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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2013
Témata:
Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky