フォロー
Brianne M Daly
Brianne M Daly
Study Coordinator, Huntsman Cancer Institute
確認したメール アドレス: hci.utah.edu
タイトル
引用先
引用先
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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論文 1–10