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Author Title Type [ Year(Asc)]
Filters: Keyword is Genome-Wide Association Study  [Clear All Filters]
2021
Horimoto ARVR, Xue D, Thornton TA, Blue EE.  2021.  Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics.. Alzheimers Res Ther. 13(1):122.
Patel D, Zhang X, Farrell JJ, Chung J, Stein TD, Lunetta KL, Farrer LA.  2021.  Cell-type-specific expression quantitative trait loci associated with Alzheimer disease in blood and brain tissue.. Transl Psychiatry. 11(1):250.
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I et al..  2021.  Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.. Nat Commun. 12(1):3417.
Marca-Ysabel MVictoria, Rajabli F, Cornejo-Olivas M, Whitehead PG, Hofmann NK, Manrique MZaida Illa, Otani DMartin Vel, Neyra AKarina Mil, Suarez SCastro, Vega MMeza et al..  2021.  Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population.. Neurobiol Aging. 101:298.e11-298.e15.
Robins C, Liu Y, Fan W, Duong DM, Meigs J, Harerimana NV, Gerasimov ES, Dammer EB, Cutler DJ, Beach TG et al..  2021.  Genetic control of the human brain proteome.. Am J Hum Genet. 108(3):400-410.
Chia R, Sabir MS, Bandres-Ciga S, Saez-Atienzar S, Reynolds RH, Gustavsson E, Walton RL, Ahmed S, Viollet C, Ding J et al..  2021.  Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.. Nat Genet. 53(3):294-303.
Yan Q, Nho K, Del-Aguila JL, Wang X, Risacher SL, Fan K-H, Snitz BE, Aizenstein HJ, Mathis CA, Lopez OL et al..  2021.  Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging.. Mol Psychiatry. 26(1):309-321.
Wang H, Bennett DA, De Jager PL, Zhang Q-Y, Zhang H-Y.  2021.  Genome-wide epistasis analysis for Alzheimer's disease and implications for genetic risk prediction.. Alzheimers Res Ther. 13(1):55.
He Z, Liu L, Wang C, Le Guen Y, Lee J, Gogarten S, Lu F, Montgomery S, Tang H, Silverman EK et al..  2021.  Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.. Nat Commun. 12(1):3152.
Baird DA, Liu JZ, Zheng J, Sieberts SK, Perumal T, Elsworth B, Richardson TG, Chen C-Y, Carrasquillo MM, Allen M et al..  2021.  Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptome.. PLoS Genet. 17(1):e1009224.
Wingo AP, Liu Y, Gerasimov ES, Gockley J, Logsdon BA, Duong DM, Dammer EB, Robins C, Beach TG, Reiman EM et al..  2021.  Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer's disease pathogenesis.. Nat Genet. 53(2):143-146.
Novikova G, Kapoor M, Tcw J, Abud EM, Efthymiou AG, Chen SX, Cheng H, Fullard JF, Bendl J, Liu Y et al..  2021.  Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes.. Nat Commun. 12(1):1610.
Rajabli F, Feliciano-Astacio BE, Cukier HN, Wang L, Griswold AJ, Hamilton-Nelson KL, Adams LD, Rodriguez VC, Mena PR, Tejada S et al..  2021.  Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus.. Neurobiol Aging. 104:115.e1-115.e7.
Blue EE, Thornton TA, Kooperberg C, Liu S, Wactawski-Wende J, Manson JA, Kuller L, Hayden K, Reiner AP.  2021.  Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women.. Alzheimers Dement. 17(2):215-225.
Kunkle BW, Schmidt M, Klein H-U, Naj AC, Hamilton-Nelson KL, Larson EB, Evans DA, De Jager PL, Crane PK, Buxbaum JD et al..  2021.  Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.. JAMA Neurol. 78(1):102-113.
Damotte V, van der Lee SJ, Chouraki V, Grenier-Boley B, Simino J, Adams H, Tosto G, White C, Terzikhan N, Cruchaga C et al..  2021.  Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.. Alzheimers Dement. 17(10):1663-1674.
Zhan L, Li J, Jew B, Sul JHoon.  2021.  Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences.. PLoS Genet. 17(9):e1009772.
Patel D, Zhang X, Farrell JJ, Lunetta KL, Farrer LA.  2021.  Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants.. Genes (Basel). 12(3)
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.
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.
2020
Lancour D, Dupuis J, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg GC, Crovella M, Farrer LA, Kasif S.  2020.  Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease.. Alzheimers Res Ther. 12(1):103.
Andrews SJ, Goate A, Anstey KJ.  2020.  Association between alcohol consumption and Alzheimer's disease: A Mendelian randomization study.. Alzheimers Dement. 16(2):345-353.
Smith JA, Zhao W, Yu M, Rumfelt KE, Moorjani P, Ganna A, Dey AB, Lee J, Kardia SLR.  2020.  Association Between Episodic Memory and Genetic Risk Factors for Alzheimer's Disease in South Asians from the Longitudinal Aging Study in India-Diagnostic Assessment of Dementia (LASI-DAD).. J Am Geriatr Soc. 68 Suppl 3:S45-S53.
Wang L, Qiao Y, Zhang H, Zhang Y, Hua J, Jin S, Liu G.  2020.  Circulating Vitamin D Levels and Alzheimer's Disease: A Mendelian Randomization Study in the IGAP and UK Biobank.. J Alzheimers Dis. 73(2):609-618.
Armstrong NJ, Mather KA, Sargurupremraj M, Knol MJ, Malik R, Satizabal CL, Yanek LR, Wen W, Gudnason VG, Dueker ND et al..  2020.  Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.. Stroke. 51(7):2111-2121.

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