Association of variants in DRD2 and GRM3 with motor and cognitive function in first-episode psychosis

European Archives of Psychiatry and Clinical Neuroscience

Volumn 264, Issue 4, 2014, Pages 345-355

  Lencer, Rebekka ^a   Bishop, Jeffrey R ^b   Harris, Margret S H ^c   Reilly, James L ^d   Patel, Shitalben ^b   Kittles, Rick ^c   Prasad, Konasale M ^e   Nimgaonkar, Vishwajit L ^e,f   Keshavan, Matcheri S ^g   Sweeney, John A ^h  

^a UNIVERSITY OF MÜNSTER   (Germany)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^c UNIVERSITY OF ILLINOIS   (United States)

^d NORTHWESTERN UNIVERSITY   (United States)

^e UNIVERSITY OF PITTSBURGH   (United States)

^f UNIVERSITY OF PITTSBURGH   (United States)

^g HARVARD MEDICAL SCHOOL   (United States)

^h UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Antipsychotic treatment effects; DRD2 gene; Eye tracking dysfunction; GRM3 gene; Intermediate phenotype; Psychotic disorders; Smooth pursuit

Indexed keywords

ARIPIPRAZOLE; CHLORPROMAZINE; DOPAMINE; DOPAMINE 2 RECEPTOR; GLUTAMIC ACID; HALOPERIDOL; METABOTROPIC RECEPTOR 3; OLANZAPINE; QUETIAPINE; RISPERIDONE; SEROTONIN UPTAKE INHIBITOR; AMPA RECEPTOR; DRD2 PROTEIN, HUMAN; GLUTAMATE RECEPTOR IONOTROPIC, AMPA 3; METABOTROPIC RECEPTOR; NEUROLEPTIC AGENT;

ADULT; ARTICLE; BIPOLAR I DISORDER; COGNITION; COGNITIVE DEFECT; CONTROLLED STUDY; DRD2 GENE; EYE MOVEMENT DISORDER; EYE TRACKING; FEMALE; FOLLOW UP; GENE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; GRM3 GENE; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MAJOR DEPRESSION; MALE; MOTOR PERFORMANCE; NEUROPHYSIOLOGY; NEUROTRANSMISSION; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOAFFECTIVE PSYCHOSIS; SCHIZOPHRENIA; SCHIZOPHRENIFORM DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM; SMOOTH PURSUIT EYE MOVEMENT; ADOLESCENT; COGNITION DISORDERS; COMPLICATION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; GENETICS; OCULAR MOTILITY DISORDERS; PSYCHOTIC DISORDERS; YOUNG ADULT;

ADOLESCENT; ADULT; ANTIPSYCHOTIC AGENTS; COGNITION DISORDERS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; OCULAR MOTILITY DISORDERS; PSYCHOTIC DISORDERS; RECEPTORS, AMPA; RECEPTORS, DOPAMINE D2; RECEPTORS, METABOTROPIC GLUTAMATE; YOUNG ADULT;

EID: 84903629425     PISSN: 09401334     EISSN: 14338491     Source Type: Journal    
DOI: 10.1007/s00406-013-0464-6     Document Type: Article

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