Dynamic DNA methylation during aging: A "prophet" of age-related outcomes
Open accessAbstract
The biological markers of aging used to predict physical health status in older people are of great interest. Telomere shortening, which occurs during the process of cell replication, was initially considered a promising biomarker for the prediction of age and age-related outcomes (e.g., diseases, longevity). However, the high instability in detection and low correlation with age-related outcomes limit the extension of telomere length to the field of prediction. Currently, a growing number of studies have shown that dynamic DNA methylation throughout human lifetime exhibits strong correlation with age and age-related outcomes. Indeed, many researchers have built age prediction models with high accuracy based on age-dependent methylation changes in certain CpG loci. For now, DNA methylation based on epigenetic clocks, namely epigenetic or DNA methylation age, serves as a new standard to track chronological age and predict biological age. Measures of age acceleration (Δage, DNA methylation age - chronological age) have been developed to assess the health status of a person. In addition, there is evidence that an accelerated epigenetic age exists in patients with certain age-related diseases (e.g., Alzheimer's disease, cardiovascular disease). In this review, we provide an overview of the dynamic signatures of DNA methylation during aging and emphasize its practical utility in the prediction of various age-related outcomes.
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Biological confounders known to affect epigenetic patterns such as age, sex, ethnicity, body mass index, smoking behavior or nutritional aspects may introduce critical biases limiting the interpretation of epigenetic data.
“Biological confounders known to affect epigenetic patterns such as age (Xiao, Wang, & Kong, 2019), sex (Yousefi et al., 2015), ethnicity (Fraser, Lam, Neumann, & Kobor, 2012), body mass index (Sayols-Baixeras et al., 2017), smoking behavior (Li et al., 2018) or nutritional aspects (Gadecka & Bielak-Zmijewska, 2019) may introduce critical biases limiting the interpretation of epigenetic data.”
From The applied implications of epigenetics in anxiety, affective and stress-related disorders - A review and synthesis on psychosocial stress, psychotherapy and prevention (2020) · cites this paper as Xiao, Wang, & Kong, 2019
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López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982 · see citing works
DNA methylation age of human tissues and cell types
Horvath, S. (2013) · Genome Biology · doi:10.1186/gb-2013-14-10-r115 · Cited by 7,075 · see citing works
Okano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143 · see citing works
DNA methylation and its basic function
Moore, L. D., Le, T., & Fan, G. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2012.112 · Cited by 4,906 · see citing works
Human DNA methylomes at base resolution show widespread epigenomic differences
Lister, R., Pelizzola, M., Dowen, R. H., Hawkins, R. D., Hon, G., Tonti-Filippini, J., Nery, J. R., Lee, L., Ye, Z., Ngo, Q.-M., et al. (2009) · Nature · doi:10.1038/nature08514 · Cited by 4,673 · see citing works
Genome-wide methylation profiles reveal quantitative views of human aging rates
Hannum, G., Guinney, J., Zhao, L., Zhang, L., Hughes, G., Sadda, S., Klotzle, B., Bibikova, M., Fan, J.-B., Gao, Y., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2012.10.016 · Cited by 4,270 · see citing works
CpG-rich islands and the function of DNA methylation
Bird, A. P. (1986) · Nature · doi:10.1038/321209a0 · Cited by 3,777 · see citing works
Ageing populations: the challenges ahead
Christensen, K., Doblhammer, G., Rau, R., & Vaupel, J. W. (2009) · The Lancet · doi:10.1016/s0140-6736(09)61460-4 · Cited by 3,764 · see citing works
Gene Silencing in Cancer in Association with Promoter Hypermethylation
Herman, J. G., & Baylin, S. B. (2003) · New England Journal of Medicine · doi:10.1056/nejmra023075 · Cited by 3,414 · see citing works
Persistent epigenetic differences associated with prenatal exposure to famine in humans
Heijmans, B. T., Tobi, E. W., Stein, A. D., Putter, H., Blauw, G. J., Susser, E. S., Slagboom, P. E., & Lumey, L. H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806560105 · Cited by 3,082 · see citing works
DNA methylation and human disease
Robertson, K. D. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1655 · Cited by 2,864 · see citing works
Geroscience: Linking Aging to Chronic Disease
Kennedy, B. K., Berger, S. L., Brunet, A., Campisi, J., Cuervo, A. M., Epel, E. S., Franceschi, C., Lithgow, G. J., Morimoto, R. I., Pessin, J. E., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.039 · Cited by 2,764 · see citing works
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
Jones, P. L., Veenstra, G. J. C., Wade, P. A., Vermaak, D., Kass, S. U., Landsberger, N., Strouboulis, J., & Wolffe, A. P. (1998) · Nature Genetics · doi:10.1038/561 · Cited by 2,734 · see citing works
Conserved role of intragenic DNA methylation in regulating alternative promoters
Maunakea, A. K., Nagarajan, R. P., Bilenky, M., Ballinger, T. J., D’Souza, C., Fouse, S. D., Johnson, B. E., Hong, C., Nielsen, C., Zhao, Y., et al. (2010) · Nature · doi:10.1038/nature09165 · Cited by 1,743 · see citing works
The coming acceleration of global population ageing
Lutz, W., Sanderson, W. C., & Scherbov, S. (2008) · Nature · doi:10.1038/nature06516 · Cited by 1,442 · see citing works
Cardiovascular disease in Europe: epidemiological update
Nichols, M. S., Townsend, N. P., Scarborough, P., & Rayner, M. (2013) · European Heart Journal · doi:10.1093/eurheartj/eht356 · Cited by 1,349 · see citing works
Cardiovascular disease in Europe 2014: epidemiological update
Nichols, M. S., Townsend, N. P., Scarborough, P., & Rayner, M. (2014) · European Heart Journal · doi:10.1093/eurheartj/ehu299 · Cited by 1,294 · see citing works
DNA methylation age of blood predicts all-cause mortality in later life
Marioni, R. E., Shah, S., McRae, A. F., Chen, B. H., Colicino, E., Harris, S. E., Gibson, J., Henders, A. K., Redmond, P., Cox, S. R., et al. (2015) · Genome Biology · doi:10.1186/s13059-015-0584-6 · Cited by 1,261 · see citing works
Gene Body Methylation Can Alter Gene Expression and Is a Therapeutic Target in Cancer
Yang, X., Han, H., De Carvalho, D. D., Lay, F. D., Jones, P. A., & Liang, G. (2014) · Cancer Cell · doi:10.1016/j.ccr.2014.07.028 · Cited by 1,199 · see citing works
DNA methylation-based measures of biological age: meta-analysis predicting time to death
Chen, B. H., Marioni, R. E., Colicino, E., Peters, M. J., Ward-Caviness, C. K., Tsai, P.-C., Roetker, N. S., Just, A. C., Demerath, E. W., Guan, W., et al. (2016) · Aging · doi:10.18632/aging.101020 · Cited by 1,126 · see citing works
Dna Hypomethylation In Cancer Cells
Ehrlich, M. (2009) · Epigenomics · doi:10.2217/epi.09.33 · Cited by 1,065 · see citing works
Amount and distribution of 5-methylcytosine in human DNA from different types of tissues or cells
Ehrlich, M., Gama-Sosa, M. A., Huang, L.-H., Midgett, R. M., Kuo, K. C., McCune, R. A., & Gehrke, C. W. (1982) · Nucleic Acids Research · doi:10.1093/nar/10.8.2709 · Cited by 1,039 · see citing works
Bocklandt, S., Lin, W., Sehl, M. E., Sánchez, F. J., Sinsheimer, J. S., Horvath, S., & Vilain, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0014821 · Cited by 1,012 · see citing works
The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation
Fuks, F., Hurd, P. J., Wolf, D., Nan, X., Bird, A. P., & Kouzarides, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210256200 · Cited by 994 · see citing works
Epigenetic mechanisms of longevity and aging
Sen, P., Shah, P. P., Nativio, R., & Berger, S. L. (2016) · Cell · doi:10.1016/j.cell.2016.07.050 · Cited by 956 · see citing works
DNA methylation and healthy human aging
Jones, M. J., Goodman, S. J., & Kobor, M. S. (2015) · Aging Cell · doi:10.1111/acel.12349 · Cited by 937 · see citing works
Small Interfering RNA-Induced Transcriptional Gene Silencing in Human Cells
Morris, K. V., Chan, S. W.-L., Jacobsen, S. E., & Looney, D. J. (2004) · Science · doi:10.1126/science.1101372 · Cited by 925 · see citing works
S‐Adenosylmetliionine and methylation
Chiang, P. K., Gordon, R. K., Tal, J., Zeng, G. C., Doctor, B. P., Pardhasaradhi, K., & McCann, P. P. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.4.8647346 · Cited by 902 · see citing works
Aging of blood can be tracked by DNA methylation changes at just three CpG sites
Weidner, C. I., Lin, Q., Koch, C., Eisele, L., Beier, F., Ziegler, P., Bauerschlag, D., Jöckel, K., Erbel, R., Mühleisen, T., et al. (2014) · Genome Biology · doi:10.1186/gb-2014-15-2-r24 · Cited by 849 · see citing works
Distinct DNA methylomes of newborns and centenarians
Heyn, H., Li, N., Ferreira, H. J., Moran, S., Pisano, D. G., Gomez, A., Diez, J., Sanchez-Mut, J. V., Setien, F., Carmona, F. J., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120658109 · Cited by 802 · see citing works
THE QUANTITATIVE SEPARATION OF PURINES, PYRIMIDINES, AND NUCLEOSIDES BY PAPER CHROMATOGRAPHY
Hotchkiss, R. D. (1948) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)57261-6 · Cited by 765 · see citing works
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domainsPreprint
Rakyan, V. K., Down, T. A., Maslau, S., Andrew, T., Yang, T.-P., Beyan, H., Whittaker, P., McCann, O. T., Finer, S., Valdes, A. M., et al. (2010) · Genome Research · doi:10.1101/gr.103101.109 · Cited by 750 · see citing works
Active DNA Demethylation Mediated by DNA Glycosylases
Zhu, J. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134205 · Cited by 746 · see citing works
Intragenic DNA methylation prevents spurious transcription initiation
Neri, F., Rapelli, S., Krepelova, A., Incarnato, D., Parlato, C., Basile, G., Maldotti, M., Anselmi, F., & Oliviero, S. (2017) · Nature · doi:10.1038/nature21373 · Cited by 739 · see citing works
Epigenetics and aging: the targets and the marks
Fraga, M. F., & Esteller, M. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.05.008 · Cited by 690 · see citing works
DNA Methylation Decreases in Aging But Not in Immortal Cells
Wilson, V. L., & Jones, P. A. (1983) · Science · doi:10.1126/science.6844925 · Cited by 649 · see citing works
The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites
Hendrich, B., Hardeland, U., Ng, H., Jiricny, J., & Bird, A. P. (1999) · Nature · doi:10.1038/45843 · Cited by 637 · see citing works
Decline in genomic DNA methylation through aging in a cohort of elderly subjects
Bollati, V., Schwartz, J. D., Wright, R. O., Litonjua, A. A., Tarantini, L., Suh, H. H., Sparrow, D., Vokonas, P., & Baccarelli, A. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.12.003 · Cited by 594 · see citing works
Perna, L., Zhang, Y., Mons, U., Holleczek, B., Saum, K.-U., & Brenner, H. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0228-z · Cited by 572 · see citing works
Marioni, R. E., Shah, S. H., McRae, A. F., Ritchie, S. J., Terrera, G. M., Harris, S. E., Gibson, J., Redmond, P. H., Cox, S. R., Pattie, A., et al. (2015) · International Journal of Epidemiology · doi:10.1093/ije/dyu277 · Cited by 559 · see citing works
Jung, M., & Pfeifer, G. P. (2015) · BMC Biology · doi:10.1186/s12915-015-0118-4 · Cited by 541 · see citing works
Menopause accelerates biological aging
Levine, M. E., Lu, A. T.-H., Chen, B. H., Hernandez, D. G., Singleton, A., Ferrucci, L., Bandinelli, S., Salfati, E., Manson, J. E., Quach, A., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1604558113 · Cited by 507 · see citing works
Pagidipati, N. J., & Gaziano, T. A. (2013) · Circulation · doi:10.1161/circulationaha.112.128413 · Cited by 504 · see citing works
Epigenetic regulation of PPARGC1A in human type 2 diabetic islets and effect on insulin secretion
Ling, C., Del Guerra, S., Lupi, R., Rönn, T., Granhall, C., Luthman, H., Masiello, P., Marchetti, P., Groop, L., & Del Prato, S. (2008) · Diabetologia · doi:10.1007/s00125-007-0916-5 · Cited by 495 · see citing works
Accelerated epigenetic aging in Down syndrome
Horvath, S., Garagnani, P., Bacalini, M. G., Pirazzini, C., Salvioli, S., Gentilini, D., Blasio, A. M. D., Giuliani, C., Tung, S., Vinters, H. V., et al. (2015) · Aging Cell · doi:10.1111/acel.12325 · Cited by 488 · see citing works
A systematic review of leukocyte telomere length and age in adults
Müezzinler, A., Zaineddin, A. K., & Brenner, H. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.01.003 · Cited by 474 · see citing works
Zannas, A. S., Arloth, J., Carrillo-Roa, T., Iurato, S., Röh, S., Ressler, K. J., Nemeroff, C. B., Smith, A. K., Bradley, B., Heim, C., et al. (2015) · Genome Biology · doi:10.1186/s13059-015-0828-5 · Cited by 469 · see citing works
CpG methylation inhibits proenkephalin gene expression and binding of the transcription factor AP-2
Comb, M., & Goodman, H. M. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.13.3975 · Cited by 422 · see citing works
Chouliaras, L., Mastroeni, D., Delvaux, E., Grover, A., Kenis, G., Hof, P. R., Steinbusch, H. W. M., Coleman, P. D., Rutten, B. P. F., & van den Hove, D. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.02.021 · Cited by 422 · see citing works
Impact of aging on DNA methylation
Richardson, B. (2003) · Ageing Research Reviews · doi:10.1016/s1568-1637(03)00010-2 · Cited by 420 · see citing works
DNA Methylation and Demethylation in Mammals
Chen, Z., & Riggs, A. D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.r110.205286 · Cited by 395 · see citing works
Multi-tissue DNA methylation age predictor in mouse
BI Ageing Clock Team, Stubbs, T. M., Bonder, M. J., Stark, A.-K., Krueger, F., von Meyenn, F., Stegle, O., & Reik, W. (2017) · Genome Biology · doi:10.1186/s13059-017-1203-5 · Cited by 384 · see citing works
Andersen, S. L., Paola Sebastiani, B., Dworkis, D. A., Feldman, L., & Perls, T. T. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr223 · Cited by 382 · see citing works
DNA methylation signatures in peripheral blood strongly predict all-cause mortality
Zhang, Y., Wilson, R., Heiss, J., Breitling, L. P., Saum, K.-U., Schöttker, B., Holleczek, B., Waldenberger, M., Peters, A., & Brenner, H. (2017) · Nature Communications · doi:10.1038/ncomms14617 · Cited by 382 · see citing works
Trowbridge, J. J., Snow, J. W., Kim, J., & Orkin, S. H. (2009) · Cell Stem Cell · doi:10.1016/j.stem.2009.08.016 · Cited by 373 · see citing works
Genomic DNA methylation decreases in response to moderate folate depletion in elderly women
Rampersaud, G. C., KAUWELL, G. P. A., Hutson, A. D., Cerda, J. J., & Bailey, L. B. (2000) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/72.4.998 · Cited by 365 · see citing works
Ischemic Heart Disease and Stroke in Relation to Blood DNA Methylation
Baccarelli, A., Wright, R. O., Bollati, V., Litonjua, A. A., Zanobetti, A., Tarantini, L., Sparrow, D., Vokonas, P., & Schwartz, J. D. (2010) · Epidemiology · doi:10.1097/ede.0b013e3181f20457 · Cited by 361 · see citing works
Ichiyama, K., Chen, T., Wang, X., Yan, X., Kim, B.-S., Tanaka, S., Ndiaye-Lobry, D., Deng, Y., Zou, Y., Zheng, P., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.005 · Cited by 327 · see citing works
Epigenetic factors in aging and longevity
Gravina, S., & Vijg, J. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0730-7 · Cited by 326 · see citing works
Centenarians: the older you get, the healthier you have been
Hitt, R. A., Young‐Xu, Y., Silver, M. H., & Perls, T. T. (1999) · The Lancet · doi:10.1016/s0140-6736(99)01987-x · Cited by 324 · see citing works
Role of DNA methylation in the regulation of transcription
Eden, S., & Cedar, H. (1994) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(05)80052-8 · Cited by 319 · see citing works
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring
Horvath, S., Pirazzini, C., Bacalini, M. G., Gentilini, D., Di Blasio, A. M., Delledonne, M., Mari, D., Arosio, B., Monti, D., Passarino, G., et al. (2015) · Aging · doi:10.18632/aging.100861 · Cited by 316 · see citing works
Frailty is associated with the epigenetic clock but not with telomere length in a German cohort
Breitling, L. P., Saum, K.-U., Perna, L., Schöttker, B., Holleczek, B., & Brenner, H. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0186-5 · Cited by 296 · see citing works
Marioni, R. E., Harris, S. E., Shah, S. H., McRae, A. F., von Zglinicki, T., Martin-Ruiz, C. M., Wray, N. R., Visscher, P. M., & Deary, I. J. (2016) · International Journal of Epidemiology · doi:10.1093/ije/dyw041 · Cited by 285 · see citing works
DNA Methylation Dynamics of Human Hematopoietic Stem Cell Differentiation
Farlik, M., Halbritter, F., Müller, F., Choudry, F., Ebert, P., Klughammer, J., Farrow, S., Santoro, A., Ciaurro, V., Mathur, A., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.10.019 · Cited by 263 · see citing works
DNA methylation levels at individual age-associated CpG sites can be indicative for life expectancy
Lin, Q., Weidner, C. I., Costa, I. G., Marioni, R. E., Ferreira, M. R. P., Deary, I. J., & Wagner, W. (2016) · Aging · doi:10.18632/aging.100908 · Cited by 247 · see citing works
Traumatic stress and accelerated DNA methylation age: a meta-analysis
Wolf, E. J., Maniates, H., Nugent, N., Maihofer, A. X., Armstrong, D., Ratanatharathorn, A., Ashley-Koch, A. E., Garrett, M., Kimbrel, N. A., Lori, A., et al. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.12.007 · Cited by 245 · see citing works
DNA methylation and autoimmune disease
Richardson, B. (2003) · Clinical Immunology · doi:10.1016/s1521-6616(03)00206-7 · Cited by 221 · see citing works
Blood Epigenetic Age may Predict Cancer Incidence and Mortality
Zheng, Y., Joyce, B. T., Colicino, E., Liu, L., Zhang, W., Dai, Q., Shrubsole, M. J., Kibbe, W. A., Gao, T., Zhang, Z., et al. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.02.008 · Cited by 219 · see citing works
Gentilini, D., Mari, D., Castaldi, D., Remondini, D., Ogliari, G., Ostan, R., Bucci, L., Sirchia, S. M., Tabano, S. M., Cavagnini, F., et al. (2012) · AGE · doi:10.1007/s11357-012-9463-1 · Cited by 211 · see citing works
Telomere Length Variations in Aging and Age-Related Diseases
Rizvi, S., Raza, S. T., & Mahdi, F. (2015) · Current Aging Science · doi:10.2174/1874609808666150122153151 · Cited by 209 · see citing works
Distinctive patterns of age-dependent hypomethylation in interspersed repetitive sequences
Jintaridth, P., & Mutirangura, A. (2010) · Physiological Genomics · doi:10.1152/physiolgenomics.00146.2009 · Cited by 205 · see citing works
Processive Methylation of Hemimethylated CpG Sites by Mouse Dnmt1 DNA Methyltransferase
Vilkaitis, G., Suetake, I., Klimašauskas, S., & Tajima, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411126200 · Cited by 192 · see citing works
Wolffe, A. P., Jones, P. L., & Wade, P. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.5894 · Cited by 186 · see citing works
The 5-Methylcytosine in DNA of Rats
Vanyushin, B. F., Nemirovskiĭ, L. E., Klimenko, V. V., Vasiliev, V. K., & Belozersky, A. N. (2009) · Gerontologia · doi:10.1159/000211967 · Cited by 184 · see citing works
Aging results in hypermethylation of ribosomal DNA in sperm and liver of male rats
Oakes, C. C., Smiraglia, D. J., Plass, C., Trasler, J. M., & Robaire, B. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437971100 · Cited by 184 · see citing works
Dugué, P., Bassett, J. K., Joo, J. E., Baglietto, L., Jung, C.-H., Wong, E. M., Fiorito, G., Schmidt, D. F., Makalic, E., Li, S., et al. (2017) · American Journal of Epidemiology · doi:10.1093/aje/kwx291 · Cited by 181 · see citing works
Obesity accelerates epigenetic aging in middle-aged but not in elderly individuals
Nevalainen, T., Kananen, L., Marttila, S., Jylhävä, J., Mononen, N., Kähönen, M. A. P., Raitakari, O. T., Hervonen, A., Jylhä, M. K., Lehtimäki, T. J., et al. (2017) · Clinical Epigenetics · doi:10.1186/s13148-016-0301-7 · Cited by 173 · see citing works
Vanyushin, B. F., Nemirovskiĭ, L. E., Klimenko, V. V., Vasiliev, V. K., & Belozersky, A. N. (1973) · PubMed · Cited by 172 · see citing works
Sato, N., Fukushima, N., Matsubayashi, H., & Goggins, M. (2003) · Oncogene · doi:10.1038/sj.onc.1207269 · Cited by 162 · see citing works
Accelerated DNA methylation age: Associations with PTSD and neural integrity
Wolf, E. J., Logue, M. W., Hayes, J. P., Sadeh, N., Schichman, S. A., Stone, A., Salat, D. H., Milberg, W., McGlinchey, R. E., & Miller, M. W. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.09.020 · Cited by 146 · see citing works
H3K4me1 marks DNA regions hypomethylated during aging in human stem and differentiated cellsPreprint
Fernandez-Fernandez, A., Bayón, G. F., Urdinguio, R. G., Toraño, E. G., García, M. G., Carella, A., Petrus-Reurer, S., Ferrero, C., Martinez-Camblor, P., Cubillo, I., et al. (2014) · Genome Research · doi:10.1101/gr.169011.113 · Cited by 139 · see citing works
Engberg, H., Oksuzyan, A., Jeune, B., Vaupel, J. W., & Christensen, K. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00474.x · Cited by 137 · see citing works
Establishment of a Normal Hematopoietic and Leukemia Stem Cell HierarchyPreprint
Chao, M. P., Seita, J., & Weissman, I. L. (2008) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2008.73.031 · Cited by 135 · see citing works
McCartney, D. L., Stevenson, A. J., Walker, R. M., Gibson, J., Morris, S. W., Campbell, A., Murray, A. D., Whalley, H. C., Porteous, D. J., McIntosh, A. M., et al. (2018) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1016/j.dadm.2018.05.006 · Cited by 134 · see citing works
TET1 is a maintenance DNA demethylase that prevents methylation spreading in differentiated cells
Jin, C., Lu, Y., Jelı́nek, J., Liang, S., Estecio, M. R., Barton, M. C., & Issa, J. J. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku372 · Cited by 130 · see citing works
Influence of ambient air pollution on global DNA methylation in healthy adults: A seasonal follow-up
Prins, S. D., Koppen, G., Jacobs, G., Dons, E., de Mieroop, E. V., Nelen, V., Fierens, F., Panis, L. I., Boever, P. D., Cox, B., et al. (2013) · Environment International · doi:10.1016/j.envint.2013.07.007 · Cited by 120 · see citing works
Case-control meta-analysis of blood DNA methylation and autism spectrum disorder
Andrews, S. V., Sheppard, B. K., Windham, G. C., Schieve, L. A., Schendel, D., Croen, L., Chopra, P., Alisch, R. S., Newschaffer, C. J., Warren, S. T., et al. (2018) · Molecular Autism · doi:10.1186/s13229-018-0224-6 · Cited by 104 · see citing works
Côté, S., Gagné‐Ouellet, V., Guay, S., Allard, C., Houde, A.-A., Perron, P., Baillargeon, J., Gaudet, D., Guérin, R., Brisson, D., et al. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0239-9 · Cited by 94 · see citing works
Lowe, R., Barton, C., Jenkins, C. A., Ernst, C., Forman, O. P., Fernandez‐Twinn, D. S., Bock, C., Rossiter, S. J., Faulkes, C. G., Ozanne, S. E., et al. (2018) · Genome biology · doi:10.1186/s13059-018-1397-1 · Cited by 89 · see citing works
Ozaki, Y., Yoshino, Y., Yamazaki, K., Sao, T., Mori, Y., Ochi, S., Yoshida, T., Mori, T., Iga, J., & Ueno, S. (2017) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2017.04.003 · Cited by 85 · see citing works
Davis, E., Humphreys, K. L., McEwen, L. M., Sacchet, M. D., Camacho, M. C., MacIsaac, J. L., Lin, D., Kobor, M. S., & Gotlib, I. H. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.188 · Cited by 79 · see citing works
Ciccarone, F., Malavolta, M., Calabrese, R., Guastafierro, T., Bacalini, M. G., Reale, A., Franceschi, C., Capri, M., Hervonen, A., Hurme, M., et al. (2016) · Aging Cell · doi:10.1111/acel.12485 · Cited by 77 · see citing works
Accelerated DNA Methylation Age: Associations With Posttraumatic Stress Disorder and Mortality
Wolf, E. J., Logue, M. W., Stoop, T. B., Schichman, S. A., Stone, A., Sadeh, N., Hayes, J. P., & Miller, M. W. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000506 · Cited by 76 · see citing works
D’Aquila, P., Rose, G., Bellizzi, D., & Passarino, G. (2012) · Maturitas · doi:10.1016/j.maturitas.2012.11.005 · Cited by 72 · see citing works
Jost, J. P., Schwarz, S., Hess, D., Angliker, H., Fuller-Pace, F. V., Stahl, H. D., Thiry, S., & Siegmann, M. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.16.3245 · Cited by 60 · see citing works
Role of DNA methylation in human age prediction
Goel, N., Karir, P., & Garg, V. K. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.08.012 · Cited by 60 · see citing works
Epigenetic aging clocks in mice and men
Wagner, W. (2017) · Genome biology · doi:10.1186/s13059-017-1245-8 · Cited by 53 · see citing works
Progress on the role of DNA methylation in aging and longevity
Xiao, F., Kong, Q., Perry, B., & He, Y. (2016) · Briefings in Functional Genomics · doi:10.1093/bfgp/elw009 · Cited by 51 · see citing works
Self-citationDevelopmental Tuning of Epigenetic Clock
Vaiserman, A. M. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00584 · Cited by 49 · see citing works
Epigenetic mechanisms in human disease.
Feinberg, A. P., Oshimura, M., & Barrett, J. C. (2002) · PubMed · Cited by 47 · see citing works
Xiao, F., He, Y., Li, Q.-G., Wu, H., Luo, L., & Kong, Q. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120388 · Cited by 46 · see citing works
Self-citationZhang, Y., Hapala, J., Brenner, H., & Wagner, W. (2017) · Clinical Epigenetics · doi:10.1186/s13148-017-0315-9 · Cited by 42 · see citing works
Age-related DNA methylation changes for forensic age-prediction
Yi, S.-H., Jia, Y.-S., Mei, K., Yang, R.-Z., & Huang, D.-X. (2015) · Zeitschrift für Rechtsmedizin · doi:10.1007/s00414-014-1100-3 · Cited by 41 · see citing works
Wu, Z., Li, X., Qin, H., Zhu, X., Xu, J., & Shi, W. (2013) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2013.04.022 · Cited by 39 · see citing works
Alu Hypomethylation in Smoke-Exposed Epithelia and Oral Squamous Carcinoma
Puttipanyalears, C., Subbalekha, K., Mutirangura, A., & Kitkumthorn, N. (2013) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2013.14.9.5495 · Cited by 30 · see citing works
Epigenetic response to environmental change: DNA methylation varies with invasion status
Schrey, A. W., Robbins, T. R., Lee, J., Dukes, D. W., Ragsdale, A. K., Thawley, C. J., & Langkilde, T. L. (2016) · Current Zoology · doi:10.1093/eep/dvw008 · Cited by 27 · see citing works
Andrews, C. P., Nettle, D., Larriva, M., Gillespie, R., Reichert, S., Brilot, B., Bedford, T., Monaghan, P., Spencer, K. A., & Melissa Bateson, B. (2017) · Royal Society Open Science · doi:10.1098/rsos.171208 · Cited by 26 · see citing works
Accelerated DNA methylation changes in middle-aged men define sexual dimorphism in human lifespans
Xiao, F., Chen, X., He, Y., & Kong, Q. (2018) · Clinical Epigenetics · doi:10.1186/s13148-018-0573-1 · Cited by 24 · see citing works
Self-citationP1‐321: EVIDENCE OF NEUROINFLAMMATION IN THE RETINA IN PRESYMPTOMATIC ALZHEIMER'S DISEASE
Lim, Y. Y., Site, M., Maruff, P. T., Getter, C., Salloway, S., Ott, B. R., Schindler, R. J., & Snyder, P. J. (2014) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2014.05.562 · Cited by 8 · see citing works
DNA methylome: Unveiling your biological age
Li, M., Liu, W., Yuan, T., Bai, R., Liu, G., Zhang, W., & Qu, J. T. (2013) · Protein & Cell · doi:10.1007/s13238-013-3913-0 · Cited by 7 · see citing works
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Aging Hallmarks and the Role of Oxidative Stress
Maldonado, E., Morales, S., Urbina, F., & Solari, A. (2023) · Antioxidants · doi:10.3390/antiox12030651 · Cited by 454 · see citing works
Cai, Y., Song, W., Li, J., Jing, Y., Liang, C., Zhang, L., Zhang, X., Zhang, W., Liu, B., An, Y., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-022-2161-3 · Cited by 436 · see citing works
Self-citationBao, H., Cao, J., Chen, M., Min, C., Chen, W., Chen, X., Chen, Y., Chen, Y., Chen, Y., Chen, Z., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2305-0 · Cited by 389 · see citing works
Self-citationInflammation and DNA damage: cause, effect or both
Pezone, A., Olivieri, F., Napoli, M. V., Procopio, A., Avvedimento, E. V., & Gabrielli, A. (2023) · Nature Reviews Rheumatology · doi:10.1038/s41584-022-00905-1 · Cited by 212 · see citing works
Schiele, M. A., Gottschalk, M. G., & Domschke, K. (2020) · Clinical Psychology Review · doi:10.1016/j.cpr.2020.101830 · Cited by 156 · see citing works
Ashapkin, V. V., Suvorov, A., Pilsner, J. R., Krawetz, S. A., & Sergeyev, O. (2022) · Human Reproduction Update · doi:10.1093/humupd/dmac033 · Cited by 143 · see citing works
The enigma and implications of brain hemispheric asymmetry in neurodegenerative diseases
Lubben, N., Ensink, E., Coetzee, G. A., & Labrie, V. (2021) · Brain Communications · doi:10.1093/braincomms/fcab211 · Cited by 132 · see citing works
Histone Modifications in Alzheimer’s Disease
Santana, D. A., Smith, M. D. A. C., & Chen, E. (2023) · Genes · doi:10.3390/genes14020347 · Cited by 109 · see citing works
Epigenetic reprogramming as a key to reverse ageing and increase longevity
Pereira, B., Correia, F. P., Alves, I. A., Costa, M., Gameiro, M. D., Martins, A. P., & Saraiva, J. A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102204 · Cited by 108 · see citing works
Pellegrini, C., Pirazzini, C., Sala, C., Sambati, L., Yusipov, I., Kalyakulina, A., Ravaioli, F., Kwiatkowska, K. M., Durso, D. F., Ivanchenko, M., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.639428 · Cited by 88 · see citing works
Epigenetics of prenatal stress in humans: the current research landscape
Dieckmann, L., & Czamara, D. (2024) · Clinical Epigenetics · doi:10.1186/s13148-024-01635-9 · Cited by 84 · see citing works
Introduction to Single-Cell DNA Methylation Profiling Methods
Ahn, J., Heo, S., Lee, J., & Bang, D. (2021) · Biomolecules · doi:10.3390/biom11071013 · Cited by 67 · see citing works
DNA methylation across the tree of life, from micro to macro-organism
NASRULLAH, N., Hussain, A., Ahmed, S., Rasool, M., & Shah, A. J. (2022) · Bioengineered · doi:10.1080/21655979.2021.2014387 · Cited by 56 · see citing works
Characteristics of epigenetic aging across gestational and perinatal tissues
Dieckmann, L., Lahti‐Pulkkinen, M., Kvist, T., Lahti, J. M. T., DeWitt, P. E., Cruceanu, C., Laivuori, H. M., Sammallahti, S., Villa, P., Suomalainen‐König, S., et al. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01080-y · Cited by 56 · see citing works
Role of primary aging hallmarks in Alzheimer´s disease
Zhao, J., & Huai, J. (2022) · Theranostics · doi:10.7150/thno.79535 · Cited by 53 · see citing works
Parrillo, L., Spinelli, R., Nicolò, A., Longo, M., Mirra, P., Raciti, G. A., Miele, C., & Bèguinot, F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20122983 · Cited by 52 · see citing works
Aging hampers neutrophil extracellular traps (NETs) efficacy
Sabbatini, M., Bona, E., Novello, G., Migliario, M., & Renò, F. (2022) · Aging Clinical and Experimental Research · doi:10.1007/s40520-022-02201-0 · Cited by 51 · see citing works
Huang, G., Liu, L., Wang, H., Gou, M., Gong, P., Tian, C., Deng, W., Yang, J., Zhou, T.-T., Xu, G.-L., et al. (2020) · iScience · doi:10.1016/j.isci.2020.100908 · Cited by 47 · see citing works
Self-citationDNA methylation changes and inflammaging in aging-associated diseases.
Alimohammadi, M., Makaremi, S., Rahimi, A., Asghariazar, V., Taghadosi, M., & Safarzadeh, E. (2022) · Epigenomics · doi:10.2217/epi-2022-0143 · Cited by 36 · see citing works
Association between depression and epigenetic age acceleration: A co‐twin control study
Liu, C., Wang, Z., Hui, Q., Goldberg, J. H., Smith, N. L., Shah, A. J., Murrah, N. V., Shallenberger, L. H., Diggers, E., Bremner, J. D., et al. (2022) · Depression and Anxiety · doi:10.1002/da.23279 · Cited by 40 · see citing works
Moreira, L., Costa, C., Pires, J., Teixeira, J. P., & Fraga, S. (2021) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2021.108385 · Cited by 34 · see citing works
Penova‐Veselinovic, B., Melton, P. E., Huang, R., Yovich, J. L., Burton, P., Wijs, L. A., & Hart, R. J. (2021) · Human Reproduction · doi:10.1093/humrep/deab078 · Cited by 33 · see citing works
G-quadruplexes and associated proteins in aging and Alzheimer’s disease
Kumar, M. J. V., Morales, R., & Tsvetkov, A. S. (2023) · Frontiers in Aging · doi:10.3389/fragi.2023.1164057 · Cited by 33 · see citing works
Talukdar, F. R., Marcillo, D. I. E., Laskar, R. S., Novoloaca, A., Cuenin, C., Sbraccia, P., Nisticò, L., Guglielmi, V., Gheit, T., Tommasino, M., et al. (2022) · Clinical Epigenetics · doi:10.1186/s13148-022-01401-9 · Cited by 32 · see citing works
Maternal DNA Methylation During Pregnancy: a Review
Das, J., & Maitra, A. (2021) · Reproductive Sciences · doi:10.1007/s43032-020-00456-4 · Cited by 29 · see citing works
Medicine and Phlebolymphology: Time to Change?
Cavezzi, A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9124091 · Cited by 28 · see citing works
Development of DNA methylation‐based epigenetic age predictors in loblolly pine ( Pinus taeda )
Gardner, S. T., Bertucci, E. M., Sutton, R., Horcher, A., Aubrey, D. P., & Parrott, B. B. (2022) · Molecular Ecology Resources · doi:10.1111/1755-0998.13698 · Cited by 28 · see citing works
Accelerated epigenetic aging and myopenia in young adult cancer survivors
Gehle, S. C., Kleissler, D., Heiling, H., Deal, A. M., Xu, Z., Miller, V. L. A., Taylor, J. A., & Smitherman, A. B. (2023) · Cancer Medicine · doi:10.1002/cam4.5908 · Cited by 27 · see citing works
Giordo, R., Posadino, A. M., Mangoni, A. A., & Pintus, G. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115732 · Cited by 27 · see citing works
Developmental programming of adult haematopoiesis system
Balistreri, C. R., Garagnani, P., Madonna, R., Vaiserman, A. M., & Melino, G. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100918 · Cited by 27 · see citing works
Epigenetic enzymes: A role in aging and prospects for pharmacological targeting
PASYUKOVA, E. G., Symonenko, A. V., Rybina, O. Y., & Vaiserman, A. M. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101312 · Cited by 27 · see citing works
Zawieja, E. E., & Chmurzyńska, A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102634 · Cited by 25 · see citing works
Function and treatment strategies of β-hydroxybutyrate in aging
Xiang, Y., Wang, Q., Lan, X., Zhang, H., & Wei, D. (2022) · Smart Materials in Medicine · doi:10.1016/j.smaim.2022.09.003 · Cited by 25 · see citing works
Gutman, D., Rivkin, E., Fadida, A., Sharvit, L. E., Hermush, V., Rubin, E., Kirshner, D., Sabin, I., Dwolatzky, T., & Atzmon, G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020615 · Cited by 25 · see citing works
Brain areas involved with obsessive-compulsive disorder present different DNA methylation modulation
de Oliveira, K. C., Camilo, C., Gastaldi, V. D., Feltrin, A. S., Lisbôa, B. C. G., de Paula, V. D. J. R., Moretto, A. C., Lafer, B., Hoexter, M. Q., Miguel, E. C., et al. (2021) · BMC Genomic Data · doi:10.1186/s12863-021-00993-0 · Cited by 24 · see citing works
miRMap: Profiling 14q32 microRNA Expression and DNA Methylation Throughout the Human Vasculature
Goossens, E. A. C., de Vries, M. R., Simons, K. H., Putter, H., Quax, P. H. A., & Nossent, A. Y. (2019) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2019.00113 · Cited by 24 · see citing works
Bertucci, E. M., Shealy, E. P., & Parrott, B. B. (2024) · Aging · doi:10.18632/aging.205503 · Cited by 22 · see citing works
Compound combinations targeting longevity: Challenges and perspectives
Rybina, O. Y., Symonenko, A. V., & PASYUKOVA, E. G. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101851 · Cited by 22 · see citing works
Epigenetic alterations—The silent indicator for early aging and age‐associated health‐risks
Dhar, P., Moodithaya, S. S., & Patil, P. (2022) · Aging Medicine · doi:10.1002/agm2.12236 · Cited by 21 · see citing works
Exercise and epigenetic ages in older adults with myeloid malignancies
Loh, K. P., Sanapala, C., Jensen‐Battaglia, M., Rana, A., Sohn, M. B., Watson, E., Gilmore, N. J., Klepin, H. D., Mendler, J. H., Liesveld, J. L., et al. (2023) · European journal of medical research · doi:10.1186/s40001-023-01145-z · Cited by 20 · see citing works
Aneuploidy and DNA Methylation as Mirrored Features of Early Human Embryo Development
Tolmacheva, E. N., Vasilyev, S. А., & Лебедев, И. Н. (2020) · Genes · doi:10.3390/genes11091084 · Cited by 20 · see citing works
Ageing-associated changes in DNA methylation in X and Y chromosomes
Kananen, L., & Marttila, S. (2021) · Epigenetics & Chromatin · doi:10.1186/s13072-021-00407-6 · Cited by 20 · see citing works
de Pontual, L., & Tomé, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073477 · Cited by 18 · see citing works
Wang, H., Xiao, F., Gao, Z., Guo, L., Yang, L., Li, G., & Kong, Q. (2024) · Aging Cell · doi:10.1111/acel.14163 · Cited by 15 · see citing works
Self-citationEffendi, W. I., & Nagano, T. (2023) · Biomedicines · doi:10.3390/biomedicines11041047 · Cited by 15 · see citing works
Shiga, M., Asari, M., Takahashi, Y., Isozaki, S., Hoshina, C., Mori, K., Namba, R., Okuda, K., & Shimizu, K. (2023) · Legal Medicine · doi:10.1016/j.legalmed.2023.102336 · Cited by 14 · see citing works
Pacetti, M., Conti, L. D., Marasco, L. E., Romano, M., Rashid, M. M., Nubiè, M., Baralle, F. E., & Baralle, M. (2022) · Disease Models & Mechanisms · doi:10.1242/dmm.049032 · Cited by 14 · see citing works
Associations of age, sex, sexual abuse, and genotype with monoamine oxidase a gene methylation
Checknita, D., Tiihonen, J., Hodgins, S., & Nilsson, K. W. (2021) · Journal of Neural Transmission · doi:10.1007/s00702-021-02403-2 · Cited by 14 · see citing works
Discovering the direct relations between nutrients and epigenetic ageing
Grootswagers, P., Bach, D., Biemans, Y., Behrouzi, P., Horvath, S., Kramer, C. S., Liu, S., Manson, J. E., Shadyab, A. H., Stewart, J. D., et al. (2024) · The journal of nutrition health & aging · doi:10.1016/j.jnha.2024.100324 · Cited by 12 · see citing works
Rössnerová, A., Hoňková, K., Chvojkova, I., Pelclová, D., Ždı́mal, V., Hubacek, J. A., Lischková, L., Vlčková, Š., Ondráček, J., Dvorackova, S., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22157834 · Cited by 12 · see citing works
Zeng, Z., Meyer, K. F., Lkhagvadorj, K., Kooistra, W., Reinders-Luinge, M., Xu, X., Huo, X., Song, J., Plösch, T., & Hylkema, M. N. (2020) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00293.2019 · Cited by 12 · see citing works
The Epigenome in Atherosclerosis
Costantino, S., & Paneni, F. (2020) · Handbook of experimental pharmacology · doi:10.1007/164_2020_422 · Cited by 12 · see citing works
Fernández-Carrión, R., Sorlí, J. V., Asensio, E. M., Pascual, E. C., Portolés, O., Álvarez‐Sala, A., Francès, F., Sabio, J. B. R., Fidalgo, J. A. P., Villamil, L. V., et al. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20043635 · Cited by 11 · see citing works
DNA methylation perturbations may link altered development and aging in the lung
Kachroo, P., Morrow, J. D., Vyhlidal, C. A., Gaedigk, R., Silverman, E. K., Weiss, S. T., Tantisira, K. G., & DeMeo, D. L. (2021) · Aging · doi:10.18632/aging.202544 · Cited by 11 · see citing works
Matsumoto, S., Tateishi‐Karimata, H., Ohyama, T., & Sugimoto, N. (2021) · RSC Advances · doi:10.1039/d1ra07201c · Cited by 11 · see citing works
Bondhus, L., Wei, A., & Arboleda, V. A. (2022) · BMC Bioinformatics · doi:10.1186/s12859-022-04899-1 · Cited by 9 · see citing works
Aronica, T. S., Carella, M., & Balistreri, C. R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073928 · Cited by 9 · see citing works
Rinaldi, M., Pezone, A., Quadrini, G. I., Abbadessa, G., Laezza, M. P., Passaro, M. L., Porcellini, A., & Costagliola, C. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1371745 · Cited by 9 · see citing works
Age-related changes in DNA methylation in a sample of elderly Brazilians
Welsh, H., Batalha, C. M. P. F., Li, W., de Souza-Pinto, N. C., Duarte, Y. A. O., Naslavsky, M. S., & Parra, E. J. (2025) · Clinical Epigenetics · doi:10.1186/s13148-025-01821-3 · Cited by 9 · see citing works
DNA methylation-based age prediction using cell separation algorithm
Jaddi, N. S., & Abadeh, M. S. (2020) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2020.103747 · Cited by 9 · see citing works
Role of TLR9 methylation on its active transcription in apical inflammation
Fernández, A., V, Astorga, J., Bordagaray, M. J., Lira, M. J., Gebicke‐Haerter, P. J., & Hernández, M. (2022) · International Endodontic Journal · doi:10.1111/iej.13745 · Cited by 9 · see citing works
Social Determinants of Health and Cerebral Small Vessel Disease: Is Epigenetics a Key Mediator?
Parodi, L., Mayerhofer, E., Narasimhalu, K., Yechoor, N., Comeau, M., Rosand, J., Langefeld, C., & Anderson, C. (2023) · Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease · doi:10.1161/jaha.123.029862 · Cited by 9 · see citing works
Genetics and Epigenetics of Alzheimer’s Disease: new Cognitive Technologies and Neurocommunication
Sirotko, I. I., Volobuev, A. N., & Иванович, Р. П. (2021) · Bulletin of Science and Practice · doi:10.33619/2414-2948/63/09 · Cited by 9 · see citing works
Morgan, A. E., Acutt, K. D., & Auley, M. T. M. (2020) · Bioscience Reports · doi:10.1042/bsr20202571 · Cited by 8 · see citing works
Shao, X., Stunff, C. L., Cheung, W., Kwan, T., Lathrop, M. G., Pastinen, T., & Bougneres, P. F. (2022) · Clinical Epigenetics · doi:10.1186/s13148-022-01281-z · Cited by 8 · see citing works
DNA methylation is regulated by both the stability and topology of G-quadruplex
Matsumoto, S., Tateishi‐Karimata, H., & Sugimoto, N. (2022) · Chemical Communications · doi:10.1039/d2cc04383a · Cited by 8 · see citing works
Han, Z., & Wen, L. (2023) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v15.i7.1149 · Cited by 8 · see citing works
Campisi, M., Cannella, L., Visioli, F., & Pavanello, S. (2025) · Advances in Nutrition · doi:10.1016/j.advnut.2025.100521 · Cited by 7 · see citing works
Montesanto, A., D’Aquila, P., Rossano, V., Passarino, G., & Bellizzi, D. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00672 · Cited by 7 · see citing works
D’Amico-Willman, K. M., Niederhuth, C. E., Sovic, M. G., Anderson, E. S., Gradziel, T. M., & Fresnedo‐Ramírez, J. (2023) · Plant Science · doi:10.1016/j.plantsci.2023.111918 · Cited by 7 · see citing works
Dash, M., Mahajan, B., Dar, G. M., Sahu, P., & Saluja, S. S. (2024) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2024.106555 · Cited by 7 · see citing works
Causal effects of cardiovascular health on five epigenetic clocks
Sung, H.-L., & Lin, W. (2024) · Clinical Epigenetics · doi:10.1186/s13148-024-01752-5 · Cited by 7 · see citing works
Innan, H., Veitia, R. A., & Govindaraju, D. R. (2019) · Human Genetics · doi:10.1007/s00439-019-02067-9 · Cited by 7 · see citing works
García-Flores, E., Calderón-Colmenero, J. E., Borgonio‐Cuadra, V. M., Sandoval, J. P., García‐Montes, J. A., Cazarín-Santos, B. G., Miranda‐Duarte, A., Gamboa‐Domínguez, A., Rodrı́guez-Pérez, J. M., & Pérez‐Hernández, N. (2023) · Cells · doi:10.3390/cells12040586 · Cited by 7 · see citing works
A new robust AI/ML based model for accurate forensic age estimation using DNA methylation markers
Mathew, J. A., Paul, G., Jacob, J., Kumar, J., Dubey, N., & Philip, N. S. (2025) · Forensic Science Medicine and Pathology · doi:10.1007/s12024-025-00985-x · Cited by 6 · see citing works
Reversing Aging and Improving Health Span in Glaucoma Patients: The Next Frontier?
Bhartiya, S., Dada, T., & Mahalingam, K. (2024) · JOURNAL OF CURRENT GLAUCOMA PRACTICE · doi:10.5005/jp-journals-10078-1451 · Cited by 6 · see citing works
Potential regulatory role of epigenetic modifications in aging-related heart failure
Lv, L., Chen, Q., Lü, J., Zhao, Q., Wang, H., Li, J., Yuan, K., & Dong, Z. (2024) · International Journal of Cardiology · doi:10.1016/j.ijcard.2024.131858 · Cited by 6 · see citing works
Self-citationMitochondrial DNA Copy Number Variations in Gastrointestinal Tract Cancers: Potential Players
Alikhani, M., Touati, E., Karimipoor, M., Vosough, M., & Mohammadi, M. (2021) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-021-00707-w · Cited by 5 · see citing works
Cellular senescence as a source of chronic microinflammation that promotes the aging process
Nakanishi, M. (2025) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.101.014 · Cited by 5 · see citing works
Completing Single-Cell DNA Methylome Profiles via Transfer Learning Together With KL-Divergence
Dodlapati, S., Jiang, Z., & Sun, J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.910439 · Cited by 5 · see citing works
Neto, S. C., Reis, A., Pinheiro, M., Ferreira, M., Neves, V., Castanho, T. C., Santos, N. C., Rodrigues, A. J., Sousa, N., Santos, M. A. S., et al. (2024) · Human Genomics · doi:10.1186/s40246-024-00640-6 · Cited by 4 · see citing works
Epigenetic Alterations in Aging: A Brief Review
Ekowati, A. L., & Siswanto, F. M. (2024) · Journal of Urban Health Research · doi:10.25170/juhr.v2i3.5759 · Cited by 4 · see citing works
Xiao, F., Wang, H., Zhao, L., Xia, T., Yang, L., Ma, S., & Kong, Q. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115158 · Cited by 4 · see citing works
Self-citationLlanquinao, J., Cicali, K. A., Jara, C., Vigil-Vásquez, C., Sjöberg-Herrera, M. K., Ricca, M., Valenzuela, S., Loyola, A., Pinti, M., Schüller, A., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-24766-2 · Cited by 3 · see citing works
Park, J., Lee, Y., & Won, C. W. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111704 · Cited by 3 · see citing works
Personalized Nutrition for Healthy Aging, A Review
Pointner, A., & Haslberger, A. G. (2022) · Springer eBooks · doi:10.1007/978-3-031-10153-3_5 · Cited by 3 · see citing works
Biomedical science limitations and flaws: why not choose wisely?
Cavezzi, A., d'Errico, G., & Colucci, R. (2022) · Journal of Theoretical and Applied Vascular Research · doi:10.24019/jtavr.142 · Cited by 3 · see citing works
Green Tea Mitigates the Hallmarks of Aging and Age-Related Multisystem Deterioration
Yilmaz, Y. N. (2013) · Aging and Disease · doi:10.14336/ad.2025.0398 · Cited by 3 · see citing works
Monroy‐Jaramillo, N., & Vázquez-Martínez, E. R. (2020) · Springer eBooks · doi:10.1007/978-3-030-40955-5_8 · Cited by 3 · see citing works
Lim, Z. M., Chew, Y. E., Guan, L., Wang, W., Mahadzir, M. D. A., Dorajoo, R., Kennedy, B. K., Sandalova, E., & Maier, A. B. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112867 · Cited by 2 · see citing works
The epigenetic control of inflammaging in skeletal muscle and adipose tissue
de Melo, D. G., Rodrigues, V. C. D. C., Pereira, G. J. D. S., Fernandes, C. J. D. C., & de Moura, L. P. (2026) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2026.112205 · Cited by 2 · see citing works
Epigenetic regulons in Alzheimer's disease
Raval, M., Mishra, S., & Tiwari, A. K. (2023) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2023.01.012 · Cited by 2 · see citing works
Obtaining Longevity Footprints in DNA Methylation Data Using Different Machine Learning Approaches
Kalyakulina, A., Yusipov, I., & Ivanchenko, M. (2023) · Healthy ageing and longevity · doi:10.1007/978-3-031-35176-1_4 · Cited by 2 · see citing works
Le, N. T., Do, T. T. H., Duong, D. M. T., Tran, D. H. N., Huynh, T. Q., Huynh, K., Nguyen, P. T., Le, M. T., & Nguyen, T. T. H. (2024) · Gene Reports · doi:10.1016/j.genrep.2024.101939 · Cited by 2 · see citing works
Okada, D. (2023) · GeroScience · doi:10.1007/s11357-023-00949-5 · Cited by 2 · see citing works
El-Ahwany, E. G., Hassan, M. N. M., Elzallat, M., Abdelsalam, L., Elsawy, M. A., & Seyam, M. (2022) · Virus Research · doi:10.1016/j.virusres.2022.198928 · Cited by 2 · see citing works
Sex-Specific Age-Related Changes in Methylation of Certain Genes
Kondakova, E. V., Vershinina, O., Lopatenko, M. V., Franceschi, C., Ivanchenko, M., & Vedunova, M. V. (2021) · Современные технологии в медицине · doi:10.17691/stm2021.13.3.03 · Cited by 2 · see citing works
Steyaert, S., Verhelle, A., & Criekinge, W. V. (2023) · medRxiv · doi:10.1101/2023.07.07.23292381 · Cited by 2 · see citing works
Sehl, M. E., Guo, W., Farrell, C., Marino, N., Henry, J. E., Storniolo, A. M., Papp, J. C., Li, J. J., Horvath, S., Pellegrini, M. A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.31.619735 · Cited by 2 · see citing works
Kaczmarek, M., & Zysek, W. (2022) · Postępy Biochemii · doi:10.18388/pb.2021_449 · Cited by 1 · see citing works
- Authors
- Xiao, F.-H., Wang, H.-T., & Kong, Q.-P.
- Affiliations
- Chinese University of Hong Kong (HK)
- Corresponding author
- Kong, Qing-Peng
- Venue
- Frontiers in Genetics
- Publisher
- Frontiers Media SA
- Published
- 2019-02-18
- Volume
- 10
- Pages
- 107-107
- ISSN
- 1664-8021 (ISSN-L)
- PMC
- PMC6387955
- OpenAlex
- W2917732063
- Cited by
- 140
- References
- 112
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 24 · 2023: 23 · 2022: 27 · 2021: 28 · 2020: 11 · 2019: 6 · 2013: 1
- FWCI
- 1.66
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- DNA methylation, aging, epigenetic clocks, DNA methylation age, biological age, accelerated aging, telomere shortening, age-related diseases, Alzheimer's disease, cardiovascular disease, age prediction model, CpG sites, aging biomarkers
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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