Detalles de la búsqueda
1.
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
; 143(18): 1845-1855, 2024 May 02.
Artículo
Inglés
| MEDLINE | ID: mdl-38320121
2.
Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.
PLoS Genet
; 19(5): e1010517, 2023 05.
Artículo
Inglés
| MEDLINE | ID: mdl-37216410
3.
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.
Am J Hum Genet
; 109(6): 1175-1181, 2022 06 02.
Artículo
Inglés
| MEDLINE | ID: mdl-35504290
4.
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Hum Mol Genet
; 31(18): 3120-3132, 2022 09 10.
Artículo
Inglés
| MEDLINE | ID: mdl-35552711
5.
Missense Genetic Variation of ICAM1 and Incident Heart Failure.
J Card Fail
; 29(8): 1163-1172, 2023 08.
Artículo
Inglés
| MEDLINE | ID: mdl-36882149
6.
Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.
Stroke
; 53(3): 875-885, 2022 03.
Artículo
Inglés
| MEDLINE | ID: mdl-34727735
7.
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.
Am J Hum Genet
; 104(2): 260-274, 2019 02 07.
Artículo
Inglés
| MEDLINE | ID: mdl-30639324
8.
Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants.
Arterioscler Thromb Vasc Biol
; 41(6): e369-e378, 2021 06.
Artículo
Inglés
| MEDLINE | ID: mdl-33910371
9.
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program.
Am J Epidemiol
; 190(10): 1977-1992, 2021 10 01.
Artículo
Inglés
| MEDLINE | ID: mdl-33861317
10.
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.
Artículo
Inglés
| MEDLINE | ID: mdl-30307499
11.
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
Blood
; 133(9): 967-977, 2019 02 28.
Artículo
Inglés
| MEDLINE | ID: mdl-30642921
12.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Artículo
Inglés
| MEDLINE | ID: mdl-29590102
13.
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.
Artículo
Inglés
| MEDLINE | ID: mdl-29750786
14.
Comparison of Proteomic Assessment Methods in Multiple Cohort Studies.
Proteomics
; 20(12): e1900278, 2020 06.
Artículo
Inglés
| MEDLINE | ID: mdl-32386347
15.
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Circulation
; 139(5): 620-635, 2019 01 29.
Artículo
Inglés
| MEDLINE | ID: mdl-30586737
16.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC Genomics
; 21(1): 228, 2020 Mar 14.
Artículo
Inglés
| MEDLINE | ID: mdl-32171239
17.
Soluble CD14 and Risk of Heart Failure and Its Subtypes in Older Adults.
J Card Fail
; 26(5): 410-419, 2020 May.
Artículo
Inglés
| MEDLINE | ID: mdl-32165348
18.
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
PLoS Genet
; 13(4): e1006760, 2017 04.
Artículo
Inglés
| MEDLINE | ID: mdl-28453575
19.
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
PLoS Genet
; 13(5): e1006728, 2017 May.
Artículo
Inglés
| MEDLINE | ID: mdl-28498854
20.
A robust and powerful two-step testing procedure for local ancestry adjusted allelic association analysis in admixed populations.
Genet Epidemiol
; 42(3): 288-302, 2018 04.
Artículo
Inglés
| MEDLINE | ID: mdl-29226381