% alzhub.org library filter % Source: https://alzhub.org/research?institution=I4210154623 % 13 entries, in the order the page lists them. Built from alzhub.org's own records. % 0 entries have no readable author in the source record and carry no author field. @article{sims2017-28714976, author = {Sims, R. and van der Lee, S. J. and Naj, A. C. and Bellenguez, C. and Badarinarayan, N. and Jakobsdottir, J. and Kunkle, B. W. and Boland, A. and others}, title = {{Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease}}, journal = {Nature genetics}, year = {2017}, doi = {10.1038/ng.3916}, pmid = {28714976}, url = {https://doi.org/10.1038/ng.3916} } @article{ferrari2014-24943344, author = {Ferrari, R. and Hernandez, D. G. and Nalls, M. A. and Rohrer, J. D. and Ramasamy, A. and Kwok, J. B. and Dobson-Stone, C. and Brooks, W. S. and others}, title = {{Frontotemporal dementia and its subtypes: a genome-wide association study}}, journal = {The Lancet. Neurology}, year = {2014}, doi = {10.1016/s1474-4422(14)70065-1}, pmid = {24943344}, url = {https://doi.org/10.1016/s1474-4422(14)70065-1} } @article{lanoiselee2017-28350801, author = {Lanoiselée, H. M. and Nicolas, G. and Wallon, D. and Rovelet-Lecrux, A. and Lacour, M. and Rousseau, S. and Richard, A. C. and Pasquier, F. and others}, title = {{APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases}}, journal = {PLoS medicine}, year = {2017}, doi = {10.1371/journal.pmed.1002270}, pmid = {28350801}, url = {https://doi.org/10.1371/journal.pmed.1002270} } @article{luo2023-37195665, author = {Luo, J. and Thomassen, J. Q. and Bellenguez, C. and Grenier-Boley, B. and de Rojas, I. and Castillo, A. and Parveen, K. and others}, title = {{Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease}}, journal = {JAMA network open}, year = {2023}, doi = {10.1001/jamanetworkopen.2023.13734}, pmid = {37195665}, url = {https://doi.org/10.1001/jamanetworkopen.2023.13734} } @article{roveletlecrux2006-16369530, author = {Rovelet-Lecrux, A. and Hannequin, D. and Raux, G. and Le Meur, N. and Laquerrière, A. and Vital, A. and Dumanchin, C. and Feuillette, S. and others}, title = {{APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy}}, journal = {Nature genetics}, year = {2006}, doi = {10.1038/ng1718}, pmid = {16369530}, url = {https://doi.org/10.1038/ng1718} } @article{cabrejo2006-16959815, author = {Cabrejo, L. and Guyant-Maréchal, L. and Laquerrière, A. and Vercelletto, M. and De la Fournière, F. and Thomas-Antérion, C. and Verny, C. and Letournel, F. and others}, title = {{Phenotype associated with APP duplication in five families}}, journal = {Brain : a journal of neurology}, year = {2006}, doi = {10.1093/brain/awl237}, pmid = {16959815}, url = {https://doi.org/10.1093/brain/awl237} } @article{bellenguez2017-28789839, author = {Bellenguez, C. and Charbonnier, C. and Grenier-Boley, B. and Quenez, O. and Le Guennec, K. and Nicolas, G. and Chauhan, G. and Wallon, D. and others}, title = {{Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls}}, journal = {Neurobiology of aging}, year = {2017}, doi = {10.1016/j.neurobiolaging.2017.07.001}, pmid = {28789839}, url = {https://doi.org/10.1016/j.neurobiolaging.2017.07.001} } @article{bousiges2018-29321140, author = {Bousiges, O. and Bombois, S. and Schraen, S. and Wallon, D. and Quillard, M. M. and Gabelle, A. and Lehmann, S. and Paquet, C. and others}, title = {{Cerebrospinal fluid Alzheimer biomarkers can be useful for discriminating dementia with Lewy bodies from Alzheimer's disease at the prodromal stage}}, journal = {Journal of neurology, neurosurgery, and psychiatry}, year = {2018}, doi = {10.1136/jnnp-2017-316385}, pmid = {29321140}, url = {https://doi.org/10.1136/jnnp-2017-316385} } @article{beaufort2026-42691466, author = {Beaufort, Q. and Charbonnier, C. and Ruellan, P. and Ozkul-Wermester, O. and Amar, V. and Turpin, D. and Quillard-Muraine, M. and Gerardin, E. and others}, title = {{Evaluation of Disease Severity Using CSF Biomarkers in Patients With Probable Cerebral Amyloid Angiopathy}}, journal = {Neurology}, year = {2026}, doi = {10.1212/wnl.0000000000218458}, pmid = {42691466}, url = {https://doi.org/10.1212/wnl.0000000000218458} } @article{roveletlecrux2015-26194182, author = {Rovelet-Lecrux, A. and Charbonnier, C. and Wallon, D. and Nicolas, G. and Seaman, M. N. and Pottier, C. and Breusegem, S. Y. and Mathur, P. P. and others}, title = {{De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease}}, journal = {Molecular psychiatry}, year = {2015}, doi = {10.1038/mp.2015.100}, pmid = {26194182}, url = {https://doi.org/10.1038/mp.2015.100} } @article{wallon2012-22475797, author = {Wallon, D. and Rousseau, S. and Rovelet-Lecrux, A. and Quillard-Muraine, M. and Guyant-Maréchal, L. and Martinaud, O. and Pariente, J. and Puel, M. and others}, title = {{The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers}}, journal = {Journal of Alzheimer's disease : JAD}, year = {2012}, doi = {10.3233/jad-2012-120172}, pmid = {22475797}, url = {https://doi.org/10.3233/jad-2012-120172} } @article{castelot2025-40336092, author = {Castelot, Romain and Zaréa, Aline and Wallon, David and Rovelet‐Lecrux, Anne and Schramm, Catherine and Quillard‐Muraine, Muriel and Beaume, Anne and Blanc, Frédéric and others}, title = {{Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer disease}}, journal = {Alzheimer s Research \& Therapy}, year = {2025}, doi = {10.1186/s13195-025-01748-0}, pmid = {40336092}, url = {https://doi.org/10.1186/s13195-025-01748-0} } @article{ulugut2025-41387629, author = {Ulugut, Hülya and Younes, Kyan and Montembeault, Maxime and Bertoux, Maxime and Irish, Muireann and Kumfor, Fiona and Fumagalli, Giorgio and Samancı, Bedia and others}, title = {{Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working Group}}, journal = {Communications Medicine}, year = {2025}, doi = {10.1038/s43856-025-01252-4}, pmid = {41387629}, url = {https://doi.org/10.1038/s43856-025-01252-4} }