Disturbed mitochondrial dynamics and neurodegenerative disorders F Burté, V Carelli, PF Chinnery, P Yu-Wai-Man Nature reviews neurology 11 (1), 11-24, 2015 | 712 | 2015 |
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis EC Genin, M Plutino, S Bannwarth, E Villa, E Cisneros‐Barroso, M Roy, ... EMBO molecular medicine 8 (1), 58-72, 2016 | 196 | 2016 |
A neurodegenerative perspective on mitochondrial optic neuropathies P Yu-Wai-Man, M Votruba, F Burté, C La Morgia, P Barboni, V Carelli Acta neuropathologica 132, 789-806, 2016 | 167 | 2016 |
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation R Spiegel, A Saada, PJ Flannery, F Burté, D Soiferman, M Khayat, ... Journal of medical genetics 53 (2), 127-131, 2016 | 115 | 2016 |
Metabolic profiling of Parkinson's disease and mild cognitive impairment F Burté, D Houghton, H Lowes, A Pyle, S Nesbitt, A Yarnall, ... Movement Disorders 32 (6), 927-932, 2017 | 80 | 2017 |
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions C Rouzier, D Moore, C Delorme, S Lacas-Gervais, S Ait-El-Mkadem, ... Human molecular genetics 26 (9), 1599-1611, 2017 | 75 | 2017 |
Alterations in the mitochondrial proteome of neuroblastoma cells in response to complex 1 inhibition F Burté, LA De Girolamo, AJ Hargreaves, EE Billett Journal of proteome research 10 (4), 1974-1986, 2011 | 70 | 2011 |
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy P Yu-Wai-Man, D Soiferman, DG Moore, F Burté, A Saada Mitochondrion 36, 36-42, 2017 | 61 | 2017 |
Malaria Induces Anemia through CD8+ T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen I Safeukui, ND Gomez, AA Adelani, F Burte, NK Afolabi, R Akondy, ... MBio 6 (1), 10.1128/mbio. 02493-14, 2015 | 55 | 2015 |
Circulatory hepcidin is associated with the anti-inflammatory response but not with iron or anemic status in childhood malaria F Burté, BJ Brown, AE Orimadegun, WA Ajetunmobi, NK Afolabi, ... Blood, The Journal of the American Society of Hematology 121 (15), 3016-3022, 2013 | 55 | 2013 |
Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria J Bachmann, F Burté, S Pramana, I Conte, BJ Brown, AE Orimadegun, ... PLoS pathogens 10 (4), e1004038, 2014 | 51 | 2014 |
Altered ceramide metabolism is a feature in the extracellular vesicle-mediated spread of alpha-synuclein in Lewy body disorders M Kurzawa-Akanbi, S Tammireddy, I Fabrik, L Gliaudelytė, MK Doherty, ... Acta neuropathologica 142, 961-984, 2021 | 42 | 2021 |
Monoamine oxidase-A promotes protective autophagy in human SH-SY5Y neuroblastoma cells through Bcl-2 phosphorylation A Ugun-Klusek, TS Theodosi, JC Fitzgerald, F Burté, C Ufer, DJ Boocock, ... Redox Biology 20, 167-181, 2019 | 40 | 2019 |
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells S Trifunov, A Pyle, ML Valentino, R Liguori, P Yu-Wai-Man, F Burté, J Duff, ... Scientific reports 8 (1), 11682, 2018 | 31 | 2018 |
The IL17F and IL17RA Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations S Marquet, I Conte, B Poudiougou, L Argiro, S Cabantous, H Dessein, ... Infection and immunity 84 (2), 590-597, 2016 | 27 | 2016 |
Severe childhood malaria syndromes defined by plasma proteome profiles F Burté, BJ Brown, AE Orimadegun, WA Ajetunmobi, F Battaglia, BK Ely, ... PLoS One 7 (12), e49778, 2012 | 21 | 2012 |
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria S Marquet, I Conte, B Poudiougou, L Argiro, H Dessein, C Couturier, ... Scientific reports 7 (1), 41636, 2017 | 17 | 2017 |
Retinal pigment epithelium extracellular vesicles are potent inducers of age‐related macular degeneration disease phenotype in the outer retina M Kurzawa‐Akanbi, P Whitfield, F Burté, PM Bertelli, V Pathak, M Doherty, ... Journal of Extracellular Vesicles 11 (12), 12295, 2022 | 16 | 2022 |
WFS1-associated optic neuropathy: genotype-phenotype correlations and disease progression A Majander, N Jurkute, F Burté, K Brock, C João, H Huang, MM Neveu, ... American Journal of Ophthalmology 241, 9-27, 2022 | 14 | 2022 |
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis SE Abah, F Burté, S Marquet, BJ Brown, F Akinkunmi, G Oyinloye, ... Scientific Reports 8 (1), 17527, 2018 | 14 | 2018 |