Nazareth S, Hayward L, Simmons E, Snir M, Hatchell KE, Rojahn S, Nussbaum RL (2021) Hereditary cancer risk using a genetic chatbot before routine care visits. Obstet Gynecol 138:860–870. https://doi.org/10.1097/AOG.0000000000004596
Article PubMed PubMed Central Google Scholar
Rao SK, Blakely LJ, Small K, Schleicher S, Natalie RDM (2024) Building efficiency and scaling with a remote genetic counseling program. Oncol (Williston Park) 38:20–25. https://doi.org/10.46883/2024.25921011
Raspa M, Moultrie R, Toth D, Haque SN (2021) Barriers and facilitators to genetic service delivery models: scoping review. Interact J Med Res 10:e23523. https://doi.org/10.2196/23523
Article PubMed PubMed Central Google Scholar
National Comprehensive Cancer Network (2025) Genetic/familial high-risk assessment: breast, ovarian, pancreatic, and prostate. https://www.nccn.org/guidelines/guidelines-detail?category=2&id=1545
Radford C, Prince A, Lewis K, Pal T (2014) Factors which impact the delivery of genetic risk assessment services focused on inherited cancer genomics: expanding the role and reach of certified genetics professionals. J Genet Couns 23:522–530. https://doi.org/10.1007/s10897-013-9668-1
Cohen SA, Huziak RC, Gustafson S, Grubs RE (2016) Analysis of advantages, limitations, and barriers of genetic counseling service delivery models. J Genet Couns 25:1010–1018. https://doi.org/10.1007/s10897-016-9932-2
Buchanan AH, Datta SK, Skinner CS, Hollowell GP, Beresford HF, Freeland T, Adams MB (2015) Randomized trial of telegenetics vs in-person cancer genetic counseling: cost, patient satisfaction and attendance. J Genet Couns 24:961–970. https://doi.org/10.1007/s10897-015-9836-6
Article PubMed PubMed Central Google Scholar
Danylchuk NR, Cook L, Shane-Carson KP, Cacioppo CN, Hardy MW, Nusbaum R, Malinowski J (2021) Telehealth for genetic counseling: a systematic evidence review. J Genet Couns 30:1361–1378. https://doi.org/10.1002/jgc4.1481
Proussaloglou EM, Koelliker EL, Laprise J, Wilbur JS, Robison K, Stuckey A, Crawford K (2024) The impact of converting to telehealth for cancer genetic counseling and testing during the COVID-19 pandemic. J Genet Couns 33:834–841. https://doi.org/10.1002/jgc4.1792
Kinney AY, Steffen LE, Brumbach BH, Kohlmann W, Du R, Lee JH, Schwartz MD (2016) Randomized noninferiority trial of telephone delivery of BRCA1/2 genetic counseling compared with in-person counseling: 1-year follow-up. J Clin Oncol 34:2914–2924. https://doi.org/10.1200/JCO.2015.65.9557
Article PubMed PubMed Central Google Scholar
Lahiri S, Mersch J, Zimmerman J, Mauer Hall C, Moriarty K, Gemmell A, Pirzadeh-Miller S (2025) Randomized control trial comparing genetic counseling service delivery models in an underserved population. J Genet Couns 34:e1975. https://doi.org/10.1002/jgc4.1975
Wang C, Lu H, Bowen DJ, Xuan Z (2023) Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: an observational study of 4 clinical workflows. Genet Med 25:100802. https://doi.org/10.1016/j.gim.2023.100802
Article CAS PubMed Google Scholar
Williams S, Ebrahimzadeh JE, Clay D, Constantino G, Heiman J, Wangensteen KJ, Katona BW (2023) Comparing telemedicine and in-person gastrointestinal cancer genetic appointment outcomes during the COVID-19 pandemic. Hered Cancer Clin Pract 21:6. https://doi.org/10.1186/s13053-023-00250-8
Article PubMed PubMed Central Google Scholar
Chapman-Davis E, Zhou ZN, Fields JC, Frey MK, Jordan B, Sapra KJ, Holcomb KM (2021) Racial and ethnic disparities in genetic testing at a hereditary breast and ovarian cancer center. J Gen Intern Med 36:35–42. https://doi.org/10.1007/s11606-020-06064-x
Peterson JM, Pepin A, Thomas R, Biagi T, Stark E, Sparks AD, Kaltman R (2020) Racial disparities in breast cancer hereditary risk assessment referrals. J Genet Couns 29:587–593. https://doi.org/10.1002/jgc4.1250
Grzymski JJ, Elhanan G, Morales Rosado JA, Smith E, Schlauch KA, Read R, Lu JT (2020) Population genetic screening efficiently identifies carriers of autosomal dominant diseases. Nat Med 26:1235–1239. https://doi.org/10.1038/s41591-020-0982-5
Article CAS PubMed Google Scholar
Abul-Husn NS, Soper ER, Odgis JA, Cullina S, Bobo D, Moscati A, Kenny EE (2019) Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. Genome Med 12:2. https://doi.org/10.1186/s13073-019-0691-1
Article CAS PubMed PubMed Central Google Scholar
Manchanda R, Blyuss O, Gaba F, Gordeev VS, Jacobs C, Burnell M, Jacobs I (2018) Current detection rates and time-to-detection of all identifiable BRCA carriers in the Greater London population. J Med Genet 55:538–545. https://doi.org/10.1136/jmedgenet-2017-105195
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