Publications

Selected publications 

(Article titles redirect to papers on publishers page)

Takahashi K, Kanerva K, Vanharanta L, Almeida-Souza L, Lietha D, Olkkonen VM, Ikonen E. ORP2 couples LDL-cholesterol transport to FAK activation by endosomal cholesterol/PI(4,5)P 2 exchange. EMBO Journal 2021.

Hu M, Cebola I, Carrat G, Jiang S, Nawaz S, Khamis A, Canouil M, Froguel P, Schulte A, Solimena M, Ibberson M, Marchetti P, Cardenas-Diaz FL, Gadue PJ, Hastoy B, Almeida-Souza L, McMahon H, Rutter GA. Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretionCell Reports 2021.

Almeida-Souza L*, Frank R, García-Nafría J, Colussi A, Gunawardana N, Johnson CM , Yu M, Howard G, Andrews B, Vallis Y, McMahon HT. A flat BAR protein promotes actin polymerisation at the base of clathrin coated pitsCell, 2018. * Lead contact 

Boucrot E, Ferreira APA, Almeida-Souza L, Debard S, Vallis Y, Howard G, Bertot L, Sauvonnet N, McMahon HT. Endophilin marks and controls a clathrin-independent endocytic pathwayNature, 2015. 

Almeida-Souza L, Asselbergh B, De Winter V, Goethals S, Timmerman V, Janssens S. HSPB1 facilitates the formation of non-centrosomal microtubulesPlos One, 2013. 

Zimon M, Baets J, Almeida-Souza L, De Vriendt E, Nikodinovic J, Parman Y, Battaloglu E, Matur Z, Guergueltcheva V, Tournev I, Auer-Grumbach M, De Rijk P, Petersen B, Müller T, Fransen E, Van Damme P, Löscher W, Barisic N, Mitrovic Z, Previtali S, Topaloglu H, Bernert G, Beleza-Meireles A, Todorovic S, Savic-Pevicevic D, Ishpekova B, Lechner S, Peeters K, Ooms T, Hahn A, Züchner S, Timmerman V, Van Dijck P, Milic Rasic V, Janecke A, De Jonghe P, Jordanova A. Loss of function mutations in HINT1 are a major cause of autosomal recessive axonal neuropathy with neuromyotoniaNature Genetics, 2012. 

Almeida-Souza L, Asselbergh B, d’Ydewalle C, Moonens K, Goethals S, de Winter V, Gevaert K, Azmi A, Timmermans JP, Irobi J, Remaut H, Van Den Bosch L, Timmerman V, Janssens S. Small heat shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy. The Journal of Neuroscience, 2011. * featured article, *comment on NEJM Dec 15 2011 

Almeida-Souza L, Goethals S, de Winter V, Dierick I, Gallardo R, Van Durme J, Irobi J, Gettemans J, Rousseau F, Schymkowitz J, Timmerman V, Janssens S. Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathyThe Journal of Biological Chemistry, 2010. 

Almeida-Souza L, Baets J. PhD survival guideEMBO reports, 2012. 

Krols M, Detry S, Asselbergh B, Almeida-Souza L, Kremer A, Lippens S, de Rycke R, De Winter V, Müller FJ, Kurth I, McMahon HT, Savvides SN, Timmerman V, Janssens S. Sensory neuropathy-causing mutations in ATL3 cause aberrant ER membrane tethering. Cell Reports. 2018. 

Full publication list:

Google Scholar profile: https://scholar.google.com/citations?user=ZRNZiXkAAAAJ&hl=en

ORCID Page: https://orcid.org/0000-0002-7169-1238