Matilde Laurá

National Hospital for Neurology and Neurosurgery

Also affiliated with University College London

Biochemistry, Genetics and Molecular BiologyMedicine

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 7 papers. Top paper: “Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study”.

Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study

Brain(2020)10.1093/brain/awaa323

N/A

0.681DataRank · unranked

93 citations

Shawna Feely, James M. Polke, Mariola Skorupinska, Laura Pérez, Rosemary Shy +55 more

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores

Neurology(2020)10.1212/wnl.0000000000009035

N/A

0DataRank · unranked

53 citations

Stefan Sillau, Gyula Acsádi, Chelsea Bacon, Kimberly Dooley, Joshua Burns +32 more

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion

Brain(2020)10.1093/brain/awz418

N/A

0DataRank · unranked

221 citations

Stefano Tozza, Wai Yan Yau, Salvatore Rossi, Sarah J. Beecroft, Zane Jaunmuktane +37 more

Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1

Brain(2023)10.1093/brain/awad203

N/A

0DataRank · unranked

11 citations

Seongsik Won, Roy Poh, Stéphanie Efthymiou, James M. Polke, Mariola Skorupinska +9 more

TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations

Brain(2024)10.1093/brain/awae201

N/A

0DataRank · unranked

6 citations

Jack K. Donohue, Maya Hoke, Simone Thomas, Margo A. Peyton, Linh K. Vo +30 more

Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability

medRxiv(2025)10.1101/2025.10.01.25336578

N/A

0DataRank · unranked

0 citations

Stefano Facchini, Arianna Manini, Ricardo Parolin Schnekenberg, Chiara Pisciotta, Stefania Magri +37 more

Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2021-327186

N/A

0DataRank · unranked

17 citations

Andrea Cortese, James M. Polke, Roy Poh, Jana Vandrovcová, Matilde Laurá +15 more