| Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia A Freischmidt, T Wieland, B Richter, W Ruf, V Schaeffer, K Müller, ... Nature neuroscience 18 (5), 631-636, 2015 | 866 | 2015 |
| Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 646 | 2018 |
| Safety and efficacy of zilucoplan in patients with generalised myasthenia gravis (RAISE): a randomised, double-blind, placebo-controlled, phase 3 study JF Howard, S Bresch, A Genge, C Hewamadduma, J Hinton, Y Hussain, ... The Lancet Neurology 22 (5), 395-406, 2023 | 102 | 2023 |
| The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations PF Pradat, E Bernard, P Corcia, P Couratier, C Jublanc, G Querin, ... Orphanet journal of rare diseases 15, 1-21, 2020 | 54 | 2020 |
| Thrombolysis for stroke caused by infective endocarditis: an illustrative case and review of the literature E Ong, L Mechtouff, E Bernard, TH Cho, LL Diallo, N Nighoghossian, ... Journal of neurology 260 (5), 1339-1342, 2013 | 54 | 2013 |
| Early illustrations of geste antagoniste in cervical and generalized dystonia E Broussolle, C Laurencin, E Bernard, S Thobois, T Danaila, P Krack Tremor and other hyperkinetic movements 5, 2015 | 52 | 2015 |
| Isotopic evidence for disrupted copper metabolism in amyotrophic lateral sclerosis L Sauzéat, E Bernard, A Perret-Liaudet, I Quadrio, A Vighetto, ... Iscience 6, 264-271, 2018 | 47 | 2018 |
| Motor neuron involvement in anti-Ma2-associated paraneoplastic neurological syndrome A Vogrig, B Joubert, A Maureille, L Thomas, E Bernard, N Streichenberger, ... Journal of Neurology 266, 398-410, 2019 | 42 | 2019 |
| Clinical and Molecular Landscape of ALS Patients with SOD1 Mutations: Novel Pathogenic Variants and Novel Phenotypes. A Single ALS Center Study E Bernard, A Pegat, J Svahn, F Bouhour, P Leblanc, S Millecamps, ... International Journal of Molecular Sciences 21 (18), 6807, 2020 | 39 | 2020 |
| Nivolumab-induced myositis: a case report and a literature review J Bourgeois-Vionnet, B Joubert, E Bernard, MA Sia, V Pante, N Fabien, ... Journal of the Neurological Sciences 387, 51-53, 2018 | 33 | 2018 |
| Isolation of exosomes and microvesicles from cell culture systems to study prion transmission P Leblanc, ZE Arellano-Anaya, E Bernard, L Gallay, M Provansal, ... Exosomes and Microvesicles: Methods and Protocols, 153-176, 2017 | 30 | 2017 |
| Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centres B Marin, E Beghi, C Vial, E Bernard, G Lautrette, P Clavelou, N Guy, ... European journal of neurology 23 (4), 787-795, 2016 | 30 | 2016 |
| Phosphorylated and aggregated TDP-43 with seeding properties are induced upon mutant Huntingtin (mHtt) polyglutamine expression in human cellular models L Coudert, T Nonaka, E Bernard, M Hasegawa, L Schaeffer, P Leblanc Cellular and Molecular Life Sciences 76, 2615-2632, 2019 | 27 | 2019 |
| Multiple sclerosis broke my heart G Androdias, E Bernard, D Biotti, N Collongues, F Durand‐Dubief, ... Annals of Neurology 81 (5), 754-758, 2017 | 26 | 2017 |
| Accuracy of distinguishing between dysembryoplastic neuroepithelial tumors and other epileptogenic brain neoplasms with [11C]methionine PET S Rheims, S Rubi, S Bouvard, E Bernard, N Streichenberger, M Guenot, ... Neuro-oncology 16 (10), 1417-1426, 2014 | 23 | 2014 |
| High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families M Benkirane, C Marelli, C Guissart, A Roubertie, E Ollagnon, A Choumert, ... Genetics in Medicine 23 (11), 2160-2170, 2021 | 18 | 2021 |
| Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS MDM Amador, F Muratet, E Teyssou, G Banneau, V Danel-Brunaud, ... Neurology: Genetics 5 (6), e374, 2019 | 18 | 2019 |
| Adenovirus COVID‐19 Vaccines and Guillain–Barré Syndrome with Facial Paralysis A Pegat, A Vogrig, C Khouri, K Masmoudi, T Vial, E Bernard Annals of Neurology 91 (1), 162, 2022 | 17 | 2022 |
| Effect of familial clustering in the genetic screening of 235 French ALS families P Corcia, W Camu, C Brulard, S Marouillat, P Couratier, ... Journal of Neurology, Neurosurgery & Psychiatry 92 (5), 479-484, 2021 | 16 | 2021 |
| Clinical phenotype and inheritance in patients with C9orf72 hexanucleotide repeat expansion: results from a large French cohort F Esselin, K Mouzat, A Polge, R Juntas-Morales, N Pageot, E De la Cruz, ... Frontiers in Neuroscience 14, 316, 2020 | 16 | 2020 |
