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% Source: https://alzhub.org/research?institution=I3019204325
% 14 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{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{holstege2022-36411364,
  author  = {Holstege, H. and Hulsman, M. and Charbonnier, C. and Grenier-Boley, B. and Quenez, O. and Grozeva, D. and van Rooij, J. G. J. and Sims, R. and others},
  title   = {{Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {2022},
  doi     = {10.1038/s41588-022-01208-7},
  pmid    = {36411364},
  url     = {https://doi.org/10.1038/s41588-022-01208-7}
}

@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{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{quenez2026-42648288,
  author  = {Quenez, O. and Schramm, C. and Cassinari, K. and Nicolas, A. and Groeneveld, J. and Huguet, G. and Grenier-Boley, B. and Hulsman, M. and Walters, G. B. and de Rojas, I. and Rovelet-Lecrux, A. and Feuillette, S. and others},
  title   = {{Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk}},
  journal = {American Journal of Human Genetics},
  year    = {2026},
  doi     = {10.1016/j.ajhg.2026.07.013},
  pmid    = {42648288},
  url     = {https://doi.org/10.1016/j.ajhg.2026.07.013}
}

@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{park2023-37081148,
  author  = {Park, M. D. and Reyes-Torres, I. and LeBerichel, J. and Hamon, P. and LaMarche, N. M. and Hegde, S. and Belabed, M. and Troncoso, L. and others},
  title   = {{TREM2 macrophages drive NK cell paucity and dysfunction in lung cancer}},
  journal = {Nature immunology},
  year    = {2023},
  doi     = {10.1038/s41590-023-01475-4},
  pmid    = {37081148},
  url     = {https://doi.org/10.1038/s41590-023-01475-4}
}

@article{pottier2012-22472873,
  author  = {Pottier, C. and Hannequin, D. and Coutant, S. and Rovelet-Lecrux, A. and Wallon, D. and Rousseau, S. and Legallic, S. and Paquet, C. and others},
  title   = {{High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease}},
  journal = {Molecular psychiatry},
  year    = {2012},
  doi     = {10.1038/mp.2012.15},
  pmid    = {22472873},
  url     = {https://doi.org/10.1038/mp.2012.15}
}

@article{dilazzaro2021-34482205,
  author  = {Di Lazzaro, V. and Bella, R. and Benussi, A. and Bologna, M. and Borroni, B. and Capone, F. and Chen, K. S. and Chen, R. and others},
  title   = {{Diagnostic contribution and therapeutic perspectives of transcranial magnetic stimulation in dementia}},
  journal = {Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology},
  year    = {2021},
  doi     = {10.1016/j.clinph.2021.05.035},
  pmid    = {34482205},
  url     = {https://doi.org/10.1016/j.clinph.2021.05.035}
}

@article{brossaud2026-41786890,
  author  = {Brossaud, Rodrigue and Oullier, Thibauld and Bessard, Anne Claire Hardy and Aubert, P. and Brossard, Lisa and Mahé, Maxime M. and Caillaud, Martial and Delfino, Giada and others},
  title   = {{The short-chain fatty acid butyrate prevents gut-brain amyloid-β pathology and neuroinflammation in an Alzheimer mouse model}},
  journal = {Molecular Psychiatry},
  year    = {2026},
  doi     = {10.1038/s41380-026-03522-6},
  pmid    = {41786890},
  url     = {https://doi.org/10.1038/s41380-026-03522-6}
}

@article{nguyen2018-29658441,
  author  = {Nguyen, J. P. and Boutoleau-Bretonniere, C. and Lefaucheur, J. P. and Suarez, A. and Gaillard, H. and Chapelet, G. and Abad, S. and Van Langhenhove, A. and others},
  title   = {{Efficacy of Transcranial Direct Current Stimulation Combined with Cognitive Training in the Treatment of Apathy in Patients with Alzheimer's Disease: Study Protocol for a Randomized Trial}},
  journal = {Reviews on recent clinical trials},
  year    = {2018},
  doi     = {10.2174/1574887113666180416153316},
  pmid    = {29658441},
  url     = {https://doi.org/10.2174/1574887113666180416153316}
}

@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{bis2020-30108311,
  author  = {Bis, J. C. and Jian, X. and Kunkle, B. W. and Chen, Y. and Hamilton-Nelson, K. L. and Bush, W. S. and Salerno, W. J. and Lancour, D. and others},
  title   = {{Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation}},
  journal = {Molecular psychiatry},
  year    = {2020},
  doi     = {10.1038/s41380-018-0112-7},
  pmid    = {30108311},
  url     = {https://doi.org/10.1038/s41380-018-0112-7}
}

@article{zarea2026-42215639,
  author  = {Zaréa, Aline and Cassinari, Kévin and Lecoquierre, François and Quenez, Olivier and Charbonnier, Camille and Schramm, Catherine and Lacour, Morgane and Rousseau, Stéphane and others},
  title   = {{Assessing the de novo paradigm in sporadic early-onset Alzheimer disease trios}},
  journal = {Molecular Psychiatry},
  year    = {2026},
  doi     = {10.1038/s41380-026-03665-6},
  pmid    = {42215639},
  url     = {https://doi.org/10.1038/s41380-026-03665-6}
}