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Paper Details

The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders.
Mol Psychiatry
8
2022
CNVs, CYP2D6, CYP2D6 genotype, Participants, SNVs, Schizophrenia, copy number variants, gene sets, indels, participants, psychosis, psychotic disorders, schizoaffective disorder, schizophrenia, single nucleotide variants
Author NameAffiliation
Anna R DochertyUniversity of Utah School of Medicine
Andrey A ShabalinUniversity of Utah School of Medicine
Gundula PovysilInstitute for Genomic Medicine, Columbia University Medical Center
Erin L HeinzenEshelman School of Pharmacy, University of North Carolina at Chapel Hill
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
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Release 1.2