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Leonardo Almeida-Souza
Leonardo Almeida-Souza
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Cited by
Cited by
Year
Endophilin marks and controls a clathrin-independent endocytic pathway
E Boucrot, APA Ferreira, L Almeida-Souza, S Debard, Y Vallis, G Howard, ...
Nature 517 (7535), 460-465, 2015
5632015
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
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
1972010
Acute injury in the peripheral nervous system triggers an alternative macrophage response
E Ydens, A Cauwels, B Asselbergh, S Goethals, L Peeraer, G Lornet, ...
Journal of neuroinflammation 9, 1-17, 2012
1722012
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
1482012
Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance
K Peeters, I Litvinenko, B Asselbergh, L Almeida-Souza, T Chamova, ...
The American Journal of Human Genetics 92 (6), 955-964, 2013
1302013
Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy
L Almeida-Souza, S Goethals, V De Winter, I Dierick, R Gallardo, ...
Journal of biological chemistry 285 (17), 12778-12786, 2010
1212010
Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy
L Almeida-Souza, B Asselbergh, C d'Ydewalle, K Moonens, S Goethals, ...
Journal of neuroscience 31 (43), 15320-15328, 2011
1162011
A Flat BAR Protein Promotes Actin Polymerization at the Base of Clathrin-Coated Pits
L Almeida-Souza, RAW Frank, J García-Nafría, A Colussi, ...
Cell 174 (2), 325-337, 2018
1072018
Mutant HSPB8 causes motor neuron-specific neurite degeneration
J Irobi, L Almeida-Souza, B Asselbergh, V De Winter, S Goethals, I Dierick, ...
Human molecular genetics 19 (16), 3254-3265, 2010
1062010
MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets
M Strazisar, S Cammaerts, K van der Ven, DA Forero, AS Lenaerts, ...
Molecular psychiatry 20 (4), 472-481, 2015
1022015
Identification and genomic characterization of a new virus (Tymoviridae Family) associated with citrus sudden death disease
W Maccheroni, MC Alegria, CC Greggio, JP Piazza, RF Kamla, ...
Journal of virology 79 (5), 3028-3037, 2005
982005
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
V Guergueltcheva, K Peeters, J Baets, C Ceuterick-de Groote, JJ Martin, ...
Neurology 77 (24), 2105-2114, 2011
622011
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach
M Zimoń, E Battaloğlu, Y Parman, S Erdem, J Baets, E De Vriendt, ...
neurogenetics 16, 33-42, 2015
462015
Microtubule dynamics in the peripheral nervous system: A matter of balance
L Almeida-Souza, V Timmerman, S Janssens
Bioarchitecture, 2011
422011
ORP2 couples LDL‐cholesterol transport to FAK activation by endosomal cholesterol/PI(4,5)P2 exchange
K Takahashi, K Kanerva, L Vanharanta, L Almeida‐Souza, D Lietha, ...
The EMBO Journal 40 (14), e106871, 2021
392021
HSPB1 facilitates ERK-mediated phosphorylation and degradation of BIM to attenuate endoplasmic reticulum stress-induced apoptosis
D Kennedy, K Mnich, D Oommen, R Chakravarthy, L Almeida-Souza, ...
Cell Death & Disease 8 (8), e3026-e3026, 2017
392017
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease
T Geuens, V De Winter, N Rajan, T Achsel, L Mateiu, L Almeida-Souza, ...
Acta neuropathologica communications 5, 1-15, 2017
362017
Disruption of Xylella fastidiosa CVC gumB and gumF genes affects biofilm formation without a detectable influence on exopolysaccharide production
LCA Souza, NA Wulff, P Gaurivaud, AG Mariano, ACD Virgílio, ...
FEMS microbiology letters 257 (2), 236-242, 2006
312006
Sensory-neuropathy-causing mutations in ATL3 cause aberrant ER membrane tethering
M Krols, S Detry, B Asselbergh, L Almeida-Souza, A Kremer, S Lippens, ...
Cell reports 23 (7), 2026-2038, 2018
282018
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