Copy number variations and cognitive phenotypes in unselected populations

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 cogn...

Full description

Saved in:

Bibliographic Details
Published in:	JAMA : the journal of the American Medical Association Vol. 313; no. 20; p. 2044
Main Authors:	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
Format:	Journal Article
Language:	English
Published:	United States 26.05.2015
Subjects:	Adolescent Adult Cognition DNA Copy Number Variations Educational Status Epilepsy - genetics Estonia Female Genome-Wide Association Study Heterozygote Humans Intellectual Disability - genetics Italy Male Mental Disorders - genetics Obesity - genetics Phenotype United Kingdom United States
ISSN:	1538-3598, 1538-3598
Online Access:	Get more information
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!