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

Mridul Johari

University of Helsinki

ORCID: 0000-0002-3549-558X

Also affiliated with The University of Western Australia, Harry Perkins Institute of Medical Research, Folkhälsans Forskningscentrum

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 6%percentile
0.252Author 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.

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127
Top 60%
0.252DataRank
Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Papers

Driven by 6 papers — median percentile 40. Top paper: “Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy”.

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127
Top 60%
0.252DataRank
Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Titin copy number variations associated with dominant inherited phenotypes

Journal of Medical Genetics(2023)10.1136/jmg-2023-109473
N/A
0DataRank · unranked
4 citations

Corinne Métay, Marco Savarese, Rabah Ben Yaou, German Demidov, Isabelle Nelson +28 more

Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum

European Journal of Human Genetics(2023)10.1038/s41431-023-01487-6
N/A
0DataRank · unranked
0 citations

Khuthala Mnika, Samuel Mawuli Adadey, Rita Barbosa‐Matos, Elena Avram, Patracia Nevondwe +14 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

Expert Panel Curation of 31 Genes in Relation to Limb Girdle Muscular Dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.03.592369
N/A
0DataRank · unranked
0 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 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