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

Qingjiong Zhang

Sun Yat-sen University

ORCID: 0000-0001-7508-848X
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

4in 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 4 indexed papers 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 8 papers. Top paper: “Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A”.

Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis(2008)10.1016/j.mrfmmm.2008.06.004
N/A
1.7DataRank · unranked
53 citations

Xiaoyun Jia, Yanli Ji, Qing-Peng Kong, Qingjiong Zhang, Yong-Gang Yao +2 more

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing

Human Genetics(2014)10.1007/s00439-014-1460-2
N/A
0.785DataRank · unranked
186 citations

Liping Guan, Tao Shen, Jianguo Zhang, Xueshan Xiao, Hui Jiang +8 more

Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation

The American Journal of Human Genetics(2008)10.1016/j.ajhg.2008.11.002
N/A
0.737DataRank · unranked
135 citations

A-Mei Zhang, Xiaoyun Jia, Ya-Ping Zhang, Xueshan Xiao, Shiqiang Li +5 more

Comprehensive Mutation Analysis by Whole-Exome Sequencing in 41 Chinese Families With Leber Congenital Amaurosis

Investigative Opthalmology & Visual Science(2013)10.1167/iovs.13-11606
N/A
0.700DataRank · unranked
105 citations

Qingyan Zhang, Tao Shen, Xueshan Xiao, Shiqiang Li, Liping Guan +8 more

Double Hyperautofluorescence Rings as a Sign ofCFAP410-related Retinopathy

Investigative Ophthalmology & Visual Science(2023)10.1167/iovs.64.15.44
N/A
0.241DataRank · unranked
4 citations

Yingwei Wang, Junwen Wang, Panfeng Wang, Qingjiong Zhang, Xueqing Li

Truncation mutations in MYRF underlie primary angle closure glaucoma

Human Genetics(2022)10.1007/s00439-022-02487-0
N/A
0DataRank · unranked
9 citations

Wenmin Sun, Huangxuan Shen, Xing Liu, Yingchen Wu, Hongmei Jiang +9 more

Systems genetics uncovers microbe-lipid-host connections in the murine gut

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.29.470403
N/A
0DataRank · unranked
0 citations

Vanessa Linke, KA Overmyer, Lindsay L. Traeger, Kazuyuki Kasahara, IJ Miller +25 more

Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants

Molecular Genetics and Genomics(2021)10.1007/s00438-021-01783-0
N/A
0DataRank · unranked
10 citations

Panfeng Wang, Xiaoyun Jia, Wenmin Sun, Shiqiang Li, Xueshan Xiao +3 more