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

Sebastian Zöllner

University of Michigan

ORCID: 0009-0005-9855-9017

Also affiliated with Statistical Research (United States)

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 1%percentile
11.7Author 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 →

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.

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534
Top 2%
9.1DataRank
Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

Papers

Driven by 22 papers — median percentile 90. Top paper: “A map of human genome variation from population-scale sequencing”.

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534
Top 2%
9.1DataRank
Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.1902766117
N/A
3.0DataRank · unranked
112 citations

Douglas P. Loesch, James A. Perry, Nancy L. Heard‐Costa, Daniel Taliun, Brian E. Cade +93 more

The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients

Cell Genomics(2023)10.1016/j.xgen.2023.100257
Top 10%
2.2DataRank
Top 10%98 citations

Lars G. Fritsche, Anita Pandit, Brett Vanderwerff, Snehal Patil, Ellen M. Schmidt +9 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3
N/A
1.6DataRank · unranked
91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithms

Genetics(2021)10.1093/genetics/iyab011
N/A
1.3DataRank · unranked
22 citations

Brett Vanderwerff, Sebastian Zöllner, Yichen Si

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115
N/A
1.2DataRank · unranked
36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 more

Mouse segmental duplication and copy number variation

Nature Genetics(2008)10.1038/ng.172
N/A
0.814DataRank · unranked
226 citations

Ze Cheng, Sebastian Zöllner, Deanna M Church, Evan E Eichler, Xinwei She

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Molecular Psychiatry(2021)10.1038/s41380-020-01006-9
N/A
0.686DataRank · unranked
22 citations

Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods +71 more

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

Cell Genomics(2023)10.1016/j.xgen.2023.100345
N/A
0.483DataRank · unranked
24 citations

Kuan-Han Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +16 more

A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.016
N/A
0.434DataRank · unranked
17 citations

Peter VandeHaar, Lars G. Fritsche, Sebastian Zöllner, Michael Boehnke, Laura J. Scott +2 more

Cohort Profile Update: The Heinz C. Prechter Longitudinal Study of Bipolar Disorder

International Journal of Epidemiology(2023)10.1093/ije/dyad109
Top 45%
0.406DataRank
Top 45%14 citations

Steve Anderau, Holli Bertram, Helen J. Burgess, Amy L. Cochran, Patricia J. Deldin +17 more

Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.008
N/A
0.292DataRank · unranked
6 citations

Stephanie M. Gogarten, Stephanie M. Fullerton, Carmen R. Isasi, Braxton D. Mitchell, Kari E. North +5 more

Multi-ancestry polygenic risk scores for venous thromboembolism

Human Molecular Genetics(2024)10.1093/hmg/ddae097
N/A
0.292DataRank · unranked
6 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +42 more

The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

medRxiv(2024)10.1101/2024.03.05.24303738
N/A
0.208DataRank · unranked
3 citations

Nuzulul Kurniansyah, Matthew Goodman, Brian Spitzer, Jiongming Wang, Adrienne M. Stilp +27 more

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

medRxiv(2023)10.1101/2023.08.21.23293271
N/A
0.165DataRank · unranked
2 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +95 more

Multi-ancestry polygenic risk scores for venous thromboembolism

medRxiv(2024)10.1101/2024.01.09.24300914
N/A
0.165DataRank · unranked
2 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +31 more

Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes

UNC Libraries(2020)10.17615/3wz8-7191
N/A
0DataRank · unranked
0 citations

Shyam Gopalakrishnan, Sebastian Zöllner, Sara A. Grimm, Matthew Zawistowski, Jun Ding +1 more

Why are rare variants hard to impute? Coalescent models reveal theoretical limits in existing algorithms

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.10.245043
N/A
0DataRank · unranked
0 citations

Brett Vanderwerff, Sebastian Zöllner, Yichen Si

Genome-wide meta-analysis identifies novel maternal risk variants and enables polygenic prediction of preeclampsia and gestational hypertension

medRxiv(2022)10.1101/2022.11.30.22282929
N/A
0DataRank · unranked
3 citations

Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy +27 more

A Stacking Framework for Polygenic Risk Prediction in Admixed Individuals

medRxiv(2024)10.1101/2024.01.31.24302103
N/A
0DataRank · unranked
0 citations

Sebastian Zöllner, Kevin Liao

Expanding biobank pharmacogenomics through machine learning calls of structural variation

Genetics(2025)10.1093/genetics/iyaf088
N/A
0DataRank · unranked
0 citations

Amy L. Pasternak, Lars G. Fritsche, Emily M. Bertucci, Snehal Patil, Michael Boehnke +5 more

The effect of mutation subtypes on the allele frequency spectrum and population genetics inference

G3 Genes Genomes Genetics(2023)10.1093/g3journal/jkad035
N/A
0DataRank · unranked
0 citations

Jedidiah Carlson, Sebastian Zöllner, Kevin Liao