Correction to: Nature Genetics https://doi.org/10.1038/s41588-024-01836-1, published online 22 July 2024.
In the version of the article initially published, the surname of Meghna Ahuja Bhasin appeared incorrectly (as Basin) and has now been amended in the HTML and PDF versions of the article.
Author information
These authors contributed equally: Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet.
These authors jointly supervised this work: Peter M. Krawitz, Tobias Haack, Nadja Ehmke, Matias Wagner.
Authors and Affiliations
Institute of Human Genetics, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Axel Schmidt, Hartmut Engels, Sophia Peters, Sugirthan Sivalingam, Claudia Perne, Elisabeth Mangold, Martina Kreiss, Kirsten Cremer, Regina C. Betz, Isabel Spier, André Heimbach, Hellen Lesmann, Sheetal Kumar & Markus Nöthen
Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Berlin, Germany
Magdalena Danyel, Felix Boschann, Henrike Lisa Sczakiel, Sarina Schwartzmann, Martin Atta Mensah, Jean Tori Pantel, Uwe Kornak, Claus-Eric Ott, Markus Schülke, Denise Horn, Stefan Mundlos & Nadja Ehmke
BIH Charité Clinician Scientist Program, Berlin Institute of Health at Charité – Universitätsmedizin Berlin, Berlin, Germany
Magdalena Danyel, Felix Boschann, Henrike Lisa Sczakiel, Martin Atta Mensah & Nadja Ehmke
Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany
Kathrin Grundmann, Martin Kehrer, German Demidov, Stefanie Beck-Wödl, Marc Sturm, Olaf Riess & Tobias Haack
Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, München, Germany
Theresa Brunet, Dominik S. Westphal, Tim Strom, Reka Kovacs, Korbinian M. Riedhammer, Katharina Mayerhanser, Elisabeth Graf, Melanie Brugger, Julia Hoefele, Ulrich Schatz, Martin Krenn, Thomas Meitinger & Matias Wagner
Institute for Genomic Statistics and Bioinformatics, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Hannah Klinkhammer, Tzung-Chien Hsieh, Alexej Knaus, Fabian Brand, Meghna Ahuja Bhasin, Pietro Incardona & Peter M. Krawitz
Institut für Medizinische Biometrie, Informatik und Epidemiologie, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Hannah Klinkhammer
Institute for Medical Genetics, Stellenbosch University, Cape Town, South Africa
Shahida Moosa
Department of Pediatrics, University Hospital Düsseldorf, Düsseldorf, Germany
Luisa Averdunk
Institute for Human Genetics and Genomic Medicine, Medical Faculty, Uniklinik RWTH Aachen University, Aachen, Germany
Jean Tori Pantel, Ingo Kurth, Miriam Elbracht, Cordula Knopp, Matthias Begemann & Florian Kraft
Core Uni Bioinformatics, Berlin Institute of Health at Charité – Universitätsmedizin Berlin, Berlin, Germany
Manuel Holtgrewe
Department of Pediatrics, Charité – Universitätsmedizin Berlin, Berlin, Germany
Annemarie Bösch, Claudia Weiß, Natalie Weinhold, Aude-Annick Suter, Corinna Stoltenburg, Julia Neugebauer, Tillmann Kallinich, Susanne Holzhauer, Christoph Bührer & Philip Bufler
Department of Pediatric Neurology, Charité – Universitätsmedizin Berlin, Berlin, Germany
Angela M. Kaindl
Center for Chronically Sick Children, Charité – Universitätsmedizin Berlin, Berlin, Germany
Angela M. Kaindl
Institute of Cell and Neurobiology, Charité – Universitätsmedizin Berlin, Berlin, Germany
Angela M. Kaindl
Department of Human Genetics, Ruhr University Bochum, Bochum, Germany
Hoa Huu Phuc Nguyen & Sabine Hoffjan
Department of Pediatrics Bochum and CeSER, Ruhr University Bochum, Bochum, Germany
Corinna Grasemann, Tobias Rothoeft, Folke Brinkmann & Nora Matar
Center for Rare Diseases, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Martin Mücke, Lorenz Grigull, Tim Bender, Christiane Stieber, Alexandra Marzena Morawiec & Sarah Bernsen
Department of Neurology, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Thomas Klockgether, Patrick Weydt, Sergio Castro-Gomez, Ahmad Aziz, Marcus Grobe-Einsler, Okka Kimmich, Xenia Kobeleva, Demet Önder & Pawel Tacik
Clinic for Internal Medicine III, University of Bonn, Medical Faculty and University Hospital Bonn, Bonn, Germany
Pantelis Karakostas & Valentin S. Schäfer
University Center for Rare Diseases, University Hospital Carl Gustav Carus, Dresden, Germany
Min Ae Lee-Kirsch, Reinhard Berner, Catharina Schuetz, Julia Körholz, Tanita Kretschmer, Nataliya Di Donato, Evelin Schröck, André Heinen, Ulrike Reuner & Amalia-Mihaela Hanßke
Department of Pediatrics, University Hospital Carl Gustav Carus, Dresden, Germany
Min Ae Lee-Kirsch, Reinhard Berner, Catharina Schuetz, Julia Körholz, Tanita Kretschmer & André Heinen
Institute for Clinical Genetics, University Hospital Carl Gustav Carus, Dresden, Germany
Nataliya Di Donato & Evelin Schröck
Department of Neurology, University Hospital Carl Gustav Carus, Dresden, Germany
Ulrike Reuner
Institute of Human Genetics, University Hospital Essen, Essen, Germany
Frank J. Kaiser, Martin Munteanu & Alma Kuechler
Department of Pediatrics II, University Hospital Essen, Essen, Germany
Eva Manka, Kiewert Cordula & Raphael Hirtz
Department of Neurology, University Hospital Halle, Halle, Germany
Elena Schlapakow
Institute of Human Genetics, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Christian Schlein, Jasmin Lisfeld, Christian Kubisch, Theresia Herget & Maja Hempel
Martin Zeitz Center for Rare Diseases, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Christian Kubisch, Maja Hempel, Christina Weiler-Normann, Kurt Ullrich, Christoph Schramm, Cornelia Rudolph, Franziska Rillig & Maximilian Groffmann
Institute of Human Genetics, Heidelberg University, Heidelberg, Germany
Maja Hempel, Alexandra Tibelius, Eva M. C. Schwaibold, Christian P. Schaaf, Michal Zawada, Lilian Kaufmann & Katrin Hinderhofer
I. Department of Medicine, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Christina Weiler-Normann & Christoph Schramm
Department of Pediatrics, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Ania Muntau
Center for Child and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany
Pamela M. Okun, Urania Kotzaeridou, Georg F. Hoffmann, Daniela Choukair & Markus Bettendorf
Institute of Human Genetics, University Hospital Schleswig-Holstein, Lübeck, Germany
Malte Spielmann & Irina Hüning
Center for Rare Diseases, University Hospital Schleswig-Holstein, Lübeck, Germany
Annekatrin Ripke, Alexander Münchau, Tobias Bäumer & Rebecca Herzog
Department of Neurology, University Hospital Schleswig-Holstein, Lübeck, Germany
Martje Pauly & Rebecca Herzog
Institute for Neurogenetics, University Hospital Schleswig-Holstein, Lübeck, Germany
Martje Pauly
Institute of Systems Motor Science, University of Lübeck, Lübeck, Germany
Alexander Münchau & Tobias Bäumer
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Katja Lohmann
Institute of Human Genetics, University of Lübeck, Lübeck, Germany
Britta Hanker
Department of Human Genetics, University Hospital Schleswig-Holstein, Lübeck, Germany
Yorck Hellenbroich
Department of Nephrology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, München, Germany
Korbinian M. Riedhammer
Institute of Neurogenomics, Helmholtz Zentrum München, München, Germany
Konrad Oexle, Nazanin Mirza-Schreiber, Riccardo Berutti & Matias Wagner
Department of Neurology, Medical University of Vienna, Wien, Austria
Martin Krenn
Department of Paediatrics, Adolescent Medicine and Neonatology, München, Germany
Christine Makowski
Dr. von Hauner Children’s Hospital, University Hospital Munich, München, Germany
Heike Weigand, Sebastian Schröder, Meino Rohlfs, Katharina Vill, Fabian Hauck, Ingo Borggraefe, Wolfgang Müller-Felber, Christoph Klein & Matias Wagner
Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany
Johannes R. Lemke, Julia Hentschel, Konrad Platzer, Vincent Strehlow & Rami Abou Jamra
Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany
Johannes R. Lemke
Center for Rare Diseases, University of Tübingen, Tübingen, Germany
Holm Graessner, Lena Zeltner & Janine Magg
Department of Neurology, University of Tübingen, Tübingen, Germany
Ludger J. Schöls
Department of Pediatric Neurology and Developmental Medicine, University of Tübingen, Tübingen, Germany
Andrea Bevot, Christiane Kehrer & Nadja Kaiser
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Ernest Turro
Berlin Centre for Rare Diseases, Charité – Universitätsmedizin Berlin, Berlin, Germany
Annette Grüters-Kieslich & Heiko Krude
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Correspondence to Peter M. Krawitz.
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Schmidt, A., Danyel, M., Grundmann, K. et al. Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings. Nat Genet 57, 1790–1791 (2025). https://doi.org/10.1038/s41588-025-02271-6
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DOI: https://doi.org/10.1038/s41588-025-02271-6
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