Marie-cecile Gaillard
Marseille, France
Last Updated: 09/26/2026
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Found 11 publications
The Orphanet Nomenclature and Classification of Rare Diseases for Improved Patient Recognition and Data Interoperability: Qualitative and Quantitative Analysis.
Journal: JMIR medical informatics
Published: September 22, 2025
Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral Dystrophy.
Journal: Scientific reports
Published: March 13, 2019
Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism.
Journal: Neurology. Genetics
Published: February 07, 2019
SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite.
Journal: Nucleic acids research
Published: September 28, 2018
Design on a Rational Basis of High-Affinity Peptides Inhibiting the Histone Chaperone ASF1.
Journal: Cell chemical biology
Published: June 13, 2018
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy.
Journal: Human mutation
Published: March 20, 2016
Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report.
Journal: BMC medical genetics
Published: February 09, 2016
SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophy.
Journal: Genome research
Published: February 05, 2015
Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers.
Journal: Neurology
Published: July 18, 2014
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy.
Journal: Human molecular genetics
Published: June 20, 2013
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Last Updated: 09/26/2026