Detalhe da pesquisa
1.
Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project.
Am J Hum Genet
; 110(7): 1034-1045, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37279760
2.
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care.
Am J Hum Genet
; 110(11): 1841-1852, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37922883
3.
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization.
Am J Hum Genet
; 108(12): 2224-2237, 2021 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34752750
4.
Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model.
Genet Med
; 25(4): 100797, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36727595
5.
Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project.
Genet Med
; 25(3): 100002, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36549595
6.
Public perspective on medications to delay Alzheimer's disease symptoms.
J Genet Couns
; 32(5): 1009-1017, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37102213
7.
Improved provider preparedness through an 8-part genetics and genomic education program.
Genet Med
; 24(1): 214-224, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906462
8.
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
; 24(5): 1130-1138, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216901
9.
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression.
J Genet Couns
; 31(1): 218-229, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34309124
10.
Do research participants share genomic screening results with family members?
J Genet Couns
; 31(2): 447-458, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665896
11.
Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance.
Genet Med
; 23(10): 1977-1983, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34113000
12.
Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insights.
Genet Med
; 23(7): 1366-1371, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33767345
13.
Airmen and health-care providers' attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project.
Genet Med
; 22(12): 2003-2010, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32807975
14.
Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing.
Value Health
; 23(5): 559-565, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32389220
15.
Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.
Genet Med
; 21(12): 2781-2790, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31189963
16.
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
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-30287922
18.
Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project.
Genet Med
; 20(9): 1069-1076, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29300387
19.
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Genet Med
; 20(10): 1186-1195, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29388940
20.
Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.
Genet Med
; 20(12): 1544-1553, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29565423