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

Ryan K. C. Yuen

University of Toronto

ORCID: 0000-0001-7273-4968

Also affiliated with Hospital for Sick Children, SickKids Foundation

NeuroscienceBiochemistry, Genetics and Molecular Biology

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
0.208Author 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.

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031
Top 65%
0.208DataRank
Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Papers

Driven by 7 papers — median percentile 35. Top paper: “C9orf72 repeat expansion creates the unstable folate-sensitive fragile site FRA9A”.

C9orf72 repeat expansion creates the unstable folate-sensitive fragile site FRA9A

NAR Molecular Medicine(2024)10.1093/narmme/ugae019
N/A
0.499DataRank · unranked
15 citations

Monika H.M. Schmidt, Natalie Shum, Tanya Prasolava, Bryanna Meikle, Stella Lanni +30 more

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

UNC Libraries(2020)10.17615/hmn0-qq55
N/A
0.483DataRank · unranked
24 citations

Dandan Cao, Irene Drmic, Yong‐hui Jiang, Christian R. Marshall, Jun Luo +27 more

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031
Top 65%
0.208DataRank
Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Recurrent repeat expansions in human cancer genomes

Nature(2022)10.1038/s41586-022-05515-1
N/A
0DataRank · unranked
89 citations

Gamze Gürsoy, Rashid Al-Abri, Ashwini Suriyaprakash, Egor Dolzhenko, Kevin Zhu +19 more

A genome-wide atlas of recurrent repeat expansions in human cancer

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.24.505159
N/A
0DataRank · unranked
1 citations

Gamze Gürsoy, Rashid Al-Abri, Ashwini Suriyaprakash, Egor Dolzhenko, Kevin Zhu +19 more

Autistic traits in myotonic dystrophy type 1 due to MBNL inhibition and RNA mis-splicing

Research Square(2023)10.21203/rs.3.rs-3221704/v1
N/A
0DataRank · unranked
3 citations

Mahreen Khan, Mariam Tadross, Adam Ciesiołka, Curtis A. Nutter, Katarzyna Taylor +6 more

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009
N/A
0DataRank · unranked
280 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more