Floriane Simonet

机构：Centre National de la Recherche Scientifique, Inserm, Institut du Thorax · ORCID：0000-0002-6366-7211

发表论文 31 篇 · 总被引 1342 次 · h-index 12

代表论文

• Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (2022 · Nature Genetics · 被引 145)
• Genetic association analyses highlight biological pathways underlying mitral valve prolapse (2015 · Nature Genetics · 被引 137)
• Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome (2015 · Human Molecular Genetics · 被引 137)
• Genetic Association Analyses Highlight IL6 , ALPL , and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis (2019 · Circulation Genomic and Precision Medicine · 被引 84)
• RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome (2019 · European Heart Journal · 被引 53)
• Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm (2018 · The American Journal of Human Genetics · 被引 50)