Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Donna J. Page(Manchester Metropolitan University), Bernard Keavney(Manchester Academic Health Science Centre), Elisavet Fotiou(Manchester Metropolitan University), Mathieu Bourgey(McGill University and Génome Québec Innovation Centre), Simon G. Williams(Manchester Metropolitan University), Martín Baron(University of Manchester), Matthieu J. Miossec(University of Oxford), Louise Sutcliffe(Manchester Metropolitan University), Connie R. Bezzina(Amsterdam Neuroscience), Jeroen Breckpot(KU Leuven), Richard M. Monaghan(Manchester Academic Health Science Centre), Sally L. Dunwoodie(Victor Chang Cardiac Research Institute), Graham Stuart(Lund University), Marc Gewillig(KU Leuven), J. David Brook(University of Nottingham), Sanjeev S. Bhaskar(Manchester Metropolitan University), Robert Eveleigh(Manchester Metropolitan University), Graeme C. Black(University of Manchester), Guillaume Bourque(Kyoto University), Kerry Setchfield(University of Nottingham), Mauro Santibanez‐Koref(Newcastle University), Alex V. Postma(Amsterdam University Medical Centers), Ana Töpf(NIHR Newcastle Biomedical Research Centre), Koenraad Devriendt(Universitair Ziekenhuis Leuven), William G. Newman(Manchester Metropolitan University), Barbara J.M. Mulder(Amsterdam UMC Location University of Amsterdam), Kathryn E. Hentges(Manchester Academic Health Science Centre), G.M. Lathrop(Emory University), Heather J. Cordell(Newcastle University), James R. Bentham(Manchester Metropolitan University), Shoumo Bhattacharya(Centre for Human Genetics), John O’Sullivan(The University of Sydney), Frances Bu’Lock(Glenfield Hospital), David S. Winlaw(Lurie Children's Hospital)
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