Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples

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; Solve-RD consortium; Stephan Ossowski; Steven Laurie; Christian Gilissen

doi:10.1038/s41431-023-01492-9

Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples

Eur J Hum Genet. 2024 Feb;32(2):248. doi: 10.1038/s41431-023-01492-9.

Authors

Robin Wijngaard^#^{1

2}, German Demidov^#³, Luke O'Gorman¹, Jordi Corominas-Galbany¹, Burcu Yaldiz¹, Wouter Steyaert^{1

4}, Elke de Boer^{1

2}, Lisenka E L M Vissers^{1

2}, Erik-Jan Kamsteeg^{1

2}, Rolph Pfundt¹, Hilde Swinkels¹, Amber den Ouden¹, Iris B A W Te Paske^{1

4}, Richarda M de Voer^{1

4}, Laurence Faivre⁵, Anne-Sophie Denommé-Pichon^{6

7}, Yannis Duffourd^{6

7}, Antonio Vitobello^{6

7}, Martin Chevarin^{6

7}, Volker Straub⁸, Ana Töpf⁸, Anneke J van der Kooi⁹, Francesca Magrinelli¹⁰, Clarissa Rocca^{11

12}, Michael G Hanna¹¹, Jana Vandrovcova¹¹; Solve-RD consortium; Stephan Ossowski³, Steven Laurie^#¹³, Christian Gilissen^#^{14

15}

Affiliations

¹ Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
² Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
³ Universitätsklinikum Tübingen - Institut für Medizinische Genetik und angewandte Genomik, Tübingen, Germany.
⁴ Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
⁵ Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs", Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU Dijon Bourgogne, Dijon, France.
⁶ UMR1231-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.
⁷ Laboratoire de Génétique chromosomique et moléculaire, UF6254 Innovation en diagnostic génomique des maladies rares, Centre Hospitalier Universitaire de Dijon, Dijon, France.
⁸ John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
⁹ Department of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands.
¹⁰ Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
¹¹ Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.
¹² Clinical Pharmacology, William Harvey Research Institute, School of Medicine and Dentistry, Queen Mary University of London, London, UK.
¹³ Centro Nacional de Análisis Genómico (CNAG), Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
¹⁴ Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. Christian.gilissen@radboudumc.nl.
¹⁵ Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands. Christian.gilissen@radboudumc.nl.

^# Contributed equally.

No abstract available

Publication types

Published Erratum