- Title
- Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2
- Creators
- Pauline Chaste - Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PennsylvaniaStephan J Sanders - Department of Genetics, Yale University School of Medicine, New Haven, ConnecticutKommu N Mohan - Department of Biological Sciences, BITS Pilani-Hyderabad Campus, Hyderabad, IndiaLambertus Klei - Department of Psychiatry, University of Pittsburgh School of Medicine, Pennsylvania, PittsburghYoueun Song - Department of Psychiatry, University of Pittsburgh School of Medicine, Pennsylvania, PittsburghMichael T Murtha - Program on Neurogenetics, Yale University School of Medicine, Connecticut, New HavenVanessa Hus - Department of Psychology, University of Michigan, Michigan, Ann ArborJennifer K Lowe - Neurogenetics Program, Department of Neurology and Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California, California, Los AngelesA. Jeremy Willsey - Department of Genetics, Yale University School of Medicine, New Haven, ConnecticutDaniel Moreno-De-Luca - Program on Neurogenetics, Yale University School of Medicine, New Haven, ConnecticutTimothy W Yu - Division of Genetics, Children's Hospital Boston, Harvard Medical School, Massachusetts, BostonEric Fombonne - Department of Psychiatry, Oregon Health & Science University, Oregon, PortlandDaniel Geschwind - Neurogenetics Program, Department of Neurology and Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California, California, Los AngelesDorothy E Grice - Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New YorkDavid H Ledbetter - Autism and Developmental Medicine Institute, Geisinger Health System, Pennsylvania, DanvilleCatherine Lord - Center for Autism and the Developing Brain, Weill Cornell Medical College, New York, White PlainsShrikant M Mane - Yale Center for Genome Analysis, Yale University, Connecticut, OrangeDonna M Martin - Departments of Pediatrics and Human Genetics, University of Michigan Medical Center, Michigan, Ann ArborEric M Morrow - Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode IslandChristopher A Walsh - Howard Hughes Medical Institute and Division of Genetics, Children's Hospital Boston, and Neurology and Pediatrics, Center for Life Sciences, Harvard Medical School, Massachusetts, BostonJames S Sutcliffe - Departments of Molecular Physiology & Biophysics and Psychiatry, Vanderbilt Brain Institute, Vanderbilt University, Tennessee, NashvilleMatthew W State - Department of Genetics, Yale University School of Medicine, New Haven, ConnecticutChrista Lese Martin - Autism and Developmental Medicine Institute, Geisinger Health System, Pennsylvania, DanvilleBernie Devlin - Department of Psychiatry, University of Pittsburgh School of Medicine, Pennsylvania, PittsburghArthur L Beaudet - Department of Human and Molecular Genetics, Baylor College of Medicine, Texas, HoustonEdwin H Cook Jr - Institute for Juvenile Research, Department of Psychiatry, University of Illinois, Illinois, ChicagoSoo-Jeong Kim - Center for Integrative Brain Research, Seattle Children's Research Institute, Department of Psychiatry and Behavioral Science, University of Washington, Washington, Seattle
- Publication Details
- Autism research, Vol.7(3), pp.355-362
- Date published
- 06/2014
- Publisher
- Blackwell Publishing Ltd
- Number of pages
- 8
- Academic Unit
- Applied Psychology (GSAPP)
- Language
- English
- Resource Type
- Journal article
- Identifiers
- 991031665478304646
Journal article
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2
Autism research, Vol.7(3), pp.355-362
06/2014
PMCID: PMC6003409
PMID: 24821083
Metrics
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