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Journal Article
Lananna BV, McKee CA, King MW, Del-Aguila JL, Dimitry JM, Farias FHG, Nadarajah CJ, Xiong DD, Guo C, Cammack AJ et al..  2020.  /YKL-40 is controlled by the astrocyte circadian clock and regulates neuroinflammation and Alzheimer's disease pathogenesis.. Sci Transl Med. 12(574)
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.
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.
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.
Lin H, Satizabal C, Xie Z, Yang Q, Huan T, Joehanes R, Wen C, Munson PJ, Beiser A, Levy D et al..  2017.  Whole blood gene expression and white matter Hyperintensities.. Mol Neurodegener. 12(1):67.
Leung YYee, Valladares O, Chou Y-F, Lin H-J, Kuzma AB, Cantwell L, Qu L, Gangadharan P, Salerno WJ, Schellenberg GD et al..  2018.  VCPA: genomic Variant Calling pipeline and data management tool for Alzheimer's Disease Sequencing Project.. Bioinformatics.
Adams S, Conner S, Himali JJ, Beiser A, Vasan RS, Seshadri S, Pase MP.  2018.  Vascular risk factor burden and new-onset depression in the community.. Prev Med. 111:348-350.
Blue EE, Yu C-E, Thornton TA, Chapman NH, Kernfeld E, Jiang N, Shively KM, Buckingham KJ, Marvin CT, Bamshad MJ et al..  2018.  Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.. Genes Brain Behav. 17(6):e12429.
Lyon MS, Andrews SJ, Elsworth B, Gaunt TR, Hemani G, Marcora E.  2021.  The variant call format provides efficient and robust storage of GWAS summary statistics.. Genome Biol. 22(1):32.
Mock C, Teylan M, Beecham G, Besser L, Cairns NJ, Crary JF, Katsumata Y, Nelson PT, Kukull W.  2020.  The Utility of the National Alzheimer's Coordinating Center's Database for the Rapid Assessment of Evolving Neuropathologic Conditions.. Alzheimer Dis Assoc Disord. 34(2):105-111.
Amlie-Wolf A, Kuksa PP, Lee C-Y, Mlynarski E, Leung YYee, San Wang L-.  2021.  Using INFERNO to Infer the Molecular Mechanisms Underlying Noncoding Genetic Associations.. Methods Mol Biol. 2254:73-91.
Bussies PL, Rajabli F, Griswold A, Dorfsman DA, Whitehead P, Adams LD, Mena PR, Cuccaro M, Haines JL, Byrd GS et al..  2020.  Use of local genetic ancestry to assess -523' and risk for Alzheimer disease.. Neurol Genet. 6(2):e404.
Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C et al..  2019.  Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.. PLoS Genet. 15(12):e1008500.
Pathak GA, Zhou Z, Silzer TK, Barber RC, Phillips NR.  2020.  Two-stage Bayesian GWAS of 9576 individuals identifies SNP regions that are targeted by miRNAs inversely expressed in Alzheimer's and cancer.. Alzheimers Dement. 16(1):162-177.
Cignarella F, Filipello F, Bollman B, Cantoni C, Locca A, Mikesell R, Manis M, Ibrahim A, Deng L, Benitez BA et al..  2020.  TREM2 activation on microglia promotes myelin debris clearance and remyelination in a model of multiple sclerosis.. Acta Neuropathol. 140(4):513-534.
He Z, McBride JD, Xu H, Changolkar L, Kim S-J, Zhang B, Narasimhan S, Gibbons GS, Guo JL, Kozak M et al..  2020.  Transmission of tauopathy strains is independent of their isoform composition.. Nat Commun. 11(1):7.
Katsumata Y, Nelson PT, Estus S, Fardo DW.  2019.  Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs.. Neurobiol Aging. 74:135-146.
Wang M, Li A, Sekiya M, Beckmann ND, Quan X, Schrode N, Fernando MB, Yu A, Zhu L, Cao J et al..  2021.  Transformative Network Modeling of Multi-omics Data Reveals Detailed Circuits, Key Regulators, and Potential Therapeutics for Alzheimer's Disease.. Neuron. 109(2):257-272.e14.
Li Z, Farias FHG, Dube U, Del-Aguila JL, Mihindukulasuriya KA, Fernández MVictoria, Ibañez L, Budde JP, Wang F, Lake AM et al..  2020.  The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion.. Acta Neuropathol. 139(1):45-61.
Goldschmidt-Clermont PJ, Volinsky FG, LaRosa SP, Gilbert JR, Pericak-Vance MA.  2020.  Time for Well-Powered Controlled Prospective Studies to Test a Causal Role for Herpes Viruses in Alzheimer's Disease Using Antiherpetic Drugs.. J Gerontol A Biol Sci Med Sci. 75(6):1058-1060.
Ramdhani S, Navarro E, Udine E, Efthymiou AG, Schilder BM, Parks M, Goate A, Raj T.  2020.  Tensor decomposition of stimulated monocyte and macrophage gene expression profiles identifies neurodegenerative disease-specific trans-eQTLs.. PLoS Genet. 16(2):e1008549.
Hsu S, Pimenova AA, Hayes K, Villa JA, Rosene MJ, Jere M, Goate AM, Karch CM.  2020.  Systematic validation of variants of unknown significance in APP, PSEN1 and PSEN2.. Neurobiol Dis. 139:104817.
Wang S, Lindroth H, Chan C, Greene R, Serrano-Andrews P, Khan S, Rios G, Jabbari S, Lim J, Saykin AJ et al..  2021.  A Systematic Review of Delirium Biomarkers and Their Alignment with the NIA-AA Research Framework.. J Am Geriatr Soc. 69(1):255-263.
Ebbert MTW, Jensen TD, Jansen-West K, Sens JP, Reddy JS, Ridge PG, Kauwe JSK, Belzil V, Pregent L, Carrasquillo MM et al..  2019.  Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight.. Genome Biol. 20(1):97.
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.


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