Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.

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Title: Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Authors: Callaghan DB; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Rogic S; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Tan PPC; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Calli K; Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada., Qiao Y; Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada., Baldwin R; Department of Biological Sciences, Brock University, St. Catharines, Canada., Jacobson M; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Belmadani M; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Holmes N; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Yu C; Medical Division, BGI-Shenzhen, Shenzhen, China., Li Y; Medical Division, BGI-Shenzhen, Shenzhen, China., Li Y; Medical Division, BGI-Shenzhen, Shenzhen, China., Kurtzke FE; Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada., Kuzeljevic B; Clinical Research Support Unit, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada., Yu AY; Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada., Hudson M; Queen's Genomics Lab at Ongwanada, Ongwanada Resource Center, Kingston, Canada.; Department of Psychiatry, Queen's University, Kingston, Canada., Mcaughton AJM; Queen's Genomics Lab at Ongwanada, Ongwanada Resource Center, Kingston, Canada.; Department of Psychiatry, Queen's University, Kingston, Canada., Xu Y; Department of Biological Sciences, Brock University, St. Catharines, Canada., Dionne-Laporte A; Montreal Neurological Institute, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Quebec, Canada., Girard S; Département des sciences fondamentales, Université du Québec à Chicoutimi, Chicoutimi, Canada., Liang P; Department of Biological Sciences, Brock University, St. Catharines, Canada., Separovic ER; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada., Liu X; Queen's Genomics Lab at Ongwanada, Ongwanada Resource Center, Kingston, Canada.; Department of Psychiatry, Queen's University, Kingston, Canada., Rouleau G; Montreal Neurological Institute, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Quebec, Canada., Pavlidis P; Michael Smith Laboratories, University of British Columbia, Vancouver, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, Canada., Lewis MES; Department of Medical Genetics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada.
Source: Clinical genetics [Clin Genet] 2019 Sep; Vol. 96 (3), pp. 199-206. Date of Electronic Publication: 2019 May 30.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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Description
ISSN:1399-0004
DOI:10.1111/cge.13556