Associated Papers
Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
Birnbaum R et al.
Jama Psychiatry, 2022
Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios.
Wu X et al.
Iscience, 2021
Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank.
Caseras X et al.
The British Journal of Psychiatry : the Journal of Mental Science, 2021
32792019 (PubMed )
Supplement: S0007125020001397sup001.zip › S0007125020001397sup003.xlsx › 2a._Surface_area
Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.
Crawford K et al.
Journal of Medical Genetics, 2019
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kendall KM et al.
Biological Psychiatry, 2017
Identification of rare copy number variants in high burden schizophrenia families.
Van Den Bossche MJ et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
Copy number variants in German patients with schizophrenia.
Priebe L et al.
Plos One, 2013
Association testing of copy number variants in schizophrenia and autism spectrum disorders.
Crespi BJ et al.
Journal of Neurodevelopmental Disorders, 2012
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