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A. K. Foreman · SciRah

Researcher profile · Semantic Scholar

A. K. Foreman

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A. K. Foreman — researcher profile on SciRah

h-index: 16
Works: 56
Citations: 1,316

Most-cited papers

Actionable exomic incidental findings in 6503 participants: challenges of variant classification
L. Amendola, M. Dorschner, P. Robertson, Joseph S. Salama +69 more
2015Genome Research367 citations Open access
Semantic Scholar
Prenatal Exome Sequencing in Anomalous Fetuses: New Opportunities and Challenges
N. Vora, B. Powell, A. Brandt, Natasha T. Strande +15 more
2017Genetics in Medicine156 citations Open access
Semantic Scholar
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
Tamara S. Roman, Stephanie B. Crowley, M. Roche, A. K. Foreman +23 more
2020American Journal of Human Genetics107 citations Open access
Semantic Scholar
A semi-quantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
J. Berg, A. K. Foreman, Julianne M. O'Daniel, J. Booker +15 more
2015Genetics in Medicine90 citations Open access
Semantic Scholar
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
L. Amendola, Kathleen Muenzen, L. Biesecker, Kevin M. Bowling +26 more
2020American Journal of Human Genetics81 citations Open access
Semantic Scholar
Clinical Validity Assessment of Genes Frequently Tested on Hereditary Breast and Ovarian Cancer Susceptibility Sequencing Panels
Kristy Lee, Bryce A. Seifert, H. Shimelis, R. Ghosh +10 more
2018Genetics in Medicine80 citations Open access
Semantic Scholar
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
N. Vora, K. Gilmore, A. Brandt, Chelsea Gustafson +10 more
2020Genetics in Medicine73 citations Open access
Semantic Scholar
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening
L. Milko, Julianne M. O'Daniel, Daniela M. DeCristo, Stephanie B. Crowley +14 more
2019Jornal de Pediatria66 citations Open access
Semantic Scholar
“Possibly positive or certainly uncertain?”: Participants’ responses to uncertain diagnostic results from exome sequencing
D. Skinner, M. Roche, K. Weck, Kelly A. Raspberry +5 more
2017Genetics in Medicine44 citations Open access
Semantic Scholar
The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study
C. Rini, Cynthia M. Khan, Elizabeth Moore, M. Roche +9 more
2017Genetics in Medicine28 citations Open access
Semantic Scholar
Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making
Daniela M. DeCristo, L. Milko, Julianne M. O'Daniel, A. K. Foreman +4 more
2021Genome Medicine26 citations Open access
Semantic Scholar
The Phenotype of Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1: Report and Review
Natario L. Couser, M. Masood, Natasha T. Strande, A. K. Foreman +8 more
2015American Journal of Medical Genetics. Part A25 citations Open access
Semantic Scholar
A Review and Definition of “Usual Care” in Genetic Counseling Trials to Standardize Use in Research
B. Biesecker, Sarah E Lillie, L. Amendola, Katherine E. Donohue +13 more
2020Journal of Genetic Counseling23 citations Open access
Semantic Scholar
The NCGENES project: exploring the new world of genome sequencing.
A. K. Foreman, Kristy Lee, James P. Evans
2013North Carolina Medical Journal20 citations
Semantic Scholar
Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes
C. Rini, G. Henderson, James P. Evans, J. Berg +5 more
2019Genetics in Medicine17 citations Open access
Semantic Scholar
Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings
M. Roche, Ida Griesemer, Cynthia M. Khan, Elizabeth Moore +9 more
2018Genetics in Medicine16 citations Open access
Semantic Scholar
A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early Check implementation
H. Cope, L. Milko, E. Jalazo, B. Crissman +19 more
2024Genetics in Medicine15 citations Open access
Semantic Scholar
An examination of the factors contributing to the expansion of subspecialty genetic counseling
Victoria C E Haverbusch, E. Heise, A. K. Foreman, N. Callanan
2019Journal of Genetic Counseling10 citations
Semantic Scholar
Congenital Midline Cervical Cleft: First Report and Genetic Analysis of Two Related Patients
M. Masood, P. Mieczkowski, Ewa P. Malc, A. K. Foreman +3 more
2020Annals of Otology, Rhinology and Laryngology9 citations Open access
Semantic Scholar
Question Prompt Lists and Caregiver Question Asking in Pediatric Specialty Appointments: A Randomized Controlled Trial
M. Waltz, Hao-Yang Yan, R. Cadigan, Courtney Canter +16 more
2023Patient Education and Counseling7 citations Open access
Semantic Scholar
ClinGen’s Pediatric Actionability Working Group: Clinical Actionability of Secondary Findings from Genome-Scale Sequencing in Children and Adolescents
J. Hunter, Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore +18 more
2022Genetics in Medicine7 citations Open access
Semantic Scholar
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
B. Staley, L. Milko, M. Waltz, Ida Griesemer +16 more
2021Trials7 citations Open access
Semantic Scholar
Genomic sequencing in diverse and underserved pediatric populations: parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results
Barbara Biesecker, Sara L. Ackerman, Kyle B. Brothers, K. East +15 more
2025Genetics in Medicine6 citations Open access
Semantic Scholar
Response of Central Giant Cell Granuloma of the Jaw to Imatinib.
Brian Tallent, R. Padilla, C. McKay, A. K. Foreman +2 more
2022Journal of pediatric hematology/oncology5 citations
Semantic Scholar
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
N. Vora, K. Gilmore, A. Brandt, Chelsea Gustafson +10 more
2020Genetics in Medicine5 citations Open access
Semantic Scholar
Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty
M. Waltz, Anya E. R. Prince, Julianne M. O'Daniel, A. K. Foreman +2 more
2020Journal of Genetic Counseling5 citations Open access
Semantic Scholar
Implementing Evidence-Based Assertions of Clinical Actionability in the Context of Secondary Findings: Updates from the ClinGen Actionability Working Group
Christine M. Pak, Marian J. Gilmore, Joanna E Bulkley, P. Chakraborty +22 more
2024Genetics in Medicine3 citations Open access
Semantic Scholar
Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial
C. Rini, M. Roche, Feng-Chang Lin, A. K. Foreman +8 more
2021Patient Education and Counseling3 citations Open access
Semantic Scholar
Community Collaboration in Public Health Genetic Literacy: Co-Designing Educational Resources for Equitable Genomics Research and Practice
J. Salunke, G. Byfield, S. Powell, D. Torres +21 more
2024medRxiv2 citations Open access
Semantic Scholar
Group-based medical mistrust in genomic medicine: Associations with patient and provider perceptions of a specialty clinical encounter
Frank Angelo, M. Waltz, Hao-Yang Yan, J. S. Berg +3 more
2024Genetics in Medicine2 citations
Semantic Scholar
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.
S. Scollon, Jill O. Robinson, Eunji Jo, Sabrina A. Suckiel +6 more
2024Genetics in Medicine2 citations
Semantic Scholar
Community Collaboration in Public Health Genetic Literacy: Methods for Co-Designing Educational Resources for Equitable Genomics Research and Practice
J. Salunke, Grace Byfield, S. Powell, D. Torres +21 more
2024Public Health Genomics2 citations Open access
Semantic Scholar
When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research
K. Bonini, L. Desrosiers-Battu, A. K. Foreman, Nuriye N Sahin-Hodoglugil +10 more
2025Genetics in medicine open1 citations Open access
Semantic Scholar
How People Undergoing Genomic Sequencing Interpret and React to Varied Secondary Findings with Limited Actionability
Hao-Yang Yan, Christine Rini, A. K. Foreman, J. S. Berg +5 more
2025Personalized Medicine1 citations Open access
Semantic Scholar
Reflections on ‘Common’ Genetic Medical History Questions: Time to Examine the What, Why, and How
M. Waltz, A. K. Foreman, Courtney Canter, R. Cadigan +1 more
2024Patient Education and Counseling1 citations Open access
Semantic Scholar
The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic Odyssey
M. Waltz, Courtney Canter, J. Bensen, J. Berg +9 more
2022Physical & Occupational Therapy in Pediatrics1 citations Open access
Semantic Scholar
Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes
C. Rini, G. Henderson, James P. Evans, J. Berg +5 more
2019Genetics in Medicine1 citations Open access
Semantic Scholar
Exploring the New World of Genome Sequencing
A. K. Foreman, Kristy Lee, James P. Evans
20131 citations
Semantic Scholar
Exome sequencing early in outpatient evaluation in NCGENES 2: Changing the course of the diagnostic odyssey?
Tamara S. Roman, S. Gray, Tam P Sneddon, A. K. Foreman +5 more
2026HGG advances0 citations Open access
Semantic Scholar
North Carolina primary care provider perspectives on expanded genomic screening in children
E. Branch, M. Roberts, M. Waltz, Neal A. deJong +7 more
2026BMC Medical Genomics0 citations Open access
Semantic Scholar
Age-Based Genomic Screening: Pediatric Providers’ Perspectives on Implementation
M. Waltz, A. K. Foreman, R. A. Gibson, S. Schilling +12 more
2025Public Health Genomics0 citations Open access
Semantic Scholar
Primary Care Provider Perspectives on Expanded Genomic Screening in Children
E. Branch, M. Roberts, M. Waltz, Neal A. deJong +7 more
2025Research Square0 citations
Semantic Scholar
P525: Exploring the Influence of Genetic Literacy on Research Participation Among Underrepresented Populations
L. Milko, G. Leon-Lozano, J. Jackson, Sharisse Jimenez +8 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
P157: Willing but not (quite) ready: Primary care provider perspectives on expanded genetic screening in children*
E. Branch, Neal A. deJong, S. Schilling, Jonathan Berg +5 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
eP442: Patients’ reaction to and interpretation of secondary genomic findings with limited or no medical actionability
Hao-Yang Yan, M. Waltz, J. Berg, A. K. Foreman +4 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar
Clinical actionability of secondary findings in the pediatric context
Kathleen E. Wallace, Kristy Lee, Marinan Gilmore, Kathleen F. Mittendorf +16 more
20210 citations
Semantic Scholar
ClinGen’s actionability working groups: development and early implementation of an assertion rubric for clinical actionability
Christine M. Pak, J. Hunter, Marian J. Gilmore, Kristy Lee +23 more
20210 citations
Semantic Scholar
The impact of COVID-19 on pediatric diagnostic odysseys
M. Waltz, J. Bensen, A. K. Foreman, Tracey L. Grant +4 more
2021Molecular Genetics and Metabolism0 citations Open access
Semantic Scholar
Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making
Daniela M. DeCristo, L. Milko, Julianne M. O'Daniel, A. K. Foreman +4 more
2021Genome Medicine0 citations Open access
Semantic Scholar
Implementing early exome sequencing to shorten the diagnostic odyssey: identifying barriers and facilitators through clinician focus groups
A. K. Foreman, Hannah Clare, J. Bensen, J. Berg +1 more
20210 citations
Semantic Scholar

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