Genetics of early-onset obsessive-compulsive disorder

European Child and Adolescent Psychiatry

Volumn 19, Issue 3, 2010, Pages 227-235

  Walitza, Susanne ^a   Wendland, Jens R ^b   Gruenblatt, Edna ^a   Warnke, Andreas ^c   Sontag, Thomas A ^d   Tucha, Oliver ^e   Lange, Klaus W ^d  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^c UNIVERSITY OF WÜRZBURG   (Germany)

^d UNIVERSITY OF REGENSBURG   (Germany)

^e UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

Brain derived neurotrophic factor; Early onset; Glutamate transporter gene; Obsessive compulsive disorder; Serotonin

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; CATECHOL METHYLTRANSFERASE; DOPAMINE 4 RECEPTOR; EXCITATORY AMINO ACID TRANSPORTER 3; NEUROTRANSMITTER; SEROTONIN 2A RECEPTOR; SEROTONIN RECEPTOR; SEROTONIN TRANSPORTER; TRYPTOPHAN HYDROXYLASE 2;

BEHAVIOR GENETICS; CHROMOSOME 9P; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DOPAMINERGIC SYSTEM; FAMILIAL DISEASE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOTYPE ENVIRONMENT INTERACTION; HUMAN; MOLECULAR GENETICS; OBSESSIVE COMPULSIVE DISORDER; ONSET AGE; PROMOTER REGION; REVIEW; SEROTONINERGIC SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; THOUGHT DISORDER; TWIN ZYGOSITY; VARIABLE NUMBER OF TANDEM REPEAT;

ADOLESCENT; CHILD; CHROMOSOME MAPPING; DISEASES IN TWINS; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; OBSESSIVE-COMPULSIVE DISORDER; PHENOTYPE;

EID: 77950860590     PISSN: 10188827     EISSN: 1435165X     Source Type: Journal    
DOI: 10.1007/s00787-010-0087-7     Document Type: Review

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