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Citation Year of Publication
Del-Aguila, Jorge L., et al. "A single-nuclei RNA sequencing study of Mendelian and sporadic AD in the human brain." Alzheimers Res Ther. 11.1 (2019): 71. 2019
Dube, Umber, et al. "An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations." Nat. Neurosci.. 22.11 (2019): 1903-1912. 2019
Dumitrescu, Logan, et al. "Sex differences in the genetic predictors of Alzheimer's pathology." Brain. 142.9 (2019): 2581-2589. 2019
Ebbert, Mark T. W., et al. "Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight." Genome Biol.. 20.1 (2019): 97. 2019
Feliciano-Astacio, Briseida E., et al. "The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach." Front Genet. 10 (2019): 538. 2019
Gardner, Olivia K., et al. "RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways." Hum. Mol. Genet.. 28.18 (2019): 3053-3061. 2019
Georgakis, Marios K., et al. "Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: Meta-Analysis of Population-Based Studies Involving 17 180 Individuals." Circ. Res.. 125.8 (2019): 773-782. 2019
González, Hector M., et al. "A research framework for cognitive aging and Alzheimer's disease among diverse US Latinos: Design and implementation of the Hispanic Community Health Study/Study of Latinos-Investigation of Neurocognitive Aging (SOL-INCA)." Alzheimers Dement. 15.12 (2019): 1624-1632. 2019
Hu, Yiming, et al. "A statistical framework for cross-tissue transcriptome-wide association analysis." Nat. Genet.. 51.3 (2019): 568-576. 2019
Huan, Tianxiao, et al. "Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease." Nat Commun. 10.1 (2019): 4267. 2019
Ji, Zheng, et al. "An Assembled Detector Based on Geometrical Constraint for Power Component Recognition." Sensors (Basel). 19.16 (2019). 2019
Katsumata, Yuriko, et al. "Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs." Neurobiol. Aging. 74 (2019): 135-146. 2019
Kowalski, Madeline H., et al. "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 (2019): e1008500. 2019
Kuksa, Pavel P., et al. "DASHR 2.0: integrated database of human small non-coding RNA genes and mature products." Bioinformatics. 35.6 (2019): 1033-1039. 2019
Larsson, Susanna C., et al. "Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study." Neurology. 92.9 (2019): e944-e950. 2019
Leonenko, Ganna, et al. "Polygenic risk and hazard scores for Alzheimer's disease prediction." Ann Clin Transl Neurol. 6.3 (2019): 456-465. 2019
Liu, Yiyuan, et al. "Promoter DNA hypermethylation - Implications for Alzheimer's disease." Neurosci. Lett.. 711 (2019): 134403. 2019
Lo, Min-Tzu, et al. "Identification of genetic heterogeneity of Alzheimer's disease across age." Neurobiol. Aging. 84 (2019): 243.e1-243.e9. 2019
Lobach, Iryna, et al. "A simple approximation to bias in the genetic effect estimates when multiple disease states share a clinical diagnosis." Genet. Epidemiol.. 43.5 (2019): 522-531. 2019
Ma, Yiyi, et al. "CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease." Aging Cell. 18.4 (2019): e12964. 2019
Mandaviya, Pooja R., et al. "Association of dietary folate and vitamin B-12 intake with genome-wide DNA methylation in blood: a large-scale epigenome-wide association analysis in 5841 individuals." Am. J. Clin. Nutr.. 110.2 (2019): 437-450. 2019
McGrath, Emer R., et al. "Circulating fibroblast growth factor 23 levels and incident dementia: The Framingham heart study." PLoS ONE. 14.3 (2019): e0213321. 2019
Mishra, Aniket, et al. "Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects." Brain. 142.4 (2019): 1009-1023. 2019
Saad, Mohamad, and Ellen M. Wijsman. "Association score testing for rare variants and binary traits in family data with shared controls." Brief. Bioinformatics. 20.1 (2019): 245-253. 2019
Sariya, Sanjeev, et al. "Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools." Front Genet. 10 (2019): 239. 2019


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