Amanda L. Bergner

Columbia University — United States

Medicine · Health Sciences

20h-index2.5kcitations61works1.82yr avg
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Research Topics

Neurofibromatosis and Schwannoma Cases(24), Genomics and Rare Diseases(16), Meningioma and schwannoma management(14), BRCA gene mutations in cancer(8), Vascular Malformations Diagnosis and Treatment(7)

Publications59 total

Inclusive genetic counseling for <scp>LGBTQ</scp> + clients: A qualitative study of reproductive genetic counselors' experiences and perspectives
Journal of Genetic Counseling·2025
Genome Sequencing for All Pregnant Persons: Navigating the Next Frontier in Prenatal Diagnosis Through Patient Reflections
Prenatal Diagnosis·2025
Barriers to the implementation of epilepsy genetic testing and counseling guidelines
Epilepsia Open·2025· 2 citedOpen Access
Loss and Grief in the Era of Genomic Medicine
2025
Prenatal Diagnostic Testing for Adult‐Onset Neurodegenerative Disease
Prenatal Diagnosis·2025
Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis
Journal of Genetic Counseling·2024· 6 citedOpen Access
Comparing the frequency of variants of uncertain significance (VUS) between ancestry groups in a paediatric epilepsy cohort
Journal of Medical Genetics·2024· 6 cited
Exploring the evolving roles of clinical geneticists and genetic counselors in the era of genomic medicine
American Journal of Medical Genetics Part A·2023· 4 cited
Patient experiences in receiving telegenetics care for inherited cardiovascular diseases
Journal of Community Genetics·2023· 1 citedOpen Access
Genetic counselors' utilization of <scp>ChatGPT</scp> in professional practice: A <scp>cross‐sectional</scp> study
American Journal of Medical Genetics Part A·2023· 11 cited
Telegenetics in cardiovascular disease: patient experience and follow-up care
Research Square (Research Square)·2023Open Access
Knowledge and beliefs about epilepsy genetics among Hispanic and <scp>non‐Hispanic</scp> patients
Epilepsia·2023· 6 citedOpen Access
Clinical utility of exome sequencing in a pediatric epilepsy cohort
Epilepsia·2023· 15 citedOpen Access
The utility of limited Spanish proficiency in interpreted genetic counseling sessions
Journal of Genetic Counseling·2023· 5 citedOpen Access
P395: Assessing the collaborative relationships among diverse stakeholders working to expand access to genetic services in Puerto Rico
Genetics in Medicine Open·2023Open Access
Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation
Genetics in Medicine·2022· 247 citedOpen Access
Genetic testing for the epilepsies: A systematic review
Epilepsia·2021· 138 cited
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination
Journal of Genetic Counseling·2021· 11 citedOpen Access
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm
Journal of Genetic Counseling·2021· 8 citedOpen Access
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
Genetics in Medicine·2021· 687 citedOpen Access
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Frequent Co-authors

Jaishri O. Blakeley(12), Vanessa L. Merker(12), Bruce R. Korf(11), D. Gareth Evans(11), Rosalie E. Ferner(10), Scott R. Plotkin(10), Dusica Babovic‐Vuksanovic(8), Justin T. Jordan(8), Victor Mautner(8), C. Oliver Hanemann(8), Matthias A. Karajannis(8), Laura M. Fayad(8), Eva Dombi(8), Robert A. Avery(7), Michael J. Fisher(7), David H. Gutmann(7), Fred G. Barker(7), Patricia Ciavarelli(7), Marco Giovannini(7), Michel Kalamarides(7)