Detalhe da pesquisa
1.
Precision medicine in 2030-seven ways to transform healthcare.
Cell
; 184(6): 1415-1419, 2021 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33740447
2.
Disease Heritability Studies Harness the Healthcare System to Achieve Massive Scale.
Cell
; 173(7): 1568-1570, 2018 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29906443
3.
The phenotype-genotype reference map: Improving biobank data science through replication.
Am J Hum Genet
; 110(9): 1522-1533, 2023 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607538
4.
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records.
PLoS Genet
; 17(6): e1009593, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34061827
5.
The Impact of COVID-19 on the All of Us Research Program.
Am J Epidemiol
; 192(1): 11-24, 2023 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36205043
6.
Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS.
Bioinformatics
; 38(8): 2297-2306, 2022 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35157022
7.
A test of automated use of electronic health records to aid in diagnosis of genetic disease.
Genet Med
; 25(12): 100966, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37622442
8.
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.
PLoS Genet
; 16(11): e1009077, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175840
9.
Antibodies to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in All of Us Research Program Participants, 2 January to 18 March 2020.
Clin Infect Dis
; 74(4): 584-590, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128970
10.
Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach.
BMC Genomics
; 23(1): 385, 2022 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35590255
11.
GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
Am J Hum Genet
; 104(3): 503-519, 2019 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30827500
12.
The "All of Us" Research Program.
N Engl J Med
; 381(7): 668-676, 2019 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31412182
13.
PheWAS-ME: a web-app for interactive exploration of multimorbidity patterns in PheWAS.
Bioinformatics
; 37(12): 1778-1780, 2021 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33051675
14.
Medical Records-Based Genetic Studies of the Complement System.
J Am Soc Nephrol
; 32(8): 2031-2047, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941608
15.
The U.S. National Library of Medicine's impact on precision and genomic medicine.
Inf Serv Use
; 42(1): 71-80, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35600119
16.
Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.
Int J Obes (Lond)
; 45(1): 155-169, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32952152
17.
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
PLoS Genet
; 14(5): e1007345, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29750786
18.
CYP2C19 Loss-of-Function is Associated with Increased Risk of Ischemic Stroke after Transient Ischemic Attack in Intracranial Atherosclerotic Disease.
J Stroke Cerebrovasc Dis
; 30(2): 105464, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246208
19.
Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects.
Circulation
; 140(4): 270-279, 2019 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31234639
20.
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways.
Kidney Int
; 97(5): 1032-1041, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32247630