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Oriol Dols-Icardo
Oriol Dols-Icardo
Sant Pau Biomedical Research Institute
Verified email at santpau.cat
Title
Cited by
Cited by
Year
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
15292019
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
3842013
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
1712011
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
1692012
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
1442014
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
1312014
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
1182014
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
1162021
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
1082013
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
1032019
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
912019
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
802018
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
782019
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
752014
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
662021
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
632022
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
632015
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
612020
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
612019
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
602020
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