Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 49, Issue 7, 2010, Pages 675-685

  Nijmeijer, Judith S ^a   Arias Vsquez, Alejandro ^b   Rommelse, Nanda N J ^b   Altink, Marieke E ^b   Anney, Richard J L ^c   Asherson, Philip ^d   Banaschewski, Tobias ^e   Buschgens, Cathelijne J M ^b   Fliers, Ellen A ^b,f   Gill, Michael ^c   Minderaa, Ruud B ^a   Poustka, Luise ^e   Sergeant, Joseph A ^g   Buitelaar, Jan K ^b   Franke, Barbara ^b   Ebstein, Richard P ^h   Miranda, Ana ⁱ   Mulas, Fernando ^j   Oades, Robert D ^k   Roeyers, Herbert ^l   Rothenberger, Aribert ^m   Sonuga Barke, Edmund J S ⁿ   Steinhausen, Hans Christoph ^o   Faraone, Stephen V ^p   Hartman, Catharina A ^a   Hoekstra, Pieter J ^a   more..

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c ST JAMES S HOSPITAL   (Ireland)

^d KING'S COLLEGE LONDON   (United Kingdom)

^e UNIVERSITY OF HEIDELBERG   (Germany)

^f Parnassia Bavo Group   (Netherlands)

^g UNIVERSITY OF AMSTERDAM   (Netherlands)

^h Sarah Herzog Memorial Hospital   (Ireland)

ⁱ UNIVERSITY OF VALENCIA   (Spain)

^j HOSPITAL UNIVERSITARIO LA FE   (Spain)

^k UNIVERSITY OF DUISBURG ESSEN   (Germany)

^l GHENT UNIVERSITY   (Belgium)

^m UNIVERSITY OF GÖTTINGEN   (Germany)

ⁿ UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^o AARHUS UNIVERSITY   (Denmark)

^p SUNY UPSTATE MEDICAL UNIVERSITY   (United States)

more..

Author keywords

ADHD; autism spectrum disorder; comorbidity; linkage

Indexed keywords

ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; CHILD; CHROMOSOME 12Q; CHROMOSOME 15Q; CHROMOSOME 16P; CHROMOSOME 18P; CHROMOSOME 7Q; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; FEMALE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC LINKAGE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIVARIATE LOGISTIC REGRESSION ANALYSIS; PLEIOTROPY; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; SCHOOL CHILD; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 18; COMMUNICATION; COMORBIDITY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LOD SCORE; MALE; PERSONALITY ASSESSMENT; POLYMORPHISM, SINGLE NUCLEOTIDE; PSYCHOMETRICS; QUANTITATIVE TRAIT LOCI; SOCIAL BEHAVIOR;

EID: 77955712869     PISSN: 08908567     EISSN: 15275418     Source Type: Journal    
DOI: 10.1097/00004583-201007000-00008     Document Type: Article

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