학술논문

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
Document Type
Article
Author
Zurek, B.Ellwanger, K.Ossowski, S.Schulze-Hentrich, J.M.Riess, O.Harmuth, T.Graessner, H.Haack, T.B.Zurek, B.Ellwanger, K.Demidov, G.Sturm, M.Vissers, L.E.L.M.de Voer, R.M.Gilissen, C.Brunner, H.G.Hoogerbrugge, N.Hoischen, A.Brunner, H.Scheffer, H.Steyaert, W.Sablauskas, K.de Voer, R.M.Kamsteeg, E.-J.te Paske, I.Janssen, E.de Boer, E.Steehouwer, M.Yaldiz, B.Kleefstra, T.van de Warrenburg, B.van Os, N.Schüle, R.Synofzik, M.Kessler, C.Wayand, M.Wilke, C.Traschütz, A.Schöls, L.Hengel, H.Heutink, P.Töpf, A.Straub, V.Bettolo, C.M.Specht, S.’t Hoen, P.A.C.Laurie, S.Matalonga, L.Beltran, S.Beltran, S.Vitobello, A.Faivre, L.Thauvin, C.Vitobello, A.Denommé-Pichon, A.-S.Duffourd, Y.Tisserant, E.Bruel, A.-L.Brookes, A.J.Veal, C.Gibson, S.Wadsley, M.Mehtarizadeh, M.Riaz, U.Warren, G.Dizjikan, F.Y.Shorter, T.Rath, A.Hanauer, M.Olry, A.Lagorce, D.Havrylenko, S.Izem, K.Rigour, F.Bonne, G.Evangelista, T.Allamand, V.Nelson, I.Yaou, R.B.Metay, C.Eymard, B.Cohen, E.Atalaia, A.Stojkovic, T.Gumus, G.Verloes, A.Swertz, M.Johansson, L.van der Velde, J.K.van der Vries, G.Neerincx, P.B.Roelofs-Prins, D.Spalding, D.Parkinson, H.Keane, T.Senf, A.Gut, I.G.Laurie, S.Piscia, D.Matalonga, L.Papakonstantinou, A.Bullich, G.Corvo, A.Garcia, C.Fernandez-Callejo, M.Hernández, C.Picó, D.Paramonov, I.Lochmüller, H.Clayton-Smith, J.Banka, S.Alexander, E.Jackson, A.Peyron, C.Pélissier, A.Gumus, G.Bros-Facer, V.Stevanin, G.Durr, A.Davoine, C.-S.Guillot-Noel, L.Heinzmann, A.Coarelli, G.Macek, M.Turnovec, M.Thomasová, D.Kremliková, R.P.Franková, V.Havlovicová, M.Kremlik, V.Robinson, P.Danis, D.Robert, G.Costa, A.Patch, C.Metcalfe, A.Hanna, M.Reilly, M.Houlden, H.Vandrovcova, J.Muntoni, F.Zaharieva, I.Sarkozy, A.Timmerman, V.Van de Vondel, L.Beijer, D.de Jonghe, P.Baets, J.Nigro, V.Banfi, S.Torella, A.Musacchia, F.Piluso, G.Castello, R.Morleo, M.Pinelli, M.Varavallo, A.Ferlini, A.Selvatici, R.Rossi, R.Neri, M.Aretz, S.Spier, I.Sommer, A.K.Peters, S.Oliveira, C.Pelaez, J.G.Matos, A.R.José, C.S.Ferreira, M.Gullo, I.Fernandes, S.Ferreira, P.Carneiro, F.Garrido, L.Köhler, S.Verloes, A.Drunat, S.Rooryck, C.Trimouille, A.De la Paz, M.P.Sánchez, E.B.Martín, E.L.Delgado, B.M.de la Rosa, F.J.A.G.Ciolfi, A.Dallapiccola, B.Pizzi, S.Radio, F.C.Tartaglia, M.Renieri, A.Benetti, E.Balicza, P.Molnar, M.J.Maver, A.Peterlin, B.Münchau, A.Lohmann, K.Herzog, R.Pauly, M.Macaya, A.Marcé-Grau, A.Osorio, A.N.de Benito, D.N.Lochmüller, H.Thompson, R.Polavarapu, K.Beeson, D.Cossins, J.Cruz, P.M.R.Hackman, P.Johari, M.Savarese, M.Udd, B.Horvath, R.Capella, G.Valle, L.Holinski-Feder, E.Laner, A.Steinke-Lange, V.Schröck, E.Rump, A.
Source
In: European Journal of Human Genetics. (European Journal of Human Genetics, 01 September 2021, 29(9):1325-1331)
Subject
Language
English
ISSN
14765438
10184813