Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

Giorgio Casari(Vita-Salute San Raffaele University), Enzo Cohen(Inserm), Isabelle Nelson(University of Bonn), Christian Gilissen(Radboud University Nijmegen), Richarda M. de Voer(Radboud University Nijmegen), Peter N. Robinson(Max Planck Institute for Molecular Genetics), Gabriel Capellá(Institut d'Investigació Biomédica de Bellvitge), Lisenka E.L.M. Vissers(Radboud University Nijmegen), Evelin Schröck(German Cancer Research Center), Carles Hernandéz-Ferrer(Boston University), Elisa Benetti, Joeri K. van der Velde(University Medical Center Groningen), Marc Tischkowitz(University of Cambridge), Elke Holinski‐Feder(Garvan Institute of Medical Research), Antonio Vitobello(Inserm), Carla Oliveíra(Universidade do Porto), Ana Töpf(Newcastle upon Tyne Hospitals NHS Foundation Trust), Andreas Rump(VKTA), Verena Steinke‐Lange(University of Cambridge), Laura Valle(Institut d'Investigació Biomédica de Bellvitge), Anne‐Sophie Denommé‐Pichon(Inserm), Ida Paramonov(Universitat Pompeu Fabra), D. Gareth Evans(Institute of Cancer Research), Shuang Li(Sun Yat-sen University), Yannis Duffourd(Radboud University Nijmegen), Rebecca Schüle(Hertie Institute for Clinical Brain Research), Daniel Danis(Inserm), Richarda de Voer(University of Bonn), Andreas Laner(Medical Genetics Center), Karolis Sablauskas(University of Helsinki), Prasanth Sivakumar(Jackson Laboratory), Steven Laurie(Centro Nacional de Análisis Genómico), Stefan Aretz(University of Bonn), Davide Piscia(Centre for Genomic Regulation), Isabel Cuesta(Instituto de Salud Carlos III), Anna Katharina Sommer(University of Bonn)
European Journal of Human Genetics
June 1, 2021
Cited by 74


Related Papers