Detalhe da pesquisa
1.
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.
Clin Genet
; 105(2): 185-189, 2024 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37904629
2.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Nature
; 504(7480): 432-6, 2013 Dec 19.
Artigo
Inglês
| MEDLINE | ID: mdl-24213632
3.
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy.
PLoS Genet
; 6(10): e1001167, 2010 Oct 21.
Artigo
Inglês
| MEDLINE | ID: mdl-20975947
4.
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
PLoS One
; 15(2): e0229472, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32059048
5.
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
PLoS One
; 12(3): e0172995, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28296976
6.
Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.
Circ Cardiovasc Genet
; 8(4): 628-36, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-26160806
7.
Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus.
Atherosclerosis
; 227(2): 244-9, 2013 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-23375685
8.
Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients.
Int J Cardiol
; 189: 105-7, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25889438