Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, Specifically Breakpoints 1 to 2

Autism Research

Volumn 7, Issue 3, 2014, Pages 355-362

  Chaste, Pauline ^a,b   Sanders, Stephan J ^c,d   Mohan, Kommu N ^e,f   Klei, Lambertus ^a   Song, Youeun ^a   Murtha, Michael T ^c   Hus, Vanessa ^g   Lowe, Jennifer K ^h   Willsey, A Jeremy ^c,d   Moreno De Luca, Daniel ^c   Yu, Timothy W ⁱ   Fombonne, Eric ^j   Geschwind, Daniel ^h   Grice, Dorothy E ^k   Ledbetter, David H ^l   Lord, Catherine ^m   Mane, Shrikant M ^c   Martin, Donna M ⁿ   Morrow, Eric M ^o,p   Walsh, Christopher A ⁱ   Sutcliffe, James S ^q   State, Matthew W ^c,d   Martin, Christa Lese ^l   Devlin, Bernie ^a   Beaudet, Arthur L ^f   Cook, Edwin H ^r   Kim, Soo Jeong ^s   more..

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b FONDATION FONDAMENTAL   (France)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e BIRLA INSTITUTE OF TECHNOLOGY AND SCIENCE   (India)

^f BAYLOR COLLEGE OF MEDICINE   (United States)

^g UNIVERSITY OF MICHIGAN   (United States)

^h UNIVERSITY OF CALIFORNIA   (United States)

ⁱ BOSTON CHILDREN S HOSPITAL   (United States)

^j OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^k MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^l GEISINGER HEALTH SYSTEM   (United States)

^m WEILL CORNELL MEDICAL COLLEGE   (United States)

ⁿ UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^o BROWN UNIVERSITY   (United States)

^p BROWN UNIVERSITY   (United States)

^q VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^r UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^s UNIVERSITY OF WASHINGTON   (United States)

more..

Author keywords

15q11.2; Autism; Deletion; Duplication; Penetrance

Indexed keywords

ADULT; ARTICLE; AUTISM; BREAKPOINT 1; BREAKPOINT 2; CHROMOSOME; CHROMOSOME 15Q; CONTROLLED STUDY; COPY NUMBER VARIATION; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENICITY; PENETRANCE; PHENOTYPE; PRACTICE GUIDELINE; PRIORITY JOURNAL; RISK FACTOR; CHILD; CHROMOSOME 15; CHROMOSOME DELETION; FEMALE; GENETIC PREDISPOSITION; GENETICS;

ADULT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE;

EID: 84902650872     PISSN: 19393792     EISSN: 19393806     Source Type: Journal    
DOI: 10.1002/aur.1378     Document Type: Article

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