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

Matthew Aguirre

Stanford University

ORCID: 0000-0001-9069-6475
Biochemistry, Genetics and Molecular Biology

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 5%percentile
0.505Author DataRank

Indexed papers

2in 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 2 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.

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.04.564839
Top 38%
0.505DataRank
Top 38%13 citations

Pagé C. Goddard, Emre Karakoç, Soumya Kundu, Stephanie M. Yan, Daniel Nachun +27 more

Papers

Driven by 16 papers — median percentile 62. Top paper: “Landscape of X chromosome inactivation across human tissues”.

Landscape of X chromosome inactivation across human tissues

bioRxiv (Cold Spring Harbor Laboratory)(2016)10.1101/073957
N/A
1.6DataRank · unranked
52 citations

Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Laura Gauthier +17 more

Genetics of 35 blood and urine biomarkers in the UK Biobank

Nature Genetics(2021)10.1038/s41588-020-00757-z
N/A
1.0DataRank · unranked
806 citations

Yosuke Tanigawa, David Amar, Nina Mars, Christian Benner, Matthew Aguirre +19 more

Erratum: Corrigendum: Landscape of X chromosome inactivation across human tissues

Nature(2018)10.1038/nature25993
N/A
0.905DataRank · unranked
15 citations

Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Laura Gauthier +17 more

Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank

Nature Genetics(2021)10.1038/s41588-021-00956-2
N/A
0.693DataRank · unranked
14 citations

Yosuke Tanigawa, David Amar, Nina Mars, Christian Benner, Matthew Aguirre +19 more

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.04.564839
Top 38%
0.505DataRank
Top 38%13 citations

Pagé C. Goddard, Emre Karakoç, Soumya Kundu, Stephanie M. Yan, Daniel Nachun +27 more

Polygenic risk modeling with latent trait-related genetic components

European Journal of Human Genetics(2021)10.1038/s41431-021-00813-0
N/A
0.442DataRank · unranked
18 citations

Yosuke Tanigawa, Guhan Venkataraman, Rob Tibshirani, Trevor Hastie, Manuel A. Rivas +1 more

Bayesian model comparison for rare-variant association studies

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.005
N/A
0.360DataRank · unranked
10 citations

Christopher DeBoever, Yosuke Tanigawa, Matthew Aguirre, Alexander Ioannidis, Hakhamanesh Mostafavi +7 more

Gene regulatory network structure informs the distribution of perturbation effects

PLOS Computational Biology(2025)10.1371/journal.pcbi.1013387
N/A
0.345DataRank · unranked
9 citations

Jeffrey P. Spence, Guy Sella, Jonathan K. Pritchard, Matthew Aguirre

Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.122.003708
N/A
0.330DataRank · unranked
8 citations

Andrew R. Harper, Matthew Aguirre, Maureen Pittman, Catherine Tcheandjieu, Dulguun Amgalan +9 more

Integration of rare large-effect expression variants improves polygenic risk prediction

medRxiv(2020)10.1101/2020.12.02.20242990
N/A
0.241DataRank · unranked
4 citations

Nicole M. Ferraro, Matthew G. Durrant, Abhiram Rao, Matthew Aguirre, Xin Li +12 more

Learning epistatic polygenic phenotypes with Boolean interactions

PLOS ONE(2024)10.1371/journal.pone.0298906
N/A
0.165DataRank · unranked
2 citations

Karl Kumbier, Aldo Cordova-Palomera, Matthew Aguirre, Omer Ronen, Chengzhong Ye +8 more

A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank

PLoS Genetics(2020)10.1371/journal.pgen.1009141
N/A
0DataRank · unranked
134 citations

Yosuke Tanigawa, Wenfei Du, Matthew Aguirre, Christopher Chang, Robert Tibshirani +3 more

Genetic determinants of interventricular septal anatomy and the risk of ventricular septal defects and hypertrophic cardiomyopathy

medRxiv(2021)10.1101/2021.04.19.21255650
N/A
0DataRank · unranked
0 citations

Andrew R. Harper, Matthew Aguirre, Maureen Pittman, Catherine Tcheandjieu, Dulguun Amgalan +9 more

Integration of rare expression outlier-associated variants improves polygenic risk prediction

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.015
N/A
0DataRank · unranked
32 citations

Nicole M. Ferraro, Qin Hui, Matthew G. Durrant, Matthew Aguirre, Yosuke Tanigawa +14 more

Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.03.007
N/A
0DataRank · unranked
65 citations

Yosuke Tanigawa, Matthew Aguirre, Gregory McInnes, Adam Lavertu, Manuel A. Rivas +1 more

A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population

PLoS Genetics(2020)10.1371/journal.pgen.1008802
N/A
0DataRank · unranked
15 citations

Matthew Aguirre, Stefan Gustafsson, Priyanka Saha, Praneetha Potiny, Melissa A Haendel +4 more