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Biblio

Author Title [ Type(Desc)] Year
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Journal Article
Guo J, Brickman AM, Manly JJ, Reitz C, Schupf N, Mayeux RP, Gu Y.  2021.  Association of Life's Simple 7 with incident dementia and its modification by the apolipoprotein E genotype.. Alzheimers Dement. 17(12):1905-1913.
Rizvi B, Lao PJ, Chesebro AG, Dworkin JD, Amarante E, Beato JM, Gutierrez J, Zahodne LB, Schupf N, Manly JJ et al..  2021.  Association of Regional White Matter Hyperintensities With Longitudinal Alzheimer-Like Pattern of Neurodegeneration in Older Adults.. JAMA Netw Open. 4(10):e2125166.
Tosto G, Vardarajan B, Sariya S, Brickman AM, Andrews H, Manly JJ, Schupf N, Reyes-Dumeyer D, Lantigua R, Bennett DA et al..  2019.  Association of Variants in PINX1 and TREM2 With Late-Onset Alzheimer Disease.. JAMA Neurol.
Avila JF, Rentería MArce, Jones RN, Vonk JMJ, Turney I, Sol K, Seblova D, Arias F, Hill-Jarrett T, Levy S-A et al..  2021.  Education differentially contributes to cognitive reserve across racial/ethnic groups.. Alzheimers Dement. 17(1):70-80.
Sharifian N, Gu Y, Manly JJ, Schupf N, Mayeux R, Brickman AM, Zahodne LB.  2020.  Linking depressive symptoms and cognitive functioning: The mediating role of leisure activity.. Neuropsychology. 34(1):107-115.
Brickman AM, Manly JJ, Honig LS, Sanchez D, Reyes-Dumeyer D, Lantigua RA, Lao PJ, Stern Y, Vonsattel JPaul, Teich AF et al..  2021.  Plasma p-tau181, p-tau217, and other blood-based Alzheimer's disease biomarkers in a multi-ethnic, community study.. Alzheimers Dement. 17(8):1353-1364.
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.
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.
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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