Genetics of syndromic and non-syndromic mitral valve prolapseThierry Le Tourneau, Jean‐Jacques Schott, Jean Mérot et al.|Heart|2018Cited by 73
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Betty Gardie, Anne Gaignerie et al.|Haematologica|2023Cited by 21
Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemiaAntoine Rimbert, Bertrand Cariou, Matthieu Pichelin et al.|Atherosclerosis|2016Cited by 17
Comprehensive <i>in silico</i> and functional studies for classification of <i>EPAS1/HIF2A</i> genetic variants identified in patients with erythrocytosisValéna Karaghiannis, Betty Gardie, Darko Maric et al.|Haematologica|2023Cited by 16
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled AnalysisSandrine Morel, Helen Kim, Isabel C. Hostettler et al.|Journal of Personalized Medicine|2022Cited by 13