Elisabeth Ollagnon
Hôpital de la Croix-Rousse(FR)Hospices Civils de Lyon(FR)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Hereditary Neurological Disorders, Mitochondrial Function and Pathology, Genetics and Neurodevelopmental Disorders, Muscle Physiology and Disorders
Most-Cited Works
- → Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy(2012)167 cited
- → Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5(2017)74 cited
- → SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia(2011)71 cited
- → SIMPLE mutation analysis in dominant demyelinating Charcot‐Marie‐Tooth disease: three novel mutations(2006)65 cited
- → Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study(2015)44 cited
- → Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias(2016)40 cited
- → Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1(2018)37 cited
- → Dysferlin deficiency treated like refractory polymyositis(2009)19 cited
- → NARP MITOCHONDRIOPATHY: AN UNUSUAL CAUSE OF PROGRESSIVE MYOCLONIC EPILEPSY(2007)15 cited
- → The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis(2023)12 cited