Detalhe da pesquisa
1.
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci.
Eur Heart J
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747976
2.
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm.
Am J Hum Genet
; 102(1): 133-141, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29304371
3.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Eur Heart J
; 40(37): 3081-3094, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31114854
4.
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Hum Mol Genet
; 24(10): 2757-63, 2015 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25650408
5.
Left Ventricular Abnormal Substrate in Brugada Syndrome.
JACC Clin Electrophysiol
; 9(10): 2041-2051, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37480873
6.
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background.
Stem Cell Res
; 59: 102647, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34999420
7.
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet
; 54(3): 232-239, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35210625
8.
Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.
Circ Genom Precis Med
; 12(10): e002617, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32141789
9.
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Nat Genet
; 54(5): 735, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35474365
10.
Dysfunction of the Voltage-Gated K+ Channel ß2 Subunit in a Familial Case of Brugada Syndrome.
J Am Heart Assoc
; 5(6)2016 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287695
11.
Fine-scale human genetic structure in Western France.
Eur J Hum Genet
; 23(6): 831-6, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25182131
12.
Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
Nat Genet
; 47(10): 1206-11, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26301497
13.
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nat Genet
; 45(9): 1044-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23872634