Detalhe da pesquisa
1.
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
; 145(12): 877-891, 2022 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34930020
2.
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
; 107(3): 432-444, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32758450
3.
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
; 150(5): 1086-1096, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35595084
4.
Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results.
Genet Med
; 24(10): 2123-2133, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943490
5.
Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.
Hum Mutat
; 42(12): 1602-1614, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34467602
6.
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
7.
A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus.
Hum Mol Genet
; 27(13): 2392-2404, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29912393
8.
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
World J Surg
; 44(1): 84-94, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31605180
9.
Probing the Virtual Proteome to Identify Novel Disease Biomarkers.
Circulation
; 138(22): 2469-2481, 2018 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-30571344
10.
Response to Li and Hopper.
Am J Hum Genet
; 108(3): 527-529, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667396
11.
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
BMC Med
; 17(1): 135, 2019 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31311600
12.
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
Am J Hum Genet
; 96(5): 731-9, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865496
13.
The IRF5-TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.
Hum Mol Genet
; 24(2): 582-96, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25205108
14.
Variant level heritability estimates of type 2 diabetes in African Americans.
Sci Rep
; 14(1): 14009, 2024 06 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38890458
15.
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations.
Nat Med
; 30(2): 480-487, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374346
16.
Evaluation of TRAF6 in a large multiancestral lupus cohort.
Arthritis Rheum
; 64(6): 1960-9, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22231568
17.
Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.
Pac Symp Biocomput
; 28: 437-448, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36540998
18.
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.
Nat Commun
; 14(1): 5562, 2023 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37689782
19.
A metadata framework for computational phenotypes.
JAMIA Open
; 6(2): ooad032, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37181728
20.
Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations.
medRxiv
; 2023 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333246