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Paper Details

Characterization of Single Gene Copy Number Variants in Schizophrenia.
Biol Psychiatry
10
2020
CNV, CNVs, ExomeDepth, Schizophrenia, Single Gene Copy Number Variants, calcium, copy number variants, gene, gene sets, rare CNVs, risk loci, schizophrenia, single-gene CNVs, single-gene deletions, voltage-gated calcium channels
Author NameAffiliation
Jin P SzatkiewiczCenter for Psychiatric Genomics, University of North Carolina
Jin P SzatkiewiczCenter for Psychiatric Genomics, University of North Carolina
Menachem FromerIcahn School of Medicine at Mount Sinai
Randal J NonnemanCenter for Psychiatric Genomics, University of North Carolina
Jessica S JohnsonIcahn School of Medicine at Mount Sinai
Eli A StahlIcahn School of Medicine at Mount Sinai
Sarah E BergenKarolinska Institutet
Christina M HultmanKarolinska Institutet
Christina M HultmanKarolinska Institutet
George KirovMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Michael C O'DonovanMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Michael J OwenMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Peter HolmansMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University
Pamela SklarIcahn School of Medicine at Mount Sinai
Patrick F SullivanCenter for Psychiatric Genomics, University of North Carolina, Karolinska Institutet
Patrick F SullivanCenter for Psychiatric Genomics, University of North Carolina, Karolinska Institutet
Shaun PurcellBrigham and Women's Hospital, Harvard Medical School
Shaun PurcellBrigham and Women's Hospital, Harvard Medical School
James J CrowleyCenter for Psychiatric Genomics, University of North Carolina, Karolinska Institutet
Douglas M RuderferVanderbilt Genetics Institute, Vanderbilt University Medical Center
Douglas M RuderferVanderbilt Genetics Institute, Vanderbilt University Medical Center
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