Brian H. Shirts

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

9.4Author 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 →

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 29 papers — median percentile 85. 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

Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

Journal of Medical Genetics(2022)10.1136/jmg-2022-108807

N/A

0.745DataRank · unranked

24 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 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

Strategies to Assess Risk for Hereditary Cancer in Primary Care Clinics

JAMA Network Open(2025)10.1001/jamanetworkopen.2025.0185

N/A

0.427DataRank · unranked

7 citations

Heather M. Harris, Sarah Knerr, Tesla Theoryn, Barbara M. Norquist, Jeannine M. Brant +11 more

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

UNC Libraries(2020)10.17615/02rz-mz46

N/A

0DataRank · unranked

0 citations

Jane Ranchalis, Mitzi L. Murray, Ann Katherine M. Foreman, Seema M. Jamal, Andrew D. Johnson +27 more

Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.001

N/A

0DataRank · unranked

128 citations

Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick +7 more

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.001

N/A

0DataRank · unranked

15 citations

Sukh Makhnoon, Brian H. Shirts, Stephanie M. Fullerton, Eric B. Larson, James D. Ralston +5 more

ClinGen CDH1 specifications for the ACMG/AMP guidelines: improvement of germline variant clinical assertions and updated curation guidelines

medRxiv(2021)10.1101/2021.11.01.21265332

N/A

0DataRank · unranked

0 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

Socioeconomic Status and Interest in Genetic Testing in a US-Based Sample

Healthcare(2022)10.3390/healthcare10050880

N/A

0DataRank · unranked

21 citations

Deborah J. Bowen, Robin L. Bennett, Kevin C. Cain, Tesla Theoryn, Mariebeth Velasquez +5 more

Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access

Genetics in Medicine(2022)10.1016/j.gim.2022.02.006

N/A

0DataRank · unranked

11 citations

Elizabeth Shuster, Michael C. Leo, Michael O. Dorschner, Bradley A. Rolf, Brian H. Shirts +73 more

Modeling the impact of data sharing on variant classification

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac232

N/A

0DataRank · unranked

6 citations

Melissa Cline, Brian H. Shirts, James Casaletto

An algorithm for optimal testing in co‐segregation analysis

Human Mutation(2022)10.1002/humu.24363

N/A

0DataRank · unranked

3 citations

John Michael O. Rañola, Annie Chen, Brian H. Shirts, Ronald W. Buie

A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian, and colorectal cancer susceptibility genes.

Journal of Clinical Oncology(2022)10.1200/jco.2022.40.16_suppl.10512

N/A

0DataRank · unranked

3 citations

Brooke Levin, Megan Ensinger, Kristin Mattie, Robert J. Volk, Zhongming Zhao +9 more

ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classification

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.009

N/A

0DataRank · unranked

87 citations

Alicia B. Byrne, Steven M Harrison, Tina Pesaran, Alejandro A. Schäffer, Brian H. Shirts +3 more

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Genetics in Medicine(2023)10.1016/j.gim.2023.100923

N/A

0DataRank · unranked

15 citations

Leslie Riddle, Galen Joseph, Laura M. Amendola, Marian J. Gilmore, Jamilyn M. Zepp +73 more

Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey

Frontiers in Oncology(2023)10.3389/fonc.2023.1141810

N/A

0DataRank · unranked

9 citations

Rachel Hodan, Linda Rodgers, Sanjeevani Arora, Francesc Balaguer, José G. Guillem +12 more

Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice Survey

JCO Precision Oncology(2023)10.1200/po.23.00440

N/A

0DataRank · unranked

3 citations

Sanjeevani Arora, Charité Ricker, Dan Li, Maheen Farooqi, Francesc Balaguer +11 more

A maternal germline mutator phenotype in a family affected by heritable colorectal cancer

medRxiv(2023)10.1101/2023.12.08.23299304

N/A

0DataRank · unranked

4 citations

Annabel C. Beichman, David Mas-Ponte, Shelby L. Hemker, Luke Zhu, Jacob O. Kitzman +3 more

Assigning credit where it’s due: An information content score to capture the clinical value of Multiplexed Assays of Variant Effect

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.20.562794

N/A

0DataRank · unranked

1 citations

Carolyn Horton, Tina Pesaran, Shawn Fayer, Lea M. Starita, Brian H. Shirts +1 more

Primary care provider practices, attitudes, and confidence with hereditary cancer risk assessment and testing: A mixed methods study

Genetics in Medicine(2024)10.1016/j.gim.2024.101307

N/A

0DataRank · unranked

7 citations

Tesla Theoryn, Emerson J. Dusic, Faith Beers, Sarah Knerr, Barbara M. Norquist +5 more

Applying health equity implementation science frameworks to population genetic screening

Frontiers in Health Services(2024)10.3389/frhs.2024.1455365

N/A

0DataRank · unranked

5 citations

Stephanie M. Fullerton, Brian H. Shirts, Annie Chen, Nora B. Henrikson, Nandana D. Rao

Assigning credit where it is due: an information content score to capture the clinical value of multiplexed assays of variant effect

BMC Bioinformatics(2024)10.1186/s12859-024-05920-5

N/A

0DataRank · unranked

1 citations

Carolyn Horton, Tina Pesaran, Shawn Fayer, Lea M. Starita, Brian H. Shirts +1 more

Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretation

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.009

N/A

0DataRank · unranked

12 citations

Runjun D. Kumar, Cristian Ovadiuc, Andrew Folta, Abbye E. McEwen, Ashley Snyder +8 more

Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications

Genetics in Medicine(2025)10.1016/j.gim.2025.101501

N/A

0DataRank · unranked

1 citations

Adriana E Sedeño Cortés, Pankhuri Gupta, Abbye E. McEwen, Eric Y. Kao, Martha Horike‐Pyne +8 more

Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival

Nature Communications(2020)10.1038/s41467-020-17386-z

N/A

0DataRank · unranked

94 citations

Tabitha A. Harrison, Amanda I. Phipps, Robert S. Steinfelder, Quang M. Trinh, Conghui Qu +71 more

Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretation

medRxiv(2025)10.1101/2025.01.25.25321117

N/A

0DataRank · unranked

2 citations

Runjun D. Kumar, Cristian Ovadiuc, Andrew Folta, Abbye E. McEwen, Ashley Snyder +6 more

Systematic misclassification of missense variants in BRCA1 and BRCA2 “coldspots”

Genetics in Medicine(2020)10.1038/s41436-019-0740-6

N/A

0DataRank · unranked

64 citations

Brian H. Shirts, Thomas P. Slavin, Tom Walsh, Mary‐Claire King, Douglas M. Fowler +2 more

Design of a study to implement population-based risk assessment for hereditary cancer genetic testing in primary care

Contemporary Clinical Trials(2020)10.1016/j.cct.2020.106257

N/A

0DataRank · unranked

13 citations

Catharine Wang, Allison Cole, Barbara M. Norquist, Sarah Knerr, Beth Devine +6 more

Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures

PLoS ONE(2020)10.1371/journal.pone.0239197

N/A

0DataRank · unranked

30 citations

Brian H. Shirts, Tom Walsh, Süleyman Gülsüner, Mary‐Claire King, Alyssa Parker +3 more

Brian H. Shirts

Indexed papers

Top data-sharing exemplar

Papers