CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Human Molecular Genetics

Volumn 23, Issue 6, 2014, Pages 1669-1676

  Rees, Elliott ^a   Walters, James T R ^a   Chambert, Kimberly D ^b   O'Dushlaine, Colm ^b   Szatkiewicz, Jin ^c   Richards, Alexander L ^a   Georgieva, Lyudmila ^a   Mahoney Davies, Gerwyn ^a   Legge, Sophie E ^a   Moran, Jennifer L ^b   Genovese, Giulio ^b   Levinson, Douglas ^d   Morris, Derek W ^e   Cormican, Paul ^e   Kendler, Kenneth S ^f   O'neill, Francis A ^g   Riley, Brien ^f   Gill, Michael ^e   Corvin, Aiden ^e   Sklar, Pamela ^h   Hultman, Christina ⁱ   Pato, Carlos ^j   Pato, Michele ^j   Sullivan, Patrick F ^c,i   Gejman, Pablo V ^k,l   Mccarroll, Steven A ^b   O'donovan, Michael C ^a   Owen, Michael J ^a   Kirov, George ^a   more..

^a CARDIFF UNIVERSITY   (United Kingdom)

^b BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^d STANFORD UNIVERSITY   (United States)

^e TRINITY COLLEGE DUBLIN   (Ireland)

^f VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^g QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^h MOUNT SINAI SCHOOL OF MEDICINE   (United States)

ⁱ KAROLINSKA INSTITUTE   (Sweden)

^j UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^k NORTHSHORE UNIVERSITY HEALTHSYSTEM   (United States)

^l UNIVERSITY OF CHICAGO   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CINGULIN LIKE 1 PROTEIN; EXCITATORY AMINO ACID TRANSPORTER 3; PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CHROMOSOME 16P; CHROMOSOME 1P; CONTROL; CONTROLLED STUDY; COPY NUMBER VARIATION; DSM-IV; EXON; FEMALE; GENE DELETION; GENE DUPLICATION; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENETIC ANALYSIS; GENETIC RISK; HERITABILITY; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; PRIORITY JOURNAL; SCHIZOPHRENIA; VERY ELDERLY; YOUNG ADULT;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 16; CYTOSKELETAL PROTEINS; DNA COPY NUMBER VARIATIONS; EXCITATORY AMINO ACID TRANSPORTER 3; FEMALE; GENE DELETION; GENE DOSAGE; GENE DUPLICATION; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; MALE; SCHIZOPHRENIA;

EID: 84894375557     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt540     Document Type: Article

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