Volgen
Jonathan Baets
Jonathan Baets
Neurogenetics group, University of Antwerp
Geverifieerd e-mailadres voor uantwerpen.be
Titel
Geciteerd door
Geciteerd door
Jaar
A de novo gain-of-function mutation in SCN11A causes loss of pain perception
E Leipold, L Liebmann, GC Korenke, T Heinrich, S Gießelmann, J Baets, ...
Nature genetics 45 (11), 1399-1404, 2013
3172013
Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial
JF Howard, V Bril, T Vu, C Karam, S Peric, T Margania, H Murai, ...
The Lancet Neurology 20 (7), 526-536, 2021
2562021
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
I Kurth, T Pamminger, JC Hennings, D Soehendra, AK Huebner, ...
Nature genetics 41 (11), 1179-1181, 2009
2412009
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
C Beetz, R Schüle, T Deconinck, KN Tran-Viet, H Zhu, BPH Kremer, ...
Brain 131 (4), 1078-1086, 2008
2042008
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy
ML Kennerson, GA Nicholson, SG Kaler, B Kowalski, JFB Mercer, J Tang, ...
The American Journal of Human Genetics 86 (3), 343-352, 2010
2022010
Genes for hereditary sensory and autonomic neuropathies: a genotype–phenotype correlation
A Rotthier, J Baets, ED Vriendt, A Jacobs, M Auer-Grumbach, N Levy, ...
Brain 132 (10), 2699-2711, 2009
2012009
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2
JB Rivière, S Ramalingam, V Lavastre, M Shekarabi, S Holbert, ...
The American Journal of Human Genetics 89 (2), 219-230, 2011
1962011
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I
A Rotthier, M Auer-Grumbach, K Janssens, J Baets, A Penno, ...
The American Journal of Human Genetics 87 (4), 513-522, 2010
1952010
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
I Gijselinck, S Van Mossevelde, J Van Der Zee, A Sieben, S Philtjens, ...
Neurology 85 (24), 2116-2125, 2015
1912015
Mechanisms of disease in hereditary sensory and autonomic neuropathies
A Rotthier, J Baets, V Timmerman, K Janssens
Nature Reviews Neurology 8 (2), 73-85, 2012
1902012
Transcriptional regulator PRDM12 is essential for human pain perception
YC Chen, M Auer-Grumbach, S Matsukawa, M Zitzelsberger, ...
Nature genetics 47 (7), 803-808, 2015
1692015
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study
I Dierick, J Baets, J Irobi, A Jacobs, E De Vriendt, T Deconinck, L Merlini, ...
Brain 131 (5), 1217-1227, 2008
1552008
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I
C Guelly, PP Zhu, L Leonardis, L Papić, J Zidar, M Schabhüttl, ...
The American Journal of Human Genetics 88 (1), 99-105, 2011
1502011
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia
M Zimoń, J Baets, L Almeida-Souza, E De Vriendt, J Nikodinovic, ...
Nature genetics 44 (10), 1080-1083, 2012
1472012
Mutations in SACS cause atypical and late-onset forms of ARSACS
J Baets, T Deconinck, K Smets, D Goossens, P Van den Bergh, K Dahan, ...
Neurology 75 (13), 1181-1188, 2010
1472010
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies
M Zimoń, J Baets, M Auer-Grumbach, J Berciano, A Garcia, E Lopez-Laso, ...
Brain 133 (6), 1798-1809, 2010
1472010
The SCN1A variant database: a novel research and diagnostic tool
LRF Claes, L Deprez, A Suls, J Baets, K Smets, T Van Dyck, T Deconinck, ...
Human mutation 30 (10), E904-E920, 2009
1452009
Genetic spectrum of hereditary neuropathies with onset in the first year of life
J Baets, T Deconinck, E De Vriendt, M Zimoń, L Yperzeele, ...
Brain 134 (9), 2664-2676, 2011
1402011
Defects of mutant DNMT1 are linked to a spectrum of neurological disorders
J Baets, X Duan, Y Wu, G Smith, WW Seeley, I Mademan, NM McGrath, ...
Brain 138 (4), 845-861, 2015
1202015
Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial
MG Hanna, UA Badrising, O Benveniste, TE Lloyd, M Needham, H Chinoy, ...
The Lancet Neurology 18 (9), 834-844, 2019
1162019
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20