Published Erratum
doi: 10.1038/s41431-021-00936-4.
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
Birte Zurek
1
, Kornelia Ellwanger
1
, Lisenka E L M Vissers
2
3
, Rebecca Schüle
4
5
, Matthis Synofzik
4
5
, Ana Töpf
6
, Richarda M de Voer
2
7
, Steven Laurie
8
, Leslie Matalonga
8
, Christian Gilissen
2
7
, Stephan Ossowski
1
, Peter A C 't Hoen
7
9
, Antonio Vitobello
10
, Julia M Schulze-Hentrich
1
, Olaf Riess
1
11
, Han G Brunner
2
3
12
, Anthony J Brookes
13
, Ana Rath
14
, Gisèle Bonne
15
, Gulcin Gumus
16
, Alain Verloes
17
, Nicoline Hoogerbrugge
2
7
, Teresinha Evangelista
15
, Tina Harmuth
1
, Morris Swertz
18
, Dylan Spalding
19
, Alexander Hoischen
2
7
20
, Sergi Beltran
8
21
22
, Holm Graessner
23
24
; Solve-RD consortium
Collaborators,
Affiliations
Collaborators
-
Solve-RD consortium:
Olaf Riess, Tobias B Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Kessler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Ludger Schöls, Holger Hengel, Peter Heutink, Han Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris Te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldiz, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, Chiara Marini Bettolo, Sabine Specht, Jill Clayton-Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Yannis Duffourd, Emilie Tisserant, Ange-Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltran, Ivo Glynne Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvo, Carles Garcia, Marcos Fernandez-Callejo, Carles Hernández, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros-Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem, Fanny Rigour, Giovanni Stevanin, Alexandra Durr, Claire-Sophie Davoine, Léna Guillot-Noel, Anna Heinzmann, Giulia Coarelli, Valérie Allamand, Isabelle Nelson, Rabah Ben Yaou, Corinne Metay, Bruno Eymard, Enzo Cohen, Antonio Atalaia, Tanya Stojkovic, Milan Macek Jr, Marek Turnovec, Dana Thomasová, Radka Pourová Kremliková, Vera Franková, Markéta Havlovicová, Vlastimil Kremlik, Helen Parkinson, Thomas Keane, Alexander Senf, Peter Robinson, Daniel Danis, Glenn Robert, Alessia Costa, Christine Patch, Mike Hanna, Henry Houlden, Mary Reilly, Jana Vandrovcova, Francesco Muntoni, Irina Zaharieva, Anna Sarkozy, Vincent Timmerman, Jonathan Baets, Liedewei Van de Vondel, Danique Beijer, Peter de Jonghe, Vincenzo Nigro, Sandro Banfi, Annalaura Torella, Francesco Musacchia, Giulio Piluso, Alessandra Ferlini, Rita Selvatici, Rachele Rossi, Marcella Neri, Stefan Aretz, Isabel Spier, Anna Katharina Sommer, Sophia Peters, Carla Oliveira, Jose Garcia Pelaez, Ana Rita Matos, Celina São José, Marta Ferreira, Irene Gullo, Susana Fernandes, Luzia Garrido, Pedro Ferreira, Fátima Carneiro, Morris A Swertz, Lennart Johansson, Joeri K van der Velde, Gerben van der Vries, Pieter B Neerincx, Dieuwke Roelofs-Prins, Sebastian Köhler, Alison Metcalfe, Alain Verloes, Séverine Drunat, Caroline Rooryck, Aurelien Trimouille, Raffaele Castello, Manuela Morleo, Michele Pinelli, Alessandra Varavallo, Manuel Posada De la Paz, Eva Bermejo Sánchez, Estrella López Martín, Beatriz Martínez Delgado, F Javier Alonso García de la Rosa, Andrea Ciolfi, Bruno Dallapiccola, Simone Pizzi, Francesca Clementina Radio, Marco Tartaglia, Alessandra Renieri, Elisa Benetti, Peter Balicza, Maria Judit Molnar, Ales Maver, Borut Peterlin, Alexander Münchau, Katja Lohmann, Rebecca Herzog, Martje Pauly, Alfons Macaya, Anna Marcé-Grau, Andres Nascimiento Osorio, Daniel Natera de Benito, Hanns Lochmüller, Rachel Thompson, Kiran Polavarapu, David Beeson, Judith Cossins, Pedro M Rodriguez Cruz, Peter Hackman, Mridul Johari, Marco Savarese, Bjarne Udd, Rita Horvath, Gabriel Capella, Laura Valle, Elke Holinski-Feder, Andreas Laner, Verena Steinke-Lange, Evelin Schröck, Andreas Rump
Affiliations
- 1 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
- 2 Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 3 Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
- 4 Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
- 5 German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
- 6 John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
- 7 Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
- 8 CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
- 9 Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 10 Inserm-University of Burgundy-Franche Comté, Dijon, France.
- 11 Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
- 12 Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
- 13 Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
- 14 INSERM, US14-Orphanet, Plateforme Maladies Rares, Paris, France.
- 15 Sorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.
- 16 EURORDIS-Rare Diseases Europe, Barcelona, Spain.
- 17 Genetics Department, APHP-Robert Debré University Hospital, Université de Paris, Paris, France.
- 18 Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
- 19 European Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, UK.
- 20 Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands.
- 21 Universitat Pompeu Fabra (UPF), Barcelona, Spain.
- 22 Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain.
- 23 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.
- 24 Centre for Rare Diseases, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.
- PMID: 34385672
- PMCID: PMC8440583
- DOI: 10.1038/s41431-021-00936-4
Item in Clipboard
Published Erratum
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
Birte Zurek et al.
Eur J Hum Genet.
2021 Sep.
Display options
Format
doi: 10.1038/s41431-021-00936-4.
Authors
Birte Zurek
1
, Kornelia Ellwanger
1
, Lisenka E L M Vissers
2
3
, Rebecca Schüle
4
5
, Matthis Synofzik
4
5
, Ana Töpf
6
, Richarda M de Voer
2
7
, Steven Laurie
8
, Leslie Matalonga
8
, Christian Gilissen
2
7
, Stephan Ossowski
1
, Peter A C 't Hoen
7
9
, Antonio Vitobello
10
, Julia M Schulze-Hentrich
1
, Olaf Riess
1
11
, Han G Brunner
2
3
12
, Anthony J Brookes
13
, Ana Rath
14
, Gisèle Bonne
15
, Gulcin Gumus
16
, Alain Verloes
17
, Nicoline Hoogerbrugge
2
7
, Teresinha Evangelista
15
, Tina Harmuth
1
, Morris Swertz
18
, Dylan Spalding
19
, Alexander Hoischen
2
7
20
, Sergi Beltran
8
21
22
, Holm Graessner
23
24
; Solve-RD consortium
Collaborators
-
Solve-RD consortium:
Olaf Riess, Tobias B Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Kessler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Ludger Schöls, Holger Hengel, Peter Heutink, Han Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris Te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldiz, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, Chiara Marini Bettolo, Sabine Specht, Jill Clayton-Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Yannis Duffourd, Emilie Tisserant, Ange-Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltran, Ivo Glynne Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvo, Carles Garcia, Marcos Fernandez-Callejo, Carles Hernández, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros-Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem, Fanny Rigour, Giovanni Stevanin, Alexandra Durr, Claire-Sophie Davoine, Léna Guillot-Noel, Anna Heinzmann, Giulia Coarelli, Valérie Allamand, Isabelle Nelson, Rabah Ben Yaou, Corinne Metay, Bruno Eymard, Enzo Cohen, Antonio Atalaia, Tanya Stojkovic, Milan Macek Jr, Marek Turnovec, Dana Thomasová, Radka Pourová Kremliková, Vera Franková, Markéta Havlovicová, Vlastimil Kremlik, Helen Parkinson, Thomas Keane, Alexander Senf, Peter Robinson, Daniel Danis, Glenn Robert, Alessia Costa, Christine Patch, Mike Hanna, Henry Houlden, Mary Reilly, Jana Vandrovcova, Francesco Muntoni, Irina Zaharieva, Anna Sarkozy, Vincent Timmerman, Jonathan Baets, Liedewei Van de Vondel, Danique Beijer, Peter de Jonghe, Vincenzo Nigro, Sandro Banfi, Annalaura Torella, Francesco Musacchia, Giulio Piluso, Alessandra Ferlini, Rita Selvatici, Rachele Rossi, Marcella Neri, Stefan Aretz, Isabel Spier, Anna Katharina Sommer, Sophia Peters, Carla Oliveira, Jose Garcia Pelaez, Ana Rita Matos, Celina São José, Marta Ferreira, Irene Gullo, Susana Fernandes, Luzia Garrido, Pedro Ferreira, Fátima Carneiro, Morris A Swertz, Lennart Johansson, Joeri K van der Velde, Gerben van der Vries, Pieter B Neerincx, Dieuwke Roelofs-Prins, Sebastian Köhler, Alison Metcalfe, Alain Verloes, Séverine Drunat, Caroline Rooryck, Aurelien Trimouille, Raffaele Castello, Manuela Morleo, Michele Pinelli, Alessandra Varavallo, Manuel Posada De la Paz, Eva Bermejo Sánchez, Estrella López Martín, Beatriz Martínez Delgado, F Javier Alonso García de la Rosa, Andrea Ciolfi, Bruno Dallapiccola, Simone Pizzi, Francesca Clementina Radio, Marco Tartaglia, Alessandra Renieri, Elisa Benetti, Peter Balicza, Maria Judit Molnar, Ales Maver, Borut Peterlin, Alexander Münchau, Katja Lohmann, Rebecca Herzog, Martje Pauly, Alfons Macaya, Anna Marcé-Grau, Andres Nascimiento Osorio, Daniel Natera de Benito, Hanns Lochmüller, Rachel Thompson, Kiran Polavarapu, David Beeson, Judith Cossins, Pedro M Rodriguez Cruz, Peter Hackman, Mridul Johari, Marco Savarese, Bjarne Udd, Rita Horvath, Gabriel Capella, Laura Valle, Elke Holinski-Feder, Andreas Laner, Verena Steinke-Lange, Evelin Schröck, Andreas Rump
Affiliations
- 1 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
- 2 Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 3 Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
- 4 Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
- 5 German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
- 6 John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
- 7 Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
- 8 CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
- 9 Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, The Netherlands.
- 10 Inserm-University of Burgundy-Franche Comté, Dijon, France.
- 11 Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
- 12 Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
- 13 Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
- 14 INSERM, US14-Orphanet, Plateforme Maladies Rares, Paris, France.
- 15 Sorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.
- 16 EURORDIS-Rare Diseases Europe, Barcelona, Spain.
- 17 Genetics Department, APHP-Robert Debré University Hospital, Université de Paris, Paris, France.
- 18 Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
- 19 European Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, UK.
- 20 Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands.
- 21 Universitat Pompeu Fabra (UPF), Barcelona, Spain.
- 22 Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain.
- 23 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.
- 24 Centre for Rare Diseases, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.
- PMID: 34385672
- PMCID: PMC8440583
- DOI: 10.1038/s41431-021-00936-4
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Erratum for
-
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.Zurek B, Ellwanger K, Vissers LELM, Schüle R, Synofzik M, Töpf A, de Voer RM, Laurie S, Matalonga L, Gilissen C, Ossowski S, 't Hoen PAC, Vitobello A, Schulze-Hentrich JM, Riess O, Brunner HG, Brookes AJ, Rath A, Bonne G, Gumus G, Verloes A, Hoogerbrugge N, Evangelista T, Harmuth T, Swertz M, Spalding D, Hoischen A, Beltran S, Graessner H; Solve-RD consortium. Zurek B, et al. Eur J Hum Genet. 2021 Sep;29(9):1325-1331. doi: 10.1038/s41431-021-00859-0. Epub 2021 Jun 1. Eur J Hum Genet. 2021. PMID: 34075208 Free PMC article.
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