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

Yiran Guo

Shanghai Jiao Tong University

ORCID: 0000-0002-6549-8589

Also affiliated with XinHua Hospital

Biochemistry, Genetics and Molecular BiologyPsychologyMedicine

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 1%percentile
16.4Author DataRank

Indexed papers

6in 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 6 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 →

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.

The diploid genome sequence of an Asian individual

Nature(2008)10.1038/nature07484
Top 1%
14.7DataRank
Top 1%964 citations

Wei Wang, Alexandra P. Lewis, Alan Hodgkinson, Geng Tian, Laurie Goodman +75 more

Papers

Driven by 22 papers — median percentile 37. Top paper: “Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants”.

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

Nature Genetics(2010)10.1038/ng.680
N/A
15.2DataRank · unranked
316 citations

Nicolas Vinckenbosch, Geng Tian, Emilia Huerta-Sanchez, Tao Jiang, Hui Jiang +33 more

The diploid genome sequence of an Asian individual

Nature(2008)10.1038/nature07484
Top 1%
14.7DataRank
Top 1%964 citations

Wei Wang, Alexandra P. Lewis, Alan Hodgkinson, Geng Tian, Laurie Goodman +75 more

Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies

Addiction Biology(2020)10.1111/adb.12880
N/A
1.4DataRank · unranked
74 citations

Emma C. Johnson, Yi‐Ling Chou, Jonathan R. I. Coleman, Laura M. Thornton, Raymond K. Walters +95 more

OpenPBTA: The Open Pediatric Brain Tumor Atlas

Cell Genomics(2023)10.1016/j.xgen.2023.100340
Top 16%
1.3DataRank
Top 16%62 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +61 more

GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

American Journal of Psychiatry(2023)10.1176/appi.ajp.21121266
N/A
0.757DataRank · unranked
154 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

Common Genetic Variation and Age of Onset of Anorexia Nervosa

Biological Psychiatry Global Open Science(2021)10.1016/j.bpsgos.2021.09.001
N/A
0.726DataRank · unranked
30 citations

Laura M. Thornton, Zeynep Yılmaz, Jessica H. Baker, Jonathan R. I. Coleman, Roger A.H. Adan +95 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003
N/A
0.564DataRank · unranked
42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

Polygenic risk for anxiety influences anxiety comorbidity and suicidal behavior in bipolar disorder

Translational Psychiatry(2020)10.1038/s41398-020-00981-5
N/A
0.515DataRank · unranked
30 citations

Kevin Zhu, Kirstin L. Purves, Christopher Song, Kwangmi Ahn, Liping Hou +41 more

Multiparametric MRI along with machine learning predicts prognosis and treatment response in pediatric low-grade glioma

Nature Communications(2025)10.1038/s41467-024-55659-z
N/A
0.434DataRank · unranked
17 citations

Adam A. Kraya, Komal S. Rathi, Meen Chul Kim, Arastoo Vossough, Nastaran Khalili +27 more

OpenPBTA: An Open Pediatric Brain Tumor Atlas

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.13.507832
Top 49%
0.363DataRank
Top 49%7 citations

Krutika S. Gaonkar, Candace L. Savonen, Stephanie J. Spielman, Chanté J. Bethell, Run Jin +59 more

Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors

medRxiv(2022)10.1101/2022.07.03.22277199
N/A
0.345DataRank · unranked
9 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

A cross-species alignment tool (CAT)

BMC Bioinformatics(2007)10.1186/1471-2105-8-349
N/A
0.241DataRank · unranked
4 citations

Liang Guan, Tao Liu, Yiran Guo, International Chicken Polymorphism Map Consortium, Jun Wang +3 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7805407
Top 78%
0.104DataRank
Top 78%1 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more

OMIC-14. OPENPBTA: AN OPEN PEDIATRIC BRAIN TUMOR ATLAS

Neuro-Oncology(2021)10.1093/neuonc/noab090.161
N/A
0.104DataRank · unranked
1 citations

Candace L. Savonen, Yuankun Zhu, Miguel A. Brown, Nhat Duong, Nighat Noureen +37 more

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

UNC Libraries(2020)10.17615/cjxw-ka66
N/A
0DataRank · unranked
0 citations

Ron C. Hoogeveen, Aaron R. Folsom, Brendan J. Keating, Andrew Johnson, Tom Palmer +17 more

Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration

UNC Libraries(2020)10.17615/wr3c-2b58
N/A
0DataRank · unranked
0 citations

Brendan J. Keating, Fotios Drenos, Vinicius Tragante, Folkert W. Asselbergs, Matthew B. Lanktree +12 more

Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

medRxiv(2020)10.1101/2020.12.01.20241281
N/A
0DataRank · unranked
29 citations

Jooeun Kang, Adrián I. Campos, Jonathan R. I. Coleman, Alexis C. Edwards, Hanga Galfalvy +95 more

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

UNC Libraries(2020)10.17615/4jbt-0545
N/A
0DataRank · unranked
3 citations

Brendan J. Keating, Kira C. Taylor, Håkon Håkonarson, Leslie A. Lange, Matthew B. Lanktree +1 more

Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.02.005
N/A
0DataRank · unranked
24 citations

Minal Menezes, Yiran Guo, Scott McLean, Håkon Håkonarson, Felicity Collins +13 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7877739
Top 100%
0DataRank
Top 100%0 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

Science Translational Medicine(2023)10.1126/scitranslmed.abo3189
N/A
0DataRank · unranked
36 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +69 more

Data underlying OpenPBTA Manuscript Figures and Molecular Alterations

Zenodo (CERN European Organization for Nuclear Research)(2023)10.5281/zenodo.7805408
Top 100%
0DataRank
Top 100%0 citations

Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chanté J. Bethell, Run Jin +63 more