Erik Fransen

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

M. Zimoń, Jonathan Baets, Leonardo Almeida‐Souza et al. · Nature Genetics · 2012 · 127 citations

Neurological Disorder, Axonal Neuropathy, Neurology +5

Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families

Caroline Van Cauwenbergh, Frauke Coppieters, Dimitri Roels et al. · PLoS ONE · 2017 · 55 citations · Full text

A New Neurological Syndrome with Mental Retardation, Choreoathetosis, and Abnormal Behavior Maps to Chromosome Xp11

Edwin Reyniers, Patrick Van Bogaert, Nils Peeters et al. · The American Journal of Human Genetics · 1999 · 41 citations · Full text

Neurological Disorder, Genetics, Social Sciences +16

Inter- and Intra-Scanner Variability of Automated Brain Volumetry on Three Magnetic Resonance Imaging Systems in Alzheimer’s Disease and Controls

Mandy Melissa Jane Wittens, Gert‐Jan Allemeersch, Diana M. Sima et al. · Frontiers in Aging Neuroscience · 2021 · 40 citations · Full text

Patterns of p53 gene mutations in head and neck cancer: full-length gene sequencing and results of primary radiotherapy.

MI Saunders, Ross MacKenzie, Richard David Shipman et al. · PubMed · 1999 · 39 citations

Pathology, Tumor Biology, Cancer-associated Virus +17