Detalhe da pesquisa
1.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046083
2.
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
3.
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 586(7831): 763-768, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057201
4.
Role of Polyunsaturated Fat in Modifying Cardiovascular Risk Associated With Family History of Cardiovascular Disease: Pooled De Novo Results From 15 Observational Studies.
Circulation
; 149(4): 305-316, 2024 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38047387
5.
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.
Hum Mol Genet
; 32(6): 1048-1060, 2023 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36444934
6.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Am J Hum Genet
; 109(5): 857-870, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385699
7.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods
; 19(12): 1599-1611, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36303018
8.
Development and Validation of a Protein Risk Score for Mortality in Heart Failure : A Community Cohort Study.
Ann Intern Med
; 177(1): 39-49, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38163367
9.
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.
Hum Mol Genet
; 31(22): 3873-3885, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766891
10.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35552711
11.
Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study.
Hum Mol Genet
; 31(20): 3566-3579, 2022 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35234888
12.
Proteomics for heart failure risk stratification: a systematic review.
BMC Med
; 22(1): 34, 2024 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38273315
13.
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.
Brain
; 146(2): 492-506, 2023 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35943854
14.
Lifestyle habits associated with cardiac conduction disease.
Eur Heart J
; 44(12): 1058-1066, 2023 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36660815
15.
Trimethylamine N-oxide is associated with long-term mortality risk: the multi-ethnic study of atherosclerosis.
Eur Heart J
; 44(18): 1608-1618, 2023 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36883587
16.
Monogenic and Polygenic Contributions to QTc Prolongation in the Population.
Circulation
; 145(20): 1524-1533, 2022 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35389749
17.
Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General Population.
Am J Kidney Dis
; 81(3): 329-335, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36241009
18.
Multiple Prior Live Births Are Associated With Cardiac Remodeling and Heart Failure Risk in Women.
J Card Fail
; 29(7): 1032-1042, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36638956
19.
Association of Immune Cell Subsets with Incident Hip Fracture: The Cardiovascular Health Study.
Calcif Tissue Int
; 113(6): 581-590, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37650930
20.
Dietary Meat, Trimethylamine N-Oxide-Related Metabolites, and Incident Cardiovascular Disease Among Older Adults: The Cardiovascular Health Study.
Arterioscler Thromb Vasc Biol
; 42(9): e273-e288, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35912635