Ann Katherine M. Foreman

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 22 papers. Top paper: “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”.

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

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

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

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

medRxiv(2020)10.1101/2020.04.25.20078931

N/A

0DataRank · unranked

5 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +18 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

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

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

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

0DataRank · unranked

7 citations

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

0DataRank · unranked

18 citations

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

Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium

Genetics in Medicine(2024)10.1016/j.gim.2024.101176

N/A

0DataRank · unranked

3 citations

Jill O. Robinson, Eunji Jo, Sabrina A. Suckiel, Laura M. Amendola, Ann Katherine M. Foreman +5 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

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

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

When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103440

N/A

0DataRank · unranked

1 citations

Lauren Desrosiers, Ann Katherine M. Foreman, Nuriye Sahin‐Hodoglugil, Mary A. Majumder, Candice R. Finnila +9 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

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

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

Human Mutation(2020)10.1002/humu.24152

N/A

0DataRank · unranked

166 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +19 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

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