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Anna Antonell
Anna Antonell
Fundació Clínic per a la Recerca Biomèdica
Verified email at clinic.cat
Title
Cited by
Cited by
Year
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
G Kleinberger, Y Yamanishi, M Suárez-Calvet, E Czirr, E Lohmann, ...
Science translational medicine 6 (243), 243ra86-243ra86, 2014
7312014
sTREM 2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early‐stage Alzheimer's disease and associate with neuronal injury markers
M Suárez‐Calvet, G Kleinberger, MÁ Araque Caballero, M Brendel, ...
EMBO molecular medicine 8 (5), 466-476, 2016
4482016
CSF biomarker variability in the Alzheimer's Association quality control program
N Mattsson, U Andreasson, S Persson, MC Carrillo, S Collins, S Chalbot, ...
Alzheimer's & Dementia 9 (3), 251-261, 2013
3972013
A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
J van der Zee, I Gijselinck, L Dillen, T Van Langenhove, J Theuns, ...
Human mutation 34 (2), 363-373, 2013
3152013
Low cerebrospinal fluid concentration of mitochondrial DNA in preclinical Alzheimer disease
P Podlesniy, J Figueiro‐Silva, A Llado, A Antonell, R Sanchez‐Valle, ...
Annals of neurology 74 (5), 655-668, 2013
2082013
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I De Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ...
Nature communications 12 (1), 3417, 2021
1722021
Partial 7q11. 23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams–Beuren syndrome neurocognitive profile
A Antonell, M Del Campo, LF Magano, L Kaufmann, JM De La Iglesia, ...
Journal of medical genetics 47 (5), 312-320, 2010
1632010
Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease
M Balasa, E Gelpi, A Antonell, MJ Rey, R Sanchez-Valle, JL Molinuevo, ...
Neurology 76 (20), 1720-1725, 2011
1592011
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
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
EL van der Ende, LH Meeter, JM Poos, JL Panman, LC Jiskoot, ...
The Lancet Neurology 18 (12), 1103-1111, 2019
1562019
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
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
MD Gallagher, E Suh, M Grossman, L Elman, L McCluskey, ...
Acta neuropathologica 127, 407-418, 2014
1422014
CSF biomarkers for the differential diagnosis of Alzheimer's disease: a large-scale international multicenter study
M Ewers, N Mattsson, L Minthon, JL Molinuevo, A Antonell, J Popp, ...
Alzheimer's & Dementia 11 (11), 1306-1315, 2015
1382015
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
Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension
M Del Campo, A Antonell, LF Magano, FJ Muñoz, R Flores, M Bayés, ...
The American Journal of Human Genetics 78 (4), 533-542, 2006
1332006
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
Cerebrospinal fluid level of YKL-40 protein in preclinical and prodromal Alzheimer's disease
A Antonell, A Mansilla, L Rami, A Lladó, A Iranzo, J Olives, M Balasa, ...
Journal of Alzheimer's Disease 42 (3), 901-908, 2014
1272014
A preliminary study of the whole-genome expression profile of sporadic and monogenic early-onset Alzheimer's disease
A Antonell, A Lladó, J Altirriba, T Botta-Orfila, M Balasa, M Fernández, ...
Neurobiology of aging 34 (7), 1772-1778, 2013
1172013
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
C Pottier, X Zhou, RB Perkerson, M Baker, GD Jenkins, DJ Serie, ...
The Lancet Neurology 17 (6), 548-558, 2018
1132018
Cognitively preserved subjects with transitional cerebrospinal fluid ss-amyloid 1-42 values have thicker cortex in Alzheimer's disease vulnerable areas
J Fortea, R Sala-Llonch, D Bartrés-Faz, A Lladó, C Solé-Padullés, ...
Biological psychiatry 70 (2), 183-190, 2011
1112011
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