Association of ADHD with genetic variants in the 5′-region of the dopamine transporter gene: Evidence for allelic heterogeneity

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 147, Issue 8, 2008, Pages 1519-1523

  Brookes, K J ^a   Xu, X ^a   Anney, R ^b   Franke, B ^c   Zhou, K ^a   Chen, Wai ^a   Banaschewski, T ^d   Buitelaar, J ^c   Ebstein, R ^e   Eisenberg, J ^f   Gill, M ^b   Miranda, A ^g   Oades, R D ^h   Roeyers, H ⁱ   Rothenberger, A ^d   Sergeant, J ^j   Sonuga Barke, E ^k   Steinhausen, H C ^l   Taylor, E ^a   Faraone, S V ^m   Asherson, P ^a   more..

^a KING'S COLLEGE LONDON   (United Kingdom)

^b ST JAMES S HOSPITAL   (Ireland)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d UNIVERSITY OF GÖTTINGEN   (Germany)

^e HERZOG HOSPITAL   (Israel)

^f GEHA MENTAL HEALTH CENTER   (Israel)

^g UNIVERSITY OF VALENCIA   (Spain)

^h UNIVERSITY HOSPITAL ESSEN   (Germany)

ⁱ GHENT UNIVERSITY   (Belgium)

^j VU UNIVERSITY AMSTERDAM   (Netherlands)

^k UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^l UNIVERSITY OF ZURICH   (Switzerland)

^m SUNY UPSTATE MEDICAL UNIVERSITY   (United States)

more..

Author keywords

Association study; Attention deficit hyperactivity disorder (ADHD); Dopamine transporter gene (DAT1)

Indexed keywords

DOPAMINE TRANSPORTER;

5' UNTRANSLATED REGION; ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; CONTROLLED STUDY; DOPAMINE TRANSPORTER GENE; GENE; GENE LOCUS; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

5' UNTRANSLATED REGIONS; ALLELES; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; DOPAMINE PLASMA MEMBRANE TRANSPORT PROTEINS; EUROPE; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENE FREQUENCY; GENETIC HETEROGENEITY; GENETIC MARKERS; GENETIC VARIATION; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MICROSATELLITE REPEATS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; RISK FACTORS;

EID: 57349124044     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30782     Document Type: Article

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