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% Source: https://alzhub.org/research?category=genetics&institution=I2803066834
% 9 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{xi2012-22964832,
  author  = {Xi, Z. and Zinman, L. and Grinberg, Y. and Moreno, D. and Sato, C. and Bilbao, J. M. and Ghani, M. and Hernández, I. and others},
  title   = {{Investigation of c9orf72 in 4 neurodegenerative disorders}},
  journal = {Archives of neurology},
  year    = {2012},
  doi     = {10.1001/archneurol.2012.2016},
  pmid    = {22964832},
  url     = {https://doi.org/10.1001/archneurol.2012.2016}
}

@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}
}