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Author Title Type [ Year(Asc)]
Filters: Keyword is Genome-Wide Association Study  [Clear All Filters]
2020
Keys KL, C Y Mak A, White MJ, Eckalbar WL, Dahl AW, Mefford J, Mikhaylova AV, Contreras MG, Elhawary JR, Eng C et al..  2020.  On the cross-population generalizability of gene expression prediction models.. PLoS Genet. 16(8):e1008927.
Ouellette AR, Neuner SM, Dumitrescu L, Anderson LC, Gatti DM, Mahoney ER, Bubier JA, Churchill G, Peters L, Huentelman MJ et al..  2020.  Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer's Dementia.. Cell Rep. 32(9):108091.
Ibañez L, Bahena JA, Yang C, Dube U, Farias FHG, Budde JP, Bergmann K, Brenner-Webster C, Morris JC, Perrin RJ et al..  2020.  Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease.. Acta Neuropathol Commun. 8(1):196.
Guerreiro R, Gibbons E, Tábuas-Pereira M, Kun-Rodrigues C, Santo GC, Bras J.  2020.  Genetic architecture of common non-Alzheimer's disease dementias.. Neurobiol Dis. 142:104946.
Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAgnes B et al..  2020.  The genetic architecture of the human cerebral cortex.. Science. 367(6484)
Hofer E, Roshchupkin GV, Adams HHH, Knol MJ, Lin H, Li S, Zare H, Ahmad S, Armstrong NJ, Satizabal CL et al..  2020.  Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.. Nat Commun. 11(1):4796.
Dumitrescu L, Mahoney ER, Mukherjee S, Lee ML, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J et al..  2020.  Genetic variants and functional pathways associated with resilience to Alzheimer's disease.. Brain. 143(8):2561-2575.
Sherva R, Gross A, Mukherjee S, Koesterer R, Amouyel P, Bellenguez C, Dufouil C, Bennett DA, Chibnik L, Cruchaga C et al..  2020.  Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways.. Alzheimers Dement. 16(8):1134-1145.
Andrews SJ, Fulton-Howard B, Goate A.  2020.  Interpretation of risk loci from genome-wide association studies of Alzheimer's disease.. Lancet Neurol. 19(4):326-335.
Strickland SL, Reddy JS, Allen M, N'songo A, Burgess JD, Corda MM, Ballard T, Wang X, Carrasquillo MM, Biernacka JM et al..  2020.  MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.. Alzheimers Dement. 16(7):983-1002.
Podleśny-Drabiniok A, Marcora E, Goate AM.  2020.  Microglial Phagocytosis: A Disease-Associated Process Emerging from Alzheimer's Disease Genetics.. Trends Neurosci. 43(12):965-979.
Tang Z-Z, Sliwoski GR, Chen G, Jin B, Bush WS, Li B, Capra JA.  2020.  PSCAN: Spatial scan tests guided by protein structures improve complex disease gene discovery and signal variant detection.. Genome Biol. 21(1):217.
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.
Hartl D, May P, Gu W, Mayhaus M, Pichler S, Spaniol C, Glaab E, Bobbili DReddy, Antony P, Koegelsberger S et al..  2020.  A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease.. Mol Psychiatry. 25(3):629-639.
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.
Kuksa PP, Lee C-Y, Amlie-Wolf A, Gangadharan P, Mlynarski EE, Chou Y-F, Lin H-J, Issen H, Greenfest-Allen E, Valladares O et al..  2020.  SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants.. Bioinformatics. 36(12):3879-3881.
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.
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.
2019
Saad M, Wijsman EM.  2019.  Association score testing for rare variants and binary traits in family data with shared controls.. Brief Bioinform. 20(1):245-253.
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV et al..  2019.  Genetic architecture of subcortical brain structures in 38,851 individuals.. Nat Genet. 51(11):1624-1636.
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A et al..  2019.  Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.. Nat Genet. 51(3):414-430.
de Vries PS, Sabater-Lleal M, Huffman JE, Marten J, Song C, Pankratz N, Bartz TM, de Haan HG, Delgado GE, Eicher JD et al..  2019.  A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.. Blood. 133(9):967-977.
Huan T, Joehanes R, Song C, Peng F, Guo Y, Mendelson M, Yao C, Liu C, Ma J, Richard M et al..  2019.  Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.. Nat Commun. 10(1):4267.
Bentley AR, Sung YJ, Brown MR, Winkler TW, Kraja AT, Ntalla I, Schwander K, Chasman DI, Lim E, Deng X et al..  2019.  Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.. Nat Genet. 51(4):636-648.
Lobach I, Kim I, Alekseyenko A, Lobach S, Zhang L.  2019.  A simple approximation to bias in the genetic effect estimates when multiple disease states share a clinical diagnosis.. Genet Epidemiol. 43(5):522-531.

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