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Mario Ezquerra
Mario Ezquerra
IDIBAPS, Fundacio Clinic de Barcelona
Verified email at clinic.ub.es
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
Disease‐specific phenotypes in dopamine neurons from human iPS‐based models of genetic and sporadic Parkinson's disease
A Sánchez‐Danés, Y Richaud‐Patin, I Carballo‐Carbajal, ...
EMBO molecular medicine 4 (5), 380-395, 2012
6262012
Cerebrospinal tau, phospho‐tau, and beta‐amyloid and neuropsychological functions in Parkinson's disease
Y Compta, MJ Martí, N Ibarretxe‐Bilbao, C Junqué, F Valldeoriola, ...
Movement disorders: official journal of the Movement Disorder Society 24 (15 …, 2009
2132009
Identification of blood serum micro‐RNAs associated with idiopathic and LRRK2 Parkinson's disease
T Botta‐Orfila, X Morató, Y Compta, JJ Lozano, N Falgas, F Valldeoriola, ...
Journal of neuroscience research 92 (8), 1071-1077, 2014
1572014
Significant association between the tau gene A0/A0 genotype and Parkinson's disease
P Pastor, M Ezquerra, E Muñoz, MJ Martí, R Blesa, E Tolosa, R Oliva
Annals of Neurology: Official Journal of the American Neurological …, 2000
1422000
Aberrant epigenome in iPSC‐derived dopaminergic neurons from Parkinson's disease patients
R Fernández‐Santiago, I Carballo‐Carbajal, G Castellano, R Torrent, ...
EMBO molecular medicine 7 (12), 1529-1546, 2015
1382015
G2019S LRRK2 mutation causing Parkinson’s disease without Lewy bodies
C Gaig, MJ Martí, M Ezquerra, MJ Rey, A Cardozo, E Tolosa
Journal of Neurology, Neurosurgery & Psychiatry 78 (6), 626-628, 2007
1372007
G2019S LRRK2 mutation causing Parkinson’s disease without Lewy bodies
C Gaig, MJ Martí, M Ezquerra, MJ Rey, A Cardozo, E Tolosa
Journal of Neurology, Neurosurgery & Psychiatry 78 (6), 626-628, 2007
1372007
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance
C Gaig, M Ezquerra, MJ Marti, E Munoz, F Valldeoriola, E Tolosa
Archives of neurology 63 (3), 377-382, 2006
1362006
Plasma miR-34a-5p and miR-545-3p as early biomarkers of Alzheimer’s disease: potential and limitations
M Cosín-Tomás, A Antonell, A Lladó, D Alcolea, J Fortea, M Ezquerra, ...
Molecular neurobiology 54, 5550-5562, 2017
1352017
Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain
A Lleó, R Blesa, R Queralt, M Ezquerra, JL Molinuevo, J Pena-Casanova, ...
Archives of neurology 59 (11), 1759-1763, 2002
1172002
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
1152021
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
KJ Billingsley, IA Barbosa, S Bandrés-Ciga, JP Quinn, VJ Bubb, ...
npj Parkinson's Disease 5 (1), 8, 2019
992019
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
Nonmotor Symptoms in LRRK2 G2019S Associated Parkinson’s Disease
C Gaig, D Vilas, J Infante, M Sierra, I Garcia-Gorostiaga, M Buongiorno, ...
PloS one 9 (10), e108982, 2014
852014
Further extension of the H1 haplotype associated with progressive supranuclear palsy
P Pastor, M Ezquerra, E Tolosa, E Muñoz, M José Martí, F Valldeoriola, ...
Movement disorders: official journal of the Movement Disorder Society 17 (3 …, 2002
842002
Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies
I Ferrer, I Hernandez, M Boada, A Llorente, MJ Rey, A Cardozo, ...
Acta neuropathologica 106, 419-435, 2003
802003
Significant changes in the tau A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection
R Oliva, E Tolosa, M Ezquerra, JL Molinuevo, F Valldeoriola, J Burguera, ...
Archives of neurology 55 (8), 1122-1124, 1998
801998
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
M Ezquerra, C Carnero, R Blesa, JL Gelpi, F Ballesta, R Oliva
Neurology 52 (3), 566-566, 1999
791999
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
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