Horvath, Steve
Altos Labs
88 papers on CoChatORCID 0000-0002-4110-3589
Most cited papers
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LINE-1 RNA causes heterochromatin erosion and is a target for amelioration of senescent phenotypes in progeroid syndromes
Della Valle, F., Reddy, P., Yamamoto, M., Liu, P., Saera-Vila, A., Bensaddek, D., Zhang, H., Prieto Martinez, J., Abassi, L., Celii, M., et al. (2022) · Science Translational Medicine
Telomeres, Telomerase, and SenescenceNuclear Structure and Function
Cited by 127
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Incorporation of a nucleoside analog maps genome repair sites in postmitotic human neurons
Reid, D. A., Reed, P. J., Schlachetzki, J. C. M., Nitulescu, I. I., Chou, G., Tsui, E. C., Jones, J. R., Chandran, S., Lu, A. T., McClain, C. A., et al. (2021) · Science
DNA Repair MechanismsDNA and Nucleic Acid Chemistry
Cited by 121
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The organization of the transcriptional network in specific neuronal classes
Winden, K. D., Oldham, M. C., Mirnics, K., Ebert, P. J., Swan, C. H., Levitt, P., Rubenstein, J. L., Horvath, S., & Geschwind, D. H. (2009) · Molecular Systems Biology
Bioinformatics and Genomic NetworksDevelopmental Biology and Gene Regulation
Cited by 112
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Transposon-triggered innate immune response confers cancer resistance to the blind mole rat
Zhao, Y., Oreskovic, E., Zhang, Q., Lu, Q., Gilman, A., Lin, Y. S., He, J., Zheng, Z., Lu, J. Y., Lee, J., et al. (2021) · Nature Immunology
Genetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence
Cited by 99
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Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome
Tian, Y., Voineagu, I., Paşca, S. P., Won, H., Chandran, V., Horvath, S., Dolmetsch, R. E., & Geschwind, D. H. (2014) · Genome Medicine
Genetics and Neurodevelopmental DisordersIon channel regulation and function
Cited by 93
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Epigenetic ageing is distinct from senescence-mediated ageing and is not prevented by telomerase expression
Kabacik, S., Horvath, S., Cohen, H., & Raj, K. (2018) · Aging
Telomeres, Telomerase, and SenescenceEpigenetics and DNA Methylation
Cited by 68
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Increased epigenetic age in normal breast tissue from luminal breast cancer patients
Hofstatter, E. W., Horvath, S., Dalela, D., Gupta, P., Chagpar, A. B., Wali, V. B., Bossuyt, V., Storniolo, A. M., Hatzis, C., Patwardhan, G., et al. (2018) · Clinical Epigenetics
Epigenetics and DNA MethylationTelomeres, Telomerase, and Senescence
Cited by 64
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Human aging DNA methylation signatures are conserved but accelerated in cultured fibroblasts
Sturm, G., Cardenas, A., Bind, M.-A., Horvath, S., Wang, S., Wang, Y., Hägg, S., Hirano, M., & Picard, M. (2019) · Epigenetics
Epigenetics and DNA MethylationTelomeres, Telomerase, and Senescence
Cited by 61
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Synchrony and asynchrony between an epigenetic clock and developmental timing
Hoshino, A., Horvath, S., Sridhar, A., Chitsazan, A., & Reh, T. A. (2019) · Scientific Reports
Epigenetics and DNA MethylationGenetics, Aging, and Longevity in Model Organisms
Cited by 55
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Coffee Consumption Is Associated with DNA Methylation Levels of Human Blood
Chuang, Y.-H., Quach, A., Absher, D., Assimes, T., Horvath, S., & Ritz, B. (2017) · European Journal of Human Genetics
Epigenetics and DNA MethylationCoffee research and impacts
Cited by 40
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Umbilical cord plasma concentrate has beneficial effects on DNA methylation GrimAge and human clinical biomarkers
Clement, J., Yan, Q., Agrawal, M., Coronado, R. E., Sturges, J. A., Horvath, M., Lu, A. T., Brooke, R. T., & Horvath, S. (2022) · Aging Cell
Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model Organisms
Cited by 34
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DNA repair‐deficient premature aging models display accelerated epigenetic age
Perez, K., Parras, A., Picó, S., Rechsteiner, C., Haghani, A., Brooke, R., Mrabti, C., Schoenfeldt, L., Horvath, S., & Ocampo, A. (2024) · Aging Cell
Epigenetics and DNA MethylationGenetics, Aging, and Longevity in Model Organisms
Cited by 31
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Reversal of ageing- and injury-induced vision loss by Tet-dependent epigenetic reprogramming
Lu, Y., Krishnan, A., Brommer, B., Tian, X., Meer, M., Vera, D. L., Wang, C., Zeng, Q., Yu, D., Bonkowski, M. S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory)
Epigenetics and DNA MethylationRetinal Development and Disorders
Cited by 20
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Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging
Paine, P. T., Rechsteiner, C., Morandini, F., Desdín-Micó, G., Mrabti, C., Parras, A., Haghani, A., Brooke, R., Horvath, S., Seluanov, A., et al. (2024) · Frontiers in Aging
Pluripotent Stem Cells ResearchTelomeres, Telomerase, and Senescence
Cited by 13
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Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging
Paine, P. T., Rechsteiner, C., Morandini, F., Desdin Mico, G., Mrabti, C., Parras, A., Haghani, A., Brooke, R., Horvath, S., Seluanov, A., et al. (2023) · Frontiers in Aging
Pluripotent Stem Cells ResearchTelomeres, Telomerase, and Senescence
Cited by 13
- Verified
Divergent age-related methylation patterns in long and short-lived mammals
Haghani, A., Wang, N., Lu, A. T., Mozhui, K., Mammalian Methylation Consortium, Raj, K., Yang, X. W., & Horvath, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory)
Epigenetics and DNA MethylationGenetics, Aging, and Longevity in Model Organisms
Cited by 9
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