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dc.contributor.authorBellenguez, Céline
dc.contributor.authorKüçükali, Fahri
dc.contributor.authorJansen, Iris E.
dc.contributor.authorKleineidam, Luca
dc.contributor.authorMoreno-Grau, Sonia
dc.contributor.authorAmin, Najaf
dc.contributor.authorNaj, Adam C.
dc.contributor.authorCampos-Martin, Rafael
dc.contributor.authorGrenier-Boley, Benjamin
dc.contributor.authorAndrade, Victor
dc.contributor.authorHolmans, Peter A.
dc.contributor.authorBoland, Anne
dc.contributor.authorDamott, Vincent
dc.contributor.authorLee, Sven J. Van Der
dc.contributor.authorCosta, Marcos R.
dc.contributor.authorKuulamaa, Teemu
dc.contributor.authorYang, Qiong
dc.contributor.authorRojas, Itziar de
dc.contributor.authorRodríguez Rodríguez, Eloy Manuel 
dc.contributor.authorBis, Joshua C.
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-03-26T17:09:02Z
dc.date.available2024-03-26T17:09:02Z
dc.date.issued2022
dc.identifier.issn1061-4036
dc.identifier.issn1546-1718
dc.identifier.urihttps://hdl.handle.net/10902/32457
dc.description.abstractCharacterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele.es_ES
dc.format.extent33 p.es_ES
dc.language.isoenges_ES
dc.publisherNature Publishing Groupes_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceNature Genetics, 2022, 54(4), 412-436es_ES
dc.titleNew insights into the genetic etiology of Alzheimer's disease and related dementiases_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1038/s41588-022-01024-zes_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1038/s41588-022-01024-z
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International