Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics

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Veröffentlicht in:	Molecular psychiatry 2013-07, Vol.18 (7), p.739-739
Hauptverfasser:	Nho, K, Corneveaux, J J, Kim, S, Lin, H, Risacher, S L, Shen, L, Swaminathan, S, Ramanan, V K, Liu, Y, Foroud, T, Inlow, M H, Siniard, A L, Reiman, R A, Aisen, P S, Petersen, R C, Green, R C, Jack, C R, Weiner, M W, Baldwin, C T, Lunetta, K, Farrer, L A, Furney, S J, Lovestone, S, Simmons, A, Mecocci, P, Vellas, B, Tsolaki, M, Kloszewska, I, Soininen, H, McDonald, B C, Farlow, M R, Ghetti, B, Huentelman, M J, Saykin, A J
Format:	Artikel
Sprache:	eng
Schlagworte:	631/208/514/1948 631/208/726/649 692/700/1421/65 Atrophy - pathology Behavioral Sciences Biological Psychology Cognitive Dysfunction - genetics Cognitive Dysfunction - pathology Exome - genetics Exome sequencing Genetic variation Genome-Wide Association Study Hippocampus - pathology Humans Identification and classification Medicine Medicine & Public Health Methods Neurogenetics Neuroimaging Neurosciences Pharmacotherapy Psychiatry
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