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Brianne M Daly
Brianne M Daly
Study Coordinator, Huntsman Cancer Institute
Verified email at hci.utah.edu
Title
Cited by
Cited by
Year
Association of Disparities in Family History and Family Cancer History in the Electronic Health Record With Sex, Race, Hispanic or Latino Ethnicity, and Language Preference in …
D Chavez-Yenter, MS Goodman, Y Chen, X Chu, RL Bradshaw, ...
JAMA Network Open 5 (10), e2234574-e2234574, 2022
322022
Interest in Cancer Predisposition Testing and Carrier Screening Offered as Part of Routine Healthcare Among an Ethnically Diverse Sample of Young Women.
KA Kaphingst, JR Bather, BM Daly, D Chavez-Yenter, A Vega, ...
Frontiers in genetics 13, 866062-866062, 2022
122022
Variability in conceptualizations and measurement of genetic literacy
BM Daly, KA Kaphingst
PEC Innovation, 100147, 2023
72023
Barriers to family history collection among Spanish-speaking primary care patients: a BRIDGE qualitative study
E Liebermann, P Taber, AS Vega, BM Daly, MS Goodman, R Bradshaw, ...
PEC Innovation 1, 100087, 2022
42022
Communication About Negative and Uncertain Results: Interactional Dilemmas During a Genetic Telehealth Consult
WA Beach, HE Canary, YW Chen, BM Daly, A Gammon, MW Savage, ...
Health Communication, 1-12, 2022
42022
Investigation of interest in and timing preference for cancer predisposition testing and expanded carrier screening among women of reproductive age
L Zhong, JR Bather, BM Daly, WK Kohlmann, MS Goodman, E Rothwell, ...
PEC Innovation 2, 100128, 2023
32023
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members
C Winskill, MS Goodman, BM Daly, A Elrick, R Mooney, W Espinel, ...
Public Health Genomics, 2023
12023
Factors affecting interest in multiple genetic tests in an ethnically diverse sample of young women: Presenter (s): Kimberly Kaphingst, University of Utah, United States
J Bather, B Daly, D Chavez-Yenter, A Vega, W Kohlmann
Patient Education and Counseling 109, 126, 2023
2023
P377: Limitations of automated approaches to utilizing the EHR to identify high-risk patients for hereditary cancer genetic testing
R Chambers, M Sigireddi, K Kaphingst, R Monahan, W Kohlmann, ...
Genetics in Medicine Open 1 (1), 2023
2023
PEC Innovation
E Liebermann, P Taber, AS Vega, BM Daly, MS Goodman, R Bradshaw
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Articles 1–10