Detalhe da pesquisa
1.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Cell
; 182(5): 1198-1213.e14, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32888493
2.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
Cell
; 182(5): 1214-1231.e11, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32888494
3.
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
; 612(7941): 720-724, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36477530
4.
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Hum Mol Genet
; 31(13): 2279-2293, 2022 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35022708
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
em Inglês
| MEDLINE | ID: mdl-34553764
6.
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
em Inglês
| MEDLINE | ID: mdl-34582791
7.
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
em Inglês
| MEDLINE | ID: mdl-33887194
8.
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(10): e1009858, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662343
9.
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
PLoS Genet
; 17(5): e1009497, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33979322
10.
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
em Inglês
| MEDLINE | ID: mdl-34779012
11.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Ophthalmology
; 129(6): 626-636, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35031440
12.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
PLoS Genet
; 15(12): e1008500, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31869403
13.
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
em Inglês
| MEDLINE | ID: mdl-34087167
14.
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.
Nature
; 483(7389): 350-4, 2012 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22343897
15.
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.
Cerebrovasc Dis
; 38(6): 433-40, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25472749
16.
Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation.
Cerebrovasc Dis
; 37(1): 57-63, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24401931
17.
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma.
Commun Biol
; 7(1): 33, 2024 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38182794
18.
Association between lifetime smoking and cutaneous squamous cell carcinoma: A 2-sample Mendelian randomization study.
JAAD Int
; 14: 69-76, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38274396
19.
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation.
Commun Biol
; 7(1): 418, 2024 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38582945
20.
Genetic analysis of a population heavy drinking phenotype identifies risk variants in whites.
J Clin Psychopharmacol
; 33(2): 206-10, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23422394