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.
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
; 612(7941): 720-724, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36477530
3.
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
; 611(7934): 115-123, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36180795
4.
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
5.
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
6.
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
em Inglês
| MEDLINE | ID: mdl-34932938
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.
Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.
Hum Mol Genet
; 31(7): 1171-1182, 2022 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34788810
9.
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
10.
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
11.
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.
Alzheimers Dement
; 20(5): 3290-3304, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511601
12.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
Hum Mol Genet
; 30(5): 393-409, 2021 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33517400
13.
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
14.
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.
Mol Psychiatry
; 27(11): 4419-4431, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35974141
15.
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.
Brain
; 145(6): 1992-2007, 2022 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511193
16.
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature
; 612(7938): E7, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36376532
17.
Serum NfL and GFAP are associated with incident dementia and dementia mortality in older adults: The cardiovascular health study.
Alzheimers Dement
; 19(12): 5672-5680, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37392405
18.
Clonal Hematopoiesis Is Associated With Higher Risk of Stroke.
Stroke
; 53(3): 788-797, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34743536
19.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-34727735
20.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-30639324