Association of Per1 and Npas2 with autistic disorder: Support for the clock genes/social timing hypothesis

Molecular Psychiatry

Volumn 12, Issue 6, 2007, Pages 581-592

  Nicholas, B ^a   Rudrasingham, V ^b   Nash, S ^a   Kirov, G ^c   Owen, M J ^b   Wimpory, D C ^a,c  

^a BANGOR UNIVERSITY   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

^c North West Wales NHS Trust   (United Kingdom)

Author keywords

Amygdala; Autistic disorder; Biological clocks; Genetics, behavioral; Memory; Sleep

Indexed keywords

PER1 PROTEIN; PROTEIN NPAS2; TRANSCRIPTION FACTOR CLOCK; UNCLASSIFIED DRUG;

AMYGDALOID NUCLEUS; ARTICLE; AUTISM; CEREBELLUM; CONTROLLED STUDY; FEMALE; GENE FUNCTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC EPISTASIS; GENETIC MARKER; HAPLOTYPE; HUMAN; HYPOTHESIS; MAJOR CLINICAL STUDY; MALE; MEMORY; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SLEEP; TIME PERCEPTION;

ADULT; AUTISTIC DISORDER; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BIOLOGICAL CLOCKS; CELL CYCLE PROTEINS; EPISTASIS, GENETIC; FEMALE; HAPLOTYPES; HUMANS; MALE; NERVE TISSUE PROTEINS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SOCIAL BEHAVIOR; TIME PERCEPTION;

EID: 34249317295     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/sj.mp.4001953     Document Type: Article

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