The Emerging Field of Neuroepigenetics

Translating the Histone Code

Jenuwein, T., & Allis, C. D. (2001) · Science · doi:10.1126/science.1063127 · Cited by 9,756 · see citing works

The language of covalent histone modifications

Strahl, B. D., & Allis, C. D. (2000) · Nature · doi:10.1038/47412 · Cited by 8,679 · see citing works

DNA methylation patterns and epigenetic memory

Bird, A. (2002) · Genes & Development · doi:10.1101/gad.947102 · Cited by 7,124 · see citing works

Epigenetic programming by maternal behavior

Weaver, I. C. G., Cervoni, N., Champagne, F. A., D'Alessio, A. C., Sharma, S., Seckl, J. R., Dymov, S., Szyf, M., & Meaney, M. J. (2004) · Nature Neuroscience · doi:10.1038/nn1276 · Cited by 6,177 · see citing works

Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1

Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836 · see citing works

Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine

Ito, S., Shen, L., Dai, Q., Wu, S. C., Collins, L. B., Swenberg, J. A., He, C., & Zhang, Y. (2011) · Science · doi:10.1126/science.1210597 · Cited by 3,451 · see citing works

The Nuclear DNA Base 5-Hydroxymethylcytosine Is Present in Purkinje Neurons and the Brain

Kriaucionis, S., & Heintz, N. (2009) · Science · doi:10.1126/science.1169786 · Cited by 2,700 · see citing works

Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification

Ito, S., D’Alessio, A. C., Taranova, O., Hong, K., Sowers, L. C., & Zhang, Y. (2010) · Nature · doi:10.1038/nature09303 · Cited by 2,542 · see citing works

Combinatorial patterns of histone acetylations and methylations in the human genome

Wang, Z., Zang, C., Rosenfeld, J. A., Schones, D. E., Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Peng, W., Zhang, M. Q., et al. (2008) · Nature Genetics · doi:10.1038/ng.154 · Cited by 2,331 · see citing works

Global epigenomic reconfiguration during mammalian brain development

Lister, R., Mukamel, E. A., Nery, J. R., Urich, M., Puddifoot, C. A., Johnson, N. D., Lucero, J., Huang, Y., Dwork, A. J., Schultz, M. D., et al. (2013) · Science · doi:10.1126/science.1237905 · Cited by 1,830 · see citing works

Hydroxylation of 5-Methylcytosine by TET1 Promotes Active DNA Demethylation in the Adult Brain

Guo, J. U., Su, Y., Zhong, C., Ming, G., & Song, H. (2011) · Cell · doi:10.1016/j.cell.2011.03.022 · Cited by 1,355 · see citing works

Lasting epigenetic influence of early-life adversity on the BDNF gene

Roth, T. L., Lubin, F. D., Funk, A. J., & Sweatt, J. D. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.11.028 · Cited by 1,273 · see citing works

Recovery of learning and memory is associated with chromatin remodelling

Fischer, A., Sananbenesi, F., Wang, X., Dobbin, M., & Tsai, L.-H. (2007) · Nature · doi:10.1038/nature05772 · Cited by 1,227 · see citing works

Covalent Modification of DNA Regulates Memory Formation

Miller, C. A., & Sweatt, J. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.022 · Cited by 1,180 · see citing works

Epigenetic Reprogramming in Plant and Animal Development

Feng, S., Jacobsen, S. E., & Reik, W. (2010) · Science · doi:10.1126/science.1190614 · Cited by 1,171 · see citing works

Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons

Feng, J., Zhou, Y., Campbell, S. L., Le, T., Li, E., Sweatt, J. D., Silva, A. J., & Fan, G. (2010) · Nature Neuroscience · doi:10.1038/nn.2514 · Cited by 1,019 · see citing works

New nomenclature for chromatin-modifying enzymes

Allis, C. D., Berger, S. L., Cote, J., Dent, S., Jenuwien, T., Kouzarides, T., Pillus, L., Reinberg, D., Shi, Y., Shiekhattar, R., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.039 · Cited by 957 · see citing works

Altered Histone Acetylation Is Associated with Age-Dependent Memory Impairment in Mice

Peleg, S., Sananbenesi, F., Zovoilis, A., Burkhardt, S., Bahari-Javan, S., Agis-Balboa, R. C., Cota, P., Wittnam, J. L., Gogol-Doering, A., Opitz, L., et al. (2010) · Science · doi:10.1126/science.1186088 · Cited by 951 · see citing works

Molecular Signals of Epigenetic States

Bonasio, R., Tu, S., & Reinberg, D. (2010) · Science · doi:10.1126/science.1191078 · Cited by 912 · see citing works

Reversal of maternal programming of stress responses in adult offspring through methyl supplementation: altering epigenetic marking later in life

Weaver, I. C. G., Champagne, F. A., Brown, S. E., Dymov, S., Sharma, S., Meaney, M. J., & Szyf, M. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3652-05.2005 · Cited by 905 · 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

Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation

Jiang, Y.-H., Armstrong, D., Albrecht, U., Atkins, C. M., Noebels, J. L., Eichele, G., Sweatt, J. D., & Beaudet, A. L. (1998) · Neuron · doi:10.1016/s0896-6273(00)80596-6 · Cited by 852 · see citing works

Histones: annotating chromatin

Campos, E. I., & Reinberg, D. (2009) · Annual Review of Genetics · doi:10.1146/annurev.genet.032608.103928 · Cited by 852 · see citing works

Epigenetic Regulation of <i>bdnf</i> Gene Transcription in the Consolidation of Fear Memory

Lubin, F. D., Roth, T. L., & Sweatt, J. D. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1786-08.2008 · Cited by 793 · 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

Inhibitors of Class 1 Histone Deacetylases Reverse Contextual Memory Deficits in a Mouse Model of Alzheimer's Disease

Kilgore, M., Miller, C. A., Fass, D. M., Hennig, K. M., Haggarty, S. J., Sweatt, J. D., & Rumbaugh, G. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.197 · Cited by 727 · see citing works

Therapeutic application of histone deacetylase inhibitors for central nervous system disorders

Kazantsev, A. G., & Thompson, L. M. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2681 · Cited by 715 · see citing works

Epigenetics: A Historical Overview

Holliday, R. (2006) · Epigenetics · doi:10.4161/epi.1.2.2762 · Cited by 712 · see citing works

Epigenetics as a unifying principle in the aetiology of complex traits and diseases

Petronis, A. (2010) · Nature · doi:10.1038/nature09230 · Cited by 682 · see citing works

Neuronal activity modifies the DNA methylation landscape in the adult brain

Guo, J. U., Ma, D. K., Mo, H., Ball, M. P., Jang, M.-H., Bonaguidi, M. A., Balazer, J. A., Eaves, H. L., Xie, B., Ford, E., et al. (2011) · Nature Neuroscience · doi:10.1038/nn.2900 · Cited by 669 · see citing works

The Language of Histone Crosstalk

Lee, J., Smith, E. R., & Shilatifard, A. (2010) · Cell · doi:10.1016/j.cell.2010.08.011 · Cited by 598 · see citing works

High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

Gregg, C., Zhang, J., Weissbourd, B., Luo, S., Schroth, G. P., Haig, D., & Dulac, C. (2010) · Science · doi:10.1126/science.1190830 · Cited by 591 · see citing works

A Role for Neuronal piRNAs in the Epigenetic Control of Memory-Related Synaptic Plasticity

Rajasethupathy, P., Antonov, I., Sheridan, R., Frey, S., Sander, C., Tuschl, T., & Kandel, E. R. (2012) · Cell · doi:10.1016/j.cell.2012.02.057 · Cited by 566 · see citing works

From neural development to cognition: unexpected roles for chromatin

Ronan, J. L., Wu, W., & Crabtree, G. R. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3413 · Cited by 544 · see citing works

Decoding the Epigenetic Language of Neuronal Plasticity

Borrelli, E., Nestler, E. J., Allis, C. D., & Sassone‐Corsi, P. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.012 · Cited by 529 · see citing works

Cortical DNA methylation maintains remote memory

Miller, C. A., Gavin, C. F., White, J. A., Parrish, R. R., Honasoge, A., Yancey, C. R., Rivera, I. M., Rubio, M. D., Rumbaugh, G., & Sweatt, J. D. (2010) · Nature Neuroscience · doi:10.1038/nn.2560 · Cited by 520 · see citing works

Epigenetic mechanisms in cognition

Day, J. J., & Sweatt, J. D. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.019 · Cited by 510 · see citing works

Epigenetic mechanisms mediating the long-term effects of maternal care on development

Champagne, F. A., & Curley, J. P. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.10.009 · Cited by 504 · see citing works

DNA methylation and memory formation

Day, J. J., & Sweatt, J. D. (2010) · Nature Neuroscience · doi:10.1038/nn.2666 · Cited by 488 · see citing works

A mechanism for memory storage insensitive to molecular turnover: a bistable autophosphorylating kinase.

Lisman, J. E. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.9.3055 · Cited by 475 · see citing works

The many faces of REST oversee epigenetic programming of neuronal genes

Ballas, N., & Mandel, G. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.08.015 · Cited by 441 · see citing works

Tet1 Is Critical for Neuronal Activity-Regulated Gene Expression and Memory Extinction

Rudenko, A., Dawlaty, M. M., Seo, J., Cheng, A. W., Meng, J., Le, T. T., Faull, K. F., Jaenisch, R., & Tsai, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.003 · Cited by 435 · see citing works

TET1 Controls CNS 5-Methylcytosine Hydroxylation, Active DNA Demethylation, Gene Transcription, and Memory Formation

Kaas, G. A., Zhong, C., Eason, D. E., Ross, D. L., Vachhani, R., Ming, G., King, J. R., Song, H., & Sweatt, J. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.032 · Cited by 411 · see citing works

Defining an epigenetic code

Turner, B. M. (2007) · Nature Cell Biology · doi:10.1038/ncb0107-2 · Cited by 392 · see citing works

Neurobiology: Memory and molecular turnover

Crick, F. (1984) · Nature · doi:10.1038/312101a0 · Cited by 392 · see citing works

Early Tagging of Cortical Networks Is Required for the Formation of Enduring Associative Memory

Lesburguères, E., Gobbo, O. L., Alaux‐Cantin, S., Hambücken, A., Trifilieff, P., & Bontempi, B. (2011) · Science · doi:10.1126/science.1196164 · Cited by 390 · see citing works

Epigenetic mechanisms in drug addiction

Renthal, W. R., & Nestler, E. J. (2008) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2008.06.004 · Cited by 383 · see citing works

Epigenetics, DNA Methylation, and Chromatin Modifying Drugs

Moshe Szyf, A. (2008) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-061008-103102 · Cited by 372 · see citing works

Sex-Specific Parent-of-Origin Allelic Expression in the Mouse Brain

Gregg, C. J., Zhang, J., Butler, J. E., Haig, D., & Dulac, C. G. (2010) · Science · doi:10.1126/science.1190831 · Cited by 347 · see citing works

Experience-Dependent Epigenetic Modifications in the Central Nervous System

Sweatt, J. D. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.09.002 · Cited by 302 · see citing works

Brain function and chromatin plasticity

Dulac, C. G. (2010) · Nature · doi:10.1038/nature09231 · Cited by 299 · see citing works

Rescue of aging-associated decline in Dnmt3a2 expression restores cognitive abilities

Oliveira, A. M. M., Hemstedt, T. J., & Bading, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3151 · Cited by 289 · see citing works

The Persistence of Long-Term Memory

Bailey, C. H., Kandel, E. R., & Si, K. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.017 · Cited by 277 · see citing works

Generation of neuronal variability and complexity

Muotri, A. R., & Gage, F. H. (2006) · Nature · doi:10.1038/nature04959 · Cited by 271 · see citing works

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse

Tate, P., Skarnes, W., & Bird, A. (1996) · Nature Genetics · doi:10.1038/ng0296-205 · Cited by 231 · see citing works

Epigenetic Alterations Are Critical for Fear Memory Consolidation and Synaptic Plasticity in the Lateral Amygdala

Monsey, M. S., Ota, K. T., Akingbade, I. F., Hong, E. S., & Schafe, G. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019958 · Cited by 215 · see citing works

DNA Methylation Regulates Cocaine-Induced Behavioral Sensitization in Mice

Anier, K., Malinovskaja, K., Aonurm‐Helm, A., Zharkovsky, A., & Kalda, A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.128 · Cited by 214 · see citing works

Reversing Neurodevelopmental Disorders in Adults

Ehninger, D., Li, W., Fox, K., Stryker, M. P., & Silva, A. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.007 · Cited by 196 · see citing works

Memory: Epigenetic mechanisms: a common theme in vertebrate and invertebrate memory formation

Levenson, J. M., & Sweatt, J. D. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-6026-6 · Cited by 178 · see citing works

MicroRNAs: regulators of neuronal fate

Sun, A. X., Crabtree, G. R., & Yoo, A. S. J. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2012.12.007 · Cited by 176 · see citing works

Epigenetic inheritance of cell differentiation status

Ng, R. K., & Gurdon, J. B. (2008) · Cell Cycle · doi:10.4161/cc.7.9.5791 · Cited by 166 · see citing works

Molecular Neurobiology of Human Cognition

Weeber, E. J., & Sweatt, J. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00634-7 · Cited by 145 · see citing works

Transgenerational Epigenetic Effects on Brain Functions

Bohacek, J., Gapp, K., Saab, B. J., & Mansuy, I. M. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.08.019 · Cited by 138 · see citing works

Epigenetic tête-à-tête: the bilateral relationship between chromatin modifications and DNA methylationThis paper is one of a selection of papers published in this Special Issue, entitled 27th International West Coast Chromatin and Chromosome Conference, and has undergone the Journal's usual peer review process.

D’Alessio, A. C., & Moshe Szyf, A. (2006) · Biochemistry and Cell Biology · doi:10.1139/o06-090 · Cited by 137 · see citing works

Epigenetic Mechanisms in Memory and Synaptic Function

Sultan, F. A., & Day, J. J. (2011) · Epigenomics · doi:10.2217/epi.11.6 · Cited by 131 · see citing works

Combinatorial chromatin modifications and memory storage: A code for memory?: Figure 1.Preprint

Wood, M. A., Hawk, J. D., & Abel, T. G. (2006) · Learning & Memory · doi:10.1101/lm.278206 · Cited by 110 · see citing works

Is there an Epigenetic Component in Long-term Memory?

Holliday, R. (1999) · Journal of Theoretical Biology · doi:10.1006/jtbi.1999.0995 · Cited by 109 · see citing works

New mechanisms in memory storage: piRNAs and epigenetics

Landry, C. D., Kandel, E. R., & Rajasethupathy, P. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.05.004 · Cited by 95 · see citing works

The prima donna of epigenetics: the regulation of gene expression by DNA methylation

Santos, K. F., Mazzola, T. N., & Carvalho, H. F. (2005) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2005001000010 · Cited by 80 · see citing works

Every methyl counts – Epigenetic calculus

Scharf, A. N. D., & Imhof, A. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.11.029 · Cited by 37 · see citing works

Lost in translation. New unexplored avenues for neuropsychopharmacology: epigenetics and microRNAs

Tardito, D., Mallei, A., & Popoli, M. (2012) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2013.749237 · Cited by 37 · see citing works

A Possible Epigenetic Mechanism for the Persistence of MemoryPreprint

SI, K., Lindquist, S., & Kandel, E. R. (2004) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2004.69.497 · Cited by 18 · see citing works

Epigenetic Regulation in the Nervous System

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Editing DNA Methylation in the Mammalian Genome

Liu, X. S., Wu, H., Ji, X., Stelzer, Y., Wu, X., Czauderna, S., Shu, J., Dadon, D., Young, R. A., & Jaenisch, R. (2016) · Cell · doi:10.1016/j.cell.2016.08.056 · Cited by 1,224 · see citing works

&lt;p&gt;Alzheimer’s disease: pathogenesis, diagnostics, and therapeutics&lt;/p&gt;

Tiwari, S., Atluri, V., Kaushik, A., Yndart, A., & Nair, M. (2019) · International Journal of Nanomedicine · doi:10.2147/ijn.s200490 · Cited by 1,308 · see citing works

The neuropharmacology of butyrate: the bread and butter of the microbiota-gut-brain axis

Stilling, R. M., van de Wouw, M., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.011 · Cited by 891 · see citing works

Microbial genes, brain &amp; behaviour – epigenetic regulation of the gut–brain axis

Stilling, R. M., Dinan, T. G., & Cryan, J. F. (2014) · Genes, Brain and Behavior · doi:10.1111/gbb.12109 · Cited by 637 · see citing works

Epigenetic and transgenerational reprogramming of brain development

Bale, T. L. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3818 · Cited by 505 · see citing works

Human cognitive aging: <i>Corriger la fortune?</i>

Lindenberger, U. (2014) · Science · doi:10.1126/science.1254403 · Cited by 414 · see citing works

Epigenetic mechanisms of chronic pain

Descalzi, G., Ikegami, D., Ushijima, T., Nestler, E. J., Zachariou, V., & Narita, M. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.02.001 · Cited by 390 · see citing works

Epigenetics of Stress-Related Psychiatric Disorders and Gene × Environment Interactions

Klengel, T., & Binder, E. B. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.036 · Cited by 353 · see citing works

DNA methylation changes in plasticity genes accompany the formation and maintenance of memory

Halder, R., Hennion, M., Vidal, R. O., Shomroni, O., Rahman, R.-U., Rajput, A., Centeno, T. P., van Bebber, F., Capece, V., Vizcaino, J. C. G., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4194 · Cited by 358 · see citing works

The emerging field of epigenetics in neurodegeneration and neuroprotection

Hwang, J.-Y., Aromolaran, K. A., & Zukin, R. S. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.46 · Cited by 343 · see citing works

Neural plasticity and behavior – sixty years of conceptual advances

Sweatt, J. D. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13580 · Cited by 341 · see citing works

Neuroimmunology and neuroepigenetics in the establishment of sex differences in the brain

McCarthy, M., Nugent, B. M., & Lenz, K. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.61 · Cited by 256 · see citing works

Applications of CRISPR–Cas systems in neuroscience

Heidenreich, M., & Zhang, F. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn.2015.2 · Cited by 282 · see citing works

Neuronal activity modifies the chromatin accessibility landscape in the adult brain

Su, Y., Shin, J., Zhong, C., Wang, S. Z., Roychowdhury, P., Lim, J., Kim, D. S., Ming, G., & Song, H. (2017) · Nature Neuroscience · doi:10.1038/nn.4494 · Cited by 234 · see citing works

Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential

Yuan, M., Yang, B., Rothschild, G., Mann, J. J., Sanford, L. D., Tang, X., Huang, C., Wang, C., & Zhang, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01519-z · Cited by 246 · see citing works

The Epigenetic Link between Prenatal Adverse Environments and Neurodevelopmental Disorders

Kundaković, M., & Jarić, I. (2017) · Genes · doi:10.3390/genes8030104 · Cited by 228 · see citing works

Epigenetic Effects of Cannabis Exposure

Szutorisz, H., & Hurd, Y. L. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.09.014 · Cited by 215 · see citing works

Epigenetic regulation and chromatin remodeling in learning and memory

Kim, S., & Kaang, B. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2016.140 · Cited by 212 · see citing works

Epigenetic editing of the Dlg4/PSD95 gene improves cognition in aged and Alzheimer’s disease mice

Bustos, F. J., Ampuero, E., Jury, N., Aguilar, R., Falahi, F., Toledo, J. A., Ahumada, J., Lata, J., Cubillos, P., Henríquez, B., et al. (2017) · Brain · doi:10.1093/brain/awx272 · Cited by 200 · see citing works

Epigenetic mechanisms in neurological and neurodegenerative diseases

Landgrave-Gómez, J., Mercado-Gómez, O. F., & Guevara‐Guzmán, R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00058 · Cited by 201 · see citing works

The Role of The RNA Demethylase FTO (Fat Mass and Obesity-Associated) and mRNA Methylation in Hippocampal Memory Formation

Walters, B. J., Mercaldo, V., Gillon, C. J., Yip, M., Neve, R. L., Boyce, F. M., Frankland, P. W., & Josselyn, S. A. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.31 · Cited by 198 · see citing works

Scrutinizing the epigenetics revolution

Meloni, M., & Testa, G. (2014) · BioSocieties · doi:10.1057/biosoc.2014.22 · Cited by 185 · see citing works

Mechanisms of Melatonin in Alleviating Alzheimer’s Disease

Shukla, M., Govitrapong, P., Boontem, P., Reiter, R., & Satayavivad, J. (2017) · Current Neuropharmacology · doi:10.2174/1570159x15666170313123454 · Cited by 173 · see citing works

Histone H3 lysine K4 methylation and its role in learning and memory

Collins, B. E., Greer, C. B., Coleman, B. C., & Sweatt, J. D. (2019) · Epigenetics & Chromatin · doi:10.1186/s13072-018-0251-8 · Cited by 194 · see citing works

Epigenetic regulation of astrocyte function in neuroinflammation and neurodegeneration

Neal, M. P., & Richardson, J. R. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.11.004 · Cited by 185 · see citing works

LSD1n is an H4K20 demethylase regulating memory formation via transcriptional elongation control

Wang, J., Telese, F., Tan, Y., Li, W., Jin, C., He, X., Basnet, H., Ma, Q., Merkurjev, D., Zhu, X., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4069 · Cited by 169 · see citing works

Multifaceted origins of sex differences in the brain

McCarthy, M. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0106 · Cited by 166 · see citing works

Immediate and deferred epigenomic signatures of in vivo neuronal activation in mouse hippocampus

Fernandez-Albert, J., Lipinski, M., Lopez-Cascales, M. T., Rowley, M. J., Martin-Gonzalez, A. M., del Blanco, B., Corces, V. G., & Barco, A. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0476-2 · Cited by 166 · see citing works

The social brain meets the reactive genome: neuroscience, epigenetics and the new social biology

Meloni, M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00309 · Cited by 158 · see citing works

Human DNA methylomes of neurodegenerative diseases show common epigenomic patterns

Sanchez-Mut, J. V., Heyn, H., Vidal, E., Morán, S., Sayols, S., Delgado‐Morales, R., Schultz, M. D., Ansoleaga, B., Garcia‐Esparcia, P., Pons‐Espinal, M., et al. (2016) · Translational Psychiatry · doi:10.1038/tp.2015.214 · Cited by 157 · see citing works

The Neuronal Activity-Driven Transcriptome

Benito, E., & Barco, Á. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8772-z · Cited by 145 · see citing works

TRIM28 Represses Transcription of Endogenous Retroviruses in Neural Progenitor Cells

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The transcription factor NRSF contributes to epileptogenesis by selective repression of a subset of target genes

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Epigenetic Etiology of Intellectual Disability

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Friends with social benefits: host-microbe interactions as a driver of brain evolution and development?

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Epigenetic Research in Neuropsychiatric Disorders: the “Tissue Issue”

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High times for cannabis: Epigenetic imprint and its legacy on brain and behavior

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The genetic basis of music ability

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Models of Intergenerational and Transgenerational Transmission of Risk for Psychopathology in Mice

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Epigenetics and EpilepsyPreprint

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Novel therapeutic approaches for disease-modification of epileptogenesis for curing epilepsy

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DNA methylation regulates neuronal glutamatergic synaptic scaling

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Neuroepigenetics of stress

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Epigenetic mechanisms of memory formation and reconsolidation

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RNA from Trained Aplysia Can Induce an Epigenetic Engram for Long-Term Sensitization in Untrained Aplysia

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Evolutionary transitions in learning and cognition

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Understanding the physical basis of memory: Molecular mechanisms of the engram

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Nutrition, the brain and cognitive decline: insights from epigenetics

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Obesity Weighs down Memory through a Mechanism Involving the Neuroepigenetic Dysregulation of Sirt1

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Identification of dynamic glucocorticoid-induced methylation changes at the FKBP5 locus

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Neuronal DNA Methyltransferases: Epigenetic Mediators between Synaptic Activity and Gene Expression?

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Epigenetic mechanisms in schizophrenia

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Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders

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Melatonin, Noncoding RNAs, Messenger RNA Stability and Epigenetics—Evidence, Hints, Gaps and Perspectives

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Epigenetic interventions for epileptogenesis: A new frontier for curing epilepsy

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MicroRNA-26a supports mammalian axon regeneration in vivo by suppressing GSK3β expression

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DNA methylation dynamics in plants and mammals: overview of regulation and dysregulation

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Drugging the pain epigenome

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Aging-related magnification of genetic effects on cognitive and brain integrity

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Epigenetic mechanisms related to cognitive decline during aging

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Opening up the DNA methylome of dementia

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Can changes in histone acetylation contribute to memory formation?

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DNA Methylation in Memory Formation

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Epigenetics and the evolution of instincts

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DNA Methylation in Neurodegenerative and Cerebrovascular Disorders

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Temporal dynamics of neurogenomic plasticity in response to social interactions in male threespined sticklebacks

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Targeted epigenomic editing ameliorates adult anxiety and excessive drinking after adolescent alcohol exposure

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Contribution of Neuroepigenetics to Huntington’s Disease

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Cognition-Enhancing Vagus Nerve Stimulation Alters the Epigenetic Landscape

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Neuroepigenetic mechanisms in disease

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The Dynamic Nature of DNA Methylation: A Role in Response to Social and Seasonal Variation

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CDYL suppresses epileptogenesis in mice through repression of axonal Nav1.6 sodium channel expression

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Experience-dependent epigenomic reorganization in the hippocampusPreprint

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Human endogenous retroviruses in neurologic disease

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Role of Epigenetic Mechanisms in Chronic Pain

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Epigenetic determinants of space radiation-induced cognitive dysfunction

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Editing the Epigenome to Tackle Brain Disorders

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Epigenetic Treatment of Neurodegenerative Disorders: Alzheimer and Parkinson Diseases

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Ketogenic diet, neuroprotection, and antiepileptogenesis

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The roles of sensitization and neuroplasticity in the long-term regulation of blood pressure and hypertension

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TET enzymes in neurophysiology and brain function

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Developmental Consequences of Intimate Partner Violence on Children

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Gene regulatory mechanisms underlying sex differences in brain development and psychiatric disease

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Oxidative DNA demethylation mediated by Tet enzymes

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Tet1 oxidase regulates neuronal gene transcription, active DNA hydroxymethylation, object location memory, and threat recognition memory

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Regulation of neural gene transcription by optogenetic inhibition of the RE1-silencing transcription factor

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Dynamic DNA methylation controls glutamate receptor trafficking and synaptic scaling

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Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue

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Early-life stress interactions with the epigenome

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Role of Microtubule-Associated Protein in Autism Spectrum Disorder

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The role of the gut microbiota in schizophrenia: Current and future perspectives

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Nuclear organization and 3D chromatin architecture in cognition and neuropsychiatric disorders

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Persistent epigenetic reprogramming of sweet taste by diet

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Exploring the Complexity of Intellectual Disability in Fetal Alcohol Spectrum Disorders

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Parent–offspring transaction: Mechanisms and the value of within family designs

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The multi-faceted impact of methamphetamine on Alzheimer's disease: From a triggering role to a possible therapeutic use.

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Histone post-translational modifications as potential therapeutic targets for pain management

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Polycomb Binding Precedes Early-Life Stress Responsive DNA Methylation at the Avp Enhancer

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Molecular windows into the human brain for psychiatric disorders

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Regulation of Gene Expression and Pain States by Epigenetic Mechanisms

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Neuroepigenetics

(n.d.)

Neuroepigenetic disorders: Progress, promises and challenges

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Epigenetic changes in the developing brain: Effects on behavior

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Epigenetic pathways through which experiences become linked with biology

McGowan, P. O., & Roth, T. L. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000206 · Cited by 72 · see citing works

The Epigenetic Switches for Neural Development and Psychiatric Disorders

Jingwen, Lv, Yong-juan, -, X., Wenhao, Zhou, Zilong, & Qiu, G. (2013)