| Giant axonal neuropathy–associated gigaxonin mutations impair intermediate filament protein degradation S Mahammad, SNP Murthy, A Didonna, B Grin, E Israeli, R Perrot, ... The Journal of clinical investigation 123 (5), 1964-1975, 2013 | 126 | 2013 |
| The promise and perils of HDAC inhibitors in neurodegeneration A Didonna, P Opal Annals of clinical and translational neurology 2 (1), 79-101, 2015 | 119 | 2015 |
| The role of neurofilament aggregation in neurodegeneration: lessons from rare inherited neurological disorders A Didonna, P Opal Molecular neurodegeneration 14 (1), 19, 2019 | 112 | 2019 |
| Hyperpolarized 13C MR metabolic imaging can detect neuroinflammation in vivo in a multiple sclerosis murine model C Guglielmetti, C Najac, A Didonna, A Van der Linden, SM Ronen, ... Proceedings of the National Academy of Sciences 114 (33), E6982-E6991, 2017 | 86 | 2017 |
| Genetic determinants of risk and progression in multiple sclerosis A Didonna, JR Oksenberg Clinica chimica acta 449, 16-22, 2015 | 79 | 2015 |
| The Genetics of Multiple Sclerosis A Didonna, JR Oksenberg Multiple Sclerosis: Perspectives in Treatment and Pathogenesis, 3-16, 2017 | 68 | 2017 |
| Mutant ataxin1 disrupts cerebellar development in spinocerebellar ataxia type 1 CR Edamakanti, J Do, A Didonna, M Martina, P Opal The Journal of clinical investigation 128 (6), 2252-2265, 2018 | 56 | 2018 |
| The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1 A Venkatraman, YS Hu, A Didonna, M Cvetanovic, A Krbanjevic, ... Human molecular genetics 23 (14), 3733-3745, 2014 | 54 | 2014 |
| Tau at the interface between neurodegeneration and neuroinflammation A Didonna Genes & Immunity 21 (5), 288-300, 2020 | 40 | 2020 |
| Post-translational modifications in neurodegeneration A Didonna, F Benetti Aims Biophysics 3 (1), 27-49, 2016 | 38 | 2016 |
| Prion protein and its role in signal transduction A Didonna Cellular and Molecular Biology Letters 18 (2), 209-230, 2013 | 33 | 2013 |
| The role of Bax and caspase-3 in doppel-induced apoptosis of cerebellar granule cells A Didonna, J Sussman, F Benetti, G Legname Prion 6 (3), 309-316, 2012 | 32 | 2012 |
| Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes NM Frederick, PV Shah, A Didonna, MR Langley, AG Kanthasamy, P Opal Human molecular genetics 28 (8), 1343-1356, 2019 | 31 | 2019 |
| Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans H Shams, X Shao, A Santaniello, G Kirkish, A Harroud, Q Ma, N Isobe, ... Brain 146 (2), 645-656, 2023 | 26 | 2023 |
| Infrared microspectroscopy: a multiple-screening platform for investigating single-cell biochemical perturbations upon prion infection A Didonna, L Vaccari, A Bek, G Legname ACS chemical neuroscience 2 (3), 160-174, 2011 | 25 | 2011 |
| Advances in sequencing technologies for understanding hereditary ataxias: a review A Didonna, P Opal JAMA neurology 73 (12), 1485-1490, 2016 | 24 | 2016 |
| A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome A Didonna, N Isobe, SJ Caillier, KH Li, AL Burlingame, SL Hauser, ... Human molecular genetics 24 (24), 7151-7158, 2015 | 24 | 2015 |
| Aberrant STAT phosphorylation signaling in peripheral blood mononuclear cells from multiple sclerosis patients E Canto, N Isobe, A Didonna, ... Journal of neuroinflammation 15, 1-11, 2018 | 22 | 2018 |
| Ataxin-1 regulates B cell function and the severity of autoimmune experimental encephalomyelitis A Didonna, E Canto Puig, Q Ma, A Matsunaga, B Ho, SJ Caillier, H Shams, ... Proceedings of the National Academy of Sciences 117 (38), 23742-23750, 2020 | 19 | 2020 |
| Specific hypomethylation programs underpin B cell activation in early multiple sclerosis Q Ma, SJ Caillier, S Muzic, ... Proceedings of the National Academy of Sciences 118 (51), e2111920118, 2021 | 17 | 2021 |
