Detalhe da pesquisa
1.
Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits.
Am J Hum Genet
; 109(1): 66-80, 2022 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34995504
2.
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.
Am J Hum Genet
; 109(10): 1727-1741, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055244
3.
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Nature
; 570(7759): 71-76, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31118516
4.
Association of structural variation with cardiometabolic traits in Finns.
Am J Hum Genet
; 108(4): 583-596, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798444
5.
SARS-CoV-2 Infection of Human Neurons Is TMPRSS2 Independent, Requires Endosomal Cell Entry, and Can Be Blocked by Inhibitors of Host Phosphoinositol-5 Kinase.
J Virol
; 97(4): e0014423, 2023 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37039676
6.
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.
PLoS Genet
; 16(9): e1009019, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32915782
7.
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.
Am J Hum Genet
; 105(4): 773-787, 2019 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31564431
8.
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Hum Genomics
; 15(1): 34, 2021 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34099068
9.
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.
Hum Mol Genet
; 28(24): 4161-4172, 2019 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31691812
10.
A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression.
Am J Hum Genet
; 102(4): 620-635, 2018 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29625024
11.
Epigenome-wide association in adipose tissue from the METSIM cohort.
Hum Mol Genet
; 27(10): 1830-1846, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29566149
12.
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Hum Mol Genet
; 27(9): 1664-1674, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29481666
13.
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.
Am J Hum Genet
; 100(3): 428-443, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28257690
14.
Rotation and torsion of the left ventricle with cardiovascular magnetic resonance tagging: comparison of two analysis methods.
BMC Med Imaging
; 20(1): 73, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32611329
15.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
PLoS Genet
; 13(10): e1007079, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29084231
16.
Circulating RNAs as predictive markers for the progression of type 2 diabetes.
J Cell Mol Med
; 23(4): 2753-2768, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30734465
17.
SIRT3 deficiency and mitochondrial protein hyperacetylation accelerate the development of the metabolic syndrome.
Mol Cell
; 44(2): 177-90, 2011 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21856199
18.
Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol.
Am J Hum Genet
; 97(6): 801-15, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26637976
19.
Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy.
J Cell Sci
; 129(14): 2732-43, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27235420
20.
Decreased plasma ß-amyloid in the Alzheimer's disease APP A673T variant carriers.
Ann Neurol
; 82(1): 128-132, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28556232