Detalhe da pesquisa
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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341765
5.
Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.
Cancer
; 128(16): 3090-3098, 2022 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35679147
6.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35522237
7.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35305866
8.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35436948
9.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689290
10.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35144679
11.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-26036338
12.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-38190737
13.
Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
Public Health Genomics
; 26(1): 135-144, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607497
14.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-37644850
15.
Development and evaluation of an exome sequencing training course for medical interpreters.
Per Med
; 19(2): 125-138, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35171038
16.
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population.
Fam Cancer
; 21(2): 167-180, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33754278
17.
Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol.
J Pers Med
; 11(11)2021 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34834546
18.
Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
AJOB Empir Bioeth
; 12(1): 1-11, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32981477
19.
Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.
Contemp Clin Trials
; 106: 106432, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33984519
20.
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study.
Public Health Genomics
; 27(1): 16-22, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38142673