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 |  |
02.07.2025
Recently accepted
Lessons learned from a muscle study in Nail-Patella syndrome Orphanet Journal of Rare Diseases ~ Paul L, Hentschel A, Depienne C, Schänzer A, Kohlschmidt N, Schara-Schmidt U, Roos A, Kölbel H mehr
28.06.2025
Recently published case report
Co-occurrence of myositis and neuropathy after anti-CD30 therapy in a late-adolescent Hodgkin lymphoma patient Acta Neuropathol Commun ~ Della Marina A, Rink L, Hentschel A, Schuendeln MM, Nelke... mehr
11.06.2025
Recently published paper
Deciphering DST-associated disorders: biallelic variants affecting DST-b cause a congenital myopathy Brain ~ Jacob M, Koelbel H, Harrer P, Kopajtich R, Munot P, Achleitner MT, Badmann S, Brugger... mehr
04.06.2025
Recently published review
Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies Ann Neurol ~ Fogel BL, Klopstock T, Lynch DR, Maltecca F, Verma M, Minassian BA, Platt FM, Gonçalves DF, Puccio H, Roos A,... mehr
31.05.2025
Recently pulished
276th ENMC International Workshop: recommendations on optimal diagnostic pathway and management strategy for patients with acute rhabdomyolysis worldwide Neuromuscul Disord ~ Kruijt N, Laforet P,... mehr
07.04.2025
Recently published paper
Mitochondrial damage is associated with an early immune response in inclusion body myositis Brain ~ Kleefeld F, Cross E, Lagos D, Walli S, Schoser B, Hentschel A, Ruck T, Nelke C, Hahn K, Hathazi... mehr
20.02.2025
Recently published paper
Multi-omics-based phenotyping of AFG3L2-mutant lymphoblasts determines key factors of a pathophysiological interplay between mitochondrial vulnerability and neurodegeneration in spastic ataxia type... mehr
19.02.2025
Recently published paper
Dominant rhabdomyolysis linked to a recurrent ATP2A2 variant reducing SERCA2 function in muscle Brain ~ Malaichamy S, Idoux R, Polavarapu K, Šikić K, Holla E, Thompson R, Spendiff S, Schänzer A,... mehr
13.02.2025
Recently accepted paper
Blood biomarker fingerprints in a cohort of patients with CHRNE-related congenital myasthenic syndrome Acta Neuropathol Commun ~ Della Marina A, Koutsoulidou A, Natera-de Benito D, Tykocinski L-O,... mehr
17.01.2025
Recently published paper
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses Nat Med. ~ Laurie S, Steyaert W, de Boer E, Polavarapu K, Schuermans N, Sommer AK, Demidov G, Ellwanger K, Paramonov I,... mehr
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