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% Source: https://alzhub.org/research?journal=Nature+genetics
% 64 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{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{savage2018-29942086,
  author  = {Savage, J. E. and Jansen, P. R. and Stringer, S. and Watanabe, K. and Bryois, J. and de Leeuw, C. A. and Nagel, M. and Awasthi, S. and others},
  title   = {{Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence}},
  journal = {Nature genetics},
  year    = {2018},
  doi     = {10.1038/s41588-018-0152-6},
  pmid    = {29942086},
  url     = {https://doi.org/10.1038/s41588-018-0152-6}
}

@article{liu2017-28092683,
  author  = {Liu, J. Z. and Erlich, Y. and Pickrell, J. K.},
  title   = {{Case-control association mapping by proxy using family history of disease}},
  journal = {Nature genetics},
  year    = {2017},
  doi     = {10.1038/ng.3766},
  pmid    = {28092683},
  url     = {https://doi.org/10.1038/ng.3766}
}

@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{stein2012-22504417,
  author  = {Stein, J. L. and Medland, S. E. and Vasquez, A. A. and Hibar, D. P. and Senstad, R. E. and Winkler, A. M. and Toro, R. and Appel, K. and others},
  title   = {{Identification of common variants associated with human hippocampal and intracranial volumes}},
  journal = {Nature genetics},
  year    = {2012},
  doi     = {10.1038/ng.2250},
  pmid    = {22504417},
  url     = {https://doi.org/10.1038/ng.2250}
}

@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{bertram2007-17192785,
  author  = {Bertram, L. and McQueen, M. B. and Mullin, K. and Blacker, D. and Tanzi, R. E.},
  title   = {{Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database}},
  journal = {Nature genetics},
  year    = {2007},
  doi     = {10.1038/ng1934},
  pmid    = {17192785},
  url     = {https://doi.org/10.1038/ng1934}
}

@article{schwartzentruber2021-33589840,
  author  = {Schwartzentruber, J. and Cooper, S. and Liu, J. Z. and Barrio-Hernandez, I. and Bello, E. and Kumasaka, N. and Young, A. M. H. and Franklin, R. J. M. and others},
  title   = {{Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes}},
  journal = {Nature genetics},
  year    = {2021},
  doi     = {10.1038/s41588-020-00776-w},
  pmid    = {33589840},
  url     = {https://doi.org/10.1038/s41588-020-00776-w}
}

@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,
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  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}
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@article{corder1994-7920638,
  author  = {Corder, E. H. and Saunders, A. M. and Risch, N. J. and Strittmatter, W. J. and Schmechel, D. E. and Gaskell, P. C. and Rimmler, J. B. and Locke, P. A. and others},
  title   = {{Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease}},
  journal = {Nature genetics},
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  title   = {{Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases}},
  journal = {Nature Genetics},
  year    = {2023},
  doi     = {10.1038/s41588-023-01300-6},
  pmid    = {36823318},
  url     = {https://doi.org/10.1038/s41588-023-01300-6}
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@article{watts2004-15034582,
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  title   = {{Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein}},
  journal = {Nature genetics},
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  doi     = {10.1038/ng1332},
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  title   = {{APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy}},
  journal = {Nature genetics},
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  title   = {{Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia}},
  journal = {Nature genetics},
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  title   = {{TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis}},
  journal = {Nature Genetics},
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@article{shade2024-39379761,
  author  = {Shade, Lincoln M P and Katsumata, Yuriko and Abner, Erin L and Aung, Khine Zin and Claas, Steven A and Qiao, Qi and Heberle, Bernardo Aguzzoli and Brandon, J Anthony and others},
  title   = {{GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia}},
  journal = {Nature genetics},
  year    = {2024},
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  pmid    = {39379761},
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  title   = {{A multiancestry polygenic risk score for Alzheimer's disease is associated with cognitive decline and neuropathological hallmarks in diverse populations}},
  journal = {Nature genetics},
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  title   = {{A map of transcriptional heterogeneity and regulatory variation in human microglia}},
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@article{bis2012-22504421,
  author  = {Bis, J. C. and DeCarli, C. and Smith, A. V. and van der Lijn, F. and Crivello, F. and Fornage, M. and Debette, S. and Shulman, J. M. and others},
  title   = {{Common variants at 12q14 and 12q24 are associated with hippocampal volume}},
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@article{hoglinger2011-21685912,
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@article{fujita2024-38514782,
  author  = {Fujita, M. and Gao, Z. and Zeng, L. and McCabe, C. and White, C. C. and Ng, B. and Green, G. S. and Rozenblatt-Rosen, O. and others},
  title   = {{Cell subtype-specific effects of genetic variation in the Alzheimer's disease brain}},
  journal = {Nature genetics},
  year    = {2024},
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