Whole genome sequencing in psychiatric disorders: the WGSPD consortium
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Whole genome sequencing in psychiatric disorders: the WGSPD consortium
Authors
Keywords
-
Journal
NATURE NEUROSCIENCE
Volume 20, Issue 12, Pages 1661-1668
Publisher
Springer Nature
Online
2017-11-09
DOI
10.1038/s41593-017-0017-9
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
- (2017) Jack A Kosmicki et al. NATURE GENETICS
- The impact of structural variation on human gene expression
- (2017) Colby Chiang et al. NATURE GENETICS
- 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
- Frequency and Complexity of De Novo Structural Mutation in Autism
- (2016) William M. Brandler et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
- (2016) Virpi M. Leppa et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder
- (2016) James J.H. Rucker et al. BIOLOGICAL PSYCHIATRY
- Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior
- (2016) Ryan N. Doan et al. CELL
- Schizophrenia
- (2016) Michael J Owen et al. LANCET
- Chromosome conformation elucidates regulatory relationships in developing human brain
- (2016) Hyejung Won et al. NATURE
- Schizophrenia risk from complex variation of complement component 4
- (2016) Aswin Sekar et al. NATURE
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- A diamond in the ruff
- (2016) NATURE GENETICS
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
- (2016) Christian R Marshall et al. NATURE GENETICS
- Advancing the understanding of autism disease mechanisms through genetics
- (2016) Luis de la Torre-Ubieta et al. NATURE MEDICINE
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
- (2016) Tarjinder Singh et al. NATURE NEUROSCIENCE
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
- (2016) Andrea Ganna et al. NATURE NEUROSCIENCE
- Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
- (2016) Giulio Genovese et al. NATURE NEUROSCIENCE
- Genetic Background Limits Generalizability of Genotype-Phenotype Relationships
- (2016) Laura J. Sittig et al. NEURON
- The Human Phenotype Ontology in 2017
- (2016) Sebastian Köhler et al. NUCLEIC ACIDS RESEARCH
- Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
- (2016) Frederick E. Dewey et al. SCIENCE
- Rett Syndrome: Crossing the Threshold to Clinical Translation
- (2016) David M. Katz et al. TRENDS IN NEUROSCIENCES
- Loss of UBE3A from TH-expressing neurons suppresses GABA co-release and enhances VTA-NAc optical self-stimulation
- (2016) Janet Berrios et al. Nature Communications
- Convergence of Advances in Genomics, Team Science, and Repositories as Drivers of Progress in Psychiatric Genomics
- (2015) Thomas Lehner et al. BIOLOGICAL PSYCHIATRY
- 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
- First glimpses of the neurobiology of autism spectrum disorder
- (2015) Stephan J Sanders CURRENT OPINION IN GENETICS & DEVELOPMENT
- Mutations in the noncoding genome
- (2015) Cheryl A. Scacheri et al. CURRENT OPINION IN PEDIATRICS
- The pluripotent regulatory circuitry connecting promoters to their long-range interacting elements
- (2015) Stefan Schoenfelder et al. GENOME RESEARCH
- Copy number variation in bipolar disorder
- (2015) E K Green et al. MOLECULAR PSYCHIATRY
- Integrative analysis of 111 reference human epigenomes
- (2015) Anshul Kundaje et al. NATURE
- Large-scale whole-genome sequencing of the Icelandic population
- (2015) Daniel F Gudbjartsson et al. NATURE GENETICS
- The PsychENCODE project
- (2015) Schahram Akbarian et al. NATURE NEUROSCIENCE
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
- (2015) Stephan J. Sanders et al. NEURON
- Hi-C Chromatin Interaction Networks Predict Co-expression in the Mouse Cortex
- (2015) Sepideh Babaei et al. PLoS Computational Biology
- A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
- (2014) Suhas S.P. Rao et al. CELL
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- The contribution of de novo coding mutations to autism spectrum disorder
- (2014) Ivan Iossifov et al. NATURE
- A framework for the interpretation of de novo mutation in human disease
- (2014) Kaitlin E Samocha et al. NATURE GENETICS
- Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci
- (2014) Susan K. Service et al. PLoS Genetics
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
- (2014) Elaine T. Lim et al. PLoS Genetics
- Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism
- (2013) Ece D. Gamsiz et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A High-Resolution Enhancer Atlas of the Developing Telencephalon
- (2013) Axel Visel et al. CELL
- Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
- (2013) A. Jeremy Willsey et al. CELL
- CNVs conferring risk of autism or schizophrenia affect cognition in controls
- (2013) Hreinn Stefansson et al. NATURE
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
- (2013) S Hong Lee et al. NATURE GENETICS
- Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
- (2013) Georg Stoll et al. NATURE NEUROSCIENCE
- Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders
- (2013) Elaine T. Lim et al. NEURON
- Using Whole-Exome Sequencing to Identify Inherited Causes of Autism
- (2013) Timothy W. Yu et al. NEURON
- Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq
- (2013) C. D. Arnold et al. SCIENCE
- Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
- (2013) Slavé Petrovski et al. PLoS Genetics
- The long-range interaction landscape of gene promoters
- (2012) Amartya Sanyal et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders
- (2012) Joseph D. Buxbaum et al. NEURON
- Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy
- (2012) G. Novarino et al. SCIENCE
- Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
- (2012) M. T. Maurano et al. SCIENCE
- Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings
- (2012) Robert A. Power et al. JAMA Psychiatry
- Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD
- (2011) Aude Saint-Pierre et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
- (2011) NATURE GENETICS
- Research Domain Criteria (RDoC): Toward a New Classification Framework for Research on Mental Disorders
- (2010) Thomas Insel et al. AMERICAN JOURNAL OF PSYCHIATRY
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors
- (2010) Gerald D. Fischbach et al. NEURON
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started