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GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia.
Shade LMP, Katsumata Y, Abner EL, Aung KZ, Claas SA, Qiao Q, Heberle BA, Brandon JA, Page ML, Hohman TJ, Mukherjee S, Mayeux RP, Farrer LA, Schellenberg GD, Haines JL, Kukull WA, Nho K, Saykin AJ, Bennett DA, Schneider JA; National Alzheimer’s Coordinating Center; Ebbert MTW, Nelson PT, Fardo DW. Shade LMP, et al. Among authors: kukull wa. Nat Genet. 2024 Nov;56(11):2407-2421. doi: 10.1038/s41588-024-01939-9. Epub 2024 Oct 8. Nat Genet. 2024. PMID: 39379761 Free PMC article.
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
Schellenberg GD, Anderson L, O'dahl S, Wisjman EM, Sadovnick AD, Ball MJ, Larson EB, Kukull WA, Martin GM, Roses AD, et al. Schellenberg GD, et al. Among authors: kukull wa. Am J Hum Genet. 1991 Sep;49(3):511-7. Am J Hum Genet. 1991. PMID: 1679288 Free PMC article.
Head injury and the risk of AD in the MIRAGE study.
Guo Z, Cupples LA, Kurz A, Auerbach SH, Volicer L, Chui H, Green RC, Sadovnick AD, Duara R, DeCarli C, Johnson K, Go RC, Growdon JH, Haines JL, Kukull WA, Farrer LA. Guo Z, et al. Among authors: kukull wa. Neurology. 2000 Mar 28;54(6):1316-23. doi: 10.1212/wnl.54.6.1316. Neurology. 2000. PMID: 10746604
292 results