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Cleo Smeets
Cleo Smeets
Institut du Cerveau - Paris Brain Institute
Verified email at icm-institute.org
Title
Cited by
Cited by
Year
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia
EAR Nibbeling, A Duarri, CC Verschuuren-Bemelmans, MR Fokkens, ...
Brain 140 (11), 2860-2878, 2017
1152017
HDAC4-myogenin axis as an important marker of HD-related skeletal muscle atrophy
M Mielcarek, M Toczek, CJLM Smeets, SA Franklin, MK Bondulich, ...
PLoS genetics 11 (3), e1005021, 2015
662015
Climbing fibers in spinocerebellar ataxia: A mechanism for the loss of motor control
C Smeets, DS Verbeek
Neurobiology of disease 88, 96-106, 2016
532016
Cerebellar ataxia and functional genomics: identifying the routes to cerebellar neurodegeneration
C Smeets, DS Verbeek
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1842 (10 …, 2014
502014
Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23
CJLM Smeets, J Jezierska, H Watanabe, A Duarri, MR Fokkens, M Meijer, ...
Brain 138 (9), 2537-2552, 2015
402015
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4. 3 channel function and gating in a dominant manner
A Duarri, MCA Lin, MR Fokkens, M Meijer, CJLM Smeets, EAR Nibbeling, ...
Cellular and molecular life sciences 72 (17), 3387-3399, 2015
332015
Altered secondary structure of Dynorphin A associates with loss of opioid signalling and NMDA-mediated excitotoxicity in SCA23
CJLM Smeets, J Zmorzyńska, MN Melo, A Stargardt, C Dooley, ...
Human molecular genetics 25 (13), 2728-2737, 2016
132016
Reply: SCA23 and prodynorphin: is it time for gene retraction?
CJLM Smeets, DS Verbeek
Brain 139 (8), e43-e43, 2016
22016
Genetic screening of glutamatergic components in cases suspected to suffer from cerebellar ataxia reveals a link with intellectual disability
C Smeets, EAR Nibbeling, MR Fokkens, D Brandenburg-Weening, F Yi, ...
The genetics of spinocerebellar ataxia and dystonia, 127, 0
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