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% Source: https://alzhub.org/research?author=Belloy+ME
% 7 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{belloy2023-37930705,
  author  = {Belloy, M. E. and Andrews, S. J. and Le Guen, Y. and Cuccaro, M. and Farrer, L. A. and Napolioni, V. and Greicius, M. D.},
  title   = {{APOE Genotype and Alzheimer Disease Risk Across Age, Sex, and Population Ancestry}},
  journal = {JAMA Neurology},
  year    = {2023},
  doi     = {10.1001/jamaneurol.2023.3599},
  pmid    = {37930705},
  url     = {https://doi.org/10.1001/jamaneurol.2023.3599}
}

@article{leguen2023-36809323,
  author  = {Le Guen, Y. and Raulin, A. C. and Logue, M. W. and Sherva, R. and Belloy, M. E. and Eger, S. J. and Chen, A. and Kennedy, G. and Kuchenbecker, L. and O'Leary, J. P. and Zhang, R. and Merritt, V. C. and others},
  title   = {{Association of African Ancestry-Specific APOE Missense Variant R145C With Risk of Alzheimer Disease}},
  journal = {JAMA},
  year    = {2023},
  doi     = {10.1001/jama.2023.0268},
  pmid    = {36809323},
  url     = {https://doi.org/10.1001/jama.2023.0268}
}

@article{bhattarai2024-38598053,
  author  = {Bhattarai, P. and Gunasekaran, T. I. and Belloy, M. E. and Reyes-Dumeyer, D. and Jülich, D. and Tayran, H. and Yilmaz, E. and Flaherty, D. and Turgutalp, B. and Sukumar, G. and Alba, C. and McGrath, E. M. and others},
  title   = {{Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer's disease}},
  journal = {Acta Neuropathologica},
  year    = {2024},
  doi     = {10.1007/s00401-024-02721-1},
  pmid    = {38598053},
  url     = {https://doi.org/10.1007/s00401-024-02721-1}
}

@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{belloy2020-32282020,
  author  = {Belloy, M. E. and Napolioni, V. and Han, S. S. and Le Guen, Y. and Greicius, M. D. and {Alzheimer’s Disease Neuroimaging Initiative}},
  title   = {{Association of Klotho-VS Heterozygosity With Risk of Alzheimer Disease in Individuals Who Carry APOE4}},
  journal = {JAMA neurology},
  year    = {2020},
  doi     = {10.1001/jamaneurol.2020.0414},
  pmid    = {32282020},
  url     = {https://doi.org/10.1001/jamaneurol.2020.0414}
}

@article{belloy2019-30844401,
  author  = {Belloy, M. E. and Napolioni, V. and Greicius, M. D.},
  title   = {{A Quarter Century of APOE and Alzheimer's Disease: Progress to Date and the Path Forward}},
  journal = {Neuron},
  year    = {2019},
  doi     = {10.1016/j.neuron.2019.01.056},
  pmid    = {30844401},
  url     = {https://doi.org/10.1016/j.neuron.2019.01.056}
}

@article{sharma2026-c65529a9,
  author  = {Sharma, R. U. and Tolosa-Tort, P. and Okorie, M. and Chatterjee, A. and Jonson, C. and Yaffe, K. and Belloy, M. E. and Andrews, S. J. and others},
  title   = {{Sex differences in genetic liability to modifiable Alzheimer’s disease risk factors}},
  journal = {medRxiv},
  year    = {2026},
  doi     = {10.64898/2026.10.01.26364536},
  url     = {https://doi.org/10.64898/2026.10.01.26364536}
}