Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms

Molecular Psychiatry

Volumn 14, Issue 8, 2009, Pages 786-795

  Holmans, P A ^a   Riley, B ^b   Pulver, A E ^c   Owen, M J ^a   Wildenauer, D B ^d,e   Gejman, P V ^f   Mowry, B J ^g   Laurent, C ^h   Kendler, K S ^b   Nestadt, G ^c   Williams, N M ^a   Schwab, S G ^d,i,j   Sanders, A R ^f   Nertney, D ^g   Mallet, J ^k   Wormley, B ^b   Lasseter, V K ^c   O'Donovan, M C ^a   Duan, J ^f   Albus, M ^l   Alexander, M ^m   Godard, S ⁿ   Ribble, R ^b   Liang, K Y ^o   Norton, N ^a   Maier, W ^a   Papadimitriou, G ^p   Walsh, D ^q   Jay, M ^h   O'Neill, A ^r   Lerer, F B ^s   Dikeos, D ^p   Crowe, R R ^t   Silverman, J M ^u   Levinson, D F ^m   more..

^a CARDIFF UNIVERSITY   (United Kingdom)

^b VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^e GRAYLANDS HOSPITAL   (Australia)

^f NORTHWESTERN UNIVERSITY   (United States)

^g UNIVERSITY OF QUEENSLAND   (Australia)

^h SORBONNE UNIVERSITÉ   (France)

ⁱ UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^j UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^k CNRS   (France)

^l KLINIKUM MÜNCHEN OST   (Germany)

^m STANFORD UNIVERSITY   (United States)

ⁿ PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^o JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^p UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

^q HEALTH RESEARCH BOARD   (Ireland)

^r QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^s HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^t UNIVERSITY OF IOWA   (United States)

^u MOUNT SINAI SCHOOL OF MEDICINE   (United States)

more..

Author keywords

Genetic predisposition to disease; Genetics; Genome; Genotype; Human; Humans; Linkage (genetics); Schizophrenia

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 10P; CHROMOSOME 12Q; CHROMOSOME 22Q; CHROMOSOME 8P; CHROMOSOME 8Q; CHROMOSOME 9Q; CONTROLLED STUDY; EUROPE; FAMILIAL DISEASE; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC MARKER; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; NRG1 GENE; PEDIGREE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOMES, HUMAN; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HUMANS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 67651177454     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2009.11     Document Type: Article

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