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Biblio

[ Author(Desc)] Title Type Year
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
K
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.
Kenny RAnne.  2020.  New Insights and Knowledge on Cognition and Dementia from Population-Based Cohort of Older Adults in India.. J Am Geriatr Soc. 68 Suppl 3:S1-S2.
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.
Kim M, Bao J, Liu K, Park B-Y, Park H, Baik JYoung, Shen L.  2021.  A structural enriched functional network: An application to predict brain cognitive performance.. Med Image Anal. 71:102026.
Kim JPyo, Kim B-H, Bice PJ, Seo SWon, Bennett DA, Saykin AJ, Nho K.  2021.  BMI1 is associated with CS8F amyloid-β and rates of cognitive decline in Alzheimer's disease.. Alzheimers Res Ther. 13(1):164.
Kirola L, Budde JP, Wang F, Norton J, Morris JC, Cruchaga C, Fernández MVictoria.  2021.  Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population.. Acta Neuropathol. 141(4):623-624.
Kling MA, Goodenowe DB, Senanayake V, MahmoudianDehkordi S, Arnold M, Massaro TJ, Baillie R, Han X, Leung Y-Y, Saykin AJ et al..  2020.  Circulating ethanolamine plasmalogen indices in Alzheimer's disease: Relation to diagnosis, cognition, and CSF tau.. Alzheimers Dement. 16(9):1234-1247.
Knopman D, Lemere CA, Lamb BT, Craft S, Gitlin LN, Golde TE, Pericak-Vance M, Sano M, Schellenberg G, Schneider JA et al..  2020.  Scientific Advising and Reviewing: On strengthening the bond between the Alzheimer's Association and the scientific community.. Alzheimers Dement. 16(7):1095-1098.
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.
Kuksa PP, Amlie-Wolf A, Katanić Ž, Valladares O, San Wang L-, Leung YYee.  2019.  DASHR 2.0: integrated database of human small non-coding RNA genes and mature products.. Bioinformatics. 35(6):1033-1039.
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.
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.
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.
Kulick ER, Wellenius GA, Boehme AK, Joyce NR, Schupf N, Kaufman JD, Mayeux R, Sacco RL, Manly JJ, Elkind MSV.  2020.  Long-term exposure to air pollution and trajectories of cognitive decline among older adults.. Neurology. 94(17):e1782-e1792.
Kulick ER, Elkind MSV, Boehme AK, Joyce NR, Schupf N, Kaufman JD, Mayeux R, Manly JJ, Wellenius GA.  2020.  Long-term exposure to ambient air pollution, APOE-ε4 status, and cognitive decline in a cohort of older adults in northern Manhattan.. Environ Int. 136:105440.
Kulminski AM, Barochia AV, Loika Y, Raghavachari N, Arbeev KG, Wojczynski MK, Thyagarajan B, Vardarajan BN, Christensen K, Yashin AI et al..  2018.  The APOE ε4 allele is associated with a reduction in FEV1/FVC in women: A cross-sectional analysis of the Long Life Family Study.. PLoS One. 13(11):e0206873.
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.
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.
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.
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.

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