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

Ruifang Sui

Chinese Academy of Medical Sciences & Peking Union Medical College

ORCID: 0000-0002-6659-0926

Also affiliated with Peking Union Medical College Hospital

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 100%percentile
0Author 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 →

Papers

Driven by 6 papers. Top paper: “Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome”.

Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome

Genetics in Medicine(2021)10.1038/s41436-021-01106-z
N/A
0.533DataRank · unranked
34 citations

Zaisheng Lin, Tian Zhu, Minjun Jin, Dan Meng, Ruida He +19 more

Systematic assessment of the contribution of structural variants to inherited retinal diseases

Human Molecular Genetics(2023)10.1093/hmg/ddad032
N/A
0.373DataRank · unranked
11 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Systematic assessment of the contribution of structural variants to inherited retinal diseases

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.02.522522
N/A
0.269DataRank · unranked
5 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Novel variants in PNPLA6 causing syndromic retinal dystrophy

Experimental Eye Research(2020)10.1016/j.exer.2020.108327
N/A
0DataRank · unranked
20 citations

Zixi Sun, Tian Zhu, Richard G. Weleber, Paul Yang, Xing Wei +3 more

Structural modeling, mutation analysis, and in vitro expression of usherin, a major protein in inherited retinal degeneration and hearing loss

Computational and Structural Biotechnology Journal(2020)10.1016/j.csbj.2020.05.025
N/A
0DataRank · unranked
16 citations

Junhuang Zou, Qian Chen, Tian Zhu, Ruifang Sui, Jun Yang +1 more

Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases

Human Molecular Genetics(2024)10.1093/hmg/ddae028
N/A
0DataRank · unranked
11 citations

Meng Wang, Hafiz Muhammad Jafar Hussain, David E Rauch, Molly Marra, Mark E. Pennesi +14 more