Detalhe da pesquisa
1.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290336
2.
IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.
J Cardiovasc Electrophysiol
; 26(7): 715-23, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25786344
3.
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Front Genet
; 13: 806429, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35154276
4.
Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis.
Sci Rep
; 10(1): 10039, 2020 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32572052
5.
A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation.
Sci Rep
; 10(1): 1453, 2020 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31996765
6.
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.
Nat Commun
; 9(1): 4316, 2018 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30333491
7.
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation.
Stem Cell Res
; 24: 29-32, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29034891
8.
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation.
Stem Cell Res
; 24: 8-11, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29034898
9.
Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.
Heart Rhythm
; 11(2): 246-51, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24144883
10.
Brugada syndrome risk loci seem protective against atrial fibrillation.
Eur J Hum Genet
; 22(12): 1357-61, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24667784
11.
Screening of the ito regulatory subunit klf15 in patients with early-onset lone atrial fibrillation.
Front Genet
; 4: 88, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23730307
12.
Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data.
Can J Cardiol
; 29(9): 1104-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23465283
13.
A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.
Cardiovasc Res
; 98(3): 488-95, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23400760
14.
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.
Eur J Hum Genet
; 21(9): 918-28, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23299917
15.
Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy.
Appl Transl Genom
; 1: 44-46, 2012 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27896052
16.
High prevalence of genetic variants previously associated with LQT syndrome in new exome data.
Eur J Hum Genet
; 20(8): 905-8, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22378279
17.
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.
Can J Cardiol
; 28(2): 196-200, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22284586