Detalhe da pesquisa
1.
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.
Cell
; 187(2): 464-480.e10, 2024 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38242088
2.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature
; 627(8003): 347-357, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374256
3.
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
4.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
; 110(10): 1704-1717, 2023 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37802043
5.
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.
Blood
; 143(18): 1845-1855, 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38320121
6.
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Nature
; 586(7831): 763-768, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057201
7.
Identification of type 2 diabetes loci in 433,540 East Asian individuals.
Nature
; 582(7811): 240-245, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32499647
8.
Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.
PLoS Genet
; 19(5): e1010517, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37216410
9.
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
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
em Inglês
| MEDLINE | ID: mdl-36303018
11.
Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease.
PLoS Genet
; 18(9): e1010294, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36048760
12.
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
13.
Differences in Metabolomic Profiles Between Black and White Women and Risk of Coronary Heart Disease: an Observational Study of Women From Four US Cohorts.
Circ Res
; 131(7): 601-615, 2022 09 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36052690
14.
Determinants of Incident Atherosclerotic Cardiovascular Disease Events Among Those With Absent Coronary Artery Calcium: Multi-Ethnic Study of Atherosclerosis.
Circulation
; 145(4): 259-267, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34879218
15.
Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease.
Circulation
; 145(5): 357-370, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34814699
16.
Epigenome-wide association study of mitochondrial genome copy number.
Hum Mol Genet
; 31(2): 309-319, 2021 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415308
17.
Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.
Hum Mol Genet
; 30(22): 2190-2204, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34165540
18.
Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction.
Hum Mol Genet
; 30(15): 1443-1456, 2021 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33856023
19.
Circulating metabolites may illustrate relationship of alcohol consumption with cardiovascular disease.
BMC Med
; 21(1): 443, 2023 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37968697
20.
Missense Genetic Variation of ICAM1 and Incident Heart Failure.
J Card Fail
; 29(8): 1163-1172, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36882149