TY  - GEN
AU  - Zurek, Birte
AU  - Ellwanger, Kornelia
AU  - Vissers, Lisenka E L M
AU  - Schüle, Rebecca
AU  - Synofzik, Matthis
AU  - Töpf, Ana
AU  - de Voer, Richarda M
AU  - Laurie, Steven
AU  - Matalonga, Leslie
AU  - Gilissen, Christian
AU  - Ossowski, Stephan
AU  - t Hoen, Peter A C
AU  - Vitobello, Antonio
AU  - Schulze-Hentrich, Julia M
AU  - Riess, Olaf
AU  - Brunner, Han G
AU  - Brookes, Anthony J
AU  - Rath, Ana
AU  - Bonne, Gisèle
AU  - Gumus, Gulcin
AU  - Verloes, Alain
AU  - Hoogerbrugge, Nicoline
AU  - Evangelista, Teresinha
AU  - Harmuth, Tina
AU  - Swertz, Morris
AU  - Spalding, Dylan
AU  - Hoischen, Alexander
AU  - Beltran, Sergi
AU  - Graessner, Holm
AU  - Solve-RD consortium
AU  - Posada De la Paz, Manuel
AU  - Bermejo-Sanchez, Eva
AU  - Lopez-Martin, Estrella
AU  - Martinez-Delgado, Beatriz
PY  - 2021
DO  - 10.1038/s41431-021-00859-0
UR  - http://hdl.handle.net/20.500.12105/15567
AB  - For the first time in Europe hundreds of rare disease (RD) experts team up to actively share and jointly analyse existing patient's data. Solve-RD is a Horizon 2020-supported EU flagship project bringing together >300 clinicians, scientists, and...
LA  - eng
PB  - Nature Publishing Group
KW  - Information Dissemination
KW  - Intersectoral Collaboration
KW  - Consensus Development Conferences as Topic
KW  - Europe
KW  - Genetic Diseases, Inborn
KW  - Genetic Testing
KW  - Humans
KW  - Rare Diseases
KW  - Exome Sequencing
TI  - Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
TY  - research article
ER  -