| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019 | 1985 | 2019 |
| Dissecting phenotypic traits linked to human resilience to Alzheimer’s pathology BG Perez-Nievas, TD Stein, HC Tai, O Dols-Icardo, TC Scotton, ... Brain 136 (8), 2510-2526, 2013 | 427 | 2013 |
| Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course N Setó‐Salvia, J Pagonabarraga, H Houlden, B Pascual‐Sedano, ... Movement Disorders 27 (3), 393-399, 2012 | 182 | 2012 |
| Dementia risk in Parkinson disease: disentangling the role of MAPT haplotypes N Setó-Salvia, J Clarimón, J Pagonabarraga, B Pascual-Sedano, ... Archives of neurology 68 (3), 359-364, 2011 | 179 | 2011 |
| Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ... JAMA neurology 78 (4), 464-472, 2021 | 152 | 2021 |
| Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia O Dols-Icardo, A García-Redondo, R Rojas-García, R Sánchez-Valle, ... Human molecular genetics 23 (3), 749-754, 2014 | 152 | 2014 |
| Assessing the role of the TREM2 p. R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia A Ruiz, O Dols-Icardo, MJ Bullido, P Pastor, E Rodríguez-Rodríguez, ... Neurobiology of aging 35 (2), 444. e1-444. e4, 2014 | 139 | 2014 |
| Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease H Holstege, M Hulsman, C Charbonnier, B Grenier-Boley, O Quenez, ... Nature genetics 54 (12), 1786-1794, 2022 | 134 | 2022 |
| Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration J Van der Zee, T Van Langenhove, GG Kovacs, L Dillen, W Deschamps, ... Acta neuropathologica 128, 397-410, 2014 | 132 | 2014 |
| A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the … SJ Van Der Lee, OJ Conway, I Jansen, MM Carrasquillo, L Kleineidam, ... Acta neuropathologica 138, 237-250, 2019 | 123 | 2019 |
| APOE4 homozygosity represents a distinct genetic form of Alzheimer’s disease J Fortea, J Pegueroles, D Alcolea, O Belbin, O Dols-Icardo, ... Nature medicine 30 (5), 1284-1291, 2024 | 113 | 2024 |
| 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 | 112 | 2013 |
| Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability RH Reynolds, J Botía, MA Nalls, J Hardy, SA Gagliano Taliun, M Ryten npj Parkinson's Disease 5 (1), 6, 2019 | 100 | 2019 |
| CSF sAPPβ, YKL-40, and NfL along the ALS-FTD spectrum I Illán-Gala, D Alcolea, V Montal, O Dols-Icardo, L Muñoz, N De Luna, ... Neurology 91 (17), e1619-e1628, 2018 | 90 | 2018 |
| The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease S Bandres‐Ciga, S Saez‐Atienzar, L Bonet‐Ponce, K Billingsley, D Vitale, ... Movement Disorders 34 (4), 460-468, 2019 | 85 | 2019 |
| Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation M Suárez-Calvet, O Dols-Icardo, A Lladó, R Sánchez-Valle, I Hernández, ... Journal of Neurology, Neurosurgery & Psychiatry 85 (6), 684-691, 2014 | 84 | 2014 |
| Pathogenic huntingtin repeat expansions in patients with frontotemporal dementia and amyotrophic lateral sclerosis R Dewan, R Chia, J Ding, RA Hickman, TD Stein, Y Abramzon, S Ahmed, ... Neuron 109 (3), 448-460. e4, 2021 | 81 | 2021 |
| Motor cortex transcriptome reveals microglial key events in amyotrophic lateral sclerosis O Dols-Icardo, V Montal, S Sirisi, G López-Pernas, L Cervera-Carles, ... Neurology: Neuroimmunology & Neuroinflammation 7 (5), e829, 2020 | 81 | 2020 |
| Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score H Iwaki, C Blauwendraat, MB Makarious, S Bandrés‐Ciga, HL Leonard, ... Movement Disorders 35 (5), 774-780, 2020 | 79 | 2020 |
| The Sant Pau Initiative on Neurodegeneration (SPIN) cohort: a data set for biomarker discovery and validation in neurodegenerative disorders D Alcolea, J Clarimón, M Carmona-Iragui, I Illán-Gala, ... Alzheimer's & Dementia: Translational Research & Clinical Interventions 5 …, 2019 | 78 | 2019 |
