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

Leslie Matalonga; Carles Hernández-Ferrer; Davide Piscia; Enzo Cohen; Isabel Cuesta; Daniel Danis; Anne Sophie Denommé-Pichon; Yannis Duffourd; Christian Gilissen; Mridul Johari; Steven Laurie; Shuang Li; Isabelle Nelson; Sophia Peters; Ida Paramonov; Sivakumar Prasanth; Peter Robinson; Karolis Sablauskas; Marco Savarese; Wouter Steyaert; Joeri K. van der Velde; Antonio Vitobello; Rebecca Schüle; Matthis Synofzik; Ana Töpf; Lisenka E.L.M. Vissers; Richarda de Voer; Stefan Aretz; Gabriel Capella; Richarda M. de Voer; Gareth Evans; Jose Garcia Pelaez; Elke Holinski-Feder; Nicoline Hoogerbrugge; Andreas Laner; Carla Oliveira; Andreas Rump; Evelin Schröck; Anna Katharina Sommer; Verena Steinke-Lange; Iris te Paske; Marc Tischkowitz; Laura Valle; Siddharth Banka; Elisa Benetti; Giorgio Casari; Andrea Ciolfi; Jill Clayton-Smith; Bruno Dallapiccola; 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; Han Brunner

doi:10.1038/s41431-021-00934-6

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

Leslie Matalonga, Carles Hernández-Ferrer, Davide Piscia, Enzo Cohen, Isabel Cuesta, Daniel Danis, Anne Sophie Denommé-Pichon, Yannis Duffourd, Christian Gilissen, Mridul Johari, Steven Laurie, Shuang Li, Isabelle Nelson, Sophia Peters, Ida Paramonov, Sivakumar Prasanth, Peter Robinson, Karolis Sablauskas, Marco Savarese, Wouter SteyaertJoeri K. van der Velde, Antonio Vitobello, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Lisenka E.L.M. Vissers, Richarda de Voer, Stefan Aretz, Gabriel Capella, Richarda M. de Voer, Gareth Evans, Jose Garcia Pelaez, Elke Holinski-Feder, Nicoline Hoogerbrugge, Andreas Laner, Carla Oliveira, Andreas Rump, Evelin Schröck, Anna Katharina Sommer, Verena Steinke-Lange, Iris te Paske, Marc Tischkowitz, Laura Valle, Siddharth Banka, Elisa Benetti, Giorgio Casari, Andrea Ciolfi, Jill Clayton-Smith, Bruno Dallapiccola, 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, Han Brunner

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

Original language	English
Pages (from-to)	1466-1469
Number of pages	4
Journal	European Journal of Human Genetics
Volume	29
Issue number	9
DOIs	https://doi.org/10.1038/s41431-021-00934-6
Publication status	Published - 1 Sept 2021

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10.1038/s41431-021-00934-6

1 Article

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
Matalonga, L., Hernandez-Ferrer, C., Piscia, D., Solve RD SNV Indel Working Group, Schuele, R., Synofzik, M., Topf, A., Vissers, L. E. L. M., de Voer, R., Solve RD DITF GENTURIS, Solve-RD DITF-ITHACA, Solve RD DITF-euroNMD, Solve-RD-DITF-RND, Tonda, R., Laurie, S., Fernandez-Callejo, M., Pico, D., Garcia-Linares, C., Papakonstantinou, A., Corvo, A., & 8 othersJoshi, R., Diez, H., Gut, I., Hoischen, A., Graessner, H., Beltran, S., Solve-RD Consortia & Brunner, H., Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1337-1347 11 p.
Research output: Contribution to journal › Article › Academic › peer-review

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Cite this

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., ... Brunner, H. (2021). Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data. European Journal of Human Genetics, 29(9), 1466-1469. https://doi.org/10.1038/s41431-021-00934-6

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

author = "Leslie Matalonga and Carles Hern{\'a}ndez-Ferrer and Davide Piscia and Enzo Cohen and Isabel Cuesta and Daniel Danis and Denomm{\'e}-Pichon, {Anne Sophie} and Yannis Duffourd and Christian Gilissen and Mridul Johari and Steven Laurie and Shuang Li and Isabelle Nelson and Sophia Peters and Ida Paramonov and Sivakumar Prasanth and Peter Robinson and Karolis Sablauskas and Marco Savarese and Wouter Steyaert and {van der Velde}, {Joeri K.} and Antonio Vitobello and Rebecca Sch{\"u}le and Matthis Synofzik and Ana T{\"o}pf and Vissers, {Lisenka E.L.M.} and {de Voer}, Richarda and Stefan Aretz and Gabriel Capella and {de Voer}, {Richarda M.} and Gareth Evans and Pelaez, {Jose Garcia} and Elke Holinski-Feder and Nicoline Hoogerbrugge and Andreas Laner and Carla Oliveira and Andreas Rump and Evelin Schr{\"o}ck and Sommer, {Anna Katharina} and Verena Steinke-Lange and Paske, {Iris te} and Marc Tischkowitz and Laura Valle and Siddharth Banka and Elisa Benetti and Giorgio Casari and Andrea Ciolfi and Jill Clayton-Smith and Bruno Dallapiccola and {Solve RD DITF-euroNMD} and {Solve RD DITF GENTURIS} and {Solve-RD DITF-ITHACA} and Solve-RD-DITF-RND and {Solve RD SNV Indel Working Group} and {SOLVE-RD Consortium} and Han Brunner",

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doi = "10.1038/s41431-021-00934-6",

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journal = "European Journal of Human Genetics",

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Matalonga, L, Hernández-Ferrer, C, Piscia, D, Cohen, E, Cuesta, I, Danis, D, Denommé-Pichon, AS, 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, van der Velde, JK, Vitobello, A, Schüle, R, Synofzik, M, Töpf, A, Vissers, LELM, de Voer, R, Aretz, S, Capella, G, de Voer, RM, Evans, G, Pelaez, JG, Holinski-Feder, E, Hoogerbrugge, N, Laner, A, Oliveira, C, Rump, A, Schröck, E, Sommer, AK, Steinke-Lange, V, Paske, IT, 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 2021, 'Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data', European Journal of Human Genetics, vol. 29, no. 9, pp. 1466-1469. https://doi.org/10.1038/s41431-021-00934-6

TY - JOUR

T1 - Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

AU - Matalonga, Leslie

AU - Hernández-Ferrer, Carles

AU - Piscia, Davide

AU - Cohen, Enzo

AU - Cuesta, Isabel

AU - Danis, Daniel

AU - Denommé-Pichon, Anne Sophie

AU - Duffourd, Yannis

AU - Gilissen, Christian

AU - Johari, Mridul

AU - Laurie, Steven

AU - Li, Shuang

AU - Nelson, Isabelle

AU - Peters, Sophia

AU - Paramonov, Ida

AU - Prasanth, Sivakumar

AU - Robinson, Peter

AU - Sablauskas, Karolis

AU - Savarese, Marco

AU - Steyaert, Wouter

AU - van der Velde, Joeri K.

AU - Vitobello, Antonio

AU - Schüle, Rebecca

AU - Synofzik, Matthis

AU - Töpf, Ana

AU - Vissers, Lisenka E.L.M.

AU - de Voer, Richarda

AU - Aretz, Stefan

AU - Capella, Gabriel

AU - de Voer, Richarda M.

AU - Evans, Gareth

AU - Pelaez, Jose Garcia

AU - Holinski-Feder, Elke

AU - Hoogerbrugge, Nicoline

AU - Laner, Andreas

AU - Oliveira, Carla

AU - Rump, Andreas

AU - Schröck, Evelin

AU - Sommer, Anna Katharina

AU - Steinke-Lange, Verena

AU - Paske, Iris te

AU - Tischkowitz, Marc

AU - Valle, Laura

AU - Banka, Siddharth

AU - Benetti, Elisa

AU - Casari, Giorgio

AU - Ciolfi, Andrea

AU - Clayton-Smith, Jill

AU - Dallapiccola, Bruno

AU - Solve RD DITF-euroNMD

AU - Solve RD DITF GENTURIS

AU - Solve-RD DITF-ITHACA

AU - Solve-RD-DITF-RND

AU - Solve RD SNV Indel Working Group

AU - SOLVE-RD Consortium

AU - Brunner, Han

PY - 2021/9/1

Y1 - 2021/9/1

U2 - 10.1038/s41431-021-00934-6

DO - 10.1038/s41431-021-00934-6

M3 - Erratum / corrigendum / retractions

SN - 1018-4813

VL - 29

SP - 1466

EP - 1469

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -