Isabell Cordts

Klinikum rechts der Isar — Germany

Medicine · Health Sciences

22h-index1.6kcitations79works6.32yr avg
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Research Topics

Neurogenetic and Muscular Disorders Research(31), Amyotrophic Lateral Sclerosis Research(23), Genetic Neurodegenerative Diseases(12), RNA modifications and cancer(10), Congenital Anomalies and Fetal Surgery(9)

Publications76 total

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia
Nature Communications·2026Open Access
EARLY-ALS: A Multicentre Study on Presymptomatic and Prodromal Amyotrophic Lateral Sclerosis
2026Open Access
Neurogenetik
Elsevier eBooks·2025
Autorinnen und Autoren
Elsevier eBooks·2025
Compound Muscle Action Potential (CMAP) Amplitude Trajectories and Pattern in Adults with 5q‐Spinal Muscular Atrophy Receiving Nusinersen Therapy: A Multicenter, Binational Observational Study
European Journal of Neurology·2025· 3 citedOpen Access
Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases
Translational Neurodegeneration·2025Open Access
The Diverse Neuromuscular Spectrum of <scp>VPS13A</scp> Disease
Annals of Clinical and Translational Neurology·2025Open Access
Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study
Journal of Neuromuscular Diseases·2025· 1 citedOpen Access
Respiratory function in 192 adult patients with spinal muscular atrophy (SMA) treated with nusinersen – a multicenter observational study
Orphanet Journal of Rare Diseases·2025· 1 citedOpen Access
Identification and validation of a tear fluid-derived protein biomarker signature in patients with amyotrophic lateral sclerosis
Acta Neuropathologica Communications·2025· 1 citedOpen Access
Repeat-associated ataxias in a German patient cohort analysed by targeted parallel long-read sequencing
Brain·2025Open Access
Detection of Amyotrophic Lateral Sclerosis with Computer Audition: An Impact Analysis of Different Speech Tasks
2025
Identification and Validation of a Tear Fluid-Derived Protein Biomarker Signature in Patients with Amyotrophic Lateral Sclerosis
2025· 1 citedOpen Access
Untersuchung von anamnestischen und klinischen Indikatoren für Dysphagien bei Motoneuronerkrankungen
Nervenheilkunde·2025
Die Selbstbewertung der Funktionsskala für Amyotrophe Lateralsklerose (ALSFRS-R) per Smartphone der Patienten ist gegenüber der klinischen Datenerfassung nicht unterlegen
Nervenheilkunde·2025Open Access
Aktualisierung des Modells pathogener CNBP Repeatexpansionen ursächlich für die Myotone Dystrophie Typ 2
Nervenheilkunde·2025
Self-assessment of amyotrophic lateral sclerosis functional rating scale on the patient’s smartphone proves to be non-inferior to clinic data capture
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration·2025· 7 citedOpen Access
Long-Term Dynamics of CSF and Serum Neurofilament Light Chain in Adult Patients With 5q Spinal Muscular Atrophy Treated With Nusinersen
Neurology·2025· 9 citedOpen Access
Shared prognostic information in amyotrophic lateral sclerosis – systematic assessment of the patients’ perception of neurofilament light chain and the ALS functional rating scale
Neurological Research and Practice·2025· 2 citedOpen Access
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD
Brain·2025· 6 citedOpen Access
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Frequent Co-authors

Marcus Deschauer(32), Paul Lingor(32), René Günther(22), Jan Christoph Koch(17), Albert C. Ludolph(17), Susanne Petri(16), Tim Hagenacker(15), Andreas Hermann(14), Tobias B. Haack(12), Olivia Schreiber‐Katz(10), Alma Osmanovic(10), Johannes Dorst(10), Thomas Meyer(10), Julian Großkreutz(9), Ute Weyen(9), Claudia D. Wurster(8), Benjamin Stolte(8), Maren Freigang(8), Daniel Zeller(8), Matthias Boentert(8)