Eva Nelis

Neuroscience · Life Sciences

38h-index7.8kcitations102works0.02yr avg
OpenAlex↗Google Scholar↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Hereditary Neurological Disorders(82), Genetic Neurodegenerative Diseases(37), Neurological diseases and metabolism(27), Botulinum Toxin and Related Neurological Disorders(13), Cellular Mechanics and Interactions(9)

Publications101 total

E-book: Neurologie - Uitgave 2023
Tijdschrift voor Geneeskunde·2023
Evaluation of sexual assault evidence collection kit: Comparison of the success rate of STR analysis of swabs versus rinses
Forensic science international. Genetics supplement series·2019· 1 cited
Evaluation of usefulness of further Y-STR analysis in sexual assault cases on PSA positive samples resulting in female autosomal STR profiling
Forensic science international. Genetics supplement series·2019· 3 citedOpen Access
Por la corriente inglesa. El uso y la importancia del inglés entre estudiantes en España y Holanda.
Utrecht University Repository (Utrecht University)·2012Open Access
PO32-FR-24 Heterozygous missense mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy or silver syndrome
Journal of the Neurological Sciences·2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Brain·2009· 92 citedOpen Access
Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity
Neuromuscular Disorders·2009· 15 cited
Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing
Human Mutation·2008· 67 cited
Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation
Journal of Neurology·2008· 43 cited
Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation
Annals of Human Genetics·2008· 161 cited
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study
Brain·2007· 122 citedOpen Access
S90L BSCL2 mutation causing Silver syndrome with optic nerve involvement
Clinical Neurophysiology·2007
NMP08 Asymptomatic Charcot Marie Tooth
European Journal of Paediatric Neurology·2007
Genotype–phenotype analysis in patients with giant axonal neuropathy (GAN)
Neuromuscular Disorders·2007· 31 cited
Hereditary Spastic Paraplegia 3A Associated With Axonal Neuropathy
Archives of Neurology·2007· 51 cited
GDAP1 mutations in Czech families with early-onset CMT
Neuromuscular Disorders·2007· 19 cited
Mutation Scanning the GJB1 Gene with High-Resolution Melting Analysis: Implications for Mutation Scanning of Genes for Charcot-Marie-Tooth Disease
Clinical Chemistry·2007· 57 cited
Volume Contents
Neuromuscular Disorders·2006Open Access
Novel mutations in the <i>HSN2</i> gene causing hereditary sensory and autonomic neuropathy type II
Neurology·2006· 40 cited
Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies
NeuroMolecular Medicine·2006· 11 cited
page 1 of 6Next →

Frequent Co-authors

Vincent Timmerman(34), Christine Van Broeckhoven(33), Peter De Jonghe(30), A. Löfgren(8), C. Ceuterick(7), Kristl G. Claeys(7), Els De Vriendt(6), Jean‐Jacques Martin(6), James R. Lupski(5), Nathalie Verpoorten(5), Jeffery M. Vance(4), Bernd Rautenstrauß(4), Stephan Züchner(3), Oleg V. Evgrafov(3), Peter Raeymaekers(3), Jurgen Del‐Favero(3), Neva E. Haites(3), Sevim Erdem‐Özdamar(3), Haluk Topaloğlu(3), Jean‐Jacques Martin(3)