Martial Mallaret

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

Martial Mallaret, Matthis Synofzik, Jae‐Ho Lee et al. · Brain · 2013 · 127 citations · Full text

Neurobiology Of Disease, Mendelian Disorder, Neurological Disorder +15

SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study

Matthis Synofzik, Katrien Smets, Martial Mallaret et al. · Brain · 2016 · 123 citations · Full text

Neurological Disorder, Genetics, Large Multi-centre Study +16

Autosomal Recessive Cerebellar Ataxia Type 3 Due to<i>ANO10</i>Mutations

M. Renaud, Mathieu Anheim, Erik‐Jan Kamsteeg et al. · JAMA Neurology · 2014 · 61 citations

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M. Renaud, Maria-Céu Moreira, B. Monga et al. · JAMA Neurology · 2018 · 37 citations · Full text

Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia

M. Renaud, Claire Guissart, Martial Mallaret et al. · Journal of Neurology · 2016 · 28 citations

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +7