Detalhe da pesquisa
1.
Insights into the Inherited Basis of Valvular Heart Disease.
Curr Cardiol Rep
; 2024 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38581562
2.
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Stroke
; 54(3): 810-818, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36655558
3.
Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci.
Circ Res
; 128(5): e84-e101, 2021 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33508947
4.
The complex genetic basis of fibromuscular dysplasia, a systemic arteriopathy associated with multiple forms of cardiovascular disease.
Clin Sci (Lond)
; 136(16): 1241-1255, 2022 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36043395
5.
Mutations in DCHS1 cause mitral valve prolapse.
Nature
; 525(7567): 109-13, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26258302
6.
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
PLoS Genet
; 12(10): e1006367, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792790
7.
A central role for GRB10 in regulation of islet function in man.
PLoS Genet
; 10(4): e1004235, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24699409
8.
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
Nat Genet
; 37(8): 863-7, 2005 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16025115
9.
Phenotypic Clusters and Multimorbidity in Hypermobile Ehlers-Danlos Syndrome.
Mayo Clin Proc Innov Qual Outcomes
; 8(3): 253-262, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38779137
10.
Genomic, Transcriptomic, and Proteomic Depiction of Induced Pluripotent Stem Cells-Derived Smooth Muscle Cells As Emerging Cellular Models for Arterial Diseases.
Hypertension
; 80(4): 740-753, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36655574
11.
Genetics and pathophysiology of mitral valve prolapse.
Front Cardiovasc Med
; 10: 1077788, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36873395
12.
Genetic mechanisms underlying arrhythmogenic mitral valve prolapse: Current and future perspectives.
Heart Rhythm O2
; 4(9): 581-591, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37744942
13.
Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI Insight
; 7(3)2022 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35132965
14.
Research Opportunities in the Treatment of Mitral Valve Prolapse: JACC Expert Panel.
J Am Coll Cardiol
; 80(24): 2331-2347, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36480975
15.
Recent Advances on the Genetics of Spontaneous Coronary Artery Dissection.
Circ Genom Precis Med
; 14(6): e003393, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34706548
16.
Plasma and genetic determinants of soluble TREM-1 and major adverse cardiovascular events in a prospective cohort of acute myocardial infarction patients. Results from the FAST-MI 2010 study.
Int J Cardiol
; 344: 213-219, 2021 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34534607
17.
Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.
Circ Genom Precis Med
; 14(5): e003148, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34461747
18.
National French registry of spontaneous coronary artery dissections: prevalence of fibromuscular dysplasia and genetic analyses.
EuroIntervention
; 17(6): 508-515, 2021 Aug 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33319763
19.
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia.
Cardiovasc Res
; 117(4): 1154-1165, 2021 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32531060
20.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
; 12(1): 24, 2021 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33402679