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1.
Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their own.
J Biomed Inform
; 149: 104568, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-38081564
2.
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024.
J Natl Compr Canc Netw
; 21(10): 1000-1010, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37856201
3.
Experiences of patients and family members with follow-up care, information needs and provider support after identification of Lynch Syndrome.
Hered Cancer Clin Pract
; 21(1): 28, 2023 Dec 19.
Article
in English
| MEDLINE | ID: mdl-38115072
4.
Increasing Skin Cancer Prevention in Young Adults: the Cumulative Impact of Personalized UV Photography and MC1R Genetic Testing.
J Cancer Educ
; 38(3): 1059-1065, 2023 06.
Article
in English
| MEDLINE | ID: mdl-36306029
5.
Cancer Risk in Patients With and Relatives of Serrated Polyposis Syndrome and Sporadic Sessile Serrated Lesions.
Am J Gastroenterol
; 117(2): 336-342, 2022 02 01.
Article
in English
| MEDLINE | ID: mdl-34889311
6.
Interactive Beliefs about Genes and Behavior Predict Improved Sun Protection Following Melanoma Genetic Counseling.
Ann Behav Med
; 56(8): 816-829, 2022 08 02.
Article
in English
| MEDLINE | ID: mdl-35179177
7.
'I had a bigger cancer risk than I thought ': The experience of receiving personalized risk information as part of a skin cancer prevention intervention in the college setting.
Health Expect
; 25(6): 2937-2949, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36225123
8.
Uptake of genetic counseling and multi-gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing.
J Genet Couns
; 31(2): 470-478, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34570943
9.
Paraganglioma and other tumour detection rates in individuals with SDHx pathogenic variants by age of diagnosis and after the age of 50.
Clin Endocrinol (Oxf)
; 95(3): 447-452, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34255389
10.
Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
J Natl Compr Canc Netw
; 19(1): 77-102, 2021 01 06.
Article
in English
| MEDLINE | ID: mdl-33406487
11.
Priority of Risk (But Not Perceived Magnitude of Risk) Predicts Improved Sun-Protection Behavior Following Genetic Counseling for Familial Melanoma.
Ann Behav Med
; 55(1): 24-40, 2021 02 12.
Article
in English
| MEDLINE | ID: mdl-32415830
12.
Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial.
BMC Health Serv Res
; 21(1): 542, 2021 Jun 02.
Article
in English
| MEDLINE | ID: mdl-34078380
13.
Patient Interactions With an Automated Conversational Agent Delivering Pretest Genetics Education: Descriptive Study.
J Med Internet Res
; 23(11): e29447, 2021 11 18.
Article
in English
| MEDLINE | ID: mdl-34792472
14.
CDKN2A testing and genetic counseling promote reductions in objectively measured sun exposure one year later.
Genet Med
; 22(1): 26-34, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31371819
15.
Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma-pheochromocytoma syndrome.
Genet Med
; 22(12): 2101-2107, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32741965
16.
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020.
J Natl Compr Canc Netw
; 18(4): 380-391, 2020 04.
Article
in English
| MEDLINE | ID: mdl-32259785
17.
A pilot study of a telehealth family-focused melanoma preventive intervention for children with a family history of melanoma.
Psychooncology
; 29(1): 148-155, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31520429
18.
Population-based relative risks for specific family history constellations of breast cancer.
Cancer Causes Control
; 30(6): 581-590, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-31030355
19.
The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population database.
BMC Cancer
; 19(1): 190, 2019 Mar 01.
Article
in English
| MEDLINE | ID: mdl-30823903
20.
Cost-effectiveness of early cancer surveillance for patients with Li-Fraumeni syndrome.
Pediatr Blood Cancer
; 66(5): e27629, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30719841