Detalhe da pesquisa
1.
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Hum Mol Genet
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747556
2.
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
3.
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
Am J Hum Genet
; 106(1): 112-120, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883642
4.
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia
; 65(3): 477-489, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34951656
5.
Urinary phthalate exposures and risk of breast cancer: the Multiethnic Cohort study.
Breast Cancer Res
; 23(1): 44, 2021 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33823904
6.
Risk of breast cancer and prediagnostic urinary excretion of bisphenol A, triclosan and parabens: The Multiethnic Cohort Study.
Int J Cancer
; 149(7): 1426-1434, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34013527
7.
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
em Inglês
| MEDLINE | ID: mdl-30307499
8.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(2): 481-8, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486782
9.
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.
Am J Hum Genet
; 99(1): 22-39, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346689
10.
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
Genet Epidemiol
; 40(6): 470-4, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229898
11.
A common TCN1 loss-of-function variant is associated with lower vitamin B12 concentration in African Americans.
Blood
; 131(25): 2859-2863, 2018 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29764838
12.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(3): 785, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588453
13.
Coronary heart disease and genetic variants with low phospholipase A2 activity.
N Engl J Med
; 372(3): 295-6, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25587968
14.
Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.
bioRxiv
; 2023 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37745480
15.
Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study.
PLoS One
; 16(7): e0249615, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34329319
16.
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
HGG Adv
; 2(2)2021 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34604815
17.
Lipoprotein-associated phospholipase A2 and risk of incident peripheral arterial disease: Findings from The Atherosclerosis Risk in Communities study (ARIC).
Atherosclerosis
; 268: 12-18, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29169030
18.
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles.
Eur J Prev Cardiol
; 24(5): 492-504, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27940953
19.
Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel ß-subunit in a case of early-onset phenotype of Liddle syndrome.
Cold Spring Harb Mol Case Stud
; 2(6): a001255, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27900368
20.
Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart Study.
Circ Cardiovasc Genet
; 9(4): 368-74, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27422940