Article
Copy number variations and cognitive phenotypes in unselected populations.
JAMA - 26 May 2015
Männik Katrin, Mägi Reedik, Macé Aurélien, Cole Ben, Guyatt Anna L, Shihab Hashem A, Maillard Anne M, Alavere Helene, Kolk Anneli, Reigo Anu, Mihailov Evelin, Leitsalu Liis, Ferreira Anne-Maud, Nõukas Margit, Teumer Alexander, Salvi Erika, Cusi Daniele, McGue Matt, Iacono William G, Gaunt Tom R, Beckmann Jacques S, Jacquemont Sébastien, Kutalik Zoltán, Pankratz Nathan, Timpson Nicholas, Metspalu Andres, Reymond Alexandre
Abstract excerpt
IMPORTANCE: The association of copy number variations (CNVs), differing numbers of copies of genetic sequence at locations in the genome, with phenotypes such as intellectual disability has been almost exclusively evaluated using clinically ascertained cohorts. The contribution of these genetic variants to cognitive phenotypes in the general population remains unclear. OBJECTIVE: To investigate the clinical...
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