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

Xueya Zhou

ORCID: 0000-0003-2350-081X
Biochemistry, Genetics and Molecular BiologyNeuroscience

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 3%percentile
1.5Author 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.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Papers

Driven by 10 papers — median percentile 86. Top paper: “Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders”.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y
N/A
0.808DataRank · unranked
218 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Recent ultra-rare inherited variants implicate new autism candidate risk genes

Nature Genetics(2021)10.1038/s41588-021-00899-8
N/A
0.749DataRank · unranked
146 citations

Tychele N. Turner, Shwetha C. Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang +38 more

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.011
N/A
0.593DataRank · unranked
51 citations

Le Xu, Lan Yu, Julia Wynn, Rebecca Hernan, Xueya Zhou +33 more

Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

UNC Libraries(2021)10.17615/j25m-xa12
N/A
0DataRank · unranked
9 citations

Jong‐Young Lee, Shengxu Li, Jyh Ming J.immy Juang, Terri L. Young, Treva Rice +95 more

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 and ALYREF as new candidate risk genes

medRxiv(2021)10.1101/2021.06.01.21257928
N/A
0DataRank · unranked
0 citations

Le Xu, Lan Yu, Julia Wynn, Rebecca Hernan, Xueya Zhou +33 more

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.

White Rose Research Online (University of Leeds, The University of Sheffield, University of York)(2021)10.17863/cam.71232
N/A
0DataRank · unranked
0 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +20 more

Rare variant analysis of 4,241 pulmonary arterial hypertension cases from an international consortium implicate FBLN2 , PDGFD and rare de novo variants in PAH

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.124255
N/A
0DataRank · unranked
4 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +19 more

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Genetics in Medicine(2020)10.1038/s41436-020-0908-0
N/A
0DataRank · unranked
37 citations

Julia Wynn, Lan Yu, Rebecca Hernan, Xueya Zhou, Vincent Duron +21 more

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Genome Medicine(2021)10.1186/s13073-021-00891-1
N/A
0DataRank · unranked
86 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +89 more