Bradford C. Powell

University of North Carolina at Chapel Hill

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 3%percentile

1.2Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228

Top 17%

1.2DataRank

Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

Papers

Driven by 21 papers — median percentile 83. Top paper: “Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies”.

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010

N/A

1.4DataRank · unranked

57 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228

Top 17%

1.2DataRank

Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation

Genetics in Medicine(2024)10.1016/j.gim.2024.101290

N/A

0.442DataRank · unranked

18 citations

Laura V. Milko, Elizabeth Jalazo, Blythe G. Crissman, Ann Katherine M. Foreman, Bradford C. Powell +18 more

Mondo: integrating disease terminology across communities

Genetics(2025)10.1093/genetics/iyaf215

N/A

0.425DataRank · unranked

16 citations

Sabrina Toro, Nicolas A Matentzoglu, Joseph E Flack, Kathleen R. Mullen, Harshad Hegde +95 more

Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

Trials(2021)10.1186/s13063-021-05341-2

N/A

0.419DataRank · unranked

10 citations

Laura V. Milko, Margaret Waltz, Ida Griesemer, Lonna Mollison, Tracey Grant +15 more

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.12.248526

N/A

0.385DataRank · unranked

12 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Question prompt lists and caregiver question asking in pediatric specialty appointments: A randomized controlled trial

Patient Education and Counseling(2023)10.1016/j.pec.2022.107620

N/A

0.312DataRank · unranked

7 citations

Haoyang Yan, R. Jean Cadigan, Courtney Canter, Lizzy Bain, Jeannette T. Bensen +15 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100120

N/A

0DataRank · unranked

12 citations

Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen +15 more

Testing and extending strategies for identifying genetic disease–related encounters in pediatric patients

Genetics in Medicine(2022)10.1016/j.gim.2021.12.001

N/A

0DataRank · unranked

1 citations

Karen Hicklin, Michael C. C. Adams, Laura Farnan, Jeannette T. Bensen, Donna Gilleskie +4 more

The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic Odyssey

Physical & Occupational Therapy In Pediatrics(2022)10.1080/01942638.2022.2138734

N/A

0DataRank · unranked

1 citations

Courtney Canter, Jeannette T. Bensen, Jonathan S. Berg, Ann Katherine M. Foreman, Tracey Grant +8 more

Implementing evidence-based assertions of clinical actionability in the context of secondary findings: Updates from the ClinGen Actionability Working Group

Genetics in Medicine(2024)10.1016/j.gim.2024.101164

N/A

0DataRank · unranked

4 citations

Marian J. Gilmore, Joanna E. Bulkley, Pranesh Chakraborty, Orit Dagan‐Rosenfeld, Ann Katherine M. Foreman +21 more

Community Collaboration in Public Health Genetic Literacy: Methods for Co-Designing Educational Resources for Equitable Genomics Research and Practice

Public Health Genomics(2024)10.1159/000543227

N/A

0DataRank · unranked

1 citations

Grace Byfield, Sabrina N. Powell, Daniel F. Torres, Grace Leon-Lozano, Jahnelle Jackson +20 more

A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation

UNC Libraries(2024)10.17615/70cp-4332

N/A

0DataRank · unranked

0 citations

Beth Lincoln Boyea, Katerina S. Kucera, Katherine G. Langley, Paul Kruszka, Jessica Ezzell Hunter +18 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

Age-Based Genomic Screening: Pediatric Providers’ Perspectives on Implementation

Public Health Genomics(2025)10.1159/000545839

N/A

0DataRank · unranked

0 citations

Ann Katherine M. Foreman, Rebecca A. Gibson, Samantha Schilling, Laura V. Milko, Rachel Phillips +11 more

Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty

Journal of Genetic Counseling(2020)10.1002/jgc4.1219

N/A

0DataRank · unranked

5 citations

Anya E. R. Prince, Julianne O’Daniel, Ann Katherine M. Foreman, Bradford C. Powell, Jonathan S. Berg +1 more

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

medRxiv(2020)10.1101/2020.02.26.20024679

N/A

0DataRank · unranked

10 citations

Stephanie B. Crowley, Myra I. Roche, Ann Katherine M. Foreman, Julianne O’Daniel, Bryce A. Seifert +22 more

Newborn Sequencing in Genomic Medicine and Public Health

UNC Libraries(2020)10.17615/p3y4-3s09

N/A

0DataRank · unranked

0 citations

Stacey Pereira, Sean D. Mooney, Anastasia L. Wise, Jennifer M. Puck, Timothy W. Yu +37 more

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

UNC Libraries(2020)10.17615/0r6z-dk65

N/A

0DataRank · unranked

0 citations

Kevin Riehle, Heidi L. Rehm, Rajarshi Ghosh, Tristan H Nelson, Aaron B. Baker +16 more

Establishing the Medical Actionability of Genomic Variants

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-111021-032401

N/A

0DataRank · unranked

25 citations

Kristy Lee, Adam H. Buchanan, Bradford C. Powell, Jessica Ezzell Hunter, Katrina A.B. Goddard

ClinGen’s Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Genetics in Medicine(2022)10.1016/j.gim.2022.02.019

N/A

0DataRank · unranked

13 citations

Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore, Kristy Lee, Christine M. Pak +17 more

Bradford C. Powell

Indexed papers

Top data-sharing exemplar

Papers