Jessica Ezzell Hunter

Also affiliated with New York University

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 24 papers — median percentile 83. Top paper: “The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation”.

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

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

Cells(2023)10.3390/cells12182330

N/A

0.637DataRank · unranked

69 citations

Dragana Protić, Emily G. Allen, Alison D. Archibald, Anna Baud, Ted W. Brown +41 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

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

An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial

Genetics in Medicine(2022)10.1016/j.gim.2022.07.025

N/A

0DataRank · unranked

13 citations

Michael C. Leo, Leslie Riddle, Cláudia Guerra, Laura M. Amendola, Marian J. Gilmore +16 more

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

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

An Examination of the Ethical and Legal Limits in Implementing “Traceback Testing” for Deceased Patients

The Journal of Law Medicine & Ethics(2022)10.1017/jme.2023.23

N/A

0DataRank · unranked

2 citations

Yolanda K. Prado, Alan F. Rope, Sheila Weinmann, Larissa L. White, Jamilyn M. Zepp +5 more

A picture is worth a thousand words: advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping

Implementation Science Communications(2023)10.1186/s43058-023-00424-4

N/A

0DataRank · unranked

35 citations

Alanna Kulchak Rahm, Marc S. Williams, Ilene Ladd, Victoria Schlieder, Jamie Atondo +11 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

Insight and Recommendations for Fragile X Premutation Associated Conditions from the 5th International Conference on FMR1 Premutation

Preprints.org(2023)10.20944/preprints202307.0605.v1

N/A

0DataRank · unranked

1 citations

Dragana Protić, Emily G. Allen, Alison D. Archibald, Anna Baud, W. Ted Brown +41 more

Genetic Testing Uptake among Ovarian Cancer Survivors in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study

Cancers(2024)10.3390/cancers16142563

N/A

0DataRank · unranked

4 citations

Jennifer Sawyer, Jamilyn M. Zepp, Yolanda K. Prado, Ana Reyes, Mahesh Maiyani +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

Identifying factors and causal chains associated with optimal implementation of Lynch syndrome tumor screening: An application of coincidence analysis

Genetics in Medicine(2024)10.1016/j.gim.2024.101201

N/A

0DataRank · unranked

4 citations

Zachary M Salvati, Jennifer L Schneider, Andrea N. Burnett‐Hartman, Mara M. Epstein, Jessica Ezzell Hunter +9 more

Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population

Translational Behavioral Medicine(2024)10.1093/tbm/ibad084

N/A

0DataRank · unranked

1 citations

Michael C. Leo, Laura M. Amendola, Katrina A.B. Goddard, Jessica Ezzell Hunter, Galen Joseph +7 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

Using Coincidence Analysis to Identify Causal Chains of Factors Associated with Implementation and Optimization of Lynch Syndrome Tumor Screening Across Multiple Health care Systems

medRxiv(2024)10.1101/2024.02.22.24301533

N/A

0DataRank · unranked

0 citations

Zachary M Salvati, Jennifer L. Schneider, Andrea N. Burnett‐Hartman, Mara M. Epstein, Jessica Ezzell Hunter +9 more

Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results

Genetics in Medicine(2025)10.1016/j.gim.2025.101363

N/A

0DataRank · unranked

3 citations

Sara Ackerman, Kyle B. Brothers, Kelly M. East, Ann Katherine M. Foreman, Lucia A. Hindorff +14 more

Primary care patient and clinician attitudes about population genomic screening, informed decision‐making needs, and the potential for Chatbot technology

Journal of Genetic Counseling(2025)10.1002/jgc4.70081

N/A

0DataRank · unranked

1 citations

Sara M. Andrews, Kristi M. Williams, Oksana Kutsa, Tarneisha Hudnell, Jennifer Brailsford +5 more

Functional and cognitive outcomes three years after COVID-19

Clinical Neurology and Neurosurgery(2025)10.1016/j.clineuro.2025.109180

N/A

0DataRank · unranked

1 citations

Thomas Wisniewski, Floyd Silva, Salma Hammam, Zariya Alvarez, Nadir Bilici +19 more

Clustering of comorbid conditions among women who carry an FMR1 premutation

Genetics in Medicine(2020)10.1038/s41436-019-0733-5

N/A

0DataRank · unranked

47 citations

Krista Charen, Heather S. Hipp, Lisa Shubeck, Ashima Amin, Weiya He +3 more

Cascade testing in an ovarian cancer traceback genetic testing program: The GRACE study experience

Journal of Genetic Counseling(2025)10.1002/jgc4.70133

N/A

0DataRank · unranked

0 citations

Heather Spencer Feigelson, Yolanda K. Prado, Ana Aurora Maldonado Reyes, Alan F. Rope, Jennifer K. Sawyer +5 more

Lessons learned about harmonizing survey measures for the CSER consortium

Journal of Clinical and Translational Science(2020)10.1017/cts.2020.41

N/A

0DataRank · unranked

34 citations

Frank Angelo, Sara Ackerman, Jonathan S. Berg, Barbara B. Biesecker, Maria I. Danila +18 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

Jessica Ezzell Hunter

Indexed papers

Top data-sharing exemplar

Papers