Jonathan Baets, Ph.D.
Affiliations: | 2011 | Universiteit Antwerpen (Belgium) |
Area:
Medicine and Surgery, Genetics, Neuroscience BiologyGoogle:
"Jonathan Baets"Mean distance: 35622
Parents
Sign in to add mentorPaul Parizel | grad student | 2011 | Universiteit Antwerpen (Belgium) | |
(Genotype phenotype correlations in hereditary neuropathies: A systematic approach.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Beijer D, Marte S, Li JC, et al. (2024) Dominant mutations causing axonal Charcot-Marie-Tooth disease expand -associated diseases. Brain Communications. 6: fcae070 |
Van de Vondel L, De Winter J, Timmerman V, et al. (2024) Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias. Trends in Neurosciences. 47: 227-238 |
Lischka A, Eggermann K, Record CJ, et al. (2023) Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies. Brain : a Journal of Neurology |
Ervilha Pereira P, Schuermans N, Meylemans A, et al. (2023) C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD. Acta Neuropathologica |
De Bleecker JL, Claeys KG, Delstanche S, et al. (2023) A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium. Acta Neurologica Belgica |
Malcorps M, Amor-Barris S, Burnyte B, et al. (2022) HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling. Orphanet Journal of Rare Diseases. 17: 374 |
Van de Vondel L, De Winter J, Beijer D, et al. (2022) De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement Disorders : Official Journal of the Movement Disorder Society |
Longo F, De Ritis D, Miluzio A, et al. (2021) Assessment of Sacsin Turnover in Patients With ARSACS: Implications for Molecular Diagnosis and Pathogenesis. Neurology |
Beijer D, Agnew T, Rack JGM, et al. (2021) Biallelic mutations in complex neuropathy affect ADP ribosylation and DNA damage response. Life Science Alliance. 4 |
Beijer D, Kim HJ, Guo L, et al. (2021) Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation. Jci Insight. 6 |