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Current Atherosclerosis Reports|April 25, 2012
Genetics of cholesterol effluxIulia Iatan, Aurélien Palmyre, Sarah Alrasheed, et al.
Chest|July 9, 2022
Myocardial Infarction in a 29-Year-Old Woman Leads to Diagnosis and Treatment of a Rare DiseaseCarma Karam, Nicolas Mansencal, Etienne Puymirat, et al.
Archives of Cardiovascular Diseases|April 26, 2024
Molecular genetic screening after non-ischaemic sudden cardiac arrest and no overt cardiomyopathy in real life: A major tool for the aetiological diagnostic work-upOrianne Weizman, Estelle Gandjbakhch, Isabelle Magnin-Poull, et al.
Prenatal Diagnosis|October 13, 2017
Prenatal molecular diagnosis in RASA1-related diseaseAurélien Palmyre, Mélanie Eyries, Marie-Victoire Senat, et al.
Human Molecular Genetics|June 14, 2015
The role of primary cilia in corpus callosum formation is mediated by production of the Gli3 repressorChristine Laclef, Isabelle Anselme, Laurianne Besse, et al.
Plos One|July 11, 2014
Collective epithelial migration drives kidney repair after acute injuryAurélien Palmyre, Jeongeun Lee, Gennadiy Ryklin, et al.
Heart Rhythm|May 16, 2026
Sudden cardiac death and major arrhythmic events in patients with Fabry disease: risk stratification in the FHFc multicenter studyYassine Temmar, Julie Proukhnitzky, Nicolas Lamblin, et al.
American Journal of Physiology. Renal Physiology|October 10, 2014
Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosisBen Fogelgren, Xiaofeng Zuo, Janine M Buonato, et al.
Plos One|January 24, 2020
Higher prevalence of splenic artery aneurysms in hereditary hemorrhagic telangiectasia: Vascular implications and risk factorsJacques Sellier, Carma Karam, Alain Beauchet, et al.
Orphanet Journal of Rare Diseases|June 10, 2025
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosisAurélien Palmyre, Fairouz Koraichi, Flavie Ader, et al.
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