PD Dr. rer. nat. Andreas Roos
Germany:
Research Coordinator / Scientific Officer - Dept. of Neuropediatrics, University of Duisburg-Essen 🡵
Project Manager - Institute of Neurology - Düsseldorf University Hospital, Heinrich-Heine-Universität Düsseldorf
![[NMD-GPS]](/.cm4all/uproc.php/0/Bilder/.Logo_NMD-GPS_150px.jpg/picture-200?_=1715988ba28 "[NMD-GPS]"){kind=logo}
Project Manager - NMD-GPS 🡵
GENOMIC AND PROTEOMIC SIGNATURES AS A GPS IN NEUROMUSCULAR DISEASES
Scientific Coordinator of the B2B-Rare-Project 🡵
Scientific Advisory Board Member of "Zusammen stark e.V."
International:
Visiting Professor - University of Belgrad
Emerging Myologist of the year 2023
Adjunct Professor - University of Ottawa 🡵
Invited Lecturer at University of Belgrade (Medical Faculty)
Welcome dear visitor
As senior scientist I am working in the field of translational medicine with a main focus on neurodegenerative and neuromuscular disorders.
In order to understand the etiology of these diseases and to obtain a full picture, my work focusses on the identification of the genetic cause as well as on the discovery of the related pathophysiological consequences. For the latter purpose, various biochemical techniques including different proteomic approaches are applied by making use of in vitro and in vivo models as well as of patient-derived material.
I'd like to invite you to discover my field activity and related projects.
Best regards
Andreas Roos
News |  |
23.01.2026
Published in Journal of Neurology
Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers J Neurol ~ Mroczek M, Preusse C, Hentschel A, Chrościńska-Krawczyk M, Bielak M, Sobolewska A, Della... mehr
16.01.2026
Published in Journal of Neuromuscular Diseases
Choosing the optimal mouse model for the study of late-onset spinal muscular atrophy: Why the 4-copy SMN2 model offers ideal translational relevance J Neuromuscul Dis ~ Leo M, Schmitt L-I, Liebig... mehr
16.01.2026
Published in Journal of Neuromuscular Diseases
Large-scale proteomics profiling of peripheral blood of DM1 patients identifies biomarkers for disease severity and functional capacity J Neuromuscul Dis ~ van As D, Claeys T, Salz R, Van Haver... mehr
07.01.2026
Published in Clinical Genetics
A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia Clin Genet ~ Kilicarslan OA, Gangfuß A, Hentschel A, Kölbel H, Muhmann D, Töpf A, Stöhr M, Chen L,... mehr
10.12.2025
Recently accepted paper in Journal of Neuromuscular Diseases
Large-scale Proteomics Profiling of Peripheral Blood of DM1 patients identifies biomarkers for disease severity and physical activity Journal of Neuromuscular Diseases ~ van As D, Claeys T, Salz R,... mehr
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