No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

European Journal of Human Genetics

Volumn 23, Issue 4, 2015, Pages 555-557

  Ruderfer, Douglas M ^a,b   Lim, Elaine T ^c   Genovese, Giulio ^b   Moran, Jennifer L ^b   Hultman, Christina M ^d   Sullivan, Patrick F ^e   McCarroll, Steven A ^b,f   Holmans, Peter ^g   Sklar, Pamela ^a   Purcell, Shaun M ^a,b,c  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

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

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d KAROLINSKA INSTITUTE   (Sweden)

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

^f HARVARD MEDICAL SCHOOL   (United States)

^g CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; CASE CONTROL STUDY; CONTROLLED STUDY; EXOME; FEMALE; GENE FREQUENCY; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; X CHROMOSOME; ALLELE; CAUCASIAN; DNA SEQUENCE; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; HETEROZYGOTE; HOMOZYGOTE; POPULATION GENETICS; STATISTICAL MODEL; SWEDEN;

ALLELES; CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXOME; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; HETEROZYGOTE; HOMOZYGOTE; HUMANS; LOGISTIC MODELS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; SEQUENCE ANALYSIS, DNA; SWEDEN;

EID: 84924652200     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2014.228     Document Type: Article

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