Detalhe da pesquisa
1.
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
Am J Hum Genet
; 107(5): 932-941, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33108757
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.
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
4.
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
5.
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
6.
Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia.
Neuropathology
; 42(1): 58-65, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34753215
7.
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
8.
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing.
J Genet Couns
; 30(3): 793-802, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33393146
9.
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
10.
The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care.
Clin Transl Sci
; 17(1): e13635, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38064200
11.
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
12.
Assessment of a Peer Physician Coaching Partnership Between a Designated Cancer Center Genetics Service and a Community Cancer Network Hospital.
JAMA Netw Open
; 6(3): e231723, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36877518
13.
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
14.
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
15.
Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432].
Contemp Clin Trials
; 114: 106682, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35123916