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.
Return of Results in Genomic Research Using Large-Scale or Whole Genome Sequencing: Toward a New Normal.
Annu Rev Genomics Hum Genet
; 24: 393-414, 2023 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36913714
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.
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
5.
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Am J Hum Genet
; 109(9): 1605-1619, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36007526
6.
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
7.
Purifying selection on noncoding deletions of human regulatory loci detected using their cellular pleiotropy.
Genome Res
; 31(6): 935-946, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33963077
8.
Prioritizing the detection of rare pathogenic variants in population screening.
Nat Rev Genet
; 24(4): 205-206, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36639513
9.
Public willingness to participate in population DNA screening in Australia.
J Med Genet
; 60(7): 662-668, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450406
10.
Familial communication and cascade testing following elective genomic testing.
J Genet Couns
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38757439
11.
The Alzheimer's Disease Neuroimaging Initiative in the era of Alzheimer's disease treatment: A review of ADNI studies from 2021 to 2022.
Alzheimers Dement
; 20(1): 652-694, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37698424
12.
Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies.
Am J Med Genet C Semin Med Genet
; 193(1): 30-43, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36738469
13.
Are we prepared to deliver gene-targeted therapies for rare diseases?
Am J Med Genet C Semin Med Genet
; 193(1): 7-12, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36691939
14.
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
15.
An Ethical Framework for Research Using Genetic Ancestry.
Perspect Biol Med
; 66(2): 225-248, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37755714
16.
Increasing participant diversity in AD research: Plans for digital screening, blood testing, and a community-engaged approach in the Alzheimer's Disease Neuroimaging Initiative 4.
Alzheimers Dement
; 19(1): 307-317, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36209495
17.
Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project.
Am J Hum Genet
; 105(1): 177-188, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31256874
18.
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
19.
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
20.
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