Detalhe da pesquisa
1.
Transcriptome-wide association study of the plasma proteome reveals cis and trans regulatory mechanisms underlying complex traits.
Am J Hum Genet
; 111(3): 445-455, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38320554
2.
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.
Am J Hum Genet
; 111(1): 133-149, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38181730
3.
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric.
Am J Hum Genet
; 111(5): 990-995, 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38636510
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.
A structural variation reference for medical and population genetics.
Nature
; 581(7809): 444-451, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32461652
6.
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
7.
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
8.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35504290
9.
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits.
Am J Hum Genet
; 109(7): 1286-1297, 2022 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35716666
10.
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
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.
The impact of Mendelian sleep and circadian genetic variants in a population setting.
PLoS Genet
; 18(9): e1010356, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36137075
13.
Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits.
PLoS Genet
; 18(12): e1010557, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36574455
14.
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
15.
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
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
em Inglês
| MEDLINE | ID: mdl-33887194
17.
Association of clonal hematopoiesis with chronic obstructive pulmonary disease.
Blood
; 139(3): 357-368, 2022 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34855941
18.
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
19.
Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease.
Circ Res
; 131(2): e51-e69, 2022 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35658476
20.
A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities.
Am J Respir Crit Care Med
; 208(7): 791-801, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37523715