klein-Tasman et al.   JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS

Validating, augmenting and refining genome-wide association signals

(2009) John P. A. Ioannidis et al.   NATURE REVIEWS GENETICS

What are maternal effects (and what are they not)?

(2009) J. B Wolf et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES