Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Birte Zurek(University of Cologne), Iris te Paske(Radboud University Nijmegen), Nicoline Hoogerbrugge(Radboud University Nijmegen), Ana Rath(Inserm), Peter A.C. ’t Hoen(Radboud University Nijmegen), Nienke van Os(Radboud University Nijmegen), Christian Gilissen(Radboud University Nijmegen), Richarda M. de Voer(Radboud University Nijmegen), Alexander Hoischen(Radboud University Nijmegen), Gisèle Bonne(Stanford University), Matthis Synofzik(German Center for Neurodegenerative Diseases), Julia M. Schulze‐Hentrich(Saarland University), Tina Harmuth(University of Tübingen), Dylan Spalding, Lisenka E.L.M. Vissers(Radboud University Nijmegen), Hans Scheffer(Radboud University Nijmegen), Leslie Matalonga(Centre for Genomic Regulation), Morris A. Swertz(University Medical Center Groningen), Peter Heutink(Parkinson's Foundation), Antonio Vitobello(Inserm), Christoph Keßler(Roche (United States)), Sergi Beltrán(Centro Nacional de Análisis Genómico), Kornelia Ellwanger(University of Hohenheim), Wouter Steyaert(Ghent University Hospital), Andreas Traschütz(German Center for Neurodegenerative Diseases), Ana Töpf(NIHR Newcastle Biomedical Research Centre), Carlo Wilke(German Center for Neurodegenerative Diseases), Lüdger Schöls(German Center for Neurodegenerative Diseases), Holm Graeßner(University Children's Hospital Tübingen), Marc Sturm(University of Tübingen), Steven Laurie(Centre for Genomic Regulation), Rebecca Schüle(Heidelberg University), Gulcin Gumus, T. Haack(University of Tübingen), Bart van de Warrenburg(Radboud University Nijmegen), Stephan Ossowski(University of Tübingen), Melanie Wayand(German Center for Neurodegenerative Diseases), Kornelia Ellwanger(University of Tübingen), Karolis Sablauskas(University of Helsinki), Holger Hengel(German Center for Neurodegenerative Diseases), German Demidov(University of Tübingen), Teresinha Evangelista, Erik-Jan Kamsteeg(Radboud University Nijmegen), Han G. Brunner(Radboud University Nijmegen), Alain Verloès(Inserm), Olaf Rieß(University of Tübingen), Anthony J. Brookes(Uppsala University)
European Journal of Human Genetics
June 1, 2021
Cited by 104


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