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1.
Engagement and return of results preferences among a primarily African American genomic sequencing research cohort.
Am J Hum Genet
; 108(5): 894-902, 2021 05 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33887195
2.
The PrU: Development and validation of a measure to assess personal utility of genomic results.
Genet Med
; 25(3): 100356, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36516964
3.
Future-oriented Emotions and Decisions to Receive Genomic Testing Results Among U.S. Adults of African Ancestry.
Ann Behav Med
; 57(5): 418-423, 2023 04 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-36356050
4.
Elective genomic testing: Practice resource of the National Society of Genetic Counselors.
J Genet Couns
; 32(2): 281-299, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36597794
5.
The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort.
Genet Med
; 24(3): 736-743, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34906458
6.
The role of future-oriented affect in engagement with genomic testing results.
J Behav Med
; 45(1): 103-114, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34480685
7.
Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial.
Am J Hum Genet
; 102(4): 540-546, 2018 04 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29526281
8.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30193136
9.
A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings.
Genet Med
; 23(12): 2260-2269, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34433902
10.
An open-source python library for detection of known and novel Kell, Duffy and Kidd variants from exome sequencing.
Vox Sang
; 116(4): 451-463, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33567470
11.
Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing.
J Behav Med
; 44(6): 860-866, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33987754
12.
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counseling.
J Genet Couns
; 30(1): 11-21, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33554391
13.
Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African-American cohort.
J Genet Couns
; 30(6): 1582-1590, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33876469
14.
Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes.
Genet Med
; 21(3): 748-752, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29997389
15.
Ethnic identity and engagement with genome sequencing research.
Genet Med
; 21(8): 1735-1743, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-30568309
16.
Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort.
Genet Med
; 21(6): 1355-1362, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30382154
17.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30287922
18.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30670880
19.
Using the diffusion of innovations model to guide participant engagement in the genomics era.
J Genet Couns
; 28(2): 419-427, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30653790
20.
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.
Am J Hum Genet
; 96(6): 913-25, 2015 Jun 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-26046366