Delphine Mavel

Publications by Year

Research Areas

Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Genomics and Phylogenetic Studies, Bacterial Genetics and Biotechnology

Most-Cited Works

• → Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia(1999)631 cited
• → Quality Assessment of Whole Genome Mapping Data in the Refined Familial Spastic Paraplegia Interval on Chromosome 14q(1998)25 cited
• → A physical map of human chromosome 14(2001)22 cited
• → A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia(1999)13 cited
• → A 10.3 kbp Segment from nprB to argJ at the 102 Region of the Bacillus Subtilis Chromosome(1997)4 cited
• → Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia(2005)