Didier Devys
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut de génétique et de biologie moléculaire et cellulaire(FR)Université de Strasbourg(FR)
Publications by Year
Research Areas
Genomics and Chromatin Dynamics, Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, RNA Research and Splicing, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Huntingtin Acts in the Nucleus to Induce Apoptosis but Death Does Not Correlate with the Formation of Intranuclear Inclusions(1998)1,585 cited
- → Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome(1991)1,491 cited
- → Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats(1996)851 cited
- → LBR and Lamin A/C Sequentially Tether Peripheral Heterochromatin and Inversely Regulate Differentiation(2013)813 cited
- → The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation(1993)779 cited
- → Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias(1995)653 cited