Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Year: 2017
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng.3863
Authors: iPSYCH-Broad Autism Group, Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm, Thomas Werge, David M Hougaard, Jacob Taylor, David Skuse, Bernie Devlin, Richard Anney, Stephan J Sanders, Somer Bishop, Preben Bo Mortensen, Anders D Børglum, George Davey Smith, Mark J Daly, Elise B Robinson
Institutions: Harvard University, Massachusetts General Hospital, Broad Institute, Stanley Center for Psychiatric Research, Stiftung Charité, Charité – Universitätsmedizin Berlin, Aarhus University, Lundbeck Foundation, Vrije Universiteit Amsterdam, Statens Serum Institut, University of Copenhagen, Mental Health Services, Brigham and Women's Hospital, University College London, University of Pittsburgh, Cardiff University, University of California, San Francisco, University of Bristol, MRC Integrative Epidemiology Unit
Language: English
Subfield: Cognitive Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
Funders: Brain and Behavior Research Foundation, Brain Research Foundation, Simons Foundation, National Alliance for Research on Schizophrenia and Depression, Broad Institute, Simons Foundation Autism Research Initiative, Lundbeckfonden, H. Lundbeck A/S, National Institutes of Health, Stanley Center for Psychiatric Research, Broad Institute, Medical Research Council, National Institute of Mental Health, National Institute of Environmental Health Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development, H2020 European Research Council
Awards: 2/7 Psychiatric Genomics Consortium: Finding Actionable Variation, 5/7 Psychiatric Genomics Consortium: Finding actionable variation, The Intellectual and Developmental Disabilities Research Center at CHOP/Penn, G2013484569, 2/3 Sequencing Autism Spectrum Disorder Extended Pedigrees, G214445032, G2223139287, The genomic bridge project (GBP), Neuroimaging genetics to study social cognitive deficits in ASD and schizophrenia, Autism Genetics Phase II: Increasing Representation of Human Diversity, G5075569525, MRC Centre for Neuropsychiatric Genetics and Genomics, The molecular genetic architecture of educational attainment and its significance for cognitive health, G6113921874, G6142233662, G7509807454, G76570769, G8147495229, 2/4-Psychiatric GWAS Consortium: Genomic Follow-Up Next-Gen Sequencing & Genotypi, G8799334662, Center of Excellence in Environmental Toxicology, G914259863
OpenAlex ID: W2616744713