Jonathan Baets
University of Antwerp(BE)Laboratoire de Psychologie des Pays de la Loire(FR)Antwerp University Hospital(BE)Province of Antwerp(BE)Université d'Angers(FR)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Mitochondrial Function and Pathology, Muscle Physiology and Disorders
Most-Cited Works
- → Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial(2021)612 cited
- → A de novo gain-of-function mutation in SCN11A causes loss of pain perception(2013)302 cited
- → Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy(2009)252 cited
- → KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2(2011)203 cited
- → Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I(2010)186 cited
- → Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy(2010)186 cited