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Cell Reports|May 12, 2015
The Nav1.9 channel is a key determinant of cold pain sensation and cold allodyniaStéphane Lolignier, Caroline Bonnet, Christelle Gaudioso, et al.
American Journal of Medical Genetics. Part A|November 22, 2016
Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencingAmandine Baurand, Sylvie Falcon-Eicher, Gabriel Laurent, et al.
Respiratory Medicine and Research|May 11, 2026
The preponderance of genetic variations in paediatric pulmonary hypertensionJulien Grynblat, Mélanie Eyries, Marine Ambar-Akkaoui, et al.
European Heart Journal|September 17, 2011
Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre studyAlban-Elouen Baruteau, Swanny Fouchard, Albin Behaghel, et al.
Nature Communications|March 4, 2025
Inhibition of the STAT3/Fanconi anemia axis is synthetic lethal with PARP inhibition in breast cancerCelia D Rouault, Lucile Bansard, Elena Martínez-Balsalobre, et al.
Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.
Research Square|April 25, 2024
Activation of lysosomal iron triggers ferroptosis in cancerRaphaël Rodriguez, Tatiana Cañeque, Leeroy Baron, et al.
European Journal of Human Genetics : EJHG|November 3, 2016
Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short statureSalima El Chehadeh, Wilhelmina S Kerstjens-Frederikse, Julien Thevenon, et al.
Nature|May 7, 2025
Activation of lysosomal iron triggers ferroptosis in cancerTatiana Cañeque, Leeroy Baron, Sebastian Müller, et al.
Circulation. Genomic and Precision Medicine|May 13, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International StudyMarine Tortigue, Lynne E Nield, Matilde Karakachoff, et al.
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