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In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

Whole genome sequencing was completed on 1,325 individuals from 602 families, identifying 27 million autosomal variants. Genetic association tests were conducted for those individuals who had been assessed for one or more of 17 endophenotypes (N range = 802–1,185). No significant associations were f...

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Τόπος έκδοσης:	Psychophysiology
Κύριοι συγγραφείς:	VRIEZE, SCOTT I., MALONE, STEPHEN M., VAIDYANATHAN, UMA, KWONG, ALAN, KANG, HYUN MIN, ZHAN, XIAOWEI, FLICKINGER, MATTHEW, IRONS, DANIEL, JUN, GOO, LOCKE, ADAM E., PISTIS, GIORGIO, PORCU, ELEONORA, LEVY, SHAWN, MYERS, RICHARD M., OETTING, WILLIAM, MCGUE, MATT, ABECASIS, GONCALO, IACONO, WILLIAM G.
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	2014
Θέματα:	Article
Διαθέσιμο Online:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4231480/ https://ncbi.nlm.nih.gov/pubmed/25387710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/psyp.12350
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In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

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