Eric Venner

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 1%percentile

11.0Author DataRank

Indexed papers

3in 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 3 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 16 papers — median percentile 88. Top paper: “Genomic data in the All of Us Research Program”.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-023-05708-y

Top 12%

1.7DataRank

Top 12%52 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +95 more

Harmonizing variant classification for return of results in the All of Us Research Program

Human Mutation(2021)10.1002/humu.24317

Top 27%

0.738DataRank

Top 27%17 citations

Christina Austin‐Tse, Serra Kim, Matthew S. Lebo, Annette Leon, David R. Murdock +8 more

Defining and Reducing Variant Classification Disparities

medRxiv(2024)10.1101/2024.04.11.24305690

N/A

0.165DataRank · unranked

2 citations

Shawn Fayer, Sriram Pendyala, Mason Post, Divya Kalra, Karynne Patterson +13 more

Exome variant discrepancies due to reference-genome differences

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.011

N/A

0DataRank · unranked

66 citations

Moez Dawood, Michael M. Khayat, Jesse Farek, Shalini N. Jhangiani, Ziad Khan +8 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study

Genetics in Medicine(2022)10.1016/j.gim.2022.01.022

N/A

0DataRank · unranked

69 citations

Steven E. Scherer, Suzette J. Bielinski, Donna M. Muzny, Leila A. Jones, John L. Black +95 more

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

Genome Medicine(2022)10.1186/s13073-022-01031-z

N/A

0DataRank · unranked

63 citations

Donna M. Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood +16 more

Empowering personalized pharmacogenomics with generative AI solutions

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae039

N/A

0DataRank · unranked

58 citations

Bo Yuan, Eric Venner, Christie M. Ballantyne, Katherine M. Robinson, James C. Coons +4 more

Tracking updates in clinical databases increases efficiency for variant reanalysis

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101841

N/A

0DataRank · unranked

3 citations

Xia Tian, Vaughan Woodzell, Richard A. Gibbs, Bo Yuan, Eric Venner +1 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011

N/A

0DataRank · unranked

112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

Celeste : A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects

medRxiv(2025)10.1101/2025.04.29.25326690

N/A

0DataRank · unranked

0 citations

Breanna Lee, Victoria Yi, Jesse Farek, Ziad Khan, Sara E. Kalla +12 more

Improving reporting standards for polygenic scores in risk prediction studies

medRxiv(2020)10.1101/2020.04.23.20077099

N/A

0DataRank · unranked

55 citations

Samuel A. Lambert, Cecelia P. Tamburro, Michael A. Iacocca, Jack W. O’Sullivan, Catherine H. Sillari +28 more

Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1130

N/A

0DataRank · unranked

5 citations

Guolian Ding, Kexin Zou, Zi-Ru Jiang, Junyu Zhang, Yun-hua Lu +7 more

Methods developed during the first National Center for Biotechnology Information Structural Variation Codeathon at Baylor College of Medicine

F1000Research(2020)10.12688/f1000research.23773.1

N/A

0DataRank · unranked

0 citations

Alejandro R. Gener, Michael M. Khayat, Adam C. English, Advait Balaji, Anbo Zhou +41 more

Eric Venner

Indexed papers

Top data-sharing exemplar

Papers