Detalhe da pesquisa
1.
Improving reporting standards for polygenic scores in risk prediction studies.
Nature
; 591(7849): 211-219, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33692554
2.
Establishing the Medical Actionability of Genomic Variants.
Annu Rev Genomics Hum Genet
; 23: 173-192, 2022 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-35363504
3.
Implementing Evidence-Based Assertions of Clinical Actionability in the Context of Secondary Findings: Updates from the ClinGen Actionability Working Group.
Genet Med
; : 101164, 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38757444
4.
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
5.
The PrU: Development and validation of a measure to assess personal utility of genomic results.
Genet Med
; 25(3): 100356, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36516964
6.
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
7.
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
8.
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
Am J Hum Genet
; 104(6): 1088-1096, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31104772
9.
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings.
Genet Med
; 24(3): 610-621, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906471
10.
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
11.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-36053287
12.
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
13.
ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents.
Genet Med
; 24(6): 1328-1335, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35341655
14.
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
J Genet Couns
; 31(1): 230-241, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34302314
15.
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
16.
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
17.
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
18.
Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
Am J Hum Genet
; 102(6): 1078-1089, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754767
19.
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Am J Hum Genet
; 103(3): 319-327, 2018 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30193136
20.
Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution.
Genet Med
; 22(6): 1094-1101, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32089547