Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: A genome-wide analysis

The Lancet

Volumn 376, Issue 9750, 2010, Pages 1401-1408

  Williams, Nigel M ^a   Zaharieva, Irina ^a   Martin, Andrew ^a   Langley, Kate ^a   Mantripragada, Kiran ^a   Fossdal, Ragnheidur ^b   Stefansson, Hreinn ^b   Stefansson, Kari ^b   Magnusson, Pall ^c   Gudmundsson, Olafur O ^c   Gustafsson, Omar ^b,d   Holmans, Peter ^a   Owen, Michael J ^a   O'Donovan, Michael ^a   Thapar, Anita ^a  

^a CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

^b DECODE GENETICS   (Iceland)

^c LANDSPITALI UNIVERSITY HOSPITAL   (Iceland)

^d OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HYPERKINESIA; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PSYCHOLOGIC ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; SOMATIC HYPERMUTATION; AUTISM; CHROMOSOME ABERRATION; CLINICAL TRIAL; COPY NUMBER VARIATION; FEMALE; GENETICS; MALE; MULTICENTER STUDY; PRESCHOOL CHILD; SCHIZOPHRENIA;

ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 78049303903     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(10)61109-9     Document Type: Article

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