Detalhe da pesquisa
1.
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet;
17(7): e1009679, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34324492
2.
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS Genet;
17(9): e1009809, 2021 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34547032
3.
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
Hum Mol Genet;
30(6): 500-513, 2021 04 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33437986
4.
Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot.
J Hum Genet;
67(10): 613-615, 2022 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35718831
5.
Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes.
J Hum Genet;
67(2): 123-125, 2022 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34493817
6.
Data-independent acquisition mass spectrometry in severe rheumatic heart disease (RHD) identifies a proteomic signature showing ongoing inflammation and effectively classifying RHD cases.
Clin Proteomics;
19(1): 7, 2022 Mar 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35317720
7.
Genetic analyses of circulating PUFA-derived mediators identifies heritable dihydroxyeicosatrienoic acid species.
Prostaglandins Other Lipid Mediat;
160: 106638, 2022 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35472599
8.
The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discrimination.
Bioinformatics;
36(7): 2217-2223, 2020 04 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31790148
9.
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Genet Med;
23(10): 1952-1960, 2021 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34113005
10.
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Circ Res;
124(4): 553-563, 2019 02 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30582441
11.
Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney.
Eur Heart J;
41(48): 4580-4588, 2020 12 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33206176
12.
Human Y Chromosome Exerts Pleiotropic Effects on Susceptibility to Atherosclerosis.
Arterioscler Thromb Vasc Biol;
39(11): 2386-2401, 2019 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31644355
13.
Global prevalence of congenital heart disease in school-age children: a meta-analysis and systematic review.
BMC Cardiovasc Disord;
20(1): 488, 2020 11 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33213369
14.
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development.
PLoS Genet;
13(10): e1007068, 2017 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29084269
15.
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.
Hum Mol Genet;
26(16): 3031-3045, 2017 08 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28521042
16.
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hum Mol Genet;
25(11): 2331-2341, 2016 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26965164
17.
Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation.
Am J Hum Genet;
97(3): 419-34, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26320892
18.
Defining the Normal Spectrum of Electrocardiographic and Left Ventricular Adaptations in Mixed-Race Male Adolescent Soccer Players.
Circulation;
143(1): 94-96, 2021 01 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33378235
19.
The Open Science of Atrial Fibrillation.
Circ Res;
126(2): 210-211, 2020 01 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31944917
20.
Myocardial ischemia and reperfusion leads to transient CD8 immune deficiency and accelerated immunosenescence in CMV-seropositive patients.
Circ Res;
116(1): 87-98, 2015 Jan 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25385851