Detalhe da pesquisa
1.
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network.
Am J Hum Genet
; 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38688278
2.
Studying the impact of translational genomic research: Lessons from eMERGE.
Am J Hum Genet
; 110(7): 1021-1033, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37343562
3.
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
4.
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Am J Hum Genet
; 110(11): 1950-1958, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37883979
5.
Returning Individual Research Results from Digital Phenotyping in Psychiatry.
Am J Bioeth
; 24(2): 69-90, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37155651
6.
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
7.
Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.
Genet Med
; 25(9): 100906, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37246632
8.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
; 25(4): 100006, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36621880
9.
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Am J Hum Genet
; 104(1): 76-93, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30609409
10.
Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.
Genet Med
; 24(6): 1297-1305, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35341654
11.
Genetic Determinants of Sudden Unexpected Death in Pediatrics.
Genet Med
; 24(4): 839-850, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35027292
12.
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
13.
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
14.
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
15.
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project.
Genet Med
; 23(7): 1372-1375, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33772220
16.
Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI).
Genet Med
; 23(2): 396-407, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33005041
17.
The Unrecognized Mortality Burden of Genetic Disorders in Infancy.
Am J Public Health
; 111(S2): S156-S162, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34314210
18.
Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study.
J Med Internet Res
; 23(3): e21023, 2021 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33724192
19.
Current Trends in Genetics and Neonatal Care.
Adv Neonatal Care
; 21(6): 473-481, 2021 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33538495
20.
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Am J Hum Genet
; 100(3): 414-427, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28190457