Vincent Timmerman
Vincent Timmerman
Verified email at molgen.vib-ua.be - Homepage
Title
Cited by
Cited by
Year
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ...
Nature genetics 36 (5), 449-451, 2004
14722004
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
YZ Chen, CL Bennett, HM Huynh, IP Blair, I Puls, J Irobi, I Dierick, A Abel, ...
The American Journal of Human Genetics 74 (6), 1128-1135, 2004
7882004
Duplication in chromosome 17p11. 2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogenduk, ...
Neuromuscular disorders 1 (2), 93-97, 1991
6621991
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
OV Evgrafov, I Mersiyanova, J Irobi, L Van Den Bosch, I Dierick, CL Leung, ...
Nature genetics 36 (6), 602-606, 2004
6252004
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy
K Verhoeven, P De Jonghe, K Coen, N Verpoorten, M Auer-Grumbach, ...
The American Journal of Human Genetics 72 (3), 722-727, 2003
4512003
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
J Irobi, K Van Impe, P Seeman, A Jordanova, I Dierick, N Verpoorten, ...
Nature genetics 36 (6), 597-601, 2004
4262004
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication
V Timmerman, E Nelis, W Van Hul, BW Nieuwenhuijsen, KL Chen, ...
Nature genetics 1 (3), 171-175, 1992
3951992
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome
C Windpassinger, M Auer-Grumbach, J Irobi, H Patel, E Petek, G Hörl, ...
Nature genetics 36 (3), 271-276, 2004
3512004
HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease
C d'Ydewalle, J Krishnan, DM Chiheb, P Van Damme, J Irobi, ...
Nature medicine 17 (8), 968, 2011
3502011
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy
A Jordanova, J Irobi, FP Thomas, P Van Dijck, K Meerschaert, M Dewil, ...
Nature genetics 38 (2), 197-202, 2006
3452006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2
K Verhoeven, KG Claeys, S Züchner, JM Schröder, J Weis, C Ceuterick, ...
Brain 129 (8), 2093-2102, 2006
3442006
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease
S Züchner, M Noureddine, M Kennerson, K Verhoeven, K Claeys, ...
Nature genetics 37 (3), 289-294, 2005
3422005
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
S Züchner, P De Jonghe, A Jordanova, KG Claeys, V Guergueltcheva, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
3242006
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot–Marie–Tooth disease
A Jordanova, P De Jonghe, CF Boerkoel, H Takashima, E De Vriendt, ...
Brain 126 (3), 590-597, 2003
2812003
The hnRNP family: insights into their role in health and disease
T Geuens, D Bouhy, V Timmerman
Human genetics 135 (8), 851-867, 2016
2402016
Molecular biological characterization of an azole-resistant Candida glabrata isolate.
P Marichal, HV Bossche, FC Odds, G Nobels, DW Warnock, ...
Antimicrobial agents and chemotherapy 41 (10), 2229-2237, 1997
2331997
Further evidence that neurofilament light chain gene mutations can cause Charcot‐Marie‐Tooth disease type 2E
P De Jonghe, I Mersivanova, E Nelis, J Del Favero, JJ Martin, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
2312001
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype
P De Jonghe, V Timmerman, C Ceuterick, E Nelis, E De Vriendt, ...
Brain 122 (2), 281-290, 1999
2271999
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, 2013
2152013
Mutations in SEPT9 cause hereditary neuralgic amyotrophy
G Kuhlenbäumer, MC Hannibal, E Nelis, A Schirmacher, N Verpoorten, ...
Nature genetics 37 (10), 1044-1046, 2005
2152005
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