Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
By C. Marshall, D. Howrigan, Daniele Merico, B. Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, D. Antaki, A. Shetty, P. Holmans, D. Pinto and 253 more. Nature Genetics, 2016
996 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/e83f0cf7766e4642baff49bdaa3c424796ab3802
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Citations in the corpus
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018, neutral): “…rare, moderate to highly penetrant copy-number variants (CNVs) and de novo CNVs are seen in SCZ patients (Gulsuner and McClellan, 2015; Kirov et al., 2012; Marshall et al., 2017; Stone et al., 2008; Szatkiewicz et al., 2014), while the involvement of CNVs in BD is less clear (Green et al., 2016).”
- Psychiatric Genomics: An Update and an Agenda (2017, positive): “Figure 2B shows significant results fromGWAS, copy number variation (CNV), and exome sequencing studies (15, 36, 37).”
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022, neutral): “Missense, MPC 2–3 (10) Missense, MPC > 3 (1) Missense, MPC > 3 (3)”