Copy number variations and cognitive phenotypes in unselected populations

IMPORTANCE: The association of rare copy number variants (CNVs) with complex disorders is almost exclusively evaluated using clinically ascertained cohorts. As a result, the contribution of these genetic variants to cognitive phenotypes in the general population remains unclear. OBJECTIVES: - To inv...

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Publicado no:JAMA
Main Authors: Männik, Katrin, Mägi, Reedik, Macé, Aurélien, Cole, Ben, Guyatt, Anna, 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4684269/
https://ncbi.nlm.nih.gov/pubmed/26010633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jama.2015.4845
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