Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

Solve-RD SNV-indel working group; Solve-RD DITF-GENTURIS; Solve-RD DITF-ITHACA; Solve-RD DITF-euroNMD; Solve-RD-DITF-RND; The Solve-RD Consortium; Leslie Matalonga; Carles Hernández; Davide Piscia; Enzo Cohen; Isabel Cuesta; Daniel Danis; Anne Sophie Denommé-Pichon; Yannis Duffourd; Christian Gilissen; Mridul Johari; Steven Laurie; Shuang Li; Leslie Matalonga; 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 Vissers; Richarda M. 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; Alexander Münchau; Alexander Münchau; Katja Lohmann; Rebecca Herzog; Martje Pauly

doi:10.1038/s41431-021-00934-6

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

Solve-RD SNV-indel working group, Solve-RD DITF-GENTURIS, Solve-RD DITF-ITHACA, Solve-RD DITF-euroNMD, Solve-RD-DITF-RND, The Solve-RD Consortium, Leslie Matalonga, Carles Hernández, Davide Piscia, Enzo Cohen, Isabel Cuesta, Daniel Danis, Anne Sophie Denommé-Pichon, Yannis Duffourd, Christian Gilissen, Mridul Johari, Steven Laurie, Shuang Li, Leslie Matalonga, Isabelle NelsonSophia 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 Vissers, Richarda M. 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, Alexander Münchau, Alexander Münchau, Katja Lohmann, Rebecca Herzog, Martje Pauly

Original language	English
Journal	European Journal of Human Genetics
Volume	29
Issue number	9
Pages (from-to)	1466-1469
Number of pages	4
ISSN	1018-4813
DOIs	https://doi.org/10.1038/s41431-021-00934-6
Publication status	Published - 09.2021

Funding

Funders	Funder number
Medical Research Council	MR/M006824/1
European Commission	305444
Horizon 2020 Framework Programme	825575

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Research Areas and Centers

Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)
Centers: Center for Rare Diseases (ZSE)

DFG Research Classification Scheme

2.23-07 Clinical Neurology, Neurosurgery and Neuroradiology

Access to Document

10.1038/s41431-021-00934-6

Cite this

Solve-RD SNV-indel working group, Solve-RD DITF-GENTURIS, Solve-RD DITF-ITHACA, Solve-RD DITF-euroNMD, Solve-RD-DITF-RND, The Solve-RD Consortium, Matalonga, L., Hernández, C., Piscia, D., Cohen, E., Cuesta, I., Danis, D., Denommé-Pichon, A. S., Duffourd, Y., Gilissen, C., Johari, M., Laurie, S., Li, S., Matalonga, L., ... Pauly, M. (2021). Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7). European Journal of Human Genetics, 29(9), 1466-1469. https://doi.org/10.1038/s41431-021-00934-6

@article{c3908708b4db46bab53b41dca67f0abb,

title = "Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)",

author = "\{Solve-RD SNV-indel working group\} and \{Solve-RD DITF-GENTURIS\} and \{Solve-RD DITF-ITHACA\} and \{Solve-RD DITF-euroNMD\} and Solve-RD-DITF-RND and \{The Solve-RD Consortium\} and Leslie Matalonga and Carles Hern{\'a}ndez 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 Leslie Matalonga 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 Lisenka Vissers and \{de Voer\}, \{Richarda M.\} 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 Alexander M{\"u}nchau and Alexander M{\"u}nchau and Katja Lohmann and Rebecca Herzog and Martje Pauly",

year = "2021",

month = sep,

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

language = "English",

volume = "29",

pages = "1466--1469",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

number = "9",

}

Solve-RD SNV-indel working group, Solve-RD DITF-GENTURIS, Solve-RD DITF-ITHACA, Solve-RD DITF-euroNMD, Solve-RD-DITF-RND, The Solve-RD Consortium, Matalonga, L, Hernández, C, Piscia, D, Cohen, E, Cuesta, I, Danis, D, Denommé-Pichon, AS, Duffourd, Y, Gilissen, C, Johari, M, Laurie, S, Li, S, Matalonga, L, 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, L, de Voer, RM, 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, Münchau, A , Münchau, A , Lohmann, K , Herzog, R & Pauly, M 2021, 'Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)', European Journal of Human Genetics, vol. 29, no. 9, pp. 1466-1469. https://doi.org/10.1038/s41431-021-00934-6

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7). / Solve-RD SNV-indel working group; Solve-RD DITF-GENTURIS; Solve-RD DITF-ITHACA et al.
In: European Journal of Human Genetics, Vol. 29, No. 9, 09.2021, p. 1466-1469.

Research output: Journal Articles › Comments/Debates

TY - JOUR

T1 - Correction to

T2 - Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

AU - Solve-RD SNV-indel working group

AU - Solve-RD DITF-GENTURIS

AU - Solve-RD DITF-ITHACA

AU - Solve-RD DITF-euroNMD

AU - Solve-RD-DITF-RND

AU - The Solve-RD Consortium

AU - Matalonga, Leslie

AU - Hernández, 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 - Matalonga, Leslie

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

AU - de Voer, Richarda M.

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 - Münchau, Alexander

AU - Lohmann, Katja

AU - Herzog, Rebecca

AU - Pauly, Martje

PY - 2021/9

Y1 - 2021/9

UR - https://www.scopus.com/pages/publications/85116958148

U2 - 10.1038/s41431-021-00934-6

DO - 10.1038/s41431-021-00934-6

M3 - Comments/Debates

C2 - 34393220

AN - SCOPUS:85116958148

SN - 1018-4813

VL - 29

SP - 1466

EP - 1469

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -

Solve-RD SNV-indel working group, Solve-RD DITF-GENTURIS, Solve-RD DITF-ITHACA, Solve-RD DITF-euroNMD, Solve-RD-DITF-RND, The Solve-RD Consortium et al. Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7). European Journal of Human Genetics. 2021 Sept;29(9):1466-1469. doi: 10.1038/s41431-021-00934-6

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

Funding

UN SDGs

Research Areas and Centers

DFG Research Classification Scheme

Access to Document

Other files and links

FOR/RU 2698: Cognitive theory for Tourette syndrome – a novel perspective

Cite this

Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

Funding

UN SDGs

Research Areas and Centers

DFG Research Classification Scheme

Access to Document

Other files and links

Projects

FOR/RU 2698: Cognitive theory for Tourette syndrome – a novel perspective

Cite this