Copy number variations and cognitive phenotypes in unselected populations

JAMA - Journal of the American Medical Association

Volumn 313, Issue 20, 2015, Pages 2044-2054

  Männik, Katrin ^a,b   Mägi, Reedik ^b   Macé, Aurélien ^b,c   Cole, Ben ^d   Guyatt, Anna L ^e   Shihab, Hashem A ^e   Maillard, Anne M ^a   Alavere, Helene ^b   Kolk, Anneli ^b,f   Reigo, Anu ^b   Mihailov, Evelin ^b   Leitsalu, Liis ^b,g   Ferreira, Anne Maud ^a,c   Nõukas, Margit ^b,g   Teumer, Alexander ^h   Salvi, Erika ⁱ   Cusi, Daniele ^i,j   McGue, Matt ^k   Iacono, William G ^k   Gaunt, Tom R ^e   Beckmann, Jacques S ^c   Jacquemont, Sebastien ^a   Kutalik, Zoltán ^a,c,l   Pankratz, Nathan ^d   Timpson, Nicholas ^e   Metspalu, Andres ^b,g   Reymond, Alexandre ^a   more..

^a UNIVERSITY OF LAUSANNE   (Switzerland)

^b UNIVERSITY OF TARTU   (Estonia)

^c SWISS INSTITUTE OF BIOINFORMATICS   (Switzerland)

^d UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF BRISTOL   (United Kingdom)

^f TARTU UNIVERSITY HOSPITAL   (Estonia)

^g UNIVERSITY OF TARTU   (Estonia)

^h UNIVERSITY MEDICINE GREIFSWALD   (Germany)

ⁱ UNIVERSITY OF MILAN   (Italy)

^j INSTITUTE OF BIOMEDICAL TECHNOLOGIES   (Italy)

^k UNIVERSITY OF MINNESOTA   (United States)

^l UNIVERSITY OF LAUSANNE   (Switzerland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; COHORT ANALYSIS; CONGENITAL MALFORMATION; COPY NUMBER VARIATION; DIAGNOSTIC TEST; EDUCATIONAL STATUS; EPILEPSY; ESTONIA; ESTONIAN (PEOPLE); FEMALE; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENERAL PRACTITIONER; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC SCREENING; GENETIC TRAIT; GENOME ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; GEOGRAPHIC DISTRIBUTION; HETEROZYGOTE; HIGH SCHOOL GRADUATE; HUMAN; HUMAN GENOME; INTELLECTUAL IMPAIRMENT; ITALY; LIFESTYLE; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; NEUROPATHY; OBESITY; PHENOTYPE; POPULATION GENETICS; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; QUESTIONNAIRE; UNITED KINGDOM; UNITED STATES; ADOLESCENT; COGNITION; GENETICS;

ADOLESCENT; ADULT; COGNITION; DNA COPY NUMBER VARIATIONS; EDUCATIONAL STATUS; EPILEPSY; ESTONIA; FEMALE; GENOME-WIDE ASSOCIATION STUDY; GREAT BRITAIN; HETEROZYGOTE; HUMANS; INTELLECTUAL DISABILITY; ITALY; MALE; MENTAL DISORDERS; OBESITY; PHENOTYPE; UNITED STATES;

EID: 84929880718     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2015.4845     Document Type: Article

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