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	SMCHD1 is involved in de novo methylation of theDUX4-encoding D4Z4 macrosatellite Camille Dion , Stéphane Roche , Camille Laberthonnière , Natacha Broucqsault , Virginie Mariot iScience, 2022, 25 (2), pp.103757. ⟨10.1093/nar/gkz005⟩ Article dans une revue hal-02002680v1
	Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells Kilian Mazaleyrat , Cherif Badja , Natacha Broucqsault , Raphaël Chevalier , Camille Laberthonnière Cells, 2020, 9 (6), pp.1531. ⟨10.3390/cells9061531⟩ Article dans une revue hal-03080368v1
	Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism Stéphane Roche , Camille Dion , Natacha Broucqsault , Camille Laberthonnière , Marie-Cécile Gaillard Neurology Genetics, 2019, 5 (6), pp.e372. ⟨10.1212/NXG.0000000000000372⟩ Article dans une revue hal-02406985v1
	Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral Dystrophy. Marie-Cécile Gaillard , Natacha Broucqsault , Julia Morere , Camille Laberthonnière , Camille Dion Scientific Reports, 2019, 1, ⟨10.1038/s41598-019-46861-x⟩ Article dans une revue hal-01951503v2

	SMCHD1 variants may induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome Camille Laberthonnière , Raphaël Chevalier , Camille Dion , Mégane Delourme , David Hirst 2022 Pré-publication, Document de travail hal-03634209v1

Frederique Magdinier