Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity

PLoS ONE

Volumn 8, Issue 3, 2013, Pages

  Walters, Robin G ^a,b   Coin, Lachlan J M ^a,c   Ruokonen, Aimo ^d,e   de Smith, Adam J ^a,f   El Sayed Moustafa, Julia S ^a   Jacquemont, Sebastien ^g   Elliott, Paul ^a   Esko, Tõnu ^h,i   Hartikainen, Anna Liisa ^d   Laitinen, Jaana ^j   Männik, Katrin ^h,k   Martinet, Danielle ^g   Meyre, David ^l,m   Nauck, Matthias ⁿ   Schurmann, Claudia ⁿ   Sladek, Rob ^o   Thorleifsson, Gudmar ^p   Thorsteinsdóttir, Unnur ^p,q   Valsesia, Armand ^k   Waeber, Gerard ^g   Zufferey, Flore ^g   Balkau, Beverley ^r   Pattou, François ^s,t   Metspalu, Andres ^h,i   Völzke, Henry ⁿ   Vollenweider, Peter ^g   Stefansson, Kári ^p,q   Järvelin, Marjo Riitta ^a,d,u   Beckmann, Jacques S ^g,k   Froguel, Philippe ^a,l   Blakemore, Alexandra I F ^a   more..

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c UNIVERSITY OF QUEENSLAND   (Australia)

^d UNIVERSITY OF OULU   (Finland)

^e OULU UNIVERSITY HOSPITAL   (Finland)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^h UNIVERSITY OF TARTU   (Estonia)

ⁱ UNIVERSITY OF TARTU   (Estonia)

^j FINNISH INSTITUTE OF OCCUPATIONAL HEALTH   (Finland)

^k UNIVERSITY OF LAUSANNE   (Switzerland)

^l INSTITUT PASTEUR DE LILLE   (France)

^m MCMASTER UNIVERSITY   (Canada)

ⁿ UNIVERSITY OF GREIFSWALD   (Germany)

^o MCGILL UNIVERSITY   (Canada)

^p DECODE GENETICS   (Iceland)

^q UNIVERSITY OF ICELAND   (Iceland)

^r CENTRE FOR RESEARCH IN EPIDEMIOLOGY AND POPULATION HEALTH   (France)

^s INSERM   (France)

^t UNIV LILLE   (France)

^u NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

ADULT; ARTICLE; BODY MASS; CASE CONTROL STUDY; CHILD; CHILDHOOD OBESITY; CHROMOSOME DELETION; CHROMOSOME DELETION 16P; COHORT ANALYSIS; CONTROLLED STUDY; FALSE POSITIVE RESULT; FAMILIAL DISEASE; FOXP2 GENE; GENE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOMIC STRUCTURAL VARIANT; HETEROZYGOTE; HUMAN; KIF2B GENE; MAJOR CLINICAL STUDY; OBESITY; PHENOTYPE; POPULATION RESEARCH; QUANTITATIVE TRAIT; REPLICATION STUDY; SH2B1 GENE; STUDY DESIGN; TWO STAGE STUDY DESIGN;

ADOLESCENT; ADULT; AGED; BODY MASS INDEX; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 16; COHORT STUDIES; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENETIC LOCI; GENOME-WIDE ASSOCIATION STUDY; HUMANS; KINESIN; MALE; MIDDLE AGED; OBESITY;

EID: 84874898385     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0058048     Document Type: Article

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