Eva Nelis

Universidad de Cantabria

Publishes on Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism. 102 papers and 7.8k citations.

102Publications

7.8kTotal Citations

Hereditary Neurological Disorders Genetic Neurodegenerative Diseases Neurological diseases and metabolism Botulinum Toxin and Related Neurological Disorders Peripheral Neuropathies and Disorders

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Top publicationsby citations

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al.|Nature Genetics|2004

Cited by 1.6kOpen Access

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

Peter Raeymaekers, Vincent Timmerman, Eva Nelis et al.|Neuromuscular Disorders|1991

Cited by 599

Estimation of the Mutation Frequenciesin Charcot-Marie-Tooth Disease Type 1and Hereditary Neuropathy withLiability to Pressure Palsies:A European Collaborative Study

Eva Nelis, Christine Van Broeckhoven|European Journal of Human Genetics|1996

Cited by 423

The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

Vincent Timmerman, Eva Nelis, Wim Van Hul et al.|Nature Genetics|1992

Cited by 391

Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Laura E. Warner, Max J. Hilz, Stanley H. Appel et al.|Neuron|1996

Cited by 363Open Access