Kristl G. Claeys

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing

Beryl B. Cummings, Jamie L. Marshall, Taru Tukiainen et al. · Science Translational Medicine · 2017 · 767 citations · Full text

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Stephan Züchner, Peter De Jonghe, Albena Jordanova et al. · Annals of Neurology · 2006 · 358 citations

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Stephan Züchner, Maher Noureddine, Marina Kennerson et al. · Nature Genetics · 2005 · 356 citations

Mendelian Disorder, Genetics, Pathogenesis +6

Mapping the parietal cortex of human and non-human primates

Guy A. Orban, Kristl G. Claeys, Koen Nelissen et al. · Neuropsychologia · 2005 · 319 citations

Parietal Cortex, Cognitive Science, Neuroanatomy +8

Regional variation of Guillain-Barré syndrome

Alex Y. Doets, Christine Verboon, Bianca van den Berg et al. · Brain · 2018 · 301 citations · Full text