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

Yun Li

Sun Yat-sen University

ORCID: 0000-0002-5361-1791

Also affiliated with The Seventh Affiliated Hospital of Sun Yat-sen University, Ocean University of China

MedicineBiochemistry, 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 5%percentile
0.530Author 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.

Common variants contribute to intrinsic human brain functional networks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.30.229914
Top 37%
0.530DataRank
Top 37%8 citations

Tengfei Li, Stephen M. Smith, Di Xiong, Xifeng Wang, Yue Yang +15 more

Papers

Driven by 5 papers — median percentile 63. Top paper: “Common variants contribute to intrinsic human brain functional networks”.

Common variants contribute to intrinsic human brain functional networks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.30.229914
Top 37%
0.530DataRank
Top 37%8 citations

Tengfei Li, Stephen M. Smith, Di Xiong, Xifeng Wang, Yue Yang +15 more

Nucleotide excision repair hotspots and coldspots of UV-induced DNA damage in the human genome

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.16.045369
N/A
0.208DataRank · unranked
3 citations

Wentao Li, Laura A Lindsey-Boltz, Yuchen Yang, Yun Li, Aziz Sancar +1 more

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

Human Genetics(2020)10.1007/s00439-020-02188-6
N/A
0DataRank · unranked
32 citations

Loukas Argyriou, Francisco Martínez‐Azorín, Susanne Morlot, Gökhan Yiğit, Teresa M. Lee +19 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita

Research Square(2022)10.21203/rs.3.rs-2121654/v1
N/A
0DataRank · unranked
0 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

Human Genetics(2023)10.1007/s00439-023-02528-2
N/A
0DataRank · unranked
6 citations

Elisabeth Schuler, Almundher Al‐Maawali, Ankur Chaurasia, Steffen Syrbe, Adila Al‐Kindi +10 more