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 | 1539 | 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 | 387 | 2013 |
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 | 171 | 2011 |
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 | 170 | 2012 |
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 | 144 | 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 | 131 | 2014 |
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 | 118 | 2014 |
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 | 116 | 2021 |
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 | 108 | 2013 |
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 | 103 | 2019 |
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 | 91 | 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 | 80 | 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 | 78 | 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 | 75 | 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 | 66 | 2021 |
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 | 65 | 2022 |
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 | 64 | 2019 |
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 | 63 | 2015 |
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 | 61 | 2020 |
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 | 60 | 2020 |