🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Isabell Cordts

ORCID: 0000-0002-2078-1997

Also affiliated with Technical University of Munich

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial”.

Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial

The Lancet Neurology(2024)10.1016/s1474-4422(24)00373-9

N/A

0.653DataRank · unranked

31 citations

Andreas Leha, Helen Bidner, Isabell Cordts, Johannes Dorst, René Günther +28 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin

Movement Disorders(2022)10.1002/mds.29071

N/A

0DataRank · unranked

22 citations

Demet Önder, Andreas Traschütz, Xenia Kobeleva, Ivan Karin, Martina Minnerop +25 more

Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD

Brain(2025)10.1093/brain/awaf021

N/A

0DataRank · unranked

7 citations

Maike F. Dohrn, Riccardo Curró, Sara Negri, Petra Laššuthová, Chiara Pisciotta +76 more

Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases

Translational Neurodegeneration(2025)10.1186/s40035-025-00516-2

N/A

0DataRank · unranked

1 citations

Wenan Chen, Joanne Wuu, Angita Jain, Jason R. Myers, Isabell Cordts +26 more