Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.
PLoS Genet
; 18(6): e1010193, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35653334
6.
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
7.
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
em Inglês
| MEDLINE | ID: mdl-34582791
8.
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
9.
NetSHy: network summarization via a hybrid approach leveraging topological properties.
Bioinformatics
; 39(1)2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36548341
10.
Association of clonal hematopoiesis with chronic obstructive pulmonary disease.
Blood
; 139(3): 357-368, 2022 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34855941
11.
Mendelian randomization in the multivariate general linear model framework.
Genet Epidemiol
; 46(1): 17-31, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34672390
12.
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
13.
Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.
Int J Obes (Lond)
; 47(2): 109-116, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36463326
14.
Plasma neurofilament light chain concentrations are elevated in youth-onset type 2 diabetes and associated with neuropathy.
J Peripher Nerv Syst
; 28(3): 460-470, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37341347
15.
Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis.
Am J Respir Crit Care Med
; 206(3): 321-336, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35536696
16.
Alpha Globin Gene Copy Number Is Associated with Prevalent Chronic Kidney Disease and Incident End-Stage Kidney Disease among Black Americans.
J Am Soc Nephrol
; 33(1): 213-224, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34706968
17.
Lung function impairment and risk of incident heart failure: the NHLBI Pooled Cohorts Study.
Eur Heart J
; 43(23): 2196-2208, 2022 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35467708
18.
Mendelian randomization study of diabetes and dementia in the Million Veteran Program.
Alzheimers Dement
; 19(10): 4367-4376, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37417779
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.
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Am J Hum Genet
; 105(1): 15-28, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31178129