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...

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Vydané v:	JAMA : the journal of the American Medical Association Ročník 313; číslo 20; s. 2044
Hlavní autori:	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
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States 26.05.2015
Predmet:	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
On-line prístup:	Zistit podrobnosti o prístupe
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