You are here

Home
Citation Year of Publication
Ma, Yiyi, et al. "Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype." JAMA Neurol (2019). 2019
Patel, Devanshi, et al. "Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry." JAMA Netw Open. 2.3 (2019): e191350. 2019
Zhang, Xiaoling, et al. "A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease." Alzheimers Dement. 15.3 (2019): 441-452. 2019
Beecham, Gary W., et al. "Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease." Neurol Genet. 4.6 (2018): e286. 2018
Bis, Joshua C., et al. "Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation." Mol. Psychiatry (2018). 2018
Blue, Elizabeth E., et al. "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 (2018): 1-17. 2018
Blue, E E., et al. "Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease." Genes Brain Behav.. 17.6 (2018): e12429. 2018
Butkiewicz, Mariusz, et al. "Functional annotation of genomic variants in studies of late-onset Alzheimer's disease." Bioinformatics. 34.16 (2018): 2724-2731. 2018
Leung, Yuk Yee, et al. "VCPA: genomic Variant Calling pipeline and data management tool for Alzheimer's Disease Sequencing Project." Bioinformatics (2018). 2018
Nafikov, Rafael A., et al. "Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP." Genet. Epidemiol.. 42.6 (2018): 500-515. 2018
Naj, Adam C., et al. "Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project." Genomics (2018). 2018
Raghavan, Neha S., et al. "Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease." Ann Clin Transl Neurol. 5.7 (2018): 832-842. 2018
Vardarajan, Badri N., et al. "Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease." Ann Clin Transl Neurol. 5.4 (2018): 406-417. 2018
Beecham, Gary W., et al. "The Alzheimer's Disease Sequencing Project: Study design and sample selection." Neurol Genet. 3.5 (2017): e194. 2017
Crane, Paul K., et al. "Alzheimer's Disease Sequencing Project discovery and replication criteria for cases and controls: Data from a community-based prospective cohort study with autopsy follow-up." Alzheimers Dement. 13.12 (2017): 1410-1413. 2017
Kunkle, Brian W., et al. "Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease." Alzheimers Dement. 12.1 (2016): 2-10. 2016
Barral, Sandra, et al. "Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease." Alzheimers Dement. 11.12 (2015): 1397-1406. 2015
Citation Year of Publication
Li, Zeran, et al. "The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion." Acta Neuropathol.. 139.1 (2020): 45-61. 2020
Blue, Elizabeth E., et al. "Local ancestry at APOE modifies Alzheimer's disease risk in Caribbean Hispanics." Alzheimers Dement. 15.12 (2019): 1524-1532. 2019
Broce, Iris J., et al. "Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer's disease." Acta Neuropathol.. 137.2 (2019): 209-226. 2019
Choi, Kyu Yeong, et al. "Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of ε4 on Alzheimer's Disease Risk in a Multiracial Sample." J Clin Med. 8.8 (2019). 2019
Conner, Sarah C., et al. "Methionine Sulfoxide Reductase-B3 Risk Allele Implicated in Alzheimer's Disease Associates with Increased Odds for Brain Infarcts." J. Alzheimers Dis.. 68.1 (2019): 357-365. 2019
Conner, Sarah C., et al. "Mid-life and late-life vascular risk factor burden and neuropathology in old age." Ann Clin Transl Neurol. 6.12 (2019): 2403-2412. 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
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
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
Liu, Yiyuan, et al. "Promoter DNA hypermethylation - Implications for Alzheimer's disease." Neurosci. Lett.. 711 (2019): 134403. 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
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
Tosto, Giuseppe, et al. "Association of Variants in PINX1 and TREM2 With Late-Onset Alzheimer Disease." JAMA Neurol (2019). 2019
Weinstein, Galit, et al. "Non-alcoholic fatty liver disease, liver fibrosis score and cognitive function in middle-aged adults: The Framingham Study." Liver Int.. 39.9 (2019): 1713-1721. 2019
Adams, Shayna, et al. "Vascular risk factor burden and new-onset depression in the community." Prev Med. 111 (2018): 348-350. 2018
Amlie-Wolf, Alexandre, et al. "INFERNO: inferring the molecular mechanisms of noncoding genetic variants." Nucleic Acids Res.. 46.17 (2018): 8740-8753. 2018
Deming, Yuetiva, et al. "Sex-specific genetic predictors of Alzheimer's disease biomarkers." Acta Neuropathol.. 136.6 (2018): 857-872. 2018

Pages

Theme by Danetsoft and Danang Probo Sayekti inspired by Maksimer