Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
Anne O’Donnell‐Luria(Broad Institute), Kirsty McWalter, Bénédicte Duban‐Bedu(Hôpital Saint-Vincent-de-Paul), Gustavo Maegawa(Johns Hopkins Medicine), Boris Keren(Sorbonne Université), Alinoë Lavillaureix(Centre National de la Recherche Scientifique), Andrea Accogli(Istituto Giannina Gaslini), Florence Démurger(Centre hospitalier Bretagne Atlantique), Lynne M. Bird(University of California San Diego), Alice Basinger(Cook Children's Medical Center), Katherine L. Helbig(School of the Art Institute of Chicago), Jordan C. Wood(Broad Institute), Abigail Sveden(Broad Institute), Marcelo Rodrigues Masruha(St Mary's Hospital), Solveig Heide(Sorbonne Université), Victor Luria(Harvard University), Claudia Bianchini(Meyer Children's Hospital), Wilfrid Carré(Station Biologique de Roscoff), Carlo Marcelis(Radboud University Nijmegen), Heather M. McLaughlin, Silvia Azzarello‐Burri(University of Zurich), Kimberly Amburgey(University of Toronto), Lynn Pais(MACOM (United States)), Aurora Currò(University of Siena), Luis Escobar(St. Vincent Hospital), Pascal Joset(University of Zurich), Lisa Culliton(Children's Mercy Hospital), Bertrand Isidor(Centre National de la Recherche Scientifique), Fernando Kok(Universidade de São Paulo), Rebecca Buchert(Institute of Human Genetics), James J. Dowling, Víctor Faùndes(University of Manchester), Alessandra Ferrarini, Rami Abou Jamra(Leipzig University), Amy R. Jonasson(University of Florida), Paul R. Mark(Spectrum Health), Perrine Charles(School of the Art Institute of Chicago), Raúl Jiménez Heredia, Xin Lü(Northeast Forestry University), Mona Hashim(Centre for Human Genetics), Ingo Helbig(Schneider Electric (France)), Delphine Héron(Sorbonne Université), Hester Y. Kroes(University Medical Center Utrecht), Tobias B. Haack, Saskia M. Maas(Academic Medical Center), Britt Marie Anderlid(Karolinska University Hospital), Helen Cox(National Health Service), Sophia Ceulemans(Rady Children's Hospital-San Diego), Christèle Dubourg(Institut de génétique et de développement de Rennes), Saga Elise Eiset(Aarhus University Hospital)
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