Detalhe da pesquisa
1.
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
2.
Design and Pilot Results from Million Veteran Program Return Of Actionable Genetic Results (MVP-ROAR) Study.
Am Heart J
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38762090
3.
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
4.
Primary care physician use of patient race and polygenic risk scores in medical decision-making.
Genet Med
; 25(4): 100800, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36748708
5.
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Am J Hum Genet
; 104(4): 578-595, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30951675
6.
Should You Recommend Direct-to-Consumer Genetic Testing for This Patient? : Grand Rounds Discussion From Beth Israel Deaconess Medical Center.
Ann Intern Med
; 173(7): 563-571, 2020 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33017547
7.
How to Quantify and Interpret Treatment Effects in Comparative Clinical Studies of COVID-19.
Ann Intern Med
; 173(8): 632-637, 2020 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32634024
8.
Association of Statin Use With All-Cause and Cardiovascular Mortality in US Veterans 75 Years and Older.
JAMA
; 324(1): 68-78, 2020 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32633800
9.
Pharmacogenetic testing in the Veterans Health Administration (VHA): policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee.
Genet Med
; 21(2): 382-390, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29858578
10.
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
11.
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
12.
A Tale of Two Scores: Comparing Coronary Artery Calcium and Polygenic Risk Scores for the Prediction of Coronary Heart Disease Events.
Clin Chem
; 70(2): 358-360, 2024 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37856688
13.
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
14.
How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation.
J Gen Intern Med
; 33(6): 877-885, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29374360
15.
Yield and bias in defining a cohort study baseline from electronic health record data.
J Biomed Inform
; 78: 54-59, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29305952
16.
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Ann Intern Med
; 167(3): 159-169, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28654958
17.
Palbociclib and Fulvestrant in Breast Cancer.
N Engl J Med
; 380(8): 796, 2019 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30789681
18.
Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study.
Genet Med
; 19(5): 537-545, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27657683
19.
How to Quantify and Interpret Treatment Effects in Comparative Clinical Studies of COVID-19.
Ann Intern Med
; 174(5): 731-732, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33999681
20.
Estimated Filtration: The Continued Need for Expert Classification of Genetic Variants.
Ann Intern Med
; 170(1): 64-65, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30477012