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Paper Details

Copy number variations and cognitive phenotypes in unselected populations.
JAMA
118
2015
250 kb) deletion, CNVs, autosomal CNVs, cognitive and psychiatric problems, congenital malformations, copy number variations, epilepsy, genetic sequence, genomic disorders, intellectual disability, intermediate, neuropathies, obesity, participants
Author NameAffiliation
Reedik MägiUniversity of Tartu
Helene AlavereUniversity of Tartu
Evelin MihailovUniversity of Tartu
Alexander TeumerInstitute for Community Medicine, University Medicine Greifswald
Erika SalviUniversity of Milan
Daniele CusiUniversity of Milan, Italy12Institute of Biomedical Technologies, Italian National Research Council
Daniele CusiUniversity of Milan, Italy12Institute of Biomedical Technologies, Italian National Research Council
Matt McGueUniversity of Minnesota
William G IaconoUniversity of Minnesota
Jacques S Beckmann
Jacques S Beckmann
Zolt??n KutalikUniversity of Lausanne, Switzerland14Institute of Social and Preventive Medicine, Lausanne University Hospital (CHUV)
Zolt??n KutalikUniversity of Lausanne, Switzerland14Institute of Social and Preventive Medicine, Lausanne University Hospital (CHUV)
Nathan PankratzUniversity of Minnesota Medical School
Nathan PankratzUniversity of Minnesota Medical School
Nicholas J TimpsonUniversity of Bristol
Andres MetspaluUniversity of Tartu, Tartu9Institute of Molecular and Cell Biology
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne
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