Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

PLoS Genetics

Volumn 12, Issue 5, 2016, Pages

  Isles, Anthony R ^a   Ingason, Andrés ^b   Lowther, Chelsea ^c   Walters, James ^a   Gawlick, Micha ^d   Stöber, Gerald ^d   Rees, Elliott ^a   Martin, Joanna ^a   Little, Rosie B ^a   Potter, Harry ^a   Georgieva, Lyudmila ^e   Pizzo, Lucilla ^f   Ozaki, Norio ^g   Aleksic, Branko ^g   Kushima, Itaru ^g   Ikeda, Masashi ^h   Iwata, Nakao ^h   Levinson, Douglas F ⁱ   Gejman, Pablo V ⁱ   Shi, Jianxin ^j   Sanders, Alan R ^k,s   Duan, Jubao ^i,k,s   Willis, Joseph ^l   Sisodiya, Sanjay ^l   Costain, Gregory ^c   Werge, Thomas M ^m   Degenhardt, Franziska ⁿ   Giegling, Ina ^o   Rujescu, Dan ^o   Hreidarsson, Stefan J ^p   Saemundsen, Evald ^p,q   Ahn, Joo Wook ^r   Ogilvie, Caroline ^r   Girirajan, Santhosh D ^f   Stefansson, Hreinn ^b   Stefansson, Kari ^b   O’Donovan, Michael C ^a   Owen, Michael J ^a   Bassett, Anne ^c   Kirov, George ^a   more..

^a CARDIFF UNIVERSITY   (United Kingdom)

^b DECODE GENETICS   (Iceland)

^c UNIVERSITY OF TORONTO   (Canada)

^d UNIVERSITY OF WÜRZBURG   (Germany)

^e OXFORD GENE TECHNOLOGY   (United Kingdom)

^f Department of Biochemistry and Molecular Biology and Department of Anthropology ^*  (United States)

^g NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^h FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

ⁱ STANFORD UNIVERSITY   (United States)

^j NATIONAL CANCER INSTITUTE   (United States)

^k NORTHSHORE UNIVERSITY HEALTHSYSTEM   (United States)

^l UNIVERSITY COLLEGE LONDON   (United Kingdom)

^m UNIVERSITY OF COPENHAGEN   (Denmark)

ⁿ UNIVERSITY OF BONN   (Germany)

^o MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^p The State Diagnostic and Counselling Centre   (Iceland)

^q UNIVERSITY OF ICELAND   (Iceland)

^r GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^s UNIVERSITY OF CHICAGO   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 15Q; CHROMOSOME DUPLICATION; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; EPIGENETICS; GENETIC RISK; GENOME IMPRINTING; HETEROZYGOTE; HUMAN; INTERSTITIAL CHROMOSOME DUPLICATION; LEARNING DISORDER; MAJOR CLINICAL STUDY; MULTIPLE MALFORMATION SYNDROME; PATHOGENICITY; PENETRANCE; SCHIZOAFFECTIVE PSYCHOSIS; SCHIZOPHRENIA; CHROMOSOME 15; FEMALE; GENETICS; HAPPY PUPPET SYNDROME; MALE; MENTAL DISEASE; PATERNAL INHERITANCE; PATHOLOGY; PHENOTYPE; PRADER WILLI SYNDROME;

ANGELMAN SYNDROME; AUTISM SPECTRUM DISORDER; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN, PAIR 15; DNA COPY NUMBER VARIATIONS; FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; NEURODEVELOPMENTAL DISORDERS; PATERNAL INHERITANCE; PHENOTYPE; PRADER-WILLI SYNDROME; SCHIZOPHRENIA;

EID: 84974566646     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1005993     Document Type: Article

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