| Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2 RJLF Lemmers, JJ Goeman, PJ van der Vliet, MP van Nieuwenhuizen, ... Human molecular genetics 24 (3), 659-669, 2015 | 181 | 2015 |
| Serum chitotriosidase activity is increased in subjects with atherosclerosis disease M Artieda, A Cenarro, A Gañán, I Jericó, C Gonzalvo, JM Casado, I Vitoria, ... Arteriosclerosis, thrombosis, and vascular biology 23 (9), 1645-1652, 2003 | 162 | 2003 |
| International Guillain‐Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in … BC Jacobs, B van den Berg, C Verboon, G Chavada, DR Cornblath, ... Journal of the Peripheral Nervous System 22 (2), 68-76, 2017 | 122 | 2017 |
| Clinical and therapeutic features of myasthenia gravis in adults based on age at onset E Cortés-Vicente, R Álvarez-Velasco, S Segovia, C Paradas, ... Neurology 94 (11), e1171-e1180, 2020 | 113 | 2020 |
| Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide A García‐Redondo, O Dols‐Icardo, R Rojas‐García, J Esteban‐Pérez, ... Human mutation 34 (1), 79-82, 2013 | 110 | 2013 |
| Clinical and myopathological evaluation of early-and late-onset subtypes of myofibrillar myopathy M Olivé, Z Odgerel, A Martínez, JJ Poza, FG Bragado, RJ Zabalza, I Jericó, ... Neuromuscular Disorders 21 (8), 533-542, 2011 | 90 | 2011 |
| DNA methylation signature of human hippocampus in Alzheimer’s disease is linked to neurogenesis M Altuna, A Urdánoz-Casado, J Sánchez-Ruiz de Gordoa, MV Zelaya, ... Clinical epigenetics 11, 1-16, 2019 | 87 | 2019 |
| Myasthenia gravis: sleep quality, quality of life, and disease severity EH Martínez‐Lapiscina, ME Erro, T Ayuso, I Jericó Muscle & nerve 46 (2), 174-180, 2012 | 74 | 2012 |
| Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness A Töpf, K Johnson, A Bates, L Phillips, KR Chao, EM England, ... Genetics in medicine 22 (9), 1478-1488, 2020 | 72 | 2020 |
| Serum neurofilament light chain predicts long-term prognosis in Guillain-Barré syndrome patients L Martín-Aguilar, P Camps-Renom, C Lleixà, E Pascual-Goñi, ... Journal of Neurology, Neurosurgery & Psychiatry 92 (1), 70-77, 2021 | 67 | 2021 |
| Neuroanatomical quantitative proteomics reveals common pathogenic biological routes between amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) MO Iridoy, I Zubiri, MV Zelaya, L Martinez, K Ausín, M Lachen-Montes, ... International journal of molecular sciences 20 (1), 4, 2018 | 67 | 2018 |
| Myasthenia gravis: descriptive analysis of life‐threatening events in a recent nationwide registry A Ramos‐Fransi, R Rojas‐García, S Segovia, C Márquez‐Infante, ... European Journal of Neurology 22 (7), 1056-1061, 2015 | 65 | 2015 |
| Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain O Dols-Icardo, I Nebot, A Gorostidi, S Ortega-Cubero, I Hernández, ... Brain 138 (12), e400-e400, 2015 | 64 | 2015 |
| Clinical characteristics and outcomes of thymoma‐associated myasthenia gravis R Álvarez‐Velasco, G Gutiérrez‐Gutiérrez, JC Trujillo, E Martínez, ... European journal of neurology 28 (6), 2083-2091, 2021 | 59 | 2021 |
| El ictus en el siglo XXI: Tratamiento de urgencia J Gállego, M Herrera, I Jericó, R Muñoz, N Aymerich, E Martínez-Vila Anales del sistema sanitario de Navarra 31, 15-29, 2008 | 59 | 2008 |
| Parkinsonism and spastic paraplegia type 7: expanding the spectrum of mitochondrial Parkinsonism B De la Casa‐Fages, G Fernández‐Eulate, J Gamez, ... Movement Disorders 34 (10), 1547-1561, 2019 | 57 | 2019 |
| Brain involvement in myotonic dystrophy type 1: a morphometric and diffusion tensor imaging study with neuropsychological correlation T Cabada, M Iridoy, I Jericó, P Lecumberri, R Seijas, A Gargallo, ... Archives of Clinical Neuropsychology 32 (4), 401-412, 2017 | 51 | 2017 |
| Expanding the clinical phenotypes of MT-ATP6 mutations E Lopez-Gallardo, S Emperador, A Solano, L Llobet, A Martín-Navarro, ... Human molecular genetics 23 (23), 6191-6200, 2014 | 43 | 2014 |
| Targeted next-generation sequencing in a large cohort of genetically undiagnosed patients with neuromuscular disorders in Spain L Gonzalez-Quereda, MJ Rodriguez, J Diaz-Manera, J Alonso-Perez, ... Genes 11 (5), 539, 2020 | 40 | 2020 |
| Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert GG Gutiérrez, J Díaz-Manera, M Almendrote, S Azriel, JE Bárcena, ... Medicina Clínica 153 (2), 82. e1-82. e17, 2019 | 37 | 2019 |
