Caroline Paternotte
Inserm(FR)Sorbonne Université(FR)Assistance Publique – Hôpitaux de Paris(FR)Genoscope(FR)Pitié-Salpêtrière Hospital(FR)
Publications by Year
Research Areas
Neurological diseases and metabolism, Hereditary Neurological Disorders, Neurogenetic and Muscular Disorders Research, RNA Research and Splicing, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia(1999)631 cited
- → A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34(2000)97 cited
- → Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias(1999)93 cited
- → Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2(1996)87 cited
- → Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.(1998)71 cited
- → Analysis of the planar cell polarity gene Vangl2 and its co‐expressed paralogue Vangl1 in neural tube defect patients(2005)55 cited