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
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
Inglês
| MEDLINE | ID: mdl-32888494
3.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-37046083
4.
A saturated map of common genetic variants associated with human height.
Nature
; 610(7933): 704-712, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36224396
5.
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
; 612(7941): 720-724, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36477530
6.
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Nature
; 590(7845): 290-299, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33568819
7.
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
; 143(18): 1845-1855, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38320121
8.
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
Inglês
| MEDLINE | ID: mdl-36444934
9.
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Am J Hum Genet
; 109(1): 81-96, 2022 01 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34932938
10.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods
; 19(12): 1599-1611, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36303018
11.
Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.
Arterioscler Thromb Vasc Biol
; 44(1): 300-313, 2024 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37916415
12.
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Nature
; 570(7759): 71-76, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31118516
13.
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
Inglês
| MEDLINE | ID: mdl-35552711
14.
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
15.
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
16.
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
17.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
; 108(4): 564-582, 2021 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33713608
18.
Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels.
Arterioscler Thromb Vasc Biol
; 43(7): e254-e269, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37128921
19.
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.
Brain
; 146(2): 492-506, 2023 02 13.
Artigo
Inglês
| MEDLINE | ID: mdl-35943854
20.
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.
Circulation
; 146(16): 1225-1242, 2022 10 18.
Artigo
Inglês
| MEDLINE | ID: mdl-36154123