Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Nature Genetics

Volumn 45, Issue 7, 2013, Pages 822-824

  Cordell, Heather J ^a   Bentham, Jamie ^b   Topf, Ana ^a   Zelenika, Diana ^c,d   Heath, Simon ^c,e   Mamasoula, Chrysovalanto ^a   Cosgrove, Catherine ^b   Blue, Gillian ^f   Granados Riveron, Javier ^g,r   Setchfield, Kerry ^g   Thornborough, Chris ^h   Breckpot, Jeroen ⁱ   Soemedi, Rachel ^a   Martin, Ruairidh ^a   Rahman, Thahira J ^a   Hall, Darroch ^a   Van Engelen, Klaartje ^j   Moorman, Antoon F M ^j   Zwinderman, Aelko H ^j   Barnett, Phil ^j   Koopmann, Tamara T ^j   Adriaens, Michiel E ^j   Varro, Andras ^k   George Jr , Alfred L ^l   Dos Remedios, Christobal ^m   Bishopric, Nanette H ⁿ   Bezzina, Connie R ^j   O'Sullivan, John ^o   Gewillig, Marc ⁱ   Bu'Lock, Frances A ^h   Winlaw, David ^f   Bhattacharya, Shoumo ^b   Devriendt, Koen ⁱ   Brook, J David ^g   Mulder, Barbara J M ^j   Mital, Seema ^p   Postma, Alex V ^j   Lathrop, G Mark ^c,d   Farrall, Martin ^b   Goodship, Judith A ^a   Keavney, Bernard D ^a,q   more..

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c DIF   (France)

^d FONDATION JEAN DAUSSET CEPH   (France)

^e Centro Nacional de Analisis Genomico   (Spain)

^f CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^g UNIVERSITY OF NOTTINGHAM   (United Kingdom)

^h UNIVERSITY HOSPITALS OF LEICESTER NHS TRUST   (United Kingdom)

ⁱ UNIVERSITY OF LEUVEN   (Belgium)

^j ACADEMIC MEDICAL CENTER   (Netherlands)

^k UNIVERSITY OF SZEGED   (Hungary)

^l VANDERBILT UNIVERSITY   (United States)

^m UNIVERSITY OF SYDNEY   (Australia)

ⁿ UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^o NEWCASTLE UPON TYNE HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^p HOSPITAL FOR SICK CHILDREN   (Canada)

^q UNIVERSITY OF MANCHESTER   (United Kingdom)

^r HOSPITAL INFANTIL DE MÉXICO FEDERICO GÓMEZ   (Mexico)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 4P; CHROMOSOME 4P16; COHORT ANALYSIS; CONGENITAL HEART DISEASE; CONTROLLED STUDY; CYANOSIS; FEMALE; GENE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HEART ATRIUM SEPTUM DEFECT; HUMAN; MAJOR CLINICAL STUDY; MSX1 GENE; NUCLEOTIDE SEQUENCE; PHENOTYPE; POPULATION RISK; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STX18 GENE;

ABNORMALITIES, MULTIPLE; ANIMALS; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 4; COHORT STUDIES; FEMALE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HEART DEFECTS, CONGENITAL; HEART DISEASES; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; MALE; MICE; PHENOTYPE;

EID: 84879687374     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2637     Document Type: Article

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