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

Kevin M. Flanigan

Nationwide Children's Hospital

ORCID: 0000-0001-6440-3376

Also affiliated with The Ohio State University

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 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 16 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

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation

Skeletal Muscle(2020)10.1186/s13395-020-00239-0

N/A

0DataRank · unranked

21 citations

Nadège Calmels, Robert B. Weiss, Laurent Tiret, Adeline Vulin, Nicolas Wein +13 more

Parent Project Muscular Dystrophy Females with Dystrophinopathy Conference, Orlando, Florida June 26 – June 27, 2019

Journal of Neuromuscular Diseases(2020)10.3233/jnd-200555

N/A

0DataRank · unranked

8 citations

Kathi Kinnett, Linda Cripe, Dongsheng Duan, Jamie L. Jackson, Joe N. Kornegay +7 more

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization.

Research Square(2020)10.21203/rs.3.rs-16251/v2

N/A

0DataRank · unranked

0 citations

Nadège Calmels, Robert B. Weiss, Laurent Tiret, Adeline Vulin, Nicolas Wein +13 more

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization.

Research Square(2020)10.21203/rs.3.rs-16251/v1

N/A

0DataRank · unranked

0 citations

Nadège Calmels, Robert B. Weiss, Laurent Tiret, Adeline Vulin, Nicolas Wein +13 more

Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy

Neuromuscular Disorders(2021)10.1016/j.nmd.2021.06.001

N/A

0DataRank · unranked

8 citations

Elaine McColl, Michael McDermott, William B. Martens, Michela Guglieri, Robert C. Griggs +42 more

Candidate gene modifiers of dystrophinopathy identified by the uniform application of genome-wide datasets to novel GWAS-identified loci

medRxiv(2021)10.1101/2021.11.03.21265899

N/A

0DataRank · unranked

2 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

medRxiv(2021)10.1101/2021.11.03.21265887

N/A

0DataRank · unranked

1 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

CRISPR-Cas9 homology-independent targeted integration of exons 1–19 restores full-length dystrophin in mice

Molecular Therapy — Methods & Clinical Development(2023)10.1016/j.omtm.2023.08.009

N/A

0DataRank · unranked

19 citations

Stefan Nicolau, Tatyana A. Vetter, G. Dufresne, E. Frair, J. Sarff +5 more

Persistence of exon 2 skipping and dystrophin expression at 18 months after U7snRNA-mediated therapy in the Dup2 mouse model

Molecular Therapy — Methods & Clinical Development(2023)10.1016/j.omtm.2023.101144

N/A

0DataRank · unranked

17 citations

A. Bradley, Tatyana A. Vetter, Jacob W. Lay, N. Rohan, E. Frair +3 more

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

European Journal of Human Genetics(2023)10.1038/s41431-023-01329-5

N/A

0DataRank · unranked

13 citations

Megan A. Waldrop, Paul T. Martin, Roxane Alles, Diane M. Dunn, Lindsay N. Alfano +7 more

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features

medRxiv(2024)10.1101/2024.09.23.24313872

N/A

0DataRank · unranked

3 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +33 more

Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.

Scientific Reports(2025)10.1038/s41598-025-23758-6

N/A

0DataRank · unranked

3 citations

Rebecca Tobin, C. Degan, Ahmed Naveed, Michela Guglieri, Albert Jiménez-Requena +88 more

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101399

N/A

0DataRank · unranked

5 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +32 more

Generation of an induced pluripotent stem cell line (NCHi023-A) from a 41-year-old male with nemaline myopathy carrying autosomal dominant ACTA1 c.809-10C>A mutation

Stem Cell Research(2025)10.1016/j.scr.2025.103701

N/A

0DataRank · unranked

0 citations

Shiqiao Ye, Jingting Zhu, Yang Yu, Hui Lin, Kevin M. Flanigan +3 more

Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy phenotype

Neuromuscular Disorders(2025)10.1016/j.nmd.2025.105416

N/A

0DataRank · unranked

0 citations

Sana Yousfi, Stefan Nicolau, Afrooz Rashnonejad, Jingting Zhu, Zarife Sahenk +6 more