Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)

Robin Wijngaard; German Demidov; Luke O’Gorman; Jordi Corominas-Galbany; Burcu Yaldiz; Wouter Steyaert; Elke de Boer; Lisenka E. L. M. Vissers; Erik-Jan Kamsteeg; Rolph Pfundt; Hilde Swinkels; Amber den Ouden; Iris B. A. W. te Paske; Richarda M. de Voer; Laurence Faivre; Anne-Sophie Denommé-Pichon; Yannis Duffourd; Antonio Vitobello; Martin Chevarin; Volker Straub; Ana Töpf; Anneke J. van der Kooi; Francesca Magrinelli; Clarissa Rocca; Michael G. Hanna; Jana Vandrovcova; Stephan Ossowski; Solve-RD consortium

doi:https://doi.org/10.1038/s41431-023-01492-9

Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)

Robin Wijngaard, German Demidov, Luke O’Gorman, Jordi Corominas-Galbany, Burcu Yaldiz, Wouter Steyaert, Elke de Boer, Lisenka E. L. M. Vissers, Erik-Jan Kamsteeg, Rolph Pfundt, Hilde Swinkels, Amber den Ouden, Iris B. A. W. te Paske, Richarda M. de Voer, Laurence Faivre, Anne-Sophie Denommé-Pichon, Yannis Duffourd, Antonio Vitobello, Martin Chevarin, Volker StraubAna Töpf, Anneke J. van der Kooi, Francesca Magrinelli, Clarissa Rocca, Michael G. Hanna, Jana Vandrovcova, Stephan Ossowski, Solve-RD consortium

Research output: Contribution to journal › Comment/Letter to the editor › Academic

1 Citation (Scopus)

Abstract

Correction to: European Journal of Human Genetics, published online 19 October 2023 In this article the full list of members of the consortium was missing. It has now been uploaded as supplementary information. The original article has been corrected.

Original language	English
Journal	European journal of human genetics
Early online date	2023
DOIs	https://doi.org/10.1038/s41431-023-01492-9
Publication status	E-pub ahead of print - 2023

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Wijngaard, R., Demidov, G., O’Gorman, L., Corominas-Galbany, J., Yaldiz, B., Steyaert, W., de Boer, E., Vissers, L. E. L. M., Kamsteeg, E.-J., Pfundt, R., Swinkels, H., den Ouden, A., te Paske, I. B. A. W., de Voer, R. M., Faivre, L., Denommé-Pichon, A.-S., Duffourd, Y., Vitobello, A., Chevarin, M., ... Solve-RD consortium (2023). Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7). European journal of human genetics. Advance online publication. https://doi.org/10.1038/s41431-023-01492-9

@article{c768702f93cb4d26bf72e70c86981381,

title = "Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)",

abstract = "Correction to: European Journal of Human Genetics, published online 19 October 2023 In this article the full list of members of the consortium was missing. It has now been uploaded as supplementary information. The original article has been corrected.",

author = "Robin Wijngaard and German Demidov and Luke O{\textquoteright}Gorman and Jordi Corominas-Galbany and Burcu Yaldiz and Wouter Steyaert and {de Boer}, Elke and Vissers, {Lisenka E. L. M.} and Erik-Jan Kamsteeg and Rolph Pfundt and Hilde Swinkels and {den Ouden}, Amber and {te Paske}, {Iris B. A. W.} and {de Voer}, {Richarda M.} and Laurence Faivre and Anne-Sophie Denomm{\'e}-Pichon and Yannis Duffourd and Antonio Vitobello and Martin Chevarin and Volker Straub and Ana T{\"o}pf and {van der Kooi}, {Anneke J.} and Francesca Magrinelli and Clarissa Rocca and Hanna, {Michael G.} and Jana Vandrovcova and Stephan Ossowski and {Solve-RD consortium} and Steven Laurie and Christian Gilissen",

note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",

year = "2023",

doi = "https://doi.org/10.1038/s41431-023-01492-9",

language = "English",

journal = "European journal of human genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

}

Wijngaard, R, Demidov, G, O’Gorman, L, Corominas-Galbany, J, Yaldiz, B, Steyaert, W, de Boer, E, Vissers, LELM, Kamsteeg, E-J, Pfundt, R, Swinkels, H, den Ouden, A, te Paske, IBAW, de Voer, RM, Faivre, L, Denommé-Pichon, A-S, Duffourd, Y, Vitobello, A, Chevarin, M, Straub, V, Töpf, A, van der Kooi, AJ, Magrinelli, F, Rocca, C, Hanna, MG, Vandrovcova, J, Ossowski, S & Solve-RD consortium 2023, 'Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)', European journal of human genetics. https://doi.org/10.1038/s41431-023-01492-9

Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7). / Wijngaard, Robin; Demidov, German; O’Gorman, Luke et al.
In: European journal of human genetics, 2023.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Correction

T2 - Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)

AU - Wijngaard, Robin

AU - Demidov, German

AU - O’Gorman, Luke

AU - Corominas-Galbany, Jordi

AU - Yaldiz, Burcu

AU - Steyaert, Wouter

AU - de Boer, Elke

AU - Vissers, Lisenka E. L. M.

AU - Kamsteeg, Erik-Jan

AU - Pfundt, Rolph

AU - Swinkels, Hilde

AU - den Ouden, Amber

AU - te Paske, Iris B. A. W.

AU - de Voer, Richarda M.

AU - Faivre, Laurence

AU - Denommé-Pichon, Anne-Sophie

AU - Duffourd, Yannis

AU - Vitobello, Antonio

AU - Chevarin, Martin

AU - Straub, Volker

AU - Töpf, Ana

AU - van der Kooi, Anneke J.

AU - Magrinelli, Francesca

AU - Rocca, Clarissa

AU - Hanna, Michael G.

AU - Vandrovcova, Jana

AU - Ossowski, Stephan

AU - Solve-RD consortium

AU - Laurie, Steven

AU - Gilissen, Christian

PY - 2023

Y1 - 2023

N2 - Correction to: European Journal of Human Genetics, published online 19 October 2023 In this article the full list of members of the consortium was missing. It has now been uploaded as supplementary information. The original article has been corrected.

AB - Correction to: European Journal of Human Genetics, published online 19 October 2023 In this article the full list of members of the consortium was missing. It has now been uploaded as supplementary information. The original article has been corrected.

UR - http://www.scopus.com/inward/record.url?scp=85176934797&partnerID=8YFLogxK

U2 - https://doi.org/10.1038/s41431-023-01492-9

DO - https://doi.org/10.1038/s41431-023-01492-9

M3 - Comment/Letter to the editor

C2 - 37973950

SN - 1018-4813

JO - European journal of human genetics

JF - European journal of human genetics

ER -

Wijngaard R, Demidov G, O’Gorman L, Corominas-Galbany J, Yaldiz B, Steyaert W et al. Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7). European journal of human genetics. 2023. Epub 2023. doi: https://doi.org/10.1038/s41431-023-01492-9

Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7)

Abstract

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