Correction to: Nature Genetics https://doi.org/10.1038/s41588-025-02290-3, published online 9 September 2025.
In the version of the article initially published, the Supplementary Information did not include the members of the Solve-RD DITF-EPICARE, Solve-RD DITF-ITHACA, Solve-RD DITF-EURO-NMD, Solve-RD DITF-RITA, Solve-RD DITF-RND and Solve-RD consortia. The Supplementary Information has now been corrected to include these lists.
Author information
Full lists of members and their affiliations appear in the Supplementary Information.
Authors and Affiliations
School of Computation, Information and Technology, Technical University of Munich, Garching, Germany
Vicente A. Yépez, Rebeka Luknárová, Felix Brechtmann, Leon Kraß, Shubhankar Londhe, Christian Mertes & Julien Gagneur
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany
German Demidov, Kornelia Ellwanger, Birte Zurek & Holm Graessner
Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain
Steven Laurie, Marc Dabad, Ida Paramonov, Daniel Picó, Davide Piscia, Emanuele Raineri, Leslie Matalonga, Sergi Beltran & Anna Esteve-Codina
Universitat de Barcelona, Barcelona, Spain
Steven Laurie, Marc Dabad, Ida Paramonov, Daniel Picó, Davide Piscia, Leslie Matalonga & Anna Esteve-Codina
Department of Genetics/Epigenetics, Faculty NT, Saarland University, Saarbrücken, Germany
Midhuna Immaculate Joseph Maran, Thomas Hentrich & Julia Schulze-Hentrich
Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands
Lydia Sagath, Bart van der Sanden, Galuh Astuti, Kornelia Neveling, Machteld M. Oud, Marloes Steehouwer, Wouter Steyaert, Lisenka E. L. M. Vissers, Christian Gilissen & Alexander Hoischen
Infection in Immunocompromised Pediatric Patients Research Group, Vall d’Hebron Research Institute, Barcelona, Spain
Laura Batlle-Masó
Pediatric Infectious Diseases and Immunodeficiencies Unit, Vall d’Hebron University Hospital, Barcelona, Spain
Laura Batlle-Masó
Division Translational Genomics of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany
Danique Beijer
RESIST—Cluster of Excellence 2155 to Hannover Medical School, Satellite Center Freiburg, Freiburg, Germany
Andrés Caballero-Oteyza
Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, Albert Ludwigs University of Freiburg, Freiburg, Germany
Andrés Caballero-Oteyza
Medical Genomics, FHU TRANSLAD, Dijon University Hospital, Dijon, France
Anne-Sophie Denommé-Pichon & Antonio Vitobello
Unit 1231 GAD Team, Inserm, Burgundy Europe University, Dijon, France
Anne-Sophie Denommé-Pichon & Antonio Vitobello
Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands
Cenna Doornbos, Wouter Steyaert, Peter-Bram t’ Hoen & Christian Gilissen
Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands
Cenna Doornbos & Peter-Bram t’ Hoen
Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium
Zakaria Eddafir
Applied Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium
Zakaria Eddafir
Neuromuscular Disorders Unit, Department of Pediatric Neurology, Hospital Sant Joan de Déu, Barcelona, Spain
Berta Estévez-Arias & Daniel Natera-de Benito
Laboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, Barcelona, Spain
Berta Estévez-Arias
Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada
Ozge Aksel Kilicarslan & Kiran Polavarapu
Division of Neurodegenerative Diseases and Movement Disorders, Department of Neurology, Faculty of Medicine, Heidelberg University Hospital, Heidelberg, Germany
Ingrid H. M. Kolen
Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany
Leon Kraß, Christian Mertes & Julien Gagneur
Computational Health Center, Helmholtz Center Munich, Neuherberg, Germany
Leon Kraß, Shubhankar Londhe & Julien Gagneur
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Katja Lohmann & Mirja Thomsen
Helmholtz Association, Munich School for Data Science, Munich, Germany
Shubhankar Londhe
Institute of Rare Diseases Research, Spanish Undiagnosed Rare Diseases Cases Program (SpainUDP), Undiagnosed Diseases Network International, Instituto de Salud Carlos III, Madrid, Spain
Estrella López-Martín & Beatriz Martínez-Delgado
Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
Kars Maassen
Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK
William Macken & Heba Morsy
CIBER of Rare Diseases (CIBERER), Madrid, Spain
Beatriz Martínez-Delgado
Department of Neuroscience and Medical Genetics, Meyer Children’s Hospital IRCCS, Florence, Italy
Davide Mei
IRCCS Istituto delle Scienze Neurologiche di Bologna, European Reference Network for Rare and Complex Epilepsies (EpiCARE), Bologna, Italy
Raffaella Minardi
Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt
Heba Morsy
Dubowitz Neuromuscular Centre, UCL Great Ormond Street Hospital, London, UK
Juliane S. Mueller
Applied Research in Neuromuscular Diseases, Institut de Recerca Sant Joan de Déu, Barcelona, Spain
Daniel Natera-de Benito
Center for Biomedical Research Network on Rare Diseases (CIBERER), ISCIII, Madrid, Spain
Daniel Natera-de Benito
Centre de Recherche en Myologie, Institut de Myologie, Inserm, Sorbonne Université, Paris, France
Isabelle Nelson
Folkhälsan Research Centre and Medicum, University of Helsinki, Helsinki, Finland
Marco Savarese
VIB-CMN, Applied and Translational Neurogenomics Group, University of Antwerp, Antwerp, Belgium
Noor Smal
Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands
Morris A. Swertz & Gerben van der Vries
John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK
Ana Töpf
Peripheral Neuropathy Research Group, University of Antwerp, Antwerp, Belgium
Liedewei Van de Vondel
Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium
Liedewei Van de Vondel
Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
Liedewei Van de Vondel
Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
Carlo Wilke
German Center for Neurodegenerative Diseases, Tübingen, Germany
Carlo Wilke
Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands
Lisenka E. L. M. Vissers
Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain
Sergi Beltran
Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, the Netherlands
Alexander Hoischen
Centre for Rare Diseases, University of Tübingen, Tübingen, Germany
Holm Graessner
- Vicente A. Yépez
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- German Demidov
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Consortia
Solve-RD DITF-EPICARE
- Zakaria Eddafir
- , Kornelia Ellwanger
- , Davide Mei
- , Raffaella Minardi
- & Noor Smal
Solve-RD DITF-ITHACA
- Anne-Sophie Denommé-Pichon
- , Estrella López-Martín
- , Beatriz Martínez-Delgado
- , Machteld M. Oud
- , Lisenka E. L. M. Vissers
- & Antonio Vitobello
Solve-RD DITF-EURO-NMD
- Ozge Aksel Kilicarslan
- , Berta Estévez-Arias
- , Juliane S. Mueller
- , Daniel Natera-de Benito
- , Isabelle Nelson
- , Kiran Polavarapu
- , Marco Savarese
- , Ana Töpf
- & Liedewei Van de Vondel
Solve-RD DITF-RITA
- Laura Batlle-Masó
- , Andrés Caballero-Oteyza
- , Alexander Hoischen
- & Kars Maassen
Solve-RD DITF-RND
- Danique Beijer
- , Holm Graessner
- , Ingrid H. M. Kolen
- , Katja Lohmann
- , Heba Morsy
- , Liedewei Van de Vondel
- & Carlo Wilke
Solve-RD consortium
- Holm Graessner
- , Birte Zurek
- , Kornelia Ellwanger
- , German Demidov
- , Julia Schulze-Hentrich
- , Ingrid H. M. Kolen
- , Carlo Wilke
- , Danique Beijer
- , Alexander Hoischen
- , Peter-Bram t’ Hoen
- , Lisenka E. L. M. Vissers
- , Christian Gilissen
- , Wouter Steyaert
- , Marloes Steehouwer
- , Kornelia Neveling
- , Bart van der Sanden
- , Lydia Sagath
- , Ana Töpf
- , Antonio Vitobello
- , Anne-Sophie Denommé-Pichon
- , Sergi Beltran
- , Steven Laurie
- , Davide Piscia
- , Leslie Matalonga
- , Daniel Picó
- , Ida Paramonov
- , Anna Esteve-Codina
- , Marc Dabad
- , Emanuele Raineri
- , Isabelle Nelson
- , Heba Morsy
- , Juliane S. Mueller
- , Liedewei Van de Vondel
- , Noor Smal
- , Morris A. Swertz
- , Gerben van der Vries
- , Ozge Aksel Kilicarslan
- , Laura Batlle-Masó
- , Andrés Caballero-Oteyza
- , Berta Estévez-Arias
- , Julien Gagneur
- , Leon Kraß
- , Katja Lohmann
- , Estrella López-Martín
- , Rebeka Luknárová
- , Beatriz Martínez-Delgado
- , Davide Mei
- , Christian Mertes
- , Daniel Natera-de Benito
- , Kiran Polavarapu
- , Marco Savarese
- & Vicente A. Yépez
Corresponding authors
Correspondence to Julien Gagneur or Holm Graessner.
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Yépez, V.A., Demidov, G., Ellwanger, K. et al. Author Correction: The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. Nat Genet 58, 231 (2026). https://doi.org/10.1038/s41588-025-02500-y
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DOI: https://doi.org/10.1038/s41588-025-02500-y
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