Detalhe da pesquisa
1.
Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction.
BMC Med Genet
; 18(1): 138, 2017 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29162046
2.
New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome.
BMC Genet
; 15: 74, 2014 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24941995
3.
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.
BMC Med Genet
; 13: 24, 2012 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22471742
4.
Screening of KCNN3 in patients with early-onset lone atrial fibrillation.
Europace
; 13(7): 963-7, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21398315
5.
Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.
Cardiology
; 118(2): 116-20, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21555883
6.
Exome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension.
Mol Genet Genomic Med
; 6(5): 835-844, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30084161
7.
Stability of Circulating Blood-Based MicroRNAs - Pre-Analytic Methodological Considerations.
PLoS One
; 12(2): e0167969, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28151938
8.
A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
PLoS One
; 12(1): e0170193, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28085969
9.
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.
Heart Rhythm
; 14(10): 1531-1538, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28549997
10.
The pathogenicity of genetic variants previously associated with left ventricular non-compaction.
Mol Genet Genomic Med
; 4(2): 135-42, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27066506
11.
Incidence and risk factors of ventricular fibrillation before primary angioplasty in patients with first ST-elevation myocardial infarction: a nationwide study in Denmark.
J Am Heart Assoc
; 4(1): e001399, 2015 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25559012
12.
Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
Circ Cardiovasc Genet
; 8(1): 64-73, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25691686
13.
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Cardiovasc Res
; 106(3): 520-9, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25691538
14.
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
15.
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
16.
Rare variants in GJA5 are associated with early-onset lone atrial fibrillation.
Can J Cardiol
; 29(1): 111-6, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23040431
17.
New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia.
Circ Cardiovasc Genet
; 6(5): 481-9, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24025405
18.
Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.
Can J Cardiol
; 28(2): 191-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22336519