Both rare and common genetic variants contribute to autism in the Faroe Islands

A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability

(2018) Theron A. Russell et al.   BIOLOGICAL PSYCHIATRY

The Heritability of Autism Spectrum Disorder

(2017) Sven Sandin et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

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

(2017) Daniel J Weiner et al.   NATURE GENETICS

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

(2017) Ryan K C Yuen et al.   NATURE NEUROSCIENCE

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

(2017)   Molecular Autism

Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications

(2017) Louisa Kalsner et al.   Molecular Genetics & Genomic Medicine

Whole-exome sequencing implicatesDGKHas a risk gene for panic disorder in the Faroese population

(2016) Noomi O. Gregersen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

GEMINI: a computationally-efficient search engine for large gene expression datasets

(2016) Timothy DeFreitas et al.   BMC BIOINFORMATICS

Spectrum of PEX1 and PEX6 variants in Heimler syndrome

(2016) Claire E L Smith et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Analysis of protein-coding genetic variation in 60,706 humans

(2016) Monkol Lek et al.   NATURE

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

(2015) Stephan J. Sanders et al.   NEURON

The intellectual disability gene Kirrel3 regulates target-specific mossy fiber synapse development in the hippocampus

(2015) E Anne Martin et al.   eLife

Autism Characteristics and Behavioural Disturbances in ∼ 500 Children with Down's Syndrome in England and Wales

(2014) Georgina Warner et al.   Autism Research

PRSice: Polygenic Risk Score software

(2014) Jack Euesden et al.   BIOINFORMATICS

Inbreeding Coefficient Estimation with Dense SNP Data: Comparison of Strategies and Application to HapMap III

(2014) Steven Gazal et al.   HUMAN HEREDITY

High inbreeding in the Faroe Islands does not appear to constitute a risk factor for multiple sclerosis

(2014) S Binzer et al.   Multiple Sclerosis Journal

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

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

RIM3  and RIM4  Are Key Regulators of Neuronal Arborization

(2013) E. Alvarez-Baron et al.   JOURNAL OF NEUROSCIENCE

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

(2013) Brett S Abrahams et al.   Molecular Autism

cPLA2α knockout mice exhibit abnormalities in the architecture and synapses of cortical neurons

(2012) Bao-Xi Qu et al.   BRAIN RESEARCH

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

(2012) Benjamin M. Neale et al.   NATURE

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

(2009) R. A. Kumar et al.   JOURNAL OF MEDICAL GENETICS

Runs of Homozygosity in European Populations

(2008) Ruth McQuillan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe Islands

(2008) T D. Hjortshoj et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry

(2008) E. M. Morrow et al.   SCIENCE