Erratum: Department of Error(S0140673612621291)(10.1016/S0140-6736(12)62129-1);Identification of risk loci with shared effects on five major psychiatric disorders: A genome-wide analysis

The Lancet

Volumn 381, Issue 9875, 2013, Pages 1371-1379

  Smoller, Jordan W ^a   Kendler, Kenneth K ^b   Craddock, Nicholas ^b   Lee, Phil Hyoun ^b   Neale, Benjamin M ^b   Nurnberger, John N ^b   Ripke, Stephan ^b   Santangelo, Susan ^b   Sullivan, Patrick S ^b   Neale, Benjamin N ^b   Purcell, Shaun ^b   Anney, Richard ^b   Buitelaar, Jan ^b   Fanous, Ayman ^b   Faraone, Stephen F ^b   Hoogendijk, Witte ^b   Lesch, Klaus Peter ^b   Levinson, Douglas L ^b   Perlis, Roy P ^b   Rietschel, Marcella ^b   Riley, Brien ^b   Sonuga Barke, Edmund ^b   Schachar, Russell ^b   Schulze, Thomas G ^b   Thapar, Anita ^b   Smoller, Jordan S ^b   Neale, Michael ^b   Perlis, Roy ^b   Bender, Patrick ^b   Cichon, Sven ^b   Daly, Mark D ^b   Kelsoe, John ^b   Lehner, Thomas ^b   Levinson, Douglas ^b   O'Donovan, Mick ^b   Gejman, Pablo ^b   Sebat, Jonathan ^b   Sklar, Pamela ^b   Devlin, Bernie ^b   Sullivan, Patrick ^b   O'Donovan, Michael ^b   more..

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL L TYPE; CACNA1C PROTEIN, HUMAN; CACNB2 PROTEIN, HUMAN;

ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; AUTOPSY; BIPOLAR DISORDER; BRAIN TISSUE; CALCIUM SIGNALING; CHROMOSOME 10Q; CHROMOSOME 3P; CONTROLLED STUDY; DIAGNOSTIC TEST ACCURACY STUDY; EUROPE; GENE EXPRESSION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; MENTAL PATIENT; ONSET AGE; PLEIOTROPY; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; RISK ASSESSMENT; SCHIZOPHRENIA; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; ADULT; CHILD; GENETICS; STATISTICAL MODEL;

ADULT; AGE OF ONSET; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; BIPOLAR DISORDER; CALCIUM CHANNELS, L-TYPE; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; DEPRESSIVE DISORDER, MAJOR; GENETIC LOCI; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LOGISTIC MODELS; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 84876296688     PISSN: 01406736     EISSN: 1474547X     Source Type: Journal    
DOI: 10.1016/S0140-6736(13)60886-7     Document Type: Erratum

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