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

Jun Shen

Mahasarakham University

ORCID: 0000-0001-8362-7535

Also affiliated with Brigham and Women's Hospital, Harvard University, Guangzhou Women and Children Medical Center, Guangzhou Medical University

NeuroscienceBiochemistry, 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 7 papers. Top paper: “Susceptibility of field populations of the diamondback moth, Plutella xylostella, to a selection of insecticides in Central China”.

Susceptibility of field populations of the diamondback moth, Plutella xylostella, to a selection of insecticides in Central China

Pesticide Biochemistry and Physiology(2016)10.1016/j.pestbp.2016.01.007
N/A
3.5DataRank · unranked
87 citations

Xiaolei Zhang, Jun Shen, Kaikai Mao, Hong You, Jianhong Li +1 more

Loss of LDAH associated with prostate cancer and hearing loss

Human Molecular Genetics(2018)10.1093/hmg/ddy310
N/A
1.0DataRank · unranked
19 citations

Ming Chen, Richard C Sallari, Maura Cotter, Kristen E. Wong, Nahid G. Robertson +32 more

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

medRxiv(2021)10.1101/2021.01.27.21250652
N/A
0DataRank · unranked
8 citations

Marina T. DiStefano, Andrea M. Oza, Madeline Y. Hughes, Emma H. Wilcox, Sarah E. Hemphill +18 more

AnFiSA: An open-source computational platform for the analysis of sequencing data for rare genetic disease

Journal of Biomedical Informatics(2022)10.1016/j.jbi.2022.104174
N/A
0DataRank · unranked
2 citations

D. Etin, S I Trifonov, Viktoria Evdokimova, V. Ulitin, Jun Shen +15 more

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time

Genetics in Medicine(2025)10.1016/j.gim.2025.101392
N/A
0DataRank · unranked
1 citations

Marina T. DiStefano, Andrea M. Oza, Pamela Ajuyah, Ryan Webb, Enyonam Edoh +76 more

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w
N/A
0DataRank · unranked
17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

Gene editing in a Myo6 semi-dominant mouse model rescues auditory function

Molecular Therapy(2021)10.1016/j.ymthe.2021.06.015
N/A
0DataRank · unranked
77 citations

Xinde Hu, Daqi Wang, Di Li, Yige Li, Fang Wang +14 more