Detalhe da pesquisa
1.
Individualized interventions for rare genetic conditions and the research-treatment spectrum: Stakeholder perspectives.
Genet Med
; 25(6): 100832, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36964709
2.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-36938783
3.
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
4.
A qualitative study of unaffected ATM and CHEK2 carriers: How participants make meaning of 'moderate risk' genetic results in a population breast cancer screening trial.
J Genet Couns
; 31(6): 1421-1433, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35877161
5.
The role of polygenic risk scores in breast cancer risk perception and decision-making.
J Community Genet
; 14(5): 489-501, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37311883
6.
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
7.
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
8.
Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.
Patient Educ Couns
; 104(5): 969-978, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33549385