Detalhe da pesquisa
1.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature
; 627(8003): 347-357, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38374256
2.
An integrative framework to prioritize genes in more than 500 loci associated with body mass index.
Am J Hum Genet
; 2024 May 09.
Artigo
Inglês
| MEDLINE | ID: mdl-38754426
3.
Genetic analyses of diverse populations improves discovery for complex traits.
Nature
; 570(7762): 514-518, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31217584
4.
Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program.
Circulation
; 147(12): 942-955, 2023 03 21.
Artigo
Inglês
| MEDLINE | ID: mdl-36802703
5.
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
; 31(3): 347-361, 2022 02 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34553764
6.
Host genetic effects in pneumonia.
Am J Hum Genet
; 108(1): 194-201, 2021 01 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33357513
7.
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Am J Hum Genet
; 108(10): 1836-1851, 2021 10 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34582791
8.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(5): 874-893, 2021 05 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33887194
9.
Incidence of adverse respiratory events after adjustment of clear fluid fasting recommendations to 1 h: a prospective, observational, multi-institutional cohort study.
Br J Anaesth
; 132(1): 66-75, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-37953199
10.
The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations.
Diabetologia
; 66(1): 116-126, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36216889
11.
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
; 46(1): 3-16, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34779012
12.
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Am J Hum Genet
; 105(1): 15-28, 2019 07 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31178129
13.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
J Hum Genet
; 67(2): 87-93, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-34376796
14.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
; 22(1): 432, 2021 Jun 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34107879
15.
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.
Hum Mol Genet
; 28(3): 515-523, 2019 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30307499
16.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29290336
17.
The role of polygenic susceptibility to obesity among carriers of pathogenic mutations in MC4R in the UK Biobank population.
PLoS Med
; 17(7): e1003196, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32692746
18.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(6): 1165, 2021 Jun 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34087167
19.
Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus.
Circ Res
; 131(3): 277-279, 2022 07 22.
Artigo
Inglês
| MEDLINE | ID: mdl-35701873
20.
Apolipoprotein E gene polymorphisms and intraventricular haemorrhage in infants born preterm: a large prospective multicentre cohort study.
Dev Med Child Neurol
; 61(3): 337-342, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30084487