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Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease.
Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, Farrer LA, St Georg-Hyslop P, Rogaeva EA. Nicolaou M, et al. Among authors: percy m. Neurogenetics. 2001 Oct;3(4):203-6. doi: 10.1007/s100480100123. Neurogenetics. 2001. PMID: 11714100
Is hemochromatosis a risk factor for Alzheimer's disease?
Connor JR, Milward EA, Moalem S, Sampietro M, Boyer P, Percy ME, Vergani C, Scott RJ, Chorney M. Connor JR, et al. Among authors: percy me. J Alzheimers Dis. 2001 Oct;3(5):471-477. doi: 10.3233/jad-2001-3506. J Alzheimers Dis. 2001. PMID: 12214033
G protein-coupled receptor (GPCR) gene variants and human genetic disease.
Thompson MD, Percy ME, Cole DEC, Bichet DG, Hauser AS, Gorvin CM. Thompson MD, et al. Among authors: percy me. Crit Rev Clin Lab Sci. 2024 Mar 18:1-30. doi: 10.1080/10408363.2023.2286606. Online ahead of print. Crit Rev Clin Lab Sci. 2024. PMID: 38497103 Review.
Tibetan PHD2, an allele with loss-of-function properties.
Song D, Navalsky BE, Guan W, Ingersoll C, Wang T, Loro E, Eeles L, Matchett KB, Percy MJ, Walsby-Tickle J, McCullagh JSO, Medina RJ, Khurana TS, Bigham AW, Lappin TR, Lee FS. Song D, et al. Among authors: percy mj. Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12230-12238. doi: 10.1073/pnas.1920546117. Epub 2020 May 15. Proc Natl Acad Sci U S A. 2020. PMID: 32414920 Free PMC article.
Retraction Note: Aluminum in Neurological and Neurodegenerative Disease.
McLachlan DRC, Bergeron C, Alexandrov PN, Walsh WJ, Pogue AI, Percy ME, Kruck TPA, Fang Z, Sharfman NM, Jaber V, Zhao Y, Li W, Lukiw WJ. McLachlan DRC, et al. Among authors: percy me. Mol Neurobiol. 2020 Mar;57(3):1779. doi: 10.1007/s12035-020-01883-9. Mol Neurobiol. 2020. PMID: 31970658 Free PMC article.
A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited GPI disorder.
Thompson MD, Knaus AA, Barshop BA, Caliebe A, Muhle H, Nguyen TTM, Baratang NV, Kinoshita T, Percy ME, Campeau PM, Murakami Y, Cole DE, Krawitz PM, Mabry CC. Thompson MD, et al. Among authors: percy me. Eur J Med Genet. 2020 Apr;63(4):103822. doi: 10.1016/j.ejmg.2019.103822. Epub 2019 Dec 2. Eur J Med Genet. 2020. PMID: 31805394
227 results