These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
231 related articles for article (PubMed ID: 27892496)
1. EWAS: epigenome-wide association studies software 1.0 - identifying the association between combinations of methylation levels and diseases. Xu J; Liu D; Zhao L; Li Y; Wang Z; Chen Y; Lei C; Gao L; Kong F; Yuan L; Jiang Y Sci Rep; 2016 Nov; 6():37951. PubMed ID: 27892496 [TBL] [Abstract][Full Text] [Related]
2. EWAS: epigenome-wide association study software 2.0. Xu J; Zhao L; Liu D; Hu S; Song X; Li J; Lv H; Duan L; Zhang M; Jiang Q; Liu G; Jin S; Liao M; Zhang M; Feng R; Kong F; Xu L; Jiang Y Bioinformatics; 2018 Aug; 34(15):2657-2658. PubMed ID: 29566144 [TBL] [Abstract][Full Text] [Related]
4. EWASdb: epigenome-wide association study database. Liu D; Zhao L; Wang Z; Zhou X; Fan X; Li Y; Xu J; Hu S; Niu M; Song X; Li Y; Zuo L; Lei C; Zhang M; Tang G; Huang M; Zhang N; Duan L; Lv H; Zhang M; Li J; Xu L; Kong F; Feng R; Jiang Y Nucleic Acids Res; 2019 Jan; 47(D1):D989-D993. PubMed ID: 30321400 [TBL] [Abstract][Full Text] [Related]
5. The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Ahsan M; Ek WE; Rask-Andersen M; Karlsson T; Lind-Thomsen A; Enroth S; Gyllensten U; Johansson Å PLoS Genet; 2017 Sep; 13(9):e1007005. PubMed ID: 28915241 [TBL] [Abstract][Full Text] [Related]
6. Blood-based epigenome-wide analyses of 19 common disease states: A longitudinal, population-based linked cohort study of 18,413 Scottish individuals. Hillary RF; McCartney DL; Smith HM; Bernabeu E; Gadd DA; Chybowska AD; Cheng Y; Murphy L; Wrobel N; Campbell A; Walker RM; Hayward C; Evans KL; McIntosh AM; Marioni RE PLoS Med; 2023 Jul; 20(7):e1004247. PubMed ID: 37410739 [TBL] [Abstract][Full Text] [Related]
7. Gaps in current methods to detect polymorphic CpGs from Illumina Infinium human methylation microarrays and exploring their potential impact in multi-EWAS analyses. Bhat B; Jones GT Epigenetics; 2023 Dec; 18(1):2281153. PubMed ID: 37983305 [TBL] [Abstract][Full Text] [Related]
8. Incorporation of DNA methylation quantitative trait loci (mQTLs) in epigenome-wide association analysis: application to birthweight effects in neonatal whole blood. Li S; Mancuso N; Metayer C; Ma X; de Smith AJ; Wiemels JL Clin Epigenetics; 2022 Dec; 14(1):158. PubMed ID: 36457128 [TBL] [Abstract][Full Text] [Related]
9. DiMmer: Discovery of Differentially Methylated Regions in Epigenome-Wide Association Study (EWAS) Data. Frisch T; Gøttcke J; Röttger R; Tan Q; Baumbach J Methods Mol Biol; 2018; 1807():51-62. PubMed ID: 30030803 [TBL] [Abstract][Full Text] [Related]
10. Gene-methylation interactions: discovering region-wise DNA methylation levels that modify SNP-associated disease risk. Romanowska J; Haaland ØA; Jugessur A; Gjerdevik M; Xu Z; Taylor J; Wilcox AJ; Jonassen I; Lie RT; Gjessing HK Clin Epigenetics; 2020 Jul; 12(1):109. PubMed ID: 32678018 [TBL] [Abstract][Full Text] [Related]
11. Computationally inferred cell-type specific epigenome-wide DNA methylation analysis unveils distinct methylation patterns among immune cells for HIV infection in three cohorts. Zhang X; Hu Y; Vandenhoudt RE; Yan C; Marconi VC; Cohen MH; Wang Z; Justice AC; Aouizerat BE; Xu K PLoS Pathog; 2024 Mar; 20(3):e1012063. PubMed ID: 38466776 [TBL] [Abstract][Full Text] [Related]
12. Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies. Rahmani E; Zaitlen N; Baran Y; Eng C; Hu D; Galanter J; Oh S; Burchard EG; Eskin E; Zou J; Halperin E Nat Methods; 2016 May; 13(5):443-5. PubMed ID: 27018579 [TBL] [Abstract][Full Text] [Related]
13. A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies. Lehne B; Drong AW; Loh M; Zhang W; Scott WR; Tan ST; Afzal U; Scott J; Jarvelin MR; Elliott P; McCarthy MI; Kooner JS; Chambers JC Genome Biol; 2015 Feb; 16(1):37. PubMed ID: 25853392 [TBL] [Abstract][Full Text] [Related]
14. Data Analysis of DNA Methylation Epigenome-Wide Association Studies (EWAS): A Guide to the Principles of Best Practice. Bhat B; Jones GT Methods Mol Biol; 2022; 2458():23-45. PubMed ID: 35103960 [TBL] [Abstract][Full Text] [Related]
15. Using epigenome-wide association scans of DNA methylation in age-related complex human traits. Tsai PC; Spector TD; Bell JT Epigenomics; 2012 Oct; 4(5):511-26. PubMed ID: 23130833 [TBL] [Abstract][Full Text] [Related]
16. EWAS Open Platform: integrated data, knowledge and toolkit for epigenome-wide association study. Xiong Z; Yang F; Li M; Ma Y; Zhao W; Wang G; Li Z; Zheng X; Zou D; Zong W; Kang H; Jia Y; Li R; Zhang Z; Bao Y Nucleic Acids Res; 2022 Jan; 50(D1):D1004-D1009. PubMed ID: 34718752 [TBL] [Abstract][Full Text] [Related]
17. EWAS Data Hub: a resource of DNA methylation array data and metadata. Xiong Z; Li M; Yang F; Ma Y; Sang J; Li R; Li Z; Zhang Z; Bao Y Nucleic Acids Res; 2020 Jan; 48(D1):D890-D895. PubMed ID: 31584095 [TBL] [Abstract][Full Text] [Related]
18. Identification of novel susceptibility methylation loci for pancreatic cancer in a two-phase epigenome-wide association study. Wang Z; Lu Y; Fornage M; Jiao L; Shen J; Li D; Wei P Epigenetics; 2022 Nov; 17(11):1357-1372. PubMed ID: 35030986 [TBL] [Abstract][Full Text] [Related]
19. Epigenome-wide association study of DNA methylation in panic disorder. Shimada-Sugimoto M; Otowa T; Miyagawa T; Umekage T; Kawamura Y; Bundo M; Iwamoto K; Tochigi M; Kasai K; Kaiya H; Tanii H; Okazaki Y; Tokunaga K; Sasaki T Clin Epigenetics; 2017; 9():6. PubMed ID: 28149334 [TBL] [Abstract][Full Text] [Related]
20. Deep molecular phenotypes link complex disorders and physiological insult to CpG methylation. Zaghlool SB; Mook-Kanamori DO; Kader S; Stephan N; Halama A; Engelke R; Sarwath H; Al-Dous EK; Mohamoud YA; Roemisch-Margl W; Adamski J; Kastenmüller G; Friedrich N; Visconti A; Tsai PC; Spector T; Bell JT; Falchi M; Wahl A; Waldenberger M; Peters A; Gieger C; Pezer M; Lauc G; Graumann J; Malek JA; Suhre K Hum Mol Genet; 2018 Mar; 27(6):1106-1121. PubMed ID: 29325019 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]