Detalhe da pesquisa
1.
Novel genes and sex differences in COVID-19 severity.
Hum Mol Genet
; 31(22): 3789-3806, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35708486
2.
The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study.
J Mol Cell Cardiol
; 102: 3-9, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27894865
3.
Medico-legal perspectives on sudden cardiac death in young athletes.
Int J Legal Med
; 131(2): 393-409, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27654714
4.
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.
Int J Legal Med
; 131(5): 1211-1219, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391405
5.
PRKG1 and genetic diagnosis of early-onset thoracic aortic disease.
Eur J Clin Invest
; 46(9): 787-94, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27442293
6.
Association between SNPs of Metalloproteinases and Prostaglandin F2α Receptor Genes and Latanoprost Response in Open-Angle Glaucoma.
Ophthalmology
; 122(5): 1040-8.e4, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25704319
7.
Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population.
Ophthalmology
; 121(1): 399-407, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24144451
8.
Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.
Electrophoresis
; 35(21-22): 3111-6, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24981977
9.
Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives.
J Am Coll Cardiol
; 83(17): 1640-1651, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658103
10.
Research update for articles published in EJCI in 2016.
Eur J Clin Invest
; 48(10): e13016, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30099749
11.
Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing.
Mol Diagn Ther
; 27(1): 105-113, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36454422
12.
Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death.
Front Med (Lausanne)
; 10: 1118585, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36844202
13.
Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype-phenotype correlation.
Eur Heart J Cardiovasc Imaging
; 25(1): 75-85, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37562008
14.
Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome.
PLoS One
; 17(3): e0263469, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35231055
15.
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula.
Am J Hum Genet
; 83(6): 725-36, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19061982
16.
Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.
Int J Legal Med
; 125(4): 565-72, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21499742
17.
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Forensic Sci Int Genet
; 52: 102478, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33588347
18.
Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy.
J Am Coll Cardiol
; 78(17): 1682-1699, 2021 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34674813
19.
A strong genetic association between the tumor necrosis factor locus and proliferative vitreoretinopathy: the retina 4 project.
Ophthalmology
; 117(12): 2417-2423.e1-2, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20663564
20.
A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.
Electrophoresis
; 31(10): 1648-55, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20486126