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Paper Details

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
PLoS Genet
45
2016
15q11, AS, ASD, DD, Isodicentric chromosome 15, MCA, Neurodevelopmental Disorders, PWS, Prader, Prader-Willi/Angelman syndrome, Prader-Willi/Angelman syndrome (PWS/, SZ, Schizophrenia, autism spectrum disorder, developmental delay, embryos, idic15, imprinted genes, learning, maternally, multiple congenital anomalies, paternal ones, patients, psychotic illness, schizophrenia
Author NameAffiliation
Norio OzakiNagoya University Graduate School of Medicine
Branko AleksicNagoya University Graduate School of Medicine
Douglas F LevinsonStanford University
Douglas F LevinsonStanford University
Pablo V GejmanStanford University
Jianxin ShiNational Cancer Institute, Medical Center Drive
Jianxin ShiNational Cancer Institute, Medical Center Drive
Alan R SandersNorthShore University HealthSystem, University of Chicago
Alan R SandersNorthShore University HealthSystem, University of Chicago
Jubao DuanStanford University
Jubao DuanNorthShore University HealthSystem, University of Chicago
Sanjay M SisodiyaUCL Institute of Neurology
Thomas WergeInstitute of Biological Psychiatry, Mental Health Services Copenhagen, University of Copenhagen
Franziska DegenhardtInstitute of Human Genetics, University of Bonn
Santhosh GirirajanUniversity Park
Hreinn Stefansson
Kari Stefansson
Kari Stefansson
Michael C O'DonovanCardiff University, Institute of Psychological Medicine and Clinical Neurosciences
Michael J OwenCardiff University, Institute of Psychological Medicine and Clinical Neurosciences
Anne S BassettClinical Genetics Research Program, University of Toronto
George KirovCardiff University, Institute of Psychological Medicine and Clinical Neurosciences
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