A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing

Molecular Psychiatry

Volumn 19, Issue 8, 2014, Pages 857-858

  Hu, X ^a,d   Zhang, B ^a   Liu, W ^a   Paciga, S ^a   He, W ^a   Lanz, T A ^a   Kleiman, R ^a,e   Dougherty, B ^a   Hall, S K ^a   Mcintosh, A M ^b   Lawrie, S M ^b   Power, A ^a   John, S L ^a   Blackwood, D ^b   St Clair, D ^c   Brandon, N J ^a,f  

^a PFIZER INC   (United States)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c UNIVERSITY OF ABERDEEN   (United Kingdom)

^d BRISTOL MYERS SQUIBB   (United States)

^e Selventa   (United States)

^f ASTRAZENECA   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIC NUCLEOTIDE PHOSPHODIESTERASE;

COPY NUMBER VARIATION; DSM-IV; EXOME; GENETIC ASSOCIATION; GENETIC CODE; GENETIC VARIABILITY; GENOTYPING TECHNIQUE; HUMAN; LETTER; MAJOR HISTOCOMPATIBILITY COMPLEX; PRIORITY JOURNAL; SCHIZOPHRENIA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; ADOLESCENT; CASE CONTROL STUDY; DNA SEQUENCE; FEMALE; GENETICS; HIGH THROUGHPUT SEQUENCING; MALE; ONSET AGE; UNITED KINGDOM; UNITED STATES; ADULT; CONTROLLED STUDY; GENE FREQUENCY; GENE SEQUENCE; MAJOR CLINICAL STUDY; STOP CODON;

ADOLESCENT; AGE OF ONSET; CASE-CONTROL STUDIES; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC VARIATION; GREAT BRITAIN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; SCHIZOPHRENIA; SEQUENCE ANALYSIS, DNA; UNITED STATES;

EID: 84905055115     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2013.131     Document Type: Letter

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