The DOI matches its Crossref record; 187 of the 188 references it cites were found in a registry or an index.
Epigenetic Mechanisms of Longevity and Aging
Open accessAbstract
Aging is an inevitable outcome of life, characterized by progressive decline in tissue and organ function and increased risk of mortality. Accumulating evidence links aging to genetic and epigenetic alterations. Given the reversible nature of epigenetic mechanisms, these pathways provide promising avenues for therapeutics against age-related decline and disease. In this review, we provide a comprehensive overview of epigenetic studies from invertebrate organisms, vertebrate models, tissues, and in vitro systems. We establish links between common operative aging pathways and hallmark chromatin signatures that can be used to identify "druggable" targets to counter human aging and age-related disease.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
Multiplex Genome Engineering Using CRISPR/Cas Systems
Cong, L., Ran, F. A., Cox, D., Lin, S., Barretto, R., Habib, N., Hsu, P. D., Wu, X., Jiang, W., Marraffini, L. A., et al. (2013) · Science · doi:10.1126/science.1231143 · Cited by 15,339
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
TOR signaling in growth and metabolism
Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787
Cancer chemopreventive activity of resveratrol, a natural product derived from grapes
Jang, M., Cai, L., Udeani, G. O., Slowing, K. V., Thomas, C. F., Beecher, C. W. W., Fong, H. H. S., Farnsworth, N. R., Kinghorn, A. D., Mehta, R. G., et al. (1997) · Science · doi:10.1126/science.275.5297.218 · Cited by 4,935
Resveratrol improves health and survival of mice on a high-calorie diet
Baur, J. A., Pearson, K. J., Price, N. L., Jamieson, H. A., Lerin, C., Kalra, A., Prabhu, V. V., Allard, J. S., Lopez-Lluch, G., Lewis, K., et al. (2006) · Nature · doi:10.1038/nature05354 · Cited by 4,290
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
Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan
Howitz, K. T., Bitterman, K. J., Cohen, H. Y., Lamming, D. W., Lavu, S., Wood, J. G., Zipkin, R. E., Chung, P., Kisielewski, A., Zhang, L.-L., et al. (2003) · Nature · doi:10.1038/nature01960 · Cited by 3,796
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders
Baker, D. J., Wijshake, T., Tchkonia, T., LeBrasseur, N. K., Childs, B. G., van de Sluis, B., Kirkland, J. L., & van Deursen, J. M. (2011) · Nature · doi:10.1038/nature10600 · Cited by 3,670
A C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387
Flagged first, then by citations
1 of the 188 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 301–400 of 962
Reducing functionally defective old HSCs alleviates aging-related phenotypes in old recipient mice
Wang, Y., Zhang, W., Zhang, C., Van, H. Q. T., Seino, T., & Zhang, Y. (2025) · Cell Research · doi:10.1038/s41422-024-01057-5 · Cited by 34
Pereira, S. M., Ribeiro, R., & Logarinho, E. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040938 · Cited by 31
Csiszár, A., Balasubramanian, P., Tarantini, S., Yabluchanskiy, A., Zhang, X. A., Springó, Z., Benbrook, D. M., Sonntag, W. E., & Ungvari, Z. I. (2019) · GeroScience · doi:10.1007/s11357-019-00064-4 · Cited by 31
Malawey, A. S., Mercati, D., Love, C. C., & Tomberlin, J. K. (2019) · Annals of the Entomological Society of America · doi:10.1093/aesa/saz045 · Cited by 30
Fate of Hematopoiesis During Aging. What Do We Really Know, and What are its Implications?
Broxmeyer, H. E., Liu, Y., Kapur, R., Orschell, C. M., Aljoufi, A., Ropa, J. P., Trinh, T. L. P., Burns, S. S., & Capitano, M. L. (2020) · Stem Cell Reviews and Reports · doi:10.1007/s12015-020-10065-y · Cited by 30
Effect of heterochromatin stability on intestinal stem cell aging in Drosophila
Jeon, H.-J., Kim, Y.-S., Kim, J., Heo, K., Pyo, J.-H., Yamaguchi, M., Park, J., & Yoo, M. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.04.001 · Cited by 31
Intrinsic and environmental basis of aging: A narrative review
Navarro, C., Salazar, J. J., Diaz, M. P., Chacín, M., Santeliz, R., Vera, I., D’Marco, L., Parra, H., Bernal, M. C., Castro, A. V., et al. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e18239 · Cited by 34
Tai, Y., Yu, Q., Tang, Y. M., Sun, W., Kelly, N. J., Okawa, S., Zhao, J., Schwantes-An, T.-H. L., Lacoux, C., Torrino, S., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.add2029 · Cited by 29
Hypoxia and aging: molecular mechanisms, diseases, and therapeutic targets
Nisar, A., Khan, S., Li, W., Hu, L., Samarawickrama, P. N., Gold, N. M., Zi, M., Mehmood, S. A., Miao, J., & He, Y. (2024) · MedComm · doi:10.1002/mco2.786 · Cited by 33
The Epigenetics of Aging in Invertebrates
Yu, G., Wu, Q., Gao, Y., Chen, M., & Yang, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184535 · Cited by 32
The epigenetic legacy of illicit drugs: developmental exposures and late-life phenotypes
Flack, N., Colwell, M., & Faulk, C. D. (2019) · Current Zoology · doi:10.1093/eep/dvz022 · Cited by 28
Giorgi, G., & Re, B. D. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03489-6 · Cited by 29
Recent Advances in Epigenetics of Age-Related Kidney Diseases
Liu, F., Chen, J., Li, Z., & Meng, X. (2022) · Genes · doi:10.3390/genes13050796 · Cited by 31
Deciphering clock genes as emerging targets against aging
Zhu, Y., Liu, Y., Escames, G., Yang, Z. Z., Zhao, H., Lu, Q., Xue, C., Xu, D., Acuña-Castroviejo, D., & Yang, Y. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101725 · Cited by 32
Amaro‐Gahete, F. J., De‐la‐O, A., Jurado‐Fasoli, L., Gutiérrez, Á., Ruiz, J. R., & Castillo, M. J. (2019) · Maturitas · doi:10.1016/j.maturitas.2019.02.001 · Cited by 31
DNA Methylation Signature of Aging: Potential Impact on the Pathogenesis of Parkinson’s Disease
Yazar, V., Dawson, V. L., Dawson, T. M., & Kang, S.-U. (2023) · Journal of Parkinson s Disease · doi:10.3233/jpd-223517 · Cited by 29
Histone deficiency and hypoacetylation in the aging retinal pigment epithelium
Dubey, S. K., Dubey, R., Prajapati, S. C., Jung, K., Mohan, K., Liu, X., Roney, J., Tian, W., Abney, J., Giarmarco, M. M., et al. (2024) · Aging Cell · doi:10.1111/acel.14108 · Cited by 30
Reactivation of retrotransposable elements is associated with environmental stress and ageing
Valle, F. D., Reddy, P., Aguirre-Vázquez, A., & Belmonte, J. C. I. (2025) · Nature Reviews Genetics · doi:10.1038/s41576-025-00829-y · Cited by 27
Gulej, R., Patai, R., Ungvari, A., Kállai, A., Tarantini, S., Yabluchanskiy, A., Huffman, D. M., Conboy, M. J., Conboy, I. M., Mika Kivimaki, B., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01657-y · Cited by 29
Accelerated lung aging and chronic obstructive pulmonary disease
Yoon, Y.-S., Jin, M., & Sin, D. D. (2019) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2019.1580576 · Cited by 26
Sleep and ageing: from human studies to rodent models
McKillop, L. E., & Vyazovskiy, V. V. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2020.03.004 · Cited by 31
MiR-199-3p enhances muscle regeneration and ameliorates aged muscle and muscular dystrophy
Fukuoka, M., Fujita, H., Numao, K., Nakamura, Y., Shimizu, H., Sekiguchi, M., & Hohjoh, H. (2021) · Communications Biology · doi:10.1038/s42003-021-01952-2 · Cited by 30
Transposons: Unexpected players in cancer
Pradhan, R. K., & Ramakrishna, W. (2021) · Gene · doi:10.1016/j.gene.2021.145975 · Cited by 31
Bengtsen, M., Winje, I. M., Eftestøl, E., Landskron, J., Sun, C., Nygård, K., Domańska, D., Millay, D. P., Meza‐Zepeda, L. A., & Gundersen, K. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009907 · Cited by 26
New insights of epigenetics in vascular and cellular senescence
Zhu, M., Ding, Q., Lin, Z., Chen, X., Chen, S., & Zhu, Y. Z. (2021) · Journal of Translational Internal Medicine · doi:10.2478/jtim-2021-0049 · Cited by 28
Reduced expression of mitochondrial complex I subunit Ndufs2 does not impact healthspan in mice
McElroy, G. S., Chakrabarty, R. P., D’Alessandro, K. B., Hu, Y., Vasan, K., Tan, J., Stoolman, J. S., Weinberg, S. E., Steinert, E. M., Reyfman, P. A., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-09074-3 · Cited by 27
Lian, W., Wu, R., Ko, J., Chen, Y., Wang, S.-Y., Yu, C.-P., Jahr, H., & Wang, F. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04985-5 · Cited by 28
Gene body DNA hydroxymethylation restricts the magnitude of transcriptional changes during aging
Occean, J. R., Yang, N., Sun, Y., Dawkins, M. S., Munk, R. B., Belair, C., Dar, S. A., Anerillas, C., Wang, L., Shi, C., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50725-y · Cited by 30
Self-citationRecent insights into the cellular and molecular determinants of aging
Ruan, L., Zhang, X., & Li, R. (2018) · Journal of Cell Science · doi:10.1242/jcs.210831 · Cited by 28
Validation and characterisation of a DNA methylation alcohol biomarker across the life course
Yousefi, P., Richmond, R. C., Langdon, R., Ness, A., Liu, C., Levy, D. A., Relton, C. L., Suderman, M. J., & Zuccolo, L. (2019) · Clinical Epigenetics · doi:10.1186/s13148-019-0753-7 · Cited by 26
Metformin: Sentinel of the Epigenetic Landscapes That Underlie Cell Fate and Identity
Menéndez, J. A. (2020) · Biomolecules · doi:10.3390/biom10050780 · Cited by 27
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 28
Gene Bookmarking by the Heat-Shock Transcription Factor Programs the Insulin-Like Signaling Pathway
Das, S., Min, S., & Prahlad, V. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.09.022 · Cited by 28
Brennan, K., Zheng, H., Fahrner, J. A., Shin, J. H., Gentles, A. J., Schaefer, B., Sunwoo, J. B., Bernstein, J. A., & Gevaert, O. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac026 · Cited by 27
Folguera-Blasco, N., Cuyàs, E., Menéndez, J. A., & Alarcón, T. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006052 · Cited by 26
Murata, Y., Ikegame, T., Koike, S., Saito, T., Ikeda, M., Sasaki, T., Iwata, N., Kasai, K., Bundo, M., & Iwamoto, K. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109855 · Cited by 29
DNA Break-Induced Epigenetic Drift as a Cause of Mammalian AgingPreprint
Hayano, M., Yang, J.-H., Bonkowski, M. S., Amorim, J. A., Ross, J. M., Coppotelli, G., Griffin, P. T., Chew, Y. C., Guo, W., Yang, X., et al. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3466338 · Cited by 27
Genetic Factors Altering Immune Responses in Atrial Fibrillation
Ninni, S., Dombrowicz, D., de Winther, M. P. J., Staels, B., Montaigne, D., & Nattel, S. (2024) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2023.12.034 · Cited by 26
m5C-Seq: Machine learning-enhanced profiling of RNA 5-methylcytosine modifications
Abbas, Z., Rehman, M. U., Tayara, H., Lee, S. W., & Chong, K. T. (2024) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2024.109087 · Cited by 26
Fountoulakis, N., Miyamoto, Y., Pavkov, M. E., Karalliedde, J. J., & Maltese, G. (2024) · Diabetic Medicine · doi:10.1111/dme.15464 · Cited by 27
Watanabe, R., Kanno, S., Roushandeh, A. M., Ui, A., & Yasui, A. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0473 · Cited by 27
Age-related changes in DNA methylation affect renal histology and post-transplant fibrosis
Heylen, L., Thienpont, B., Busschaert, P., Sprangers, B., Kuypers, D. R. J., Moisse, M., Lerut, E., Lambrechts, D., & Naesens, M. (2019) · Kidney International · doi:10.1016/j.kint.2019.06.018 · Cited by 29
Fan, C., Zhao, C., Zhang, F., Kesarwani, M., Tu, Z., Cai, X., Davis, A. K., Xu, L., Hochstetler, C. L., Chen, X., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2020102118 · Cited by 27
Single-Cell Analysis of the Transcriptome and Epigenome
Mazan-Mamczarz, K., Ha, J., De, S., & Sen, P. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1831-8_3 · Cited by 27
Self-citationHow can we modulate aging through nutrition and physical exercise? An epigenetic approach
Rajado, A. T., Silva, N., Esteves, F., Brito, D. V. C., Binnie, A., Araújo, I. M., Nóbrega, C., Bragança, J., & Castelo‐Branco, P. (2023) · Aging · doi:10.18632/aging.204668 · Cited by 32
Alzheimer’s Disease: the Potential of Epigenetic Treatments and Current Clinical Candidates
Coneys, R., & Wood, I. C. (2020) · Neurodegenerative Disease Management · doi:10.2217/nmt-2019-0034 · Cited by 26
Acevedo, A., Torres, F., Kiwi, M., Baeza‐Lehnert, F., Barros, L. F., Lee‐Liu, D., & González-Billault, C. E. (2023) · Aging · doi:10.18632/aging.204663 · Cited by 27
Cell reprogramming: Therapeutic potential and the promise of rejuvenation for the aging brain
López-León, M., Outeiro, T. F., & Goya, R. G. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.09.002 · Cited by 27
Epigenetic‐based therapy for colorectal cancer: Prospect and involved mechanisms
Rezapour, S., Hosseinzadeh, E., Marofi, F., & Hassanzadeh, A. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28658 · Cited by 25
Perner, F., & Armstrong, S. A. (2020) · Cells · doi:10.3390/cells9122721 · Cited by 25
Epigenetic modifications of histones during osteoblast differentiation
Adithya, S. P., Balagangadharan, K., & Selvamurugan, N. (2021) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2021.194780 · Cited by 25
Life-long microbiome rejuvenation improves intestinal barrier function and inflammaging in mice
Sommer, F., Bernardes, J. P., Best, L., Sommer, N., Hamm, J., Messner, B., López-Agudelo, V. A., Fazio, A., Μαρίνος, Γ., Kadibalban, A. S., et al. (2025) · Microbiome · doi:10.1186/s40168-025-02089-8 · Cited by 26
Responders and non-responders to influenza vaccination: A DNA methylation approach on blood cells
Gensous, N., Franceschi, C., Blomberg, B. B., Pirazzini, C., Ravaioli, F., Gentilini, D., Blasio, A. M. D., Garagnani, P., Frasca, D., & Bacalini, M. G. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.01.019 · Cited by 24
DNA Damage and the Aging Epigenome
Siametis, A., Niotis, G., & Garinis, G. A. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.10.006 · Cited by 24
Region-specific H3K9me3 gain in aged somatic tissues in Caenorhabditis elegans
Li, C.-L. F., Pu, M., Wang, W., Chaturbedi, A., Emerson, F. J., & Lee, S. S. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009432 · Cited by 22
Involvement of lncRNA TUG1 in HIV-1 Tat-Induced Astrocyte Senescence
Pillai, P. P., Kannan, M., Sil, S., Singh, S., Thangaraj, A., Chivero, E. T., Dagur, R. S., Tripathi, A., Hu, G., Periyasamy, P., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054330 · Cited by 24
Shen, X., Gao, X., Luo, Y., Xu, Q., Fan, Y., Hong, S., Huang, Z., Liu, X., Wang, Q., Chen, Z., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00453-7 · Cited by 23
Saito, T., Braun, P., Daniel, S., Jellison, S. S., Hellman, M. M., Shinozaki, E., Lee, S., Cho, H. R., Yoshino, A., Toda, H., et al. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.06.003 · Cited by 24
DNA Break-Induced Epigenetic Drift as a Cause of Mammalian AgingPreprint
Hayano, M., Yang, J.-H., Bonkowski, M. S., Amorim, J. A., Ross, J. M., Coppotelli, G., Griffin, P. T., Chew, Y. C., Guo, W., Yang, X., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/808659 · Cited by 24
LINE-1 transposable element renaissance in aging and age-related diseases
Li, X., Yu, H., Li, D., & Liu, N. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102440 · Cited by 23
Transposable element 5mC methylation state of blood cells predicts age and disease
Morandini, F., Lu, J. Y., Rechsteiner, C., Shadyab, A. H., Casanova, R., Snively, B. M., Seluanov, A., & Gorbunova, V. A. (2024) · Nature Aging · doi:10.1038/s43587-024-00757-2 · Cited by 28
How age affects human hematopoietic stem and progenitor cells and the strategies to mitigate aging
Li, X., Wang, J., Hu, L., & Cheng, T. (2025) · Experimental Hematology · doi:10.1016/j.exphem.2025.104711 · Cited by 25
Molecular mechanisms regulating lifespan and environmental stress responses
Kishimoto, S., Uno, M., & Nishida, E. (2018) · Inflammation and Regeneration · doi:10.1186/s41232-018-0080-y · Cited by 23
Wang, H., Zhu, X., Shen, J., Zhao, E.-F., He, D., Shen, H., Liu, H., & Zhou, Y. (2019) · BMC Genomics · doi:10.1186/s12864-019-6089-z · Cited by 23
Regulatory Mechanisms of Mitochondrial Function and Cardiac Aging
Lin, R., & Kerkelä, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041359 · Cited by 23
Carty, B. L., Dattoli, A. A., & Dunleavy, E. M. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009247 · Cited by 23
A putative role for lncRNAs in epigenetic regulation of memory
Irwin, A. B., Bahabry, R., & Lubin, F. D. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105184 · Cited by 23
Scrutinizing the Therapeutic Potential of PROTACs in the Management of Alzheimer’s Disease
Bhatia, S., Singh, M., Singh, T., & Singh, V. (2023) · Neurochemical Research · doi:10.1007/s11064-022-03722-w · Cited by 22
The nuclear-mitochondrial crosstalk in aging: From mechanisms to therapeutics
Feng, Y., & Lu, Y. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.03.012 · Cited by 23
Genome and Epigenome Editing in Mechanistic Studies of Human Aging and Aging-Related Disease
Lau, C., & Suh, Y. (2016) · Gerontology · doi:10.1159/000452972 · Cited by 22
Translational control in cell ageing: an update
Woodward, K., & Shirokikh, N. E. (2021) · Biochemical Society Transactions · doi:10.1042/bst20210844 · Cited by 21
Herp, D., Ridinger, J., Robaa, D., Shinsky, S. A., Schmidtkunz, K., Yesiloglu, T. Z., Bayer, T., Steimbach, R. R., Herbst‐Gervasoni, C. J., Merz, A., et al. (2022) · ChemBioChem · doi:10.1002/cbic.202200180 · Cited by 22
The Double-Edged Role of Extracellular Vesicles in the Hallmarks of Aging
Romero-García, N., Huete-Acevedo, J., Mas‐Bargues, C., Sanz‐Ros, J., Dromant, M., & Borrás, C. (2023) · Biomolecules · doi:10.3390/biom13010165 · Cited by 25
METTL3 promotes the malignancy of non-small cell lung cancer by N6-methyladenosine modifying SFRP2
Zhao, S., Song, P., Zhou, G. Q., Zhang, D., & Hu, Y. (2023) · Cancer Gene Therapy · doi:10.1038/s41417-023-00614-1 · Cited by 22
Zhou, L., Zhong, Y., Wang, F., Guo, Y., Mao, R., Xie, H., Zhang, Y., & Li, J. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.90459 · Cited by 22
Social Environment and Epigenetics
Merrill, S. M., Gladish, N., & Kobor, M. S. (2019) · Current topics in behavioral neurosciences · doi:10.1007/7854_2019_114 · Cited by 24
Cell-to-cell variation in gene expression and the aging process
Mendenhall, A., Martin, G. M., Kaeberlein, M. R., & Anderson, R. M. (2021) · GeroScience · doi:10.1007/s11357-021-00339-9 · Cited by 23
Bellver‐Sanchís, A., Pallàs, M., & Griñán‐Ferré, C. (2021) · Epigenomes · doi:10.3390/epigenomes5020015 · Cited by 23
Zhang, H., Zhou, H., Shen, X. M., Lin, X., Zhang, Y., Sun, Y., Zhou, Y., Zhang, L., & Zhang, D. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1276707 · Cited by 25
Ferreira, F. J., Galhardo, M., Nogueira, J. M., Teixeira, J., Logarinho, E., & Bessa, J. (2025) · Nature Communications · doi:10.1038/s41467-025-57503-4 · Cited by 27
Nassir, C. M. N. C. M., Damodaran, T. K., Yusof, S. R., Norazit, A., Chilla, G. S. V. N., Huen, I., Nagaraja, B. P. K., Ibrahim, N. M., & Mustapha, M. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13081207 · Cited by 22
Balamurli, G., Liew, A. Q. X., Tee, W., & Pervaiz, S. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103441 · Cited by 23
Targeting chromatin aging - The epigenetic impact of longevity-associated interventions
Field, A. E., & Adams, P. D. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.12.010 · Cited by 22
Telomeric epigenetic response mediated by Gadd45a regulates stem cell aging and lifespan
Diao, D., Wang, H., Li, T., Shi, Z., Jin, X., Sperka, T., Zhu, X., Zhang, M., Yang, F., Cong, Y., et al. (2018) · EMBO Reports · doi:10.15252/embr.201745494 · Cited by 22
Gensous, N., Ravaioli, F., Pirazzini, C., Gramignoli, R., Ellis, E. C. S., Storci, G., Capri, M., Strom, S. C., Laconi, E., Franceschi, C., et al. (2020) · Nutrients · doi:10.3390/nu12020277 · Cited by 21
Rejuvenation by Partial Reprogramming of the Epigenome
Mendelsohn, A. R., Larrick, J. W., & Lei, J. L. (2017) · Rejuvenation Research · doi:10.1089/rej.2017.1958 · Cited by 22
Targeting the chromatin remodeler BAZ2B mitigates hepatic senescence and MASH fibrosis
Tu, C., Cheng, Q., Li, S., Lin, D.-Y., Liu, Z.-Y., Ouyang, W.-G., Kang, X.-L., Chen, F., Song, S., & Cai, S. (2025) · Nature Aging · doi:10.1038/s43587-025-00862-w · Cited by 21
Meta-epigenetic shifts in T cell aging and aging-related dysfunction
Rousseau, L., Hajdu, K. L., & Ho, P. (2025) · Journal of Biomedical Science · doi:10.1186/s12929-025-01146-6 · Cited by 21
Hiding in Plain Sight: Virtually Unrecognizable Memory Phenotype CD8+ T cells
Thiele, D., Gruta, N. L. L., Nguyen, A., & Hussain, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228626 · Cited by 23
Ghosh, I., Liu, C. S., Swardfager, W., Lanctôt, K. L., & Anderson, N. D. (2021) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2021.103683 · Cited by 20
Histone deacetylase 4 reverses cellular senescence via DDIT4 in dermal fibroblasts
Lee, Y., Song, M. J., Park, J. H., Shin, M. H., Kim, M., Hwang, D., Lee, D. H., & Chung, J. H. (2022) · Aging · doi:10.18632/aging.204118 · Cited by 20
Cheng, M.-D., Li, C., Pei, X.-Y., Zhang, Y., Jia, D., Zuo, Y.-B., Cai, S., Li, P., Xin, H., & Zhang, Y. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.115391 · Cited by 20
Fanjul, V., Jorge, I., Camafeita, E., Macías, Á., González‐Gómez, C., Barettino, A., Dorado, B., Andrés‐Manzano, M. J., Rivera, J., Vázquez, J., et al. (2020) · Aging Cell · doi:10.1111/acel.13203 · Cited by 21
Church, M. C., Workman, J. L., & Suganuma, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910274 · Cited by 19
Exploring Epigenetic Modifications as Potential Biomarkers and Therapeutic Targets in Glaucoma
Tonti, E., dell’Omo, R., Filippelli, M., Spadea, L., Salati, C., Gagliano, C., Musa, M., & Zeppieri, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052822 · Cited by 20
Aldehyde Dehydrogenase 2 (ALDH2) and Aging: Is There a Sensible Link?
Wu, N. N., & Ren, J. T. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-6260-6_15 · Cited by 19
Epigenetics and Vascular Senescence–Potential New Therapeutic Targets?
Ding, Q., Shao, C., Rose, P., & Zhu, Y. Z. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.535395 · Cited by 20
Influence of anaerobic and aerobic exercise on age-related pathways in skeletal muscle
Navas‐Enamorado, I., Bernier, M., Brea‐Calvo, G., & de Cabo, R. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.04.005 · Cited by 21
Regulating translation in aging: from global to gene-specific mechanisms
Solyga, M., Majumdar, A., & Besse, F. (2024) · EMBO Reports · doi:10.1038/s44319-024-00315-2 · Cited by 23
Comparative performance evaluation of bisulfite- and enzyme-based DNA conversion methods
Simons, R. B., Karkala, F., Kukk, M. M., Adams, H. H. H., Kayser, M., & Vidaki, A. (2025) · Clinical Epigenetics · doi:10.1186/s13148-025-01855-7 · Cited by 20
Metadata
- Authors
- Sen, P., Shah, P. P., Nativio, R., & Berger, S. L.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Berger, Shelley L.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2016-08
- Volume
- 166
- Issue
- 4
- Pages
- 822-839
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5821249
- OpenAlex
- W2517275410
- Cited by
- 956
- References
- 188
- Citations by year
- 2026: 76 · 2025: 96 · 2024: 111 · 2023: 116 · 2022: 97 · 2021: 128 · 2020: 113 · 2019: 87 · 2018: 76 · 2017: 51 · 2016: 5
- FWCI
- 7.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- American Heart Association
- National Institutes of Health (4r01ns078283-05)
- National Institute on Aging (P01AG031862)
- National Institute of Neurological Disorders and Stroke (R01-NS078283)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- aging, longevity, epigenetic mechanisms, chromatin signatures, age-related diseases, anti-aging therapeutics, druggable targets, invertebrate models, vertebrate models, tissue aging
- MeSH terms
- Aging, Animals, Histones, Humans, Longevity, DNA Methylation, Chromatin Assembly and Disassembly, Epigenesis, Genetic
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review