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

Giacomo P. Comi

University of Milan

ORCID: 0000-0002-1383-5248

Also affiliated with Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Ospedale Maggiore, Istituti di Ricovero e Cura a Carattere Scientifico

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 3%percentile

1.6Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy

Journal of Comparative Effectiveness Research(2020)10.2217/cer-2020-0095

Top 13%

1.6DataRank

Top 13%63 citations

Richard J. Barohn, Enrico Bertini, B. Chabrol, Giacomo P. Comi, Basil T. Darras +32 more

Papers

Driven by 13 papers — median percentile 87. Top paper: “Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy”.

Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy

Journal of Comparative Effectiveness Research(2020)10.2217/cer-2020-0095

Top 13%

1.6DataRank

Top 13%63 citations

Richard J. Barohn, Enrico Bertini, B. Chabrol, Giacomo P. Comi, Basil T. Darras +32 more

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Neuron(2020)10.1016/j.neuron.2020.11.005

N/A

0DataRank · unranked

83 citations

Ruth Chia, Jinhui Ding, Richard A. Hickman, Thor D. Stein, Yevgeniya Abramzon +95 more

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51046

N/A

0DataRank · unranked

45 citations

Maria Grazia D’Angelo, Matteo Villa, Aurora Fusto, Sara Vianello, Beatrice Merlo +36 more

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA Neurology(2021)10.1001/jamaneurol.2021.2598

N/A

0DataRank · unranked

85 citations

Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon +87 more

Transcriptome deregulation of peripheral monocytes in GBA -related Parkinson’s disease

medRxiv(2021)10.1101/2021.12.22.21267952

N/A

0DataRank · unranked

2 citations

Ricardo A. Vialle, Elisa Navarro, Evan Udine, Kátia de Paiva Lopes, Amanda Allan +16 more

Transcriptome deregulation of peripheral monocytes and whole blood in GBA-related Parkinson’s disease

Molecular Neurodegeneration(2022)10.1186/s13024-022-00554-8

N/A

0DataRank · unranked

34 citations

Ricardo A. Vialle, Elisa Navarro, Evan Udine, Kátia de Paiva Lopes, Jack Humphrey +17 more

Genetic modifiers of upper limb function in Duchenne muscular dystrophy

Journal of Neurology(2022)10.1007/s00415-022-11133-8

N/A

0DataRank · unranked

7 citations

Aurora Fusto, Sara Vianello, Matteo Villa, J.A. Janik, Grazia D’Angelo +28 more

Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study

Neurology and Therapy(2023)10.1007/s40120-023-00444-1

N/A

0DataRank · unranked

54 citations

Claudio Bruno, Tina Duong, Dirk Fischer, Eugenio Mercuri, Janbernd Kirschner +93 more

Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease

Annals of Neurology(2024)10.1002/ana.27071

N/A

0DataRank · unranked

6 citations

Jonathan Shintaku, Javier Ramón, Eliana Barriocanal‐Casado, Alba Pesini, Russell P. Saneto +23 more

The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy

medRxiv(2024)10.1101/2024.03.29.24304673

N/A

0DataRank · unranked

2 citations

Véronique Bolduc, Fady Guirguis, Sandra Donkervoort, Ying Hu, Rotem Orbach +64 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease

Molecular Neurobiology(2020)10.1007/s12035-020-01926-1

N/A

0DataRank · unranked

382 citations

Alessio Di Fonzo, Stefania Corti, Giacomo P. Comi, Nereo Bresolin, Eliezer Masliah +1 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more