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For: Guastafierro T, Bacalini MG, Marcoccia A, Gentilini D, Pisoni S, Di Blasio AM, Corsi A, Franceschi C, Raimondo D, Spanò A, Garagnani P, Bondanini F. Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome. Clin Epigenetics 2017;9:92. [PMID: 28861129 DOI: 10.1186/s13148-017-0389-4] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
Number Citing Articles
1 Franceschi C, Garagnani P, Morsiani C, Conte M, Santoro A, Grignolio A, Monti D, Capri M, Salvioli S. The Continuum of Aging and Age-Related Diseases: Common Mechanisms but Different Rates. Front Med (Lausanne) 2018;5:61. [PMID: 29662881 DOI: 10.3389/fmed.2018.00061] [Cited by in Crossref: 226] [Cited by in F6Publishing: 206] [Article Influence: 56.5] [Reference Citation Analysis]
2 Sadikovic B, Aref-Eshghi E, Levy MA, Rodenhiser D. DNA methylation signatures in mendelian developmental disorders as a diagnostic bridge between genotype and phenotype. Epigenomics 2019;11:563-75. [PMID: 30875234 DOI: 10.2217/epi-2018-0192] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
3 Ciccarone F, Tagliatesta S, Caiafa P, Zampieri M. DNA methylation dynamics in aging: how far are we from understanding the mechanisms? Mechanisms of Ageing and Development 2018;174:3-17. [DOI: 10.1016/j.mad.2017.12.002] [Cited by in Crossref: 71] [Cited by in F6Publishing: 64] [Article Influence: 17.8] [Reference Citation Analysis]
4 Chen Z, Gao W, Pu L, Zhang L, Han G, Zuo X, Zhang Y, Li X, Shen H, Wu J, Wang X. PRDM8 exhibits antitumor activities toward hepatocellular carcinoma by targeting NAP1L1. Hepatology 2018;68:994-1009. [PMID: 29572888 DOI: 10.1002/hep.29890] [Cited by in Crossref: 22] [Cited by in F6Publishing: 21] [Article Influence: 5.5] [Reference Citation Analysis]
5 Poot M. Scratching the Surface of Werner Syndrome and Human Ageing. Mol Syndromol 2017;9:1-4. [PMID: 29456476 DOI: 10.1159/000484424] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Haghshenas S, Bhai P, Aref-Eshghi E, Sadikovic B. Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders. Int J Mol Sci 2020;21:E9303. [PMID: 33291301 DOI: 10.3390/ijms21239303] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Cacabelos R, Cacabelos P, Carril JC. Epigenetics and Pharmacoepigenetics of Age-Related Neurodegenerative Disorders. Pharmacoepigenetics. Elsevier; 2019. pp. 903-50. [DOI: 10.1016/b978-0-12-813939-4.00038-3] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
8 Wang M, Kong W, He B, Li Z, Song H, Shi P, Wang J. Vitamin D and the promoter methylation of its metabolic pathway genes in association with the risk and prognosis of tuberculosis. Clin Epigenetics 2018;10:118. [PMID: 30208925 DOI: 10.1186/s13148-018-0552-6] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.8] [Reference Citation Analysis]
9 Reilly J, Kerkhof J, Sadikovic B. EpiSigns. Advances in Molecular Pathology 2020;3:29-39. [DOI: 10.1016/j.yamp.2020.07.018] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Harishankar M, Sampath P, Sriram M, Raghuraman R, Athikesavan V, Chinnayan P, Velayutham B, Putcha UK, Tripathy SP, Ranganathan UD, Selvaraj P, Bethunaickan R. Association of CYP2R1 gene polymorphisms in pulmonary tuberculosis. Meta Gene 2021;28:100875. [DOI: 10.1016/j.mgene.2021.100875] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Franceschi C, Garagnani P, Parini P, Giuliani C, Santoro A. Inflammaging: a new immune–metabolic viewpoint for age-related diseases. Nat Rev Endocrinol 2018;14:576-90. [DOI: 10.1038/s41574-018-0059-4] [Cited by in Crossref: 567] [Cited by in F6Publishing: 536] [Article Influence: 141.8] [Reference Citation Analysis]
12 Giuliani C, Garagnani P, Franceschi C. Genetics of Human Longevity Within an Eco-Evolutionary Nature-Nurture Framework. Circ Res 2018;123:745-72. [PMID: 30355083 DOI: 10.1161/CIRCRESAHA.118.312562] [Cited by in Crossref: 43] [Cited by in F6Publishing: 18] [Article Influence: 14.3] [Reference Citation Analysis]
13 Haghshenas S, Levy MA, Kerkhof J, Aref-Eshghi E, McConkey H, Balci T, Siu VM, Skinner CD, Stevenson RE, Sadikovic B, Schwartz C. Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type. Int J Mol Sci 2021;22:1111. [PMID: 33498634 DOI: 10.3390/ijms22031111] [Reference Citation Analysis]
14 Wang J, Zhang J, Ma D, Li X. The Potential Role of CERS1 in Autophagy Through PI3K/AKT Signaling Pathway in Hypophysoma. Technol Cancer Res Treat 2020;19:1533033820977536. [PMID: 33267708 DOI: 10.1177/1533033820977536] [Reference Citation Analysis]
15 Hu X, Tang L, Wang L, Wu FX, Li M. MADA: a web service for analysing DNA methylation array data. BMC Bioinformatics 2020;21:403. [PMID: 33203349 DOI: 10.1186/s12859-020-03734-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Castagna A, Gareri P, Falvo F, Sestito S, Rocca M, Pensabene L, Concolino D, Coppolino G, Ruotolo G. Werner syndrome: a rare mutation. Aging Clin Exp Res 2019;31:425-9. [PMID: 29876830 DOI: 10.1007/s40520-018-0982-1] [Reference Citation Analysis]
17 Zhang TP, Li HM, Huang Q, Wang L, Li XM. Vitamin D Metabolic Pathway Genes Polymorphisms and Their Methylation Levels in Association With Rheumatoid Arthritis. Front Immunol 2021;12:731565. [PMID: 34925313 DOI: 10.3389/fimmu.2021.731565] [Reference Citation Analysis]
18 Kim JL, Mestre B, Shin SH, Futerman AH. Ceramide synthases: Reflections on the impact of Dr. Lina M. Obeid. Cell Signal 2021;82:109958. [PMID: 33607256 DOI: 10.1016/j.cellsig.2021.109958] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
19 Maierhofer A, Flunkert J, Oshima J, Martin GM, Poot M, Nanda I, Dittrich M, Müller T, Haaf T. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes. Aging Cell 2019;18:e12995. [PMID: 31259468 DOI: 10.1111/acel.12995] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 5.0] [Reference Citation Analysis]