Detecting Large Copy Number Variants Using Exome Genotyping Arrays In a Large Swedish Schizophrenia Sample

Although copy number variants (CNVs) are important in genomic medicine, CNVs have not been systematically assessed for many complex traits. Several large rare CNVs increase risk for schizophrenia (SCZ) and autism and often demonstrate pleiotropic effects; however, their frequencies in the general po...

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Bibliografiska uppgifter
Huvudupphovsmän: Szatkiewicz, Jin P., Neale, Benjamin M., O'Dushlaine, Colm, Fromer, Menachem, Goldstein, Jacqueline I., Moran, Jennifer L., Chambert, Kimberly, Kähler, Anna, Magnusson, Patrik KE, Hultman, Christina M., Sklar, Pamela, Purcell, Shaun, McCarroll, Steven A., Sullivan, Patrick F.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3966073/
https://ncbi.nlm.nih.gov/pubmed/23938935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2013.98
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