Pau Pastor
Pau Pastor
Associate Professor
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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
24412013
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
4122011
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550-554, 2014
3712014
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
3622017
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
3192019
Structural brain changes in Parkinson disease with dementia: a voxel-based morphometry study
C Summerfield, C Junqué, E Tolosa, P Salgado-Pineda, B Gómez-Ansón, ...
Archives of neurology 62 (2), 281-285, 2005
2852005
PINK1-linked parkinsonism is associated with Lewy body pathology
L Samaranch, O Lorenzo-Betancor, JM Arbelo, I Ferrer, E Lorenzo, ...
Brain 133 (4), 1128-1142, 2010
2052010
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty, JSK Kauwe, S Shears, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
2052006
Frontotemporal dementia and its subtypes: a genome-wide association study
R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ...
The Lancet Neurology 13 (7), 686-699, 2014
1932014
Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene
P Pastor, E Pastor, C Carnero, R Vela, T García, G Amer, E Tolosa, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
1832001
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
RJ Guerreiro, M Baquero, R Blesa, M Boada, JM Brás, MJ Bullido, ...
Neurobiology of aging 31 (5), 725-731, 2010
1812010
Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindred
P Pastor, CM Roe, A Villegas, G Bedoya, S Chakraverty, G García, ...
Annals of neurology 54 (2), 163-169, 2003
1742003
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies
J Bras, R Guerreiro, L Darwent, L Parkkinen, O Ansorge, V Escott-Price, ...
Human molecular genetics 23 (23), 6139-6146, 2014
1632014
Amygdalar and hippocampal MRI volumetric reductions in Parkinson's disease with dementia
C Junqué, B Ramírez‐Ruiz, E Tolosa, C Summerfield, MJ Martí, P Pastor, ...
Movement disorders: official journal of the Movement Disorder Society 20 (5 …, 2005
1612005
A novel Alzheimer disease locus located near the gene encoding tau protein
G Jun, CA Ibrahim-Verbaas, M Vronskaya, JC Lambert, J Chung, AC Naj, ...
Molecular psychiatry 21 (1), 108-117, 2016
1522016
TREM2 is associated with the risk of Alzheimer's disease in Spanish population
BA Benitez, B Cooper, P Pastor, SC Jin, E Lorenzo, S Cervantes, ...
Neurobiology of aging 34 (6), 1711. e15-1711. e17, 2013
1382013
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
1212000
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
1082019
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease
JJ Zarranz, I Ferrer, E Lezcano, MI Forcadas, B Eizaguirre, B Atares, ...
Neurology 64 (9), 1578-1585, 2005
1022005
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease
V Escott-Price, C Bellenguez, LS Wang, SH Choi, D Harold, L Jones, ...
PloS one 9 (6), e94661, 2014
962014
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