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

Līvija Medne

Children's Hospital of Philadelphia

ORCID: 0000-0002-3836-4294
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 5%percentile
0.367Author 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 →

Top data-sharing exemplar

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

A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51834
Top 49%
0.367DataRank
Top 49%6 citations

Pomi Yun, Safoora Syeda, Abhinandan Batra, Andrew J. Bradley, Sandra Donkervoort +17 more

Papers

Driven by 7 papers — median percentile 51. Top paper: “A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy”.

A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51834
Top 49%
0.367DataRank
Top 49%6 citations

Pomi Yun, Safoora Syeda, Abhinandan Batra, Andrew J. Bradley, Sandra Donkervoort +17 more

POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern

Acta Neuropathologica(2020)10.1007/s00401-019-02117-6
N/A
0DataRank · unranked
39 citations

Macarena Cabrera‐Serrano, Katherine Johnson, Ashutosh Pandey, Atsuko Ito, Eloy Rivas +22 more

Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium

Journal of Clinical Investigation(2021)10.1172/jci145700
N/A
0DataRank · unranked
24 citations

Sandra Donkervoort, Josine M. de Winter, Stefan Conijn, Leon P. L. Begthel, Benno Küsters +20 more

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

Brain(2020)10.1093/brain/awaa420
N/A
0DataRank · unranked
56 citations

Rauan Kaiyrzhanov, Yaqun Zou, Sahar Da’as, Reza Maroofian, Sandra Donkervoort +91 more

CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability

Developmental Biology(2023)10.1016/j.ydbio.2023.04.006
N/A
0DataRank · unranked
27 citations

Mehreen Pasha, María Elena Guerra, Stephen Viviano, Weidong Ji, Monica Konstantino +7 more

Unusually severe muscular dystrophy upon in-frame deletion of the dystrophin rod domain and lack of compensation by membrane-localized utrophin

Med(2023)10.1016/j.medj.2023.02.005
N/A
0DataRank · unranked
8 citations

Joachim Schessl, Yaqun Zou, Michele Yang, Peter Heydemann, Robert Sufit +6 more

PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care

BMC Medical Informatics and Decision Making(2022)10.1186/s12911-022-01927-1
N/A
0DataRank · unranked
18 citations

Anbumalar Singaravelu, Dennis M. Driscoll, Leonard Minkovsky, Ingo Helbig, Līvija Medne +4 more