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% Source: https://alzhub.org/research?category=genetics&institution=I189158943
% 10 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{piccio2016-26754641,
  author  = {Piccio, L. and Deming, Y. and Del-Águila, J. L. and Ghezzi, L. and Holtzman, D. M. and Fagan, A. M. and Fenoglio, C. and Galimberti, D. and others},
  title   = {{Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status}},
  journal = {Acta neuropathologica},
  year    = {2016},
  doi     = {10.1007/s00401-016-1533-5},
  pmid    = {26754641},
  url     = {https://doi.org/10.1007/s00401-016-1533-5}
}

@article{antolini2021-34531298,
  author  = {Antolini, L. and DiFrancesco, J. C. and Zedde, M. and Basso, G. and Arighi, A. and Shima, A. and Cagnin, A. and Caulo, M. and others},
  title   = {{Spontaneous ARIA-like Events in Cerebral Amyloid Angiopathy-Related Inflammation: A Multicenter Prospective Longitudinal Cohort Study}},
  journal = {Neurology},
  year    = {2021},
  doi     = {10.1212/wnl.0000000000012778},
  pmid    = {34531298},
  url     = {https://doi.org/10.1212/wnl.0000000000012778}
}

@article{leguen2022-35639372,
  author  = {Le Guen, Y. and Belloy, M. E. and Grenier-Boley, B. and de Rojas, I. and Castillo-Morales, A. and Jansen, I. and Nicolas, A. and Bellenguez, C. and others},
  title   = {{Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease}},
  journal = {JAMA neurology},
  year    = {2022},
  doi     = {10.1001/jamaneurol.2022.1166},
  pmid    = {35639372},
  url     = {https://doi.org/10.1001/jamaneurol.2022.1166}
}

@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{genin2011-21556001,
  author  = {Genin, E. and Hannequin, D. and Wallon, D. and Sleegers, K. and Hiltunen, M. and Combarros, O. and Bullido, M. J. and Engelborghs, S. and others},
  title   = {{APOE and Alzheimer disease: a major gene with semi-dominant inheritance}},
  journal = {Molecular psychiatry},
  year    = {2011},
  doi     = {10.1038/mp.2011.52},
  pmid    = {21556001},
  url     = {https://doi.org/10.1038/mp.2011.52}
}

@article{lambert2009-19734903,
  author  = {Lambert, J. C. and Heath, S. and Even, G. and Campion, D. and Sleegers, K. and Hiltunen, M. and Combarros, O. and Zelenika, D. and others},
  title   = {{Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {2009},
  doi     = {10.1038/ng.439},
  pmid    = {19734903},
  url     = {https://doi.org/10.1038/ng.439}
}

@article{thomassen2026-42736378,
  author  = {Thomassen, J. Q. and Leonard, H. and Ulms, B. and Grenier-Boley, B. and Heikkinen, S. and Garcia-González, P. and Castillo-Morales, A. and Kikuchi, M. and Gim, J. and Cao, H. and Küçükali, F. and Amin, N. and others},
  title   = {{APOE-stratified genome-wide association analyses provide insights into the genetic etiology of Alzheimers's disease}},
  journal = {Nature genetics},
  year    = {2026},
  doi     = {10.1038/s41588-026-02713-9},
  pmid    = {42736378},
  url     = {https://doi.org/10.1038/s41588-026-02713-9}
}

@article{quadri2018-29887161,
  author  = {Quadri, M. and Mandemakers, W. and Grochowska, M. M. and Masius, R. and Geut, H. and Fabrizio, E. and Breedveld, G. J. and Kuipers, D. and others},
  title   = {{LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study}},
  journal = {The Lancet. Neurology},
  year    = {2018},
  doi     = {10.1016/s1474-4422(18)30179-0},
  pmid    = {29887161},
  url     = {https://doi.org/10.1016/s1474-4422(18)30179-0}
}

@article{benussi2025-41102550,
  author  = {Benussi, Alberto and Agosta, Federica and Alfano, Alba Rosa and Antico, Antonio and Bellelli, Giuseppe and Bonanni, Laura and Bottini, Gabriella and Bozzali, Marco and others},
  title   = {{Italian intersocietal recommendations for restructuring the diagnostic-therapeutic pathway for the implementation and appropriate use of anti-amyloid monoclonal antibodies in Alzheimer’s disease}},
  journal = {Neurological Sciences},
  year    = {2025},
  doi     = {10.1007/s10072-025-08576-y},
  pmid    = {41102550},
  url     = {https://doi.org/10.1007/s10072-025-08576-y}
}

@article{frisoni1994-7951679,
  author  = {Frisoni, G. B. and Calabresi, L. and Geroldi, C. and Bianchetti, A. and D'Acquarica, A. L. and Govoni, S. and Sirtori, C. R. and others},
  title   = {{Apolipoprotein E epsilon 4 allele in Alzheimer's disease and vascular dementia}},
  journal = {Dementia (Basel, Switzerland)},
  year    = {1994},
  doi     = {10.1159/000106730},
  pmid    = {7951679},
  url     = {https://doi.org/10.1159/000106730}
}