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Author Title [ Type(Desc)] Year
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Journal Article
Sariya S, Felsky D, Reyes-Dumeyer D, Lali R, Lantigua RA, Vardarajan B, Jimenez-Velazquez IZ, Haines JL, Shellenberg GD, Pericak-Vance MA et al..  2021.  Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics.. Ann Neurol. 90(3):366-376.
Choi KYeong, Lee JJae, Gunasekaran TIniyan, Kang S, Lee W, Jeong J, Lim HJae, Zhang X, Zhu C, Won S-Y et al..  2019.  Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of ε4 on Alzheimer's Disease Risk in a Multiracial Sample.. J Clin Med. 8(8)
Zhao L, Zhang Z, Rodriguez SMBarral, Vardarajan BN, Renton AE, Goate AM, Mayeux R, Wang GT, Leal SM.  2020.  A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease.. Eur J Hum Genet. 28(12):1734-1742.
Beecham GW, Vardarajan B, Blue E, Bush W, Jaworski J, Barral S, DeStefano A, Hamilton-Nelson K, Kunkle B, Martin ER et al..  2018.  Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease.. Neurol Genet. 4(6):e286.
Zhang X, Zhu C, Beecham G, Vardarajan BN, Ma Y, Lancour D, Farrell JJ, Chung J, Mayeux R, Haines JL et al..  2019.  A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease.. Alzheimers Dement. 15(3):441-452.
Sariya S, Lee JH, Mayeux R, Vardarajan BN, Reyes-Dumeyer D, Manly JJ, Brickman AM, Lantigua R, Medrano M, Jimenez-Velazquez IZ et al..  2019.  Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools.. Front Genet. 10:239.
Fan CChieh, Banks SJ, Thompson WK, Chen C-H, McEvoy LK, Tan CHong, Kukull W, Bennett DA, Farrer LA, Mayeux R et al..  2020.  Sex-dependent autosomal effects on clinical progression of Alzheimer's disease.. Brain. 143(7):2272-2280.
Sharifian N, Zaheed AB, Morris EP, Sol K, Manly JJ, Schupf N, Mayeux R, Brickman AM, Zahodne LB.  2021.  Social network characteristics moderate associations between cortical thickness and cognitive functioning in older adults.. Alzheimers Dement.
Tang M, Alaniz MEugenia, Felsky D, Vardarajan B, Reyes-Dumeyer D, Lantigua R, Medrano M, Bennett DA, De Jager PL, Mayeux R et al..  2020.  Synonymous variants associated with Alzheimer disease in multiplex families.. Neurol Genet. 6(4):e450.
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE et al..  2018.  Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.. Mol Psychiatry.
Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj A et al..  2018.  Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.. Ann Clin Transl Neurol. 5(4):406-417.
Raghavan NS, Brickman AM, Andrews H, Manly JJ, Schupf N, Lantigua R, Wolock CJ, Kamalakaran S, Petrovski S, Tosto G et al..  2018.  Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease.. Ann Clin Transl Neurol. 5(7):832-842.

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