T. Ooms

CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila

K. Fischbeck, T. Godenschwege, P. D. Rijk, 2014, Neurobiology of Disease.

Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy

T. Hornemann, B. Asselbergh, D. Blocquel, 2017, Neurology.

Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance.

B. Asselbergh, V. Timmerman, T. Ooms, 2013, American journal of human genetics.

Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot–Marie–Tooth neuropathy

T. Godenschwege, K. Norga, P. Callaerts, 2009, Proceedings of the National Academy of Sciences.

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

P. D. Rijk, S. Züchner, Y. Parman, 2012, Nature Genetics.

Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot–Marie–Tooth neuropathy

K. Norga, P. Callaerts, V. Timmerman, 2009, Proceedings of the National Academy of Sciences.