Detalles de la búsqueda
1.
Blood-based colorectal cancer screening in an integrated health system: a randomised trial of patient adherence.
Gut
; 73(4): 622-628, 2024 Mar 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38176899
2.
Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.
Breast Cancer Res Treat
; 201(3): 461-470, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37470892
3.
Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.
Genet Med
; 25(11): 100923, 2023 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37421176
4.
Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience.
Am J Med Genet A
; 191(2): 391-399, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36341765
5.
Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome.
J Genet Couns
; 32(4): 870-886, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36938783
6.
Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.
Cancer
; 128(16): 3090-3098, 2022 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35679147
7.
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.
Genet Med
; 24(8): 1664-1674, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35522237
8.
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.
Genet Med
; 24(6): 1196-1205, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35305866
9.
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.
Genet Med
; 24(11): 2228-2239, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36053287
10.
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.
Hered Cancer Clin Pract
; 20(1): 17, 2022 Apr 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-35436948
11.
Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.
Hered Cancer Clin Pract
; 20(1): 22, 2022 Jun 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35689290
12.
Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.
Hered Cancer Clin Pract
; 20(1): 7, 2022 Feb 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35144679
13.
A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
J Genet Couns
; 30(1): 42-50, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33278053
14.
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.
Hered Cancer Clin Pract
; 17: 31, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31890059
15.
Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators.
Genet Med
; 18(2): 152-61, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25880440
16.
Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.
Cancer
; 121(18): 3281-9, 2015 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26036338
17.
Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population.
Transl Behav Med
; 2024 Jan 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-38190737
18.
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
Public Health Genomics
; 26(1): 135-144, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37607497
19.
Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.
Cancer Med
; 12(18): 19112-19125, 2023 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-37644850
20.
Development and evaluation of an exome sequencing training course for medical interpreters.
Per Med
; 19(2): 125-138, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-35171038