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% Source: https://alzhub.org/research?institution=I4210134576&score_min=67
% 6 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{kunkle2019-30820047,
  author  = {Kunkle, B. W. and Grenier-Boley, B. and Sims, R. and Bis, J. C. and Damotte, V. and Naj, A. C. and Boland, A. and Vronskaya, M. and others},
  title   = {{Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing}},
  journal = {Nature genetics},
  year    = {2019},
  doi     = {10.1038/s41588-019-0358-2},
  pmid    = {30820047},
  url     = {https://doi.org/10.1038/s41588-019-0358-2}
}

@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{pottier2025-40280976,
  author  = {Pottier, Cyril P. and Küçükali, Fahri and Baker, Matt C. and Batzler, Anthony and Jenkins, Gregory D. and van Blitterswijk, Marka and Vicente, Cristina T. and De Coster, Wouter and others},
  title   = {{Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing}},
  journal = {Nature Communications},
  year    = {2025},
  doi     = {10.1038/s41467-025-59216-0},
  pmid    = {40280976},
  url     = {https://doi.org/10.1038/s41467-025-59216-0}
}

@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{majounie2012-22406228,
  author  = {Majounie, E. and Renton, A. E. and Mok, K. and Dopper, E. G. and Waite, A. and Rollinson, S. and Chiò, A. and Restagno, G. and others},
  title   = {{Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study}},
  journal = {The Lancet. Neurology},
  year    = {2012},
  doi     = {10.1016/s1474-4422(12)70043-1},
  pmid    = {22406228},
  url     = {https://doi.org/10.1016/s1474-4422(12)70043-1}
}

@article{young2018-30323170,
  author  = {Young, A. L. and Marinescu, R. V. and Oxtoby, N. P. and Bocchetta, M. and Yong, K. and Firth, N. C. and Cash, D. M. and Thomas, D. L. and others},
  title   = {{Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference}},
  journal = {Nature communications},
  year    = {2018},
  doi     = {10.1038/s41467-018-05892-0},
  pmid    = {30323170},
  url     = {https://doi.org/10.1038/s41467-018-05892-0}
}