Detalhe da pesquisa
1.
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
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.
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
5.
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.
J Genet Couns
; 2023 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37667436
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35679147
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.
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
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-36053287
10.
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
11.
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
12.
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
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33278053
14.
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1100-1110, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30287922
15.
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1261-1262, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30670880
16.
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
17.
Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing.
J Genet Couns
; 27(4): 823-833, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29423569
18.
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
J Genet Couns
; 27(5): 1220-1227, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29497922
19.
Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing.
J Genet Couns
; 26(5): 971-979, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28315134
20.
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
Am J Med Genet A
; 170(3): 574-82, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26792268