Julianne O’Daniel

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 100%percentile

0Author 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.

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

Papers

Driven by 18 papers — median percentile 0. Top paper: “ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines”.

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8

N/A

2.6DataRank · unranked

85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 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

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

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663

N/A

0.269DataRank · unranked

5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial

Patient Education and Counseling(2021)10.1016/j.pec.2021.04.026

N/A

0.216DataRank · unranked

3 citations

Myra I. Roche, Feng‐Chang Lin, Ann Katherine M. Foreman, Cynthia M. Khan, Ida Griesemer +7 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

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

UNC Libraries(2023)10.17615/41hv-ah02

N/A

0DataRank · unranked

0 citations

A.K.M. Foreman, Brooke S. Staley, Jeannette T. Bensen, Lindsay Mollison, Jonathan S. Berg +15 more

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

UNC Libraries(2023)10.17615/znkm-v920

N/A

0DataRank · unranked

0 citations

Kristen Hassmiller Lich, R. Jean Cadigan, Jeannette T. Bensen, Adriana Navas, Margaret Waltz +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

Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

Patient Education and Counseling(2024)10.1016/j.pec.2024.108190

N/A

0DataRank · unranked

1 citations

Ann Katherine M. Foreman, Courtney Canter, R. Jean Cadigan, Julianne O’Daniel, Margaret Waltz

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

UNC Libraries(2024)10.17615/tpm5-8x49

N/A

0DataRank · unranked

0 citations

Michael E. Mahla, Suzanne C. O’Neill, Feng Lin, Geoffrey L. Smith, B. F. Leach +15 more

Reflections on ‘common’ genetic medical history questions: Time to examine the what, why, and how

UNC Libraries(2025)10.17615/v4m0-jg74

N/A

0DataRank · unranked

0 citations

Ann Katherine M. Foreman, Margaret Waltz, R. Jean Cadigan, Courtney Canter, Julianne O’Daniel

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

How people undergoing genomic sequencing interpret and react to varied secondary findings with limited actionability

Personalized Medicine(2025)10.1080/17410541.2025.2476392

N/A

0DataRank · unranked

0 citations

Christine Rini, Ann Katherine M. Foreman, Jonathan S. Berg, Gail E. Henderson, Kristy Lee +4 more

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

UNC Libraries(2020)10.17615/0tee-nv95

N/A

0DataRank · unranked

1 citations

Christa Lese Martin, Evans, James P., Meredith Weaver, Katrina A.B. Goddard, Margaret Piper +19 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

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

Application of a framework to guide genetic testing communication across clinical indications

Genome Medicine(2021)10.1186/s13073-021-00887-x

N/A

0DataRank · unranked

30 citations

Eric P. Tricou, Kelly E. Ormond, Juliann M. Savatt, Curtis R. Coughlin, W. Andrew Faucett +11 more

Julianne O’Daniel

Indexed papers

Top data-sharing exemplar

Papers