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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.
Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C et al..  2018.  Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.. Dement Geriatr Cogn Disord. 45(1-2):1-17.
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.
DeMichele-Sweet MAnn A, Klei L, Creese B, Harwood JC, Weamer EA, McClain L, Sims R, Hernández I, Moreno-Grau S, Tarraga L et al..  2021.  Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.. Mol Psychiatry. 26(10):5797-5811.
van der Lee SJ, Knol MJ, Chauhan G, Satizabal CL, Smith AVernon, Hofer E, Bis JC, Hibar DP, Hilal S, van den Akker EB et al..  2019.  A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.. Commun Biol. 2:285.
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.
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.
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.
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.
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.
Kunkle BW, Jaworski J, Barral S, Vardarajan B, Beecham GW, Martin ER, Cantwell LS, Partch A, Bird TD, Raskind WH et al..  2016.  Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.. Alzheimers Dement. 12(1):2-10.
Nho K, Nudelman K, Allen M, Hodges A, Kim S, Risacher SL, Apostolova LG, Lin K, Lunnon K, Wang X et al..  2020.  Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology.. Alzheimers Dement. 16(9):1213-1223.
Kunji K, Ullah E, Nato AQ, Wijsman EM, Saad M.  2018.  GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data.. Bioinformatics. 34(9):1591-1593.
Fulton-Howard B, Goate AM, Adelson RP, Koppel J, Gordon ML, Barzilai N, Atzmon G, Davies P, Freudenberg-Hua Y.  2021.  Greater effect of polygenic risk score for Alzheimer's disease among younger cases who are apolipoprotein E-ε4 carriers.. Neurobiol Aging. 99:101.e1-101.e9.
Marioni RE, Harris SE, Zhang Q, McRae AF, Hagenaars SP, W Hill D, Davies G, Ritchie CW, Gale CR, Starr JM et al..  2018.  GWAS on family history of Alzheimer's disease.. Transl Psychiatry. 8(1):99.
Wheeler NR, Benchek P, Kunkle BW, Hamilton-Nelson KL, Warfe M, Fondran JR, Haines JL, Bush WS.  2020.  Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies.. Pac Symp Biocomput. 25:523-534.
Smith EE, Biessels GJan, De Guio F, de Leeuw FErik, Duchesne S, Düring M, Frayne R, M Ikram A, Jouvent E, MacIntosh BJ et al..  2019.  Harmonizing brain magnetic resonance imaging methods for vascular contributions to neurodegeneration.. Alzheimers Dement (Amst). 11:191-204.
Wu HMan, Goate AM, O'Reilly PF.  2021.  Heterogeneous effects of genetic risk for Alzheimer's disease on the phenome.. Transl Psychiatry. 11(1):406.
Ewers M, Biechele G, Suárez-Calvet M, Sacher C, Blume T, Morenas-Rodriguez E, Deming Y, Piccio L, Cruchaga C, Kleinberger G et al..  2020.  Higher CSF sTREM2 and microglia activation are associated with slower rates of beta-amyloid accumulation.. EMBO Mol Med. 12(9):e12308.
Kuksa PP, Amlie-Wolf A, Hwang Y-C, Valladares O, Gregory BD, San Wang L-.  2020.  HIPPIE2: a method for fine-scale identification of physically interacting chromatin regions.. NAR Genom Bioinform. 2(2):lqaa022.
Kuksa PP, Li F, Kannan S, Gregory BD, Leung YYee, San Wang L-.  2020.  HiPR: High-throughput probabilistic RNA structure inference.. Comput Struct Biotechnol J. 18:1539-1547.
Farron MR, Kabeto MU, Dey ABallav, Banerjee J, Levine DA, Langa KM.  2020.  Hypertension and Cognitive Health Among Older Adults in India.. J Am Geriatr Soc. 68 Suppl 3:S29-S35.
Lo M-T, Kauppi K, Fan C-C, Sanyal N, Reas ET, Sundar VS, Lee W-C, Desikan RS, McEvoy LK, Chen C-H.  2019.  Identification of genetic heterogeneity of Alzheimer's disease across age.. Neurobiol Aging. 84:243.e1-243.e9.
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.

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