Detalhe da pesquisa
1.
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
2.
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
3.
"Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients.
Hered Cancer Clin Pract
; 21(1): 24, 2023 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37978552
4.
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
5.
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
6.
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
7.
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
8.
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
9.
Clustering of comorbid conditions among women who carry an FMR1 premutation.
Genet Med
; 22(4): 758-766, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31896764
10.
Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders.
Genet Med
; 21(11): 2561-2568, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31028355
11.
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.
Hered Cancer Clin Pract
; 17: 31, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31890059
12.
Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.
Hum Mutat
; 39(11): 1677-1685, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30311382
13.
Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts.
BMC Health Serv Res
; 18(1): 824, 2018 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-30376847
14.
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.
Genet Med
; 18(12): 1258-1268, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27124788
15.
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
16.
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
17.
The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.
Genet Med
; 15(9): 698-705, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23558253
18.
A picture is worth a thousand words: advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping.
Implement Sci Commun
; 4(1): 43, 2023 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37098602
19.
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Cells
; 12(18)2023 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37759552
20.
The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.
Behav Genet
; 42(3): 415-22, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22101959