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% 23 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{naj2011-21460841,
  author  = {Naj, A. C. and Jun, G. and Beecham, G. W. and Wang, L. S. and Vardarajan, B. N. and Buros, J. and Gallins, P. J. and Buxbaum, J. D. and others},
  title   = {{Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {2011},
  doi     = {10.1038/ng.801},
  pmid    = {21460841},
  url     = {https://doi.org/10.1038/ng.801}
}

@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{wightman2021-34493870,
  author  = {Wightman, D. P. and Jansen, I. E. and Savage, J. E. and Shadrin, A. A. and Bahrami, S. and Holland, D. and Rongve, A. and Børte, S. and others},
  title   = {{A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {2021},
  doi     = {10.1038/s41588-021-00921-z},
  pmid    = {34493870},
  url     = {https://doi.org/10.1038/s41588-021-00921-z}
}

@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{jansen2019-30617256,
  author  = {Jansen, Iris E. and Savage, Jeanne E. and Watanabe, Kyoko and Bryois, Julien and Williams, Dylan M. and Steinberg, Stacy and Sealock, Julia and Karlsson, Ida and others},
  title   = {{Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk}},
  journal = {Nature Genetics},
  year    = {2019},
  doi     = {10.1038/s41588-018-0311-9},
  pmid    = {30617256},
  url     = {https://doi.org/10.1038/s41588-018-0311-9}
}

@article{vandeerlin2010-20154673,
  author  = {Van Deerlin, V. M. and Sleiman, P. M. and Martinez-Lage, M. and Chen-Plotkin, A. and Wang, L. S. and Graff-Radford, N. R. and Dickson, D. W. and Rademakers, R. and others},
  title   = {{Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions}},
  journal = {Nature genetics},
  year    = {2010},
  doi     = {10.1038/ng.536},
  pmid    = {20154673},
  url     = {https://doi.org/10.1038/ng.536}
}

@article{bellenguez2022-35379992,
  author  = {Bellenguez, C. and Küçükali, F. and Jansen, I. E. and Kleineidam, L. and Moreno-Grau, S. and Amin, N. and Naj, A. C. and Campos-Martin, R. and others},
  title   = {{New insights into the genetic etiology of Alzheimer's disease and related dementias}},
  journal = {Nature genetics},
  year    = {2022},
  doi     = {10.1038/s41588-022-01024-z},
  pmid    = {35379992},
  url     = {https://doi.org/10.1038/s41588-022-01024-z}
}

@article{lambert2013-24162737,
  author  = {Lambert, Jean‐Charles and Ibrahim‐Verbaas, Carla A. and Harold, Denise H. and Naj, Adam Christian and Sims, Rebecca and Bellenguez, Céline and others},
  title   = {{Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease}},
  journal = {Nature Genetics},
  year    = {2013},
  doi     = {10.1038/ng.2802},
  pmid    = {24162737},
  url     = {https://doi.org/10.1038/ng.2802}
}

@article{harold2009-19734902,
  author  = {Harold, Denise H. and Abraham, Richard and Hollingworth, Paul and Sims, Rebecca and Gerrish, Amy and Hamshere, Marian L. and Pahwa, Jaspreet Singh and Moskvina, Valentina and others},
  title   = {{Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease}},
  journal = {Nature Genetics},
  year    = {2009},
  doi     = {10.1038/ng.440},
  pmid    = {19734902},
  url     = {https://doi.org/10.1038/ng.440}
}

@article{study2011-21460840,
  author  = {{the Alzheimer's Disease Neuroimaging Initiative} and Hollingworth, Paul and Harold, Denise H. and Sims, Rebecca and Gerrish, Amy and Lambert, Jean‐Charles and Carrasquillo, Minerva M. and Abraham, Richard and others},
  title   = {{Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease}},
  journal = {Nature Genetics},
  year    = {2011},
  doi     = {10.1038/ng.803},
  pmid    = {21460840},
  url     = {https://doi.org/10.1038/ng.803}
}

@article{vanes2009-19734901,
  author  = {van Es, M. A. and Veldink, J. H. and Saris, C. G. and Blauw, H. M. and van Vught, P. W. and Birve, A. and Lemmens, R. and Schelhaas, H. J. and others},
  title   = {{Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis}},
  journal = {Nature genetics},
  year    = {2009},
  doi     = {10.1038/ng.442},
  pmid    = {19734901},
  url     = {https://doi.org/10.1038/ng.442}
}

@article{chia2021-33589841,
  author  = {Chia, R. and Sabir, M. S. and Bandres-Ciga, S. and Saez-Atienzar, S. and Reynolds, R. H. and Gustavsson, E. and Walton, R. L. and Ahmed, S. and others},
  title   = {{Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture}},
  journal = {Nature genetics},
  year    = {2021},
  doi     = {10.1038/s41588-021-00785-3},
  pmid    = {33589841},
  url     = {https://doi.org/10.1038/s41588-021-00785-3}
}

@article{study2009-591259cf,
  author  = {{the European Alzheimer's Disease Initiative Investigators} and Lambert, Jean‐Charles and Heath, Simon Charles and Even, Gaël and Campion, Dominique and Sleegers, Kristel and Hiltunen, Mikko and Combarros, Onofre 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},
  url     = {https://doi.org/10.1038/ng.439}
}

@article{nicolas2025-40533518,
  author  = {Nicolas, A. and Sherva, R. and Grenier-Boley, B. and Kim, Y. and Kikuchi, M. and Timsina, J. and de Rojas, I. and Dalmasso, M. C. and Zhou, X. and Le Guen, Y. and Arboleda-Bustos, C. E. and Camargos Bicalho, M. A. and others},
  title   = {{Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations}},
  journal = {Nature genetics},
  year    = {2025},
  doi     = {10.1038/s41588-025-02227-w},
  pmid    = {40533518},
  url     = {https://doi.org/10.1038/s41588-025-02227-w}
}

@article{rogaeva2007-17220890,
  author  = {Rogaeva, E. and Meng, Y. and Lee, J. H. and Gu, Y. and Kawarai, T. and Zou, F. and Katayama, T. and Baldwin, C. T. and others},
  title   = {{The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease}},
  journal = {Nature genetics},
  year    = {2007},
  doi     = {10.1038/ng1943},
  pmid    = {17220890},
  url     = {https://doi.org/10.1038/ng1943}
}

@article{watts2004-15034582,
  author  = {Watts, G. D. and Wymer, J. and Kovach, M. J. and Mehta, S. G. and Mumm, S. and Darvish, D. and Pestronk, A. and Whyte, M. P. and others},
  title   = {{Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein}},
  journal = {Nature genetics},
  year    = {2004},
  doi     = {10.1038/ng1332},
  pmid    = {15034582},
  url     = {https://doi.org/10.1038/ng1332}
}

@article{hendriks1992-1303239,
  author  = {Hendriks, L. and van Duijn, C. M. and Cras, P. and Cruts, M. and Van Hul, W. and van Harskamp, F. and Warren, A. and McInnis, M. G. and others},
  title   = {{Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene}},
  journal = {Nature genetics},
  year    = {1992},
  doi     = {10.1038/ng0692-218},
  pmid    = {1303239},
  url     = {https://doi.org/10.1038/ng0692-218}
}

@article{kurniansyah2026-42661068,
  author  = {Kurniansyah, N. and Tasaki, S. and Rehman, H. and Zhu, C. and Farrell, J. and Sherva, R. and Hauger, R. and Merritt, V. C. and Panizzon, M. and Zhang, R. and Gaziano, J. M. and Gim, J. and others},
  title   = {{A multiancestry polygenic risk score for Alzheimer's disease is associated with cognitive decline and neuropathological hallmarks in diverse populations}},
  journal = {Nature genetics},
  year    = {2026},
  doi     = {10.1038/s41588-026-02722-8},
  pmid    = {42661068},
  url     = {https://doi.org/10.1038/s41588-026-02722-8}
}

@article{gitler2009-19182805,
  author  = {Gitler, A. D. and Chesi, A. and Geddie, M. L. and Strathearn, K. E. and Hamamichi, S. and Hill, K. J. and Caldwell, K. A. and Caldwell, G. A. and others},
  title   = {{Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity}},
  journal = {Nature genetics},
  year    = {2009},
  doi     = {10.1038/ng.300},
  pmid    = {19182805},
  url     = {https://doi.org/10.1038/ng.300}
}

@article{yang2023-37735198,
  author  = {Yang, X. and Wen, J. and Yang, H. and Jones, I. R. and Zhu, X. and Liu, W. and Li, B. and Clelland, C. D. and others},
  title   = {{Functional characterization of Alzheimer's disease genetic variants in microglia}},
  journal = {Nature genetics},
  year    = {2023},
  doi     = {10.1038/s41588-023-01506-8},
  pmid    = {37735198},
  url     = {https://doi.org/10.1038/s41588-023-01506-8}
}

@article{vanduijn1994-8075646,
  author  = {van Duijn, C. M. and de Knijff, P. and Cruts, M. and Wehnert, A. and Havekes, L. M. and Hofman, A. and Van Broeckhoven, C.},
  title   = {{Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's disease}},
  journal = {Nature genetics},
  year    = {1994},
  doi     = {10.1038/ng0594-74},
  pmid    = {8075646},
  url     = {https://doi.org/10.1038/ng0594-74}
}

@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}
}