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References

  1. Haverfield, E. V., Esplin, E. D., Aguilar, S. J., Hatchell, K. E., Ormond, K. E., Hanson-Kahn, A., ... & Nussbaum, R. L. (2021). Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study. BMC medicine, 19, 1-10. https://doi.org/10.1186/s12916-021-01999-2

  2. Punj, S., Akkari, Y., Huang, J., Yang, F., Creason, A., Pak, C., ... & Richards, C. S. (2018). Preconception carrier screening by genome sequencing: results from the clinical laboratory. The American Journal of Human Genetics, 102(6), 1078-1089. https://doi.org/10.1016/j.ajhg.2018.04.004

  3. Samadder, N. J., Riegert-Johnson, D., Boardman, L., Rhodes, D., Wick, M., Okuno, S., ... & Stewart, A. K. (2021). Comparison of universal genetic testing vs guideline-directed targeted testing for patients with hereditary cancer syndrome. JAMA oncology, 7(2), 230-237. https://doi.org/10.1001/jamaoncol.2020.6252

  4. American College of Obstetrics and Gynecology. (2017). Committee Opinion No. 691: Carrier Screening for Genetic Conditions. Obstetrics and Gynecology, 129(3), e41-e55. https://doi.org/10.1097/AOG.0000000000001952

  5. Scheuner, M. T., Sales, P., Hoggatt, K., Zhang, N., Whooley, M. A., & Kelley, M. J. (2023). Genetics professionals are key to the integration of genetic testing within the practice of frontline clinicians. Genetics in Medicine, 25(1), 103-114. https://doi.org/10.1016/j.gim.2022.09.012

  6. Mikat-Stevens, N. A., Larson, I. A., & Tarini, B. A. (2015). Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature. Genetics in Medicine, 17(3), 169-176. https://doi.org/10.1038/gim.2014.101

  7. Bellcross, C. A., Peipins, L. A., McCarty, F. A., Rodriguez, J. L., Hawkins, N. A., Hensley Alford, S., & Leadbetter, S. (2015). Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system. Genetics in Medicine, 17(1), 43-50.​ https://doi.org/10.1038/gim.2014.68

  8. Linfield, D. T., Rothberg, M. B., Pfoh, E. R., Noss, R., Cassard, L., Powers, J. C., ... & Martinez, K. A. (2022). Primary care physician referral practices regarding BRCA1/2 genetic counseling in a major health system. Breast Cancer Research and Treatment, 195(2), 153-160. https://doi.org/10.1007/s10549-022-06523-5

  9. Neprash, H. T., Everhart, A., McAlpine, D., Smith, L. B., Sheridan, B., & Cross, D. A. (2021). Measuring primary care exam length using electronic health record data. Medical care, 59(1), 62-66. https://doi.org/10.1097/MLR.0000000000001450

  10. American Society of Breast Surgeons. (2019). Clinical consensus statement: Genetic testing for hereditary breast cancer. https://www.breastsurgeons.org/news/?id=17

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