Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis

Published:2019-11-04 Issue:12 Volume:6 Page:2384-2394
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Naumann Marcel¹²³^ORCID,Peikert Kevin¹³,Günther Rene¹²,Kooi Anneke J.⁴,Aronica Eleonora⁵,Hübers Annemarie⁶,Danel Veronique⁷,Corcia Philippe⁷,Pan‐Montojo Francisco⁸,Cirak Sebahattin⁹¹⁰,Haliloglu Göknur¹¹,Ludolph Albert C.⁶,Goswami Anand¹²,Andersen Peter M.¹³,Prudlo Johannes³¹⁴¹⁵,Wegner Florian¹⁶,Van Damme Philip¹⁷¹⁸,Weishaupt Jochen H.⁶,Hermann Andreas¹²³¹⁴¹⁹^ORCID

Affiliation:

1. Department of Neurology Technische Universität Dresden Dresden Germany

2. German Center for Neurodegenerative Diseases (DZNE) Dresden Germany

3. Translational Neurodegeneration Section “Albrecht‐Kossel” Department of Neurology University Medical Center Rostock University of Rostock Rostock 18147Germany

4. Department of Neurology Amsterdam UMC Academic Medical Centre Amsterdam Neuroscience University of Amsterdam Amsterdam the Netherlands

5. Amsterdam UMC Department of (Neuro)Pathology Amsterdam Neuroscience University of Amsterdam Amsterdam The Netherlands

6. Department of Neurology German Center for Neurodegenerative Diseases University of Ulm Ulm Germany

7. Centre expert pour la SLA et les maladies du motoneurone hôpital SALENGRO CHU Lille France

8. Department of Neurology Klinikum der Universität München Munich Cluster for Systems Neurology SyNergy Munich 81377Germany

9. Division of Pediatric Neurology Department of Pediatrics University Hospital Cologne Cologne Germany

10. Center for Molecular Medicine University of Cologne Cologne Germany

11. Department of Pediatric Neurology Hacettepe University Children’s Hospital Ankara 06100Turkey

12. Institute of Neuropathology RWTH Aachen University Hospital Aachen 3052074Germany

13. Institute of Pharmacology and Clinical Neuroscience Umeå University Umeå SE‐90185Sweden

14. German Center for Neurodegenerative Diseases (DZNE) Rostock/Greifswald Rostock 18147Germany

15. Department of Neurology University of Rostock Rostock Germany

16. Department of Neurology Hannover Medical School Hannover Germany

17. Department of Neurology University Hospitals Leuven Leuven Belgium

18. Department for Neuroscience VIB‐KU Leuven Center for Brain & Disease Research Leuven Belgium

19. Center for Transdisciplinary Neurosciences Rostock (CTNR) University Medical Center Rostock University of Rostock Rostock18147Germany

Funder

Knut och Alice Wallenbergs Stiftelse

Deutsche Forschungsgemeinschaft

NOMIS Stiftung

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.50930

Reference30 articles.

1. Amyotrophic Lateral Sclerosis

2. State of play in amyotrophic lateral sclerosis genetics

3. Comprehensive analysis of the mutation spectrum in 301 German ALS families

4. Truncating mutations in FUS / TLS give rise to a more aggressive ALS ‐phenotype than missense mutations: a clinico‐genetic study in G ermany

5. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients

Cited by 47 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis;Journal of Neurology;2023-11-06

2. FUS gene mutation in amyotrophic lateral sclerosis: a new case report and systematic review;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-11-05

3. French National Protocol for genetic of amyotrophic lateral sclerosis;Revue Neurologique;2023-11

4. Targeted Protein Relocalization via Protein Transport Coupling;2023-10-04

5. Multiomics Approach Reveal Novel Insights in FUS Driven Juvenile Amyotrophic Lateral Sclerosis: A Family Quartet Analysis;Annals of Neurosciences;2023-10-02