Detalhe da pesquisa
1.
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
PLoS Genet
; 17(4): e1009503, 2021 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-33822779
2.
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
PLoS Genet
; 16(4): e1008629, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32282858
3.
Targeting skeletal muscle mitochondrial health in obesity.
Clin Sci (Lond)
; 136(14): 1081-1110, 2022 07 29.
Artigo
Inglês
| MEDLINE | ID: mdl-35892309
4.
A Common Polymorphism in the FADS1 Locus Links miR1908 to Low-Density Lipoprotein Cholesterol Through BMP1.
Arterioscler Thromb Vasc Biol
; 41(8): 2252-2262, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34134519
5.
2018 George Lyman Duff Memorial Lecture: Genetics and Genomics of Coronary Artery Disease: A Decade of Progress.
Arterioscler Thromb Vasc Biol
; 39(10): 1925-1937, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31462092
6.
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling.
Circulation
; 137(3): 222-232, 2018 01 16.
Artigo
Inglês
| MEDLINE | ID: mdl-28982690
7.
The selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) paradigm: conceptual framework and therapeutic potential : A consensus statement from the International Atherosclerosis Society (IAS) and the Residual Risk Reduction Initiative (R3i) Foundation.
Cardiovasc Diabetol
; 18(1): 71, 2019 06 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31164165
8.
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.
Circ Res
; 121(1): 81-88, 2017 Jun 23.
Artigo
Inglês
| MEDLINE | ID: mdl-28506971
9.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Nature
; 504(7480): 432-6, 2013 Dec 19.
Artigo
Inglês
| MEDLINE | ID: mdl-24213632
10.
Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages.
Am J Hum Genet
; 97(2): 228-37, 2015 Aug 06.
Artigo
Inglês
| MEDLINE | ID: mdl-26166477
11.
Genetically determined height and coronary artery disease.
N Engl J Med
; 372(17): 1608-18, 2015 Apr 23.
Artigo
Inglês
| MEDLINE | ID: mdl-25853659
12.
Genetics of Coronary Artery Disease.
Circ Res
; 118(4): 564-78, 2016 Feb 19.
Artigo
Inglês
| MEDLINE | ID: mdl-26892958
13.
Role of Tribbles Pseudokinase 1 (TRIB1) in human hepatocyte metabolism.
Biochim Biophys Acta
; 1862(2): 223-32, 2016 02.
Artigo
Inglês
| MEDLINE | ID: mdl-26657055
14.
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
Hum Mol Genet
; 24(2): 559-71, 2015 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25187575
15.
IRF2BP2 Reduces Macrophage Inflammation and Susceptibility to Atherosclerosis.
Circ Res
; 117(8): 671-83, 2015 Sep 25.
Artigo
Inglês
| MEDLINE | ID: mdl-26195219
16.
Functional Analysis of a Novel Genome-Wide Association Study Signal in SMAD3 That Confers Protection From Coronary Artery Disease.
Arterioscler Thromb Vasc Biol
; 36(5): 972-83, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26966274
17.
Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease.
PLoS Genet
; 10(7): e1004502, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25033284
18.
Distribution and medical impact of loss-of-function variants in the Finnish founder population.
PLoS Genet
; 10(7): e1004494, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25078778
19.
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.
JAMA
; 317(9): 937-946, 2017 03 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28267856
20.
Acylcarnitines: potential implications for skeletal muscle insulin resistance.
FASEB J
; 29(1): 336-45, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25342132