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 | 582 | 2015 |
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 | 208 | 2010 |
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 | 206 | 2010 |
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 | 180 | 2012 |
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 | 154 | 2012 |
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 | 132 | 2013 |
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 | 125 | 2010 |
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 | 119 | 2011 |
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 | 111 | 2018 |
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 | 107 | 2010 |
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 | 106 | 2015 |
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 | 98 | 2005 |
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 | 64 | 2011 |
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 | 46 | 2015 |
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 | 44 | 2021 |
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 | 43 | 2017 |
Microtubule dynamics in the peripheral nervous system: A matter of balance L Almeida-Souza, V Timmerman, S Janssens Bioarchitecture, 2011 | 42 | 2011 |
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 | 37 | 2017 |
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 | 32 | 2018 |
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 | 31 | 2006 |