Hypoxia and Environmental Epigenetics

Regulation of chromatin by histone modifications

Bannister, A. J., & Kouzarides, T. (2011) · Cell Research · doi:10.1038/cr.2011.22 · Cited by 6,012 · see citing works

Hypoxia-inducible factors in physiology and medicine

Semenza, G. L. (2012) · Cell · doi:10.1016/j.cell.2012.01.021 · Cited by 3,645 · see citing works

Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse

McGowan, P. O., Sasaki, A., D'Alessio, A. C., Dymov, S., Labonté, B., Szyf, M., Turecki, G., & Meaney, M. J. (2009) · Nature Neuroscience · doi:10.1038/nn.2270 · Cited by 3,531 · 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

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

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

Weber, M., Hellmann, I., Stadler, M. B., Ramos, L., Pääbo, S., Rebhan, M., & Schübeler, D. (2007) · Nature Genetics · doi:10.1038/ng1990 · Cited by 2,267 · see citing works

TET enzymes, TDG and the dynamics of DNA demethylation

Kohli, R. M., & Zhang, Y. (2013) · Nature · doi:10.1038/nature12750 · Cited by 1,623 · see citing works

Epigenetic inheritance at the agouti locus in the mouse

Morgan, H. D., Sutherland, H. G. E., Martin, D. I. K., & Whitelaw, E. (1999) · Nature Genetics · doi:10.1038/15490 · Cited by 1,476 · see citing works

Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development

Dolinoy, D. C., Huang, D., & Jirtle, R. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703739104 · Cited by 1,369 · see citing works

Genetic Evidence for High-Altitude Adaptation in Tibet

Simonson, T. S., Yang, Y., Huff, C. D., Yun, H., Qin, G., Witherspoon, D. J., Bai, Z., Lorenzo, F. R., Xing, J., Jorde, L. B., et al. (2010) · Science · doi:10.1126/science.1189406 · Cited by 1,227 · see citing works

Sex-specific, male-line transgenerational responses in humans

The ALSPAC Study Team, Pembrey, M. E., Bygren, L. O., Kaati, G., Edvinsson, S., Northstone, K., Sjöström, M., & Golding, J. (2006) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201538 · Cited by 1,150 · see citing works

Integration of Oxygen Signaling at the Consensus HRE

Wenger, R. H., Stiehl, D. P., & Camenisch, G. (2005) · Science's STKE · doi:10.1126/stke.3062005re12 · Cited by 1,032 · see citing works

Maternal Genistein Alters Coat Color and Protects Avy Mouse Offspring from Obesity by Modifying the Fetal Epigenome

Dolinoy, D. C., Weidman, J. R., Waterland, R. A., & Jirtle, R. L. (2006) · Environmental Health Perspectives · doi:10.1289/ehp.8700 · Cited by 932 · see citing works

Transgenerational effects of prenatal exposure to the Dutch famine on neonatal adiposity and health in later life

Painter, R., Osmond, C., Gluckman, P., Hanson, M., Phillips, D., & Roseboom, T. (2008) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2008.01822.x · Cited by 733 · see citing works

Transgenerational Epigenetic Effects

Youngson, N. A., & Whitelaw, E. (2008) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164445 · Cited by 575 · see citing works

Genome-wide Association of Hypoxia-inducible Factor (HIF)-1α and HIF-2α DNA Binding with Expression Profiling of Hypoxia-inducible Transcripts

Mole, D. R., Blancher, C., Copley, R. R., Pollard, P. J., Gleadle, J. M., Ragoussis, J., & Ratcliffe, P. J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m901790200 · Cited by 552 · see citing works

Transgenerational response to nutrition, early life circumstances and longevity

Kaati, G., Bygren, L. O., Pembrey, M., & Sjöström, M. (2007) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201832 · Cited by 500 · see citing works

Transgenerational effects of prenatal exposure to the 1944–45 Dutch famine

Veenendaal, M., Painter, R., de Rooij, Sr., Bossuyt, P., van der Post, J., Gluckman, P., Hanson, M., & Roseboom, T. (2013) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.12136 · Cited by 477 · see citing works

Factors underlying variable DNA methylation in a human community cohort

Lam, L. L., Emberly, E., Fraser, H. B., Neumann, S. M., Chen, E., Miller, G. E., & Kobor, M. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121249109 · Cited by 476 · see citing works

Feeding pregnant rats a protein-restricted diet persistently alters the methylation of specific cytosines in the hepatic PPARα promoter of the offspring

Lillycrop, K. A., Phillips, E. S., Torrens, C., Hanson, M. A., Jackson, A. A., & Burdge, G. C. (2008) · British Journal Of Nutrition · doi:10.1017/s0007114507894438 · Cited by 461 · see citing works

Sequential ChIP-bisulfite sequencing enables direct genome-scale investigation of chromatin and DNA methylation cross-talk

Brinkman, A. B., Gu, H., Bartels, S. J. J., Zhang, Y., Matarese, F., Simmer, F., Marks, H., Bock, C., Gnirke, A., Meissner, A., et al. (2012) · Genome Research · doi:10.1101/gr.133728.111 · Cited by 413 · see citing works

Molecular Biology of Erythropoietin

JELKMANN, W. E. B. (2004) · Internal Medicine · doi:10.2169/internalmedicine.43.649 · Cited by 380 · see citing works

The effect of high altitude and other risk factors on birthweight: independent or interactive effects?

Jensen, G. M., & MOORE, L. G. (1997) · American Journal of Public Health · doi:10.2105/ajph.87.6.1003 · Cited by 355 · see citing works

Environmental Epigenetics and Its Implication on Disease Risk and Health Outcomes

Ho, S., Johnson, A. D., Tarapore, P., Janakiram, V., Zhang, X., & Leung, Y. (2012) · ILAR Journal · doi:10.1093/ilar.53.3-4.289 · Cited by 316 · see citing works

Monozygotic Twins Exhibit Numerous Epigenetic Differences: Clues to Twin Discordance?

Petronis, A., Gottesman, I. I., Kan, P., Kennedy, J. L., Basile, V. S., Paterson, A. D., & Popendikytė, V. (2003) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a006988 · Cited by 312 · see citing works

Non‐coding RNAs: Meet thy masters

Costa, F. F. (2010) · BioEssays · doi:10.1002/bies.200900112 · Cited by 310 · see citing works

Maternal Care, Gene Expression, and the Development of Individual Differences in Stress Reactivity

Francis, D. D., Champagne, F. A., Liu, D., & Meaney, M. J. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08106.x · Cited by 291 · see citing works

Intrauterine Growth Restriction, Preeclampsia, and Intrauterine Mortality at High Altitude in Bolivia

Keyes, L. E., Armaza, F. J., Niermeyer, S., Vargas, E., Young, D. A., & Moore, L. G. (2003) · Pediatric Research · doi:10.1203/01.pdr.0000069846.64389.dc · Cited by 285 · see citing works

Hypoxia induces a novel signature of chromatin modifications and global repression of transcription

Johnson, A. B., Denko, N., & Barton, M. C. (2008) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2008.01.001 · Cited by 250 · see citing works

Carcinogenic metals and the epigenome: understanding the effect of nickel, arsenic, and chromium

Chervona, Y., Arita, A., & Costa, M. (2012) · Metallomics · doi:10.1039/c2mt20033c · Cited by 240 · see citing works

Epigenomic disruption: The effects of early developmental exposures

Bernal, A. J., & Jirtle, R. L. (2010) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.20685 · Cited by 236 · see citing works

SILENCING OF THE MAMMALIAN X CHROMOSOME

Chow, J., Yen, Z., Ziesche, S. M., & Brown, C. J. (2005) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.6.080604.162350 · Cited by 215 · see citing works

Maternal Adaptation to High-altitude Pregnancy: An Experiment of Nature—A Review

Moore, L. G., Shriver, M., Bemis, L., Hickler, B., Wilson, M., Brutsaert, T., Parra, E., & Vargas, E. (2004) · Placenta · doi:10.1016/j.placenta.2004.01.008 · Cited by 210 · see citing works

Epigenetics and twins: three variations on the theme

Petronis, A. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.04.010 · Cited by 193 · see citing works

The case for transgenerational epigenetic inheritance in humans

Morgan, D. K., & Whitelaw, E. (2008) · Mammalian Genome · doi:10.1007/s00335-008-9124-y · Cited by 161 · see citing works

Epigenetics: The epicenter of the hypoxic response

Watson, J. A., Watson, C. J., McCann, A. H., & Baugh, J. A. (2010) · Epigenetics · doi:10.4161/epi.5.4.11684 · Cited by 161 · see citing works

Nitric oxide in adaptation to altitude

Beall, C. M., Laskowski, D. M., & ERZURUM, S. C. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.12.028 · Cited by 146 · see citing works

Sensing hypoxia: physiology, genetics and epigenetics

Prabhakar, N. R. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.247759 · Cited by 142 · see citing works

Epigenetic regulation of hypoxic sensing disrupts cardiorespiratory homeostasis

Nanduri, J., Makarenko, V. V., Reddy, V. D., Yuan, G., Pawar, A., Wang, N., Khan, S. A., Zhang, X., Kinsman, B. J., Peng, Y., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120600109 · Cited by 137 · see citing works

Mechanisms of X-chromosome inactivation

Samuel, C. C. (2006) · Frontiers in bioscience · doi:10.2741/1842 · Cited by 108 · see citing works

Fetal growth restriction: a workshop report

Cetin, I., Foidart, J., Miozzo, M. R., Raun, T., Jansson, T., Tsatsaris, V., Reik, W., Cross, J. C., Mouzon, S. H., Illsley, N. P., et al. (2004) · Placenta · doi:10.1016/j.placenta.2004.02.004 · Cited by 107 · see citing works

Transmission of raised blood pressure and endothelial dysfunction to the F2generation induced by maternal protein restriction in the F0, in the absence of dietary challenge in the F1generation

Torrens, C., Poston, L., & Hanson, M. A. (2008) · British Journal Of Nutrition · doi:10.1017/s0007114508921747 · Cited by 99 · see citing works

Epigenetics of the vascular endothelium

Yan, M. S.-C., Matouk, C. C., & Marsden, P. A. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00131.2010 · Cited by 89 · see citing works

Maternal protein restriction with or without folic acid supplementation during pregnancy alters the hepatic transcriptome in adult male rats

Lillycrop, K. A., Rodford, J., Garratt, E. S., Slater-Jefferies, J. L., Godfrey, K. M., Gluckman, P. D., Hanson, M. A., & Burdge, G. C. (2010) · British Journal Of Nutrition · doi:10.1017/s0007114509993795 · Cited by 87 · see citing works

DNA methylation represses the expression of the human erythropoietin gene by two different mechanisms

Yin, H., & Blanchard, K. L. (2000) · Blood · doi:10.1182/blood.v95.1.111 · Cited by 82 · see citing works

Evidence for a Genetic Basis for Altitude Illness: 2010 Update

MacInnis, M. J., Koehle, M. S., & Rupert, J. L. (2010) · High Altitude Medicine & Biology · doi:10.1089/ham.2010.1030 · Cited by 80 · see citing works

Epigenetics: New Questions on the Response to Hypoxia

Perez-Perri, J. I., Acevedo, J. M., & Wappner, P. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12074705 · Cited by 79 · see citing works

NO sparks off chromatin: Tales of a multifaceted epigenetic regulator

Illi, B., Colussi, C., Grasselli, A., Farsetti, A., Capogrossi, M. C., & Gaetano, C. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.05.003 · Cited by 74 · see citing works

Hypoxia‐induced erythropoietin expression in human neuroblastoma requires a methylation free HIF‐1 binding site

Rössler, J. K., Stolze, I. P., Frede, S., Freitag, P., Schweigerer, L., Havers, W., & Fandrey, J. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20133 · Cited by 63 · see citing works

Female Resistance to Hypoxia: Does It Explain the Sex Difference in Mortality Rates?

Mage, D. T., & Donner, M. E. (2006) · Journal of Women s Health · doi:10.1089/jwh.2006.15.786 · Cited by 60 · see citing works

Evidence that parent‐of‐origin affects birth‐weight reductions at high altitude

Bennett, A., Sain, S. R., Vargas, E., & MOORE, L. G. (2008) · American Journal of Human Biology · doi:10.1002/ajhb.20784 · Cited by 52 · see citing works

BRG1 and BRM Chromatin-Remodeling Complexes Regulate the Hypoxia Response by Acting as Coactivators for a Subset of Hypoxia-Inducible Transcription Factor Target Genes

Sena, J. A., Wang, L., & Hu, C. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00731-13 · Cited by 52 · see citing works

Nitric Oxide during Altitude Acclimatization

Janocha, A. J., Koch, C. D., Tiso, M., Ponchia, A., Doctor, A., Gibbons, L. B., Gaston, B. M., Beall, C. M., & ERZURUM, S. C. (2011) · New England Journal of Medicine · doi:10.1056/nejmc1107887 · Cited by 51 · see citing works

Gene Expression Patterns in the Hypoxic Murine Placenta: A Role in Epigenesis?

Gheorghe, C. P., Mohan, S., Oberg, K. C., & Longo, L. D. (2007) · Reproductive Sciences · doi:10.1177/1933719107302860 · Cited by 51 · see citing works

Brahma-related gene 1 (Brg1) epigenetically regulates CAM activation during hypoxic pulmonary hypertension

Chen, D., Fang, F., Yang, Y., Chen, J., Xu, G., Xu, Y., & Gao, Y. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt214 · Cited by 47 · see citing works

Gene Polymorphisms and High-Altitude Pulmonary Edema Susceptibility: A 2011 Update

Luo, Y., Zou, Y., & Gao, Y. (2012) · Respiration · doi:10.1159/000336625 · Cited by 37 · see citing works

Epigenetic Silencing of Erythropoietin in Human Cancers

Steinmann, K., Richter, A. M., & Dammann, R. (2011) · Genes & Cancer · doi:10.1177/1947601911405043 · Cited by 36 · see citing works

Meta-Analysis Using a Novel Database, miRStress, Reveals miRNAs That Are Frequently Associated with the Radiation and Hypoxia Stress-Responses

Jacobs, L., Bewicke-Copley, F., Poolman, M., Pink, R., Mulcahy, L. A., Baker, I. R., Beaman, E., Brooks, T., Caley, D., Cowling, W., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080844 · Cited by 30 · see citing works

Pulmonary Hypertension in High-Altitude Dwellers: Novel Mechanisms, Unsuspected Predisposing Factors

Scherrer, U., Turini, P., Thalmann, S., Hutter, D., Salmón, C. S., Stüber, T., Shaw, S., Jayet, P., Sartori-Cucchia, C., Villena, M., et al. (2007) · Springer eBooks · doi:10.1007/978-0-387-34817-9_23 · Cited by 28 · see citing works

Pleiotropic role of histone deacetylases in the regulation of human adult erythropoiesis

Yamamura, K., Ohishi, K., Katayama, N., Yu, Z., Kato, K., Masuya, M., Fujieda, A., Sugimoto, Y., Miyata, E., Shibasaki, T., et al. (2006) · British Journal of Haematology · doi:10.1111/j.1365-2141.2006.06275.x · Cited by 28 · see citing works

NO points to epigenetics in vascular development

Illi, B., Colussi, C., Rosati, J. D., Spallotta, F., Nanni, S., Farsetti, A., Capogrossi, M. C., & Gaetano, C. (2011) · Cardiovascular Research · doi:10.1093/cvr/cvr056 · Cited by 23 · see citing works

Environmental influence on epigenetic inheritance at the Avy allele

Martin, D. I. K., Cropley, J. E., & Suter, C. M. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2008.00057.x · Cited by 21 · see citing works

Twin Studies in Altitude and Hypoxia Research

MacLeod, K. E., MacInnis, M. J., Manokhina, I., & Rupert, J. L. (2013) · Aviation Space and Environmental Medicine · doi:10.3357/asem.3569.2013 · Cited by 9 · see citing works

Placental Origins of Chronic Disease

Burton, G. J., Fowden, A. L., & Thornburg, K. L. (2016) · Physiological Reviews · doi:10.1152/physrev.00029.2015 · Cited by 717 · 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

Epigenetic changes by DNA methylation in chronic and intermittent hypoxia

Nanduri, J., Semenza, G. L., & Prabhakar, N. R. (2017) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00325.2017 · Cited by 83 · 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

Role of Epigenetics in the Regulation of Immune Functions of the Skin

Sawada, Y., & Gallo, R. L. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.10.012 · Cited by 51 · see citing works

Non-Random Genome Editing and Natural Cellular Engineering in Cognition-Based Evolution

Miller, W. B., Enguita, F. J., & Leitão, A. L. (2021) · Cells · doi:10.3390/cells10051125 · Cited by 47 · see citing works

Genetic variants at the EGLN1 locus associated with high‐altitude adaptation in Tibetans are absent or found at low frequency in highland Andeans

Heinrich, E. C., Wu, L., Lawrence, E. S., Cole, A. M., Anza‐Ramirez, C., Villafuerte, F. C., & Simonson, T. S. (2019) · Annals of Human Genetics · doi:10.1111/ahg.12299 · Cited by 45 · see citing works

DNA Methylation Changes Are Associated With an Incremental Ascent to High Altitude

Childebayeva, A., Harman, T. S., Weinstein, J. B., Goodrich, J. M., Dolinoy, D. C., Day, T. A., Bigham, A. W., & Brutsaert, T. D. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.01062 · Cited by 45 · see citing works

Seq-ing Higher Ground: Functional Investigation of Adaptive Variation Associated With High-Altitude Adaptation

Hall, J. E., Lawrence, E. S., Simonson, T. S., & Fox, K. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00471 · Cited by 32 · see citing works

Targeting the Mild-Hypoxia Driving Force for Metabolic and Muscle Transcriptional Reprogramming of Gilthead Sea Bream (Sparus aurata) Juveniles

Naya-Català, F., Martos-Sitcha, J. A., Heras, V. D. L., Simó‐Mirabet, P., Calduch-Giner, J. À., & Pérez‐Sánchez, J. (2021) · Biology · doi:10.3390/biology10050416 · Cited by 27 · see citing works

Hypobaric hypoxia exposure alters transcriptome in mouse testis and impairs spermatogenesis in offspring

Li, S., & Yang, Q. (2022) · Gene · doi:10.1016/j.gene.2022.146390 · Cited by 22 · see citing works

Long-Term Health Outcomes in High-Altitude Pulmonary Hypertension

Robinson, J. C., Abbott, C., Meadows, C. A., Roach, R. C., Honigman, B., & Bull, T. (2017) · High Altitude Medicine & Biology · doi:10.1089/ham.2016.0098 · Cited by 22 · see citing works

Hypoxia Increases ATX Expression by Histone Crotonylation in a HIF-2α-Dependent Manner

Qu, M., Yang, L., Wang, Y., Yin, N., Zhang, X., & Zhang, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087031 · Cited by 20 · see citing works

Evolved changes in breathing and CO2sensitivity in deer mice native to high altitudes

Ivy, C. M., & Scott, G. R. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00220.2018 · Cited by 20 · see citing works

Exposomes to Exosomes: Exosomes as Tools to Study Epigenetic Adaptive Mechanisms in High-Altitude Humans

Padmasekar, M., Savai, R., Seeger, W., & Pullamsetti, S. S. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18168280 · Cited by 18 · see citing works

Effect of mindfulness meditation protocol in subjects with various psychometric characteristics at high altitude

Bhanushali, D., Tyagi, R., Limaye, N., & Anand, A. (2020) · Brain and Behavior · doi:10.1002/brb3.1604 · Cited by 16 · see citing works

Transcriptomic profiling of Gh/Igf system reveals a prompted tissue-specific differentiation and novel hypoxia responsive genes in gilthead sea bream

Naya-Català, F., Simó‐Mirabet, P., Calduch-Giner, J. À., & Pérez‐Sánchez, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-95408-6 · Cited by 16 · see citing works

Heterogeneity of treatment effect: the case for individualising oxygen therapy in critically ill patients

Martín, D., & Grocott, M. P. W. (2025) · Critical Care · doi:10.1186/s13054-025-05254-5 · Cited by 9 · see citing works

Demethylation of the hypoxia induction factor 1 binding site of GPX3 at excess blood ammonia in propionic acidemia

Item, C. B., Schanzer, A., Metz, T., Greber‐Platzer, S., & Lischka, J. (2019) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2019.02.005 · Cited by 2 · see citing works

Comparison of hypoxia- and hyperoxia-induced alteration of epigene expression pattern in lungs of Pleurodeles waltl and Mus musculus

Hasan, M. M., Sekiya, R., Zhang, X., Yassouf, M. Y., & Li, T. (2024) · PLoS ONE · doi:10.1371/journal.pone.0299661 · Cited by 1 · see citing works

DNA methylated alleles of the phenylalanine hydroxylase promoter remodeled at elevated phenylalanine levels in newborns with hyperphenylalaninemia

Item, C. B., Farhadi, S., Schanzer, A., & Greber‐Platzer, S. (2017) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2017.04.001 · Cited by 1 · see citing works

The Two Genomes of Gilthead Sea Bream (Sparus aurata): a Multi-Omics and Holobiont Approach

Naya-Català, F. (2024) · doi:10.4995/thesis/10251/205692

Genome-wide DNA methylation changes after 24 hours at high altitude

Frost, S., Pham, K., & Heinrich, E. C. (2026) · Current Zoology · doi:10.1093/eep/dvag004

The significance of epigenetic mechanisms of physiological adaptation to hypoxia in the search for key points of influence on hypoxia-dependent pathological processes

Yasinska, O. V. (2023) · DSpace BSMU

Environmental stressors and the epigenome

Hala, D. N., Huggett, D. B., & Burggren, W. W. (2012) · Drug Discovery Today Technologies · doi:10.1016/j.ddtec.2012.05.004 · Cited by 30 · see citing works

Epigenetic modification of gene expression during human acclimatization to hypobaric hypoxia (885.4)

Julian, C. G., Subudhi, A. W., Evero, O., Pedersen, B. S., Dvorkin, D., Lovering, A. T., & Roach, R. C. (2014) · The FASEB Journal · doi:10.1096/fasebj.28.1_supplement.885.4 · Cited by 1 · see citing works

Paternal hypoxia exposure primes offspring for increased hypoxia resistance

Ragsdale, A. K., Ortega‐Recalde, O., Dutoit, L., Besson, A. A., Chia, J. H. Z., King, T. M., Nakagawa, S., Hickey, A. J., Gemmell, N. J., Hore, T. A., et al. (2022) · BMC Biology · doi:10.1186/s12915-022-01389-x · Cited by 33 · see citing works

Epigenetics: The epicenter of the hypoxic response

Watson, J. A., Watson, C. J., McCann, A. H., & Baugh, J. A. (2010) · Epigenetics · doi:10.4161/epi.5.4.11684 · Cited by 161 · see citing works