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

Leslie Matalonga, Carles Hernandez-Ferrer, Davide Piscia, Solve RD SNV Indel Working Group, Rebecca Schuele, Matthis Synofzik, Ana Topf, Lisenka E. L. M. Vissers, Richarda de Voer, Solve RD DITF GENTURIS, Solve-RD DITF-ITHACA, Solve RD DITF-euroNMD, Solve-RD-DITF-RND, Raul Tonda, Steven Laurie, Marcos Fernandez-Callejo, Daniel Pico, Carles Garcia-Linares, Anastasios Papakonstantinou, Alberto CorvoRicky Joshi, Hector Diez, Ivo Gut, Alexander Hoischen, Holm Graessner, Sergi Beltran*, Solve-RD Consortia, Han Brunner

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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  • 2021

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

    Matalonga, L., Hernández-Ferrer, C., Piscia, D., Cohen, E., Cuesta, I., Danis, D., Denommé-Pichon, A. S., Duffourd, Y., Gilissen, C., Johari, M., Laurie, S., Li, S., Nelson, I., Peters, S., Paramonov, I., Prasanth, S., Robinson, P., Sablauskas, K., Savarese, M., Steyaert, W., & 36 othersvan der Velde, J. K., Vitobello, A., Schüle, R., Synofzik, M., Töpf, A., Vissers, L. E. L. M., de Voer, R., Aretz, S., Capella, G., de Voer, R. M., Evans, G., Pelaez, J. G., Holinski-Feder, E., Hoogerbrugge, N., Laner, A., Oliveira, C., Rump, A., Schröck, E., Sommer, A. K., Steinke-Lange, V., Paske, I. T., Tischkowitz, M., Valle, L., Banka, S., Benetti, E., Casari, G., Ciolfi, A., Clayton-Smith, J., Dallapiccola, B., Solve RD DITF-euroNMD, Solve RD DITF GENTURIS, Solve-RD DITF-ITHACA, Solve-RD-DITF-RND, Solve RD SNV Indel Working Group, SOLVE-RD Consortium & Brunner, H., 1 Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1466-1469 4 p.

    Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

    Open Access