% alzhub.org library filter
% Source: https://alzhub.org/research?author=Bellenguez+C&score_min=67
% 5 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{bellenguez2026-6dc8c8dc,
  author  = {Bellenguez, C. and Lambert, J. C. and others},
  title   = {{Consensus meta-analysis of genome-wide association studies for Alzheimer's disease and related dementias}},
  journal = {Nature Genetics},
  year    = {2026}
}

@article{bellenguez2022-afeff1fb,
  author  = {Bellenguez, C. and Küçükali, F. and Jansen, I. E. and Kleineidam, L. and Moreno-Grau, S. and others},
  title   = {{New insights into the genetic etiology of Alzheimer's disease and related dementias}},
  journal = {Nature Genetics},
  year    = {2022},
  pmid    = {35379992}
}

@article{dourlen2017-27113998,
  author  = {Dourlen, P. and Fernandez-Gomez, F. J. and Dupont, C. and Grenier-Boley, B. and Bellenguez, C. and Obriot, H. and Caillierez, R. and Sottejeau, Y. and others},
  title   = {{Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology}},
  journal = {Molecular psychiatry},
  year    = {2017},
  doi     = {10.1038/mp.2016.59},
  pmid    = {27113998},
  url     = {https://doi.org/10.1038/mp.2016.59}
}

@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}
}