DNA methylation and epigenetic control of cellular differentiation

DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development

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

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

DNA methylation landscapes: Provocative insights from epigenomics

Suzuki, M. M., & Bird, A. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2341 · Cited by 3,039 · see citing works

Perceptions of epigenetics

Bird, A. (2007) · Nature · doi:10.1038/nature05913 · Cited by 3,011 · see citing works

Genome-Wide Evolutionary Analysis of Eukaryotic DNA Methylation

Zemach, A., McDaniel, I. E., Silva, P., & Zilberman, D. (2010) · Science · doi:10.1126/science.1186366 · Cited by 1,796 · see citing works

Inherited epigenetic variation — revisiting soft inheritance

Richards, E. J. (2006) · Nature reviews genetics · doi:10.1038/nrg1834 · Cited by 1,200 · see citing works

Cyclical DNA methylation of a transcriptionally active promoter

Métivier, R., Gallais, R., Tiffoche, C., Péron, C. L., Jurkowska, R., Carmouche, R. P., Ibberson, D., Baráth, P., Demay, F., Reid, G., et al. (2008) · Nature · doi:10.1038/nature06544 · Cited by 942 · see citing works

Nuclear Reprogramming of Somatic Cells After Fusion with Human Embryonic Stem Cells

Cowan, C. A., Atienza, J., Melton, D. A., & Eggan, K. C. (2005) · Science · doi:10.1126/science.1116447 · Cited by 932 · see citing works

Neuronal Activity–Induced Gadd45b Promotes Epigenetic DNA Demethylation and Adult Neurogenesis

Dengke, K., Jang, M., Guo, J. U., Kitabatake, Y., Chang, M.-L., Pow-anpongkul, N., Flavell, R. A., Lu, B., Ming, G., & Song, H. (2009) · Science · doi:10.1126/science.1166859 · Cited by 929 · see citing works

The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatin

Nagano, T., Mitchell, J. A., Sanz, L. A., Pauler, F. M., Ferguson‐Smith, A. C., Feil, R., & Fraser, P. (2008) · Science · doi:10.1126/science.1163802 · Cited by 907 · see citing works

Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency

Popp, C., Dean, W., Feng, S., Cokus, S. J., Andrews, S., Pellegrini, M. A., Jacobsen, S. E., & Reik, W. (2010) · Nature · doi:10.1038/nature08829 · Cited by 860 · see citing works

Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells

Stadtfeld, M., Apostolou, E., Akutsu, H., Fukuda, A., Follett, P., Natesan, S., Kono, T., Shioda, T., & Hochedlinger, K. (2010) · Nature · doi:10.1038/nature09017 · Cited by 801 · see citing works

Rethinking how DNA methylation patterns are maintained

Jones, P. A., & Liang, G. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2651 · Cited by 767 · see citing works

Gadd45a promotes epigenetic gene activation by repair-mediated DNA demethylation

Barreto, G., Schäfer, A., Marhold, J., Stach, D., Swaminathan, S. K., Handa, V., Doederlein, G., Maltry, N., Wu, W., Lyko, F., et al. (2007) · Nature · doi:10.1038/nature05515 · Cited by 753 · see citing works

Reprogramming towards pluripotency requires AID-dependent DNA demethylation

Bhutani, N., Brady Jennifer, J., Damian, M., Sacco, A., Corbel, S. Y., & Blau, H. M. (2009) · Nature · doi:10.1038/nature08752 · Cited by 676 · see citing works

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

Sahoo, T., del Gaudio, D., German, J. R., Shinawi, M. S., Peters, S. U., Person, R., Garnica, A. D., Cheung, S. W., & Beaudet, A. L. (2008) · Nature Genetics · doi:10.1038/ng.158 · Cited by 672 · see citing works

DNA Demethylation in Zebrafish Involves the Coupling of a Deaminase, a Glycosylase, and Gadd45

Rai, K., Huggins, I. J., James, S. R., Karpf, A. R., Jones, D. A., & Cairns, B. R. (2008) · Cell · doi:10.1016/j.cell.2008.11.042 · Cited by 657 · see citing works

Parental origin of sequence variants associated with complex diseases

DIAGRAM Consortium, Kong, A., Steinthorsdottir, V., Masson, G., Thorleifsson, G., Sulem, P., Besenbacher, S., Jonasdottir, A., Sigurdsson, A., Kristinsson, K. T., et al. (2009) · Nature · doi:10.1038/nature08625 · Cited by 553 · see citing works

DNA methylation protects hematopoietic stem cell multipotency from myeloerythroid restriction

Bröske, A.-M., Vockentanz, L., Kharazi, S., Huska, M. R., Mancini, E., Scheller, M., Kuhl, C., Enns, A., Prinz, M., Jaenisch, R., et al. (2009) · Nature Genetics · doi:10.1038/ng.463 · Cited by 478 · see citing works

The SRA domain of UHRF1 flips 5-methylcytosine out of the DNA helix

Hashimoto, H., Horton, J. R., Zhang, X., Bostick, M. L., Jacobsen, S. E., & Cheng, X. (2008) · Nature · doi:10.1038/nature07280 · Cited by 448 · see citing works

Promoter CpG Methylation Contributes to ES Cell Gene Regulation in Parallel with Oct4/Nanog, PcG Complex, and Histone H3 K4/K27 Trimethylation

Fouse, S. D., Shen, Y., Pellegrini, M. A., Cole, S. W., Meissner, A., Neste, L. V., Jaenisch, R., & Fan, G. (2008) · Cell stem cell · doi:10.1016/j.stem.2007.12.011 · Cited by 447 · see citing works

DNMT1 maintains progenitor function in self-renewing somatic tissue

Sen, G. L., Reuter, J., Webster, D. E., Zhu, L., & Khavari, P. A. (2010) · Nature · doi:10.1038/nature08683 · Cited by 423 · see citing works

Genomic patterns of DNA methylation: targets and function of an epigenetic mark

Weber, M., & Schübeler, D. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.04.011 · Cited by 387 · see citing works

DNA Methyltransferase 1 Is Essential for and Uniquely Regulates Hematopoietic Stem and Progenitor Cells

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

Isolation and Initial Characterization of a Novel Zinc Finger Gene, DNMT3L, on 21q22.3, Related to the Cytosine-5- Methyltransferase 3 Gene Family

Aapola, U., Shibuya, K., Scott, H. S., Ollila, J., Vihinen, M., Heino, M., Shintani, A., Kawasaki, K., Minoshima, S., Krohn, K. J. E., et al. (2000) · Genomics · doi:10.1006/geno.2000.6168 · Cited by 317 · see citing works

CDK4 coexpression with Ras generates malignant human epidermal tumorigenesis

Lazarov, M. E., Kubo, Y., Cai, T., Dajee, M., Tarutani, M., Lin, Q., Fang, M., Tao, S., Green, C. L., & Khavari, P. A. (2002) · Nature Medicine · doi:10.1038/nm779 · Cited by 201 · see citing works

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

Gaston, V., Bouc, Y. L., Soupre, V., Bürglen, L., Donadieu, J., Oro, H., Audry, G., Vazquez, M., & Gicquel, C. (2001) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200649 · Cited by 173 · see citing works

Mammalian Cytosine DNA Methyltransferase Dnmt1: Enzymatic Mechanism, Novel Mechanism-Based Inhibitors, and RNA-directed DNA Methylation

Svedružić, Ž. M. (2008) · Current Medicinal Chemistry · doi:10.2174/092986708783330700 · Cited by 57 · see citing works

DNA Cytosine Demethylation: Are We Getting Close?

Jiricny, J., & Menigatti, M. (2008) · Cell · doi:10.1016/j.cell.2008.12.008 · Cited by 32 · see citing works

DNA methylation arrays as surrogate measures of cell mixture distribution

Houseman, E. A., Accomando, W. P., Koestler, D. C., Christensen, B. C., Marsit, C. J., Nelson, H. H., Wiencke, J. K., & Kelsey, K. T. (2012) · BMC Bioinformatics · doi:10.1186/1471-2105-13-86 · Cited by 3,175 · see citing works

Reference-free cell mixture adjustments in analysis of DNA methylation data

Houseman, E. A., Molitor, J., & Marsit, C. J. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu029 · Cited by 441 · see citing works

Epigenetics and depression

Penner-Goeke, S., & Binder, E. B. (2019) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2019.21.4/ebinder · Cited by 254 · see citing works

Reference-free deconvolution of DNA methylation data and mediation by cell composition effects

Houseman, E. A., Kile, M. L., Christiani, D. C., Ince, T. A., Kelsey, K. T., & Marsit, C. J. (2016) · BMC Bioinformatics · doi:10.1186/s12859-016-1140-4 · Cited by 249 · see citing works

Genome-wide promoter DNA methylation dynamics of human hematopoietic progenitor cells during differentiation and aging

Bocker, M., Hellwig, I., Breiling, A., Eckstein, V., Ho, A. D., & Lyko, F. (2011) · Blood · doi:10.1182/blood-2011-01-331926 · Cited by 195 · see citing works

Cell-type deconvolution from DNA methylation: a review of recent applications

Titus, A., Gallimore, R. M., Salas, L. A., & Christensen, B. C. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx275 · Cited by 185 · see citing works

Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence

Mulder, R. H., Neumann, A., Cecil, C. A. M., Walton, E., Houtepen, L. C., Simpkin, A. J., Rijlaarsdam, J., Heijmans, B. T., Gaunt, T. R., Felix, J. F., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddaa280 · Cited by 165 · see citing works

Human Genetic Adaptation to High Altitude: Evidence from the Andes

Julian, C. G., & MOORE, L. G. (2019) · Genes · doi:10.3390/genes10020150 · Cited by 162 · see citing works

An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies

McGregor, K., Bernatsky, S., Colmegna, I., Hudson, M., Pastinen, T., Labbe, A., & Greenwood, C. M. T. (2016) · Genome biology · doi:10.1186/s13059-016-0935-y · Cited by 150 · see citing works

Determination of DNA and RNA Methylation in Circulating Tumor Cells by Mass Spectrometry

Huang, W., Qi, C.-B., Lv, S.-W., Xie, M., Feng, Y., Huang, W., & Yuan, B. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b03962 · Cited by 148 · see citing works

DNA Methylation in Whole Blood: Uses and Challenges

Houseman, E. A., Kim, S., Kelsey, K. T., & Wiencke, J. K. (2015) · Current Environmental Health Reports · doi:10.1007/s40572-015-0050-3 · Cited by 147 · see citing works

Quantitative reconstruction of leukocyte subsets using DNA methylation

Accomando, W. P., Wiencke, J. K., Houseman, E. A., Nelson, H. H., & Kelsey, K. T. (2014) · Genome biology · doi:10.1186/gb-2014-15-3-r50 · Cited by 147 · see citing works

Leishmania donovani Infection Causes Distinct Epigenetic DNA Methylation Changes in Host Macrophages

Marr, A. K., MacIsaac, J. L., Jiang, R., Airo, A. M., Kobor, M. S., & McMaster, W. R. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004419 · Cited by 126 · see citing works

Epigenetic Regulation of Gene Expression in Keratinocytes

Botchkarev, V. A., Gdula, M. R., Mardaryev, A. N., Sharov, A. A., & Fessing, M. Y. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2012.182 · Cited by 127 · see citing works

Cell-composition effects in the analysis of DNA methylation array data: a mathematical perspective

Houseman, E. A., Kelsey, K. T., Wiencke, J. K., & Marsit, C. J. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0527-y · Cited by 123 · see citing works

Divergent cytosine DNA methylation patterns in single‐cell, soybean root hairs

Hossain, M. S., Kawakatsu, T., Kim, K. D., Zhang, N., Nguyen, C. T., Khan, S. M., Batek, J. M., Joshi, T., Schmutz, J., Grimwood, J., et al. (2017) · New Phytologist · doi:10.1111/nph.14421 · Cited by 101 · see citing works

Saliva cell type DNA methylation reference panel for epidemiological studies in children

Middleton, L. Y. M., Dou, J., Fisher, J., Heiss, J. A., Nguyen, V. K., Just, A. C., Faul, J. D., Ware, E. B., Mitchell, C. M., Colacino, J. A., et al. (2021) · Epigenetics · doi:10.1080/15592294.2021.1890874 · Cited by 87 · see citing works

DNA Methylation in Zebrafish

Goll, M. G., & Halpern, M. E. (2011) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-387685-0.00005-6 · Cited by 87 · see citing works

Methylation Dynamics of RASSF1A and Its Impact on Cancer

Malpeli, G., Innamorati, G., Decimo, I., Bencivenga, M., Kamdje, A. H. N., Perris, R., & Bassi, C. (2019) · Cancers · doi:10.3390/cancers11070959 · Cited by 79 · see citing works

Epigenetics and Autoimmune Diseases

Quintero-Ronderos, P., & Montoya-Ortiz, G. (2012) · Autoimmune Diseases · doi:10.1155/2012/593720 · Cited by 79 · see citing works

Protective effect of quercetin, EGCG, catechin and betaine against oxidative stress induced by ethanol in vitro

Oliva, J., Bardag‐Gorce, F., Tillman, B. C., & French, S. W. (2011) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2011.02.006 · Cited by 77 · see citing works

Epigenomics and human adaptation to high altitude

Julian, C. G. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00351.2017 · Cited by 75 · see citing works

CK19 and Glypican 3 Expression Profiling in the Prognostic Indication for Patients with HCC after Surgical Resection

Feng, J., Zhu, R., Chang, C. H., Yu, L., Cao, F., Zhu, G., Chen, F., Xia, H., Lv, F., Zhang, S., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151501 · Cited by 73 · see citing works

The mechanisms and potential of stem cell therapy for penile fibrosis

Milenkovic, U., Albersen, M., & Castiglione, F. (2018) · Nature reviews. Urology · doi:10.1038/s41585-018-0109-7 · Cited by 61 · see citing works

Impacts of air pollution, temperature, and relative humidity on leukocyte distribution: An epigenetic perspective

Gao, X., Colicino, E., Shen, J., Kioumourtzoglou, M.-A., Just, A. C., Nwanaji‐Enwerem, J. C., Coull, B. A., Lin, X., Vokonas, P., Zheng, Y., et al. (2019) · Environment International · doi:10.1016/j.envint.2019.02.053 · Cited by 68 · see citing works

Deconvolution of cellular subsets in human tissue based on targeted DNA methylation analysis at individual CpG sites

Schmidt, M. F., Maié, T., Dahl, E., Costa, I. G., & Wagner, W. (2020) · BMC Biology · doi:10.1186/s12915-020-00910-4 · Cited by 67 · see citing works

Epigenetics and developmental plasticity across species

Champagne, F. A. (2012) · Developmental Psychobiology · doi:10.1002/dev.21036 · Cited by 68 · see citing works

Cbx4 maintains the epithelial lineage identity and cell proliferation in the developing stratified epithelium

Mardaryev, A. N., Liu, B., Rapisarda, V., Poterlowicz, K., Malashchuk, I., Rudolf, J., Sharov, A. A., Jahoda, C. A. B., Fessing, M. Y., Benitah, S. A., et al. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201506065 · Cited by 67 · see citing works

HOME: a histogram based machine learning approach for effective identification of differentially methylated regions

Srivastava, A., Karpievitch, Y. V., Eichten, S. R., Borevitz, J., & Lister, R. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-2845-y · Cited by 62 · see citing works

The Epigenetic Regulation of Wound Healing

Lewis, C. J., Mardaryev, A. N., Sharov, A. A., Fessing, M. Y., & Botchkarev, V. A. (2014) · Advances in Wound Care · doi:10.1089/wound.2014.0522 · Cited by 62 · see citing works

Decreased NK Cells in Patients with Head and Neck Cancer Determined in Archival DNA

Accomando, W. P., Wiencke, J. K., Houseman, E. A., Butler, R. A., Zheng, S., Nelson, H. H., & Kelsey, K. T. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-12-1008 · Cited by 60 · see citing works

Multi-omic underpinnings of epigenetic aging and human longevity

Mavromatis, L. A., Rosoff, D. B., Bell, A. S., Jung, J., Wagner, J., & Lohoff, F. W. (2023) · Nature Communications · doi:10.1038/s41467-023-37729-w · Cited by 61 · see citing works

The Yin and Yang of Chromatin Dynamics In Stem Cell Fate Selection

Adam, R. C., & Fuchs, E. V. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.11.002 · Cited by 58 · see citing works

Epigenetic Mechanisms of Epidermal Differentiation

Moltrasio, C., Romagnuolo, M., & Marzano, A. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094874 · Cited by 57 · see citing works

Pregnancy-Induced Noncoding RNA (PINC) Associates with Polycomb Repressive Complex 2 and Regulates Mammary Epithelial Differentiation

Shore, A. N., Kabotyanski, E. B., Roarty, K. P., Smith, M. A., Zhang, Y., Creighton, C. J., Dinger, M. E., & Rosen, J. M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002840 · Cited by 56 · see citing works

An Exploratory Association Study of Alcohol Use Disorder and DNA Methylation

Hagerty, S. L., Bidwell, L. C., Harlaar, N., & Hutchison, K. E. (2016) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13138 · Cited by 54 · see citing works

Genopolitics and the Science of Genetics

CHARNEY, E., & ENGLISH, W. (2013) · American Political Science Review · doi:10.1017/s0003055413000099 · Cited by 51 · see citing works

Epigenetic Mechanisms in DNA Double Strand Break Repair: A Clinical Review

Fernandez, A., O’Leary, C. G., O'Byrne, K. J., Burgess, J. T., Richard, D. J., & Suraweera, A. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.685440 · Cited by 51 · see citing works

A comparison of DNA methylation specific droplet digital PCR (ddPCR) and real time qPCR with flow cytometry in characterizing human T cells in peripheral blood

Wiencke, J. K., Bracci, P. M., Hsuang, G., Zheng, S., Hansen, H. M., Wrensch, M., Rice, T., Eliot, M., & Kelsey, K. T. (2014) · Epigenetics · doi:10.4161/15592294.2014.967589 · Cited by 51 · see citing works

Cell Types in Environmental Epigenetic Studies: Biological and Epidemiological Frameworks

Campbell, K. A., Colacino, J. A., Park, S. K., & Bakulski, K. M. (2020) · Current Environmental Health Reports · doi:10.1007/s40572-020-00287-0 · Cited by 44 · see citing works

EGLN2 DNA methylation and expression interact with HIF1A to affect survival of early-stage NSCLC

Zhang, R., Lai, L., He, J., Chen, C., You, D., Duan, W., Dong, X., Zhu, Y., Lin, L., Shen, S., et al. (2019) · Epigenetics · doi:10.1080/15592294.2019.1573066 · Cited by 50 · see citing works

Epigenetic Regulation of Epidermal DifferentiationPreprint

Perdigoto, C. N., Valdés, V. J., Bardot, E., & Ezhkova, E. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a015263 · Cited by 50 · see citing works

Epigenetic clocks in the pediatric population: when and why they tick?

Wang, J., & Zhou, W. (2021) · Chinese Medical Journal · doi:10.1097/cm9.0000000000001723 · Cited by 47 · see citing works

Cancer Is to Embryology as Mutation Is to Genetics: Hypothesis of the Cancer as Embryological Phenomenon

Cofré, J., & Abdelhay, E. S. F. W. (2017) · The Scientific World JOURNAL · doi:10.1155/2017/3578090 · Cited by 42 · see citing works

Argonaute 4 as an Effector Protein in RNA-Directed DNA Methylation in Human Cells

Chalertpet, K., Pin-on, P., Aporntewan, C., Patchsung, M., Ingrungruanglert, P., Israsena, N., & Mutirangura, A. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00645 · Cited by 43 · see citing works

Epigenetic control in skin development, homeostasis and injury repair

Kang, S., Chovatiya, G. L., & Tumbar, T. (2019) · Experimental Dermatology · doi:10.1111/exd.13872 · Cited by 43 · see citing works

Microfluidics for genome-wide studies involving next generation sequencing

Ma, S., Murphy, T. W., & Lu, C. (2017) · Biomicrofluidics · doi:10.1063/1.4978426 · Cited by 41 · see citing works

Large intestine embryogenesis: Molecular pathways and related disorders (Review)

Kostouros, A., Koliarakis, I., Natsis, K. S., Spandidos, D. A., Tsatsakis, A. M., & Tsiaoussis, J. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4583 · Cited by 44 · see citing works

Locus-Specific Differential DNA Methylation and Urinary Arsenic: An Epigenome-Wide Association Study in Blood among Adults with Low-to-Moderate Arsenic Exposure

Bozack, A. K., Domingo‐Relloso, A., Haack, K., Gamble, M. V., Téllez-Plaza, M., Umans, J. G., Best, L. G., Yracheta, J., Gribble, M. O., Cárdenas, A., et al. (2020) · Environmental Health Perspectives · doi:10.1289/ehp6263 · Cited by 42 · see citing works

Empirical comparison of reduced representation bisulfite sequencing and Infinium BeadChip reproducibility and coverage of DNA methylation in humans

Carmona, J. J., Accomando, W. P., Binder, A. M., Hutchinson, J. N., Pantano, L., Izzi, B., Just, A. C., Lin, X., Schwartz, J. D., Vokonas, P., et al. (2017) · npj Genomic Medicine · doi:10.1038/s41525-017-0012-9 · Cited by 41 · see citing works

Linking Prenatal Environmental Exposures to Lifetime Health with Epigenome-Wide Association Studies: State-of-the-Science Review and Future Recommendations

Bakulski, K. M., Blostein, F., & London, S. J. (2023) · Environmental Health Perspectives · doi:10.1289/ehp12956 · Cited by 38 · see citing works

PDGFRβ Expression and Function in Fibroblasts Derived from Pluripotent Cells is Linked to DNA Demethylation

Hewitt, K. J., Shamis, Y., Knight, E. B., Smith, A., Maione, A. G., Alt‐Holland, A., Sheridan, S. D., Haggarty, S. J., & Garlick, J. A. (2012) · Journal of Cell Science · doi:10.1242/jcs.099192 · Cited by 38 · see citing works

Recent Advances in Genetic and Epigenetic Modulation of Animal Exposure to High Temperature

Wu, J., Zhang, W., & Li, C. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00653 · Cited by 36 · see citing works

A Role for Epigenetics in Psoriasis: Methylated Cytosine–Guanine Sites Differentiate Lesional from Nonlesional Skin and from Normal Skin

Gudjonsson, J. E., & Krueger, G. G. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.364 · Cited by 34 · see citing works

Alcohol abuse and cigarette smoking are associated with global DNA hypermethylation: Results from the German Investigation on Neurobiology in Alcoholism (GINA)

Semmler, A., Heese, P., Stoffel‐Wagner, B., Muschler, M. A. N., Heberlein, A., Bigler, L., Prost, J., Frieling, H., Kornhuber, J., Banger, M., et al. (2015) · Alcohol · doi:10.1016/j.alcohol.2015.01.004 · Cited by 32 · see citing works

Neurons versus Networks: The Interplay between Individual Neurons and Neural Networks in Cognitive Functions

Arshavsky, Y. I. (2016) · The Neuroscientist · doi:10.1177/1073858416670124 · Cited by 31 · see citing works

Cellular reprogramming to reset epigenetic signatures

Hewitt, K. J., & Garlick, J. A. (2012) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2012.08.002 · Cited by 30 · see citing works

Unsupervised deep learning with variational autoencoders applied to breast tumor genome-wide DNA methylation data with biologic feature extractionPreprint

Titus, A., Wilkins, O. M., Bobak, C. A., & Christensen, B. C. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/433763 · Cited by 30 · see citing works

Methylation in MAD1L1 is associated with the severity of suicide attempt and phenotypes of depression

Sokolov, A. V., Manu, D.-M., Nordberg, D. O. T., Boström, A. E. D., Jokinen, J., & Schiöth, H. B. (2023) · Clinical Epigenetics · doi:10.1186/s13148-022-01394-5 · Cited by 29 · see citing works

Epigenomics, Pharmacoepigenomics, and Personalized Medicine in Cervical Cancer

Kabekkodu, S. P., Chakrabarty, S., Ghosh, S., Brand, A. M., & Satyamoorthy, K. (2017) · Public Health Genomics · doi:10.1159/000475804 · Cited by 29 · see citing works

A review of epigenetic regulation in wound healing: Implications for the future of wound care

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Epigenetic and metabolic regulation of epidermal homeostasis

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