Neuropsychological endophenotypes in attention-deficit/hyperactivity disorder: A review of genetic association studies

European Archives of Psychiatry and Clinical Neuroscience

Volumn 261, Issue 8, 2011, Pages 583-594

  Kebir, Oussama ^a   Joober, Ridha ^b,c,d  

^a INSERM   (France)

^b MCGILL UNIVERSITY   (Canada)

^c MCGILL UNIVERSITY   (Canada)

^d DOUGLAS MENTAL HEALTH UNIVERSITY INSTITUTE   (Canada)

Author keywords

ADHD; Association study; Cognitive; Genetics; Neuropsychological endophenotype

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; CATECHOL METHYLTRANSFERASE; DOPAMINE 4 RECEPTOR; DOPAMINE BETA MONOOXYGENASE; DOPAMINE TRANSPORTER;

ATTENTION DEFICIT DISORDER; COGNITION; DATA BASE; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC SUSCEPTIBILITY; HUMAN; HYPERACTIVITY; MEDLINE; NEUROPSYCHOLOGY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; REVIEW;

ALLELES; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CATECHOL O-METHYLTRANSFERASE; DOPAMINE BETA-HYDROXYLASE; DOPAMINE PLASMA MEMBRANE TRANSPORT PROTEINS; ENDOPHENOTYPES; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; HETEROZYGOTE; HUMANS; MINISATELLITE REPEATS; MONOAMINE OXIDASE; NEUROPSYCHOLOGICAL TESTS; PHENOTYPE; POLYMORPHISM, GENETIC; REACTION TIME; RECEPTORS, DOPAMINE D4;

EID: 80051553157     PISSN: 09401334     EISSN: 14338491     Source Type: Journal    
DOI: 10.1007/s00406-011-0207-5     Document Type: Review

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