18/18 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Martínez de Paz A, Khajavi L, Martin H, Claveria-Gimeno R, Tom Dieck S, Cheema MS, Sanchez-Mut JV, Moksa MM, Carles A, Brodie NI, Sheikh TI, Freeman ME, Petrotchenko EV, Borchers CH, Schuman EM, et al. MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2. Epigenetics & Chromatin. 12: 63. PMID 31601272 DOI: 10.1186/s13072-019-0298-1  0.36
2018 Sanchez-Mut JV, Heyn H, Silva BA, Dixsaut L, Garcia-Esparcia P, Vidal E, Sayols S, Glauser L, Monteagudo-Sánchez A, Perez-Tur J, Ferrer I, Monk D, Schneider B, Esteller M, Gräff J. PM20D1 is a quantitative trait locus associated with Alzheimer's disease. Nature Medicine. PMID 29736028 DOI: 10.1038/s41591-018-0013-y  0.56
2017 Frangeul L, Kehayas V, Sanchez-Mut JV, Fièvre S, Krishna-K K, Pouchelon G, Telley L, Bellone C, Holtmaat A, Gräff J, Macklis JD, Jabaudon D. Input-dependent regulation of excitability controls dendritic maturation in somatosensory thalamocortical neurons. Nature Communications. 8: 2015. PMID 29222517 DOI: 10.1038/s41467-017-02172-1  0.36
2017 Sanchez-Mut JV, Heyn H, Vidal E, Delgado-Morales R, Moran S, Sayols S, Sandoval J, Ferrer I, Esteller M, Gräff J. Whole Genome Grey and White matter DNA Methylation Profiles in Dorsolateral Prefrontal cortex. Synapse (New York, N.Y.). PMID 28105729 DOI: 10.1002/syn.21959  0.56
2016 Alelú-Paz R, Carmona FJ, Sanchez-Mut JV, Cariaga-Martínez A, González-Corpas A, Ashour N, Orea MJ, Escanilla A, Monje A, Guerrero Márquez C, Saiz-Ruiz J, Esteller M, Ropero S. Epigenetics in Schizophrenia: A Pilot Study of Global DNA Methylation in Different Brain Regions Associated with Higher Cognitive Functions. Frontiers in Psychology. 7: 1496. PMID 27746755 DOI: 10.3389/fpsyg.2016.01496  0.52
2016 Heyn H, Vidal E, Ferreira HJ, Vizoso M, Sayols S, Gomez A, Moran S, Boque-Sastre R, Guil S, Martinez-Cardus A, Lin CY, Royo R, Sanchez-Mut JV, Martinez R, Gut M, et al. Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer. Genome Biology. 17: 11. PMID 26813288 DOI: 10.1186/s13059-016-0879-2  0.44
2016 Sanchez-Mut JV, Heyn H, Vidal E, Moran S, Sayols S, Delgado-Morales R, Schultz MD, Ansoleaga B, Garcia-Esparcia P, Pons-Espinal M, de Lagran MM, Dopazo J, Rabano A, Avila J, Dierssen M, et al. Human DNA methylomes of neurodegenerative diseases show common epigenomic patterns. Translational Psychiatry. 6: e718. PMID 26784972 DOI: 10.1038/tp.2015.214  0.56
2015 Sanchez-Mut JV, Gräff J. Epigenetic Alterations in Alzheimer's Disease. Frontiers in Behavioral Neuroscience. 9: 347. PMID 26734709 DOI: 10.3389/fnbeh.2015.00347  0.36
2015 Sáez MA, Fernández-Rodríguez J, Moutinho C, Sanchez-Mut JV, Gomez A, Vidal E, Petazzi P, Szczesna K, Lopez-Serra P, Lucariello M, Lorden P, Delgado-Morales R, de la Caridad OJ, Huertas D, Gelpí JL, et al. Mutations in JMJD1C are involved in Rett syndrome and intellectual disability. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26181491 DOI: 10.1038/gim.2015.100  0.44
2014 Heyn H, Sayols S, Moutinho C, Vidal E, Sanchez-Mut JV, Stefansson OA, Nadal E, Moran S, Eyfjord JE, Gonzalez-Suarez E, Pujana MA, Esteller M. Linkage of DNA methylation quantitative trait loci to human cancer risk. Cell Reports. 7: 331-8. PMID 24703846 DOI: 10.1016/j.celrep.2014.03.016  0.56
2014 Sanchez-Mut JV, Aso E, Heyn H, Matsuda T, Bock C, Ferrer I, Esteller M. Promoter hypermethylation of the phosphatase DUSP22 mediates PKA-dependent TAU phosphorylation and CREB activation in Alzheimer's disease. Hippocampus. 24: 363-8. PMID 24436131 DOI: 10.1002/hipo.22245  0.44
2014 Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simón C, Moore H, Harness JV, Keirstead H, Sanchez-Mut JV, Kaneki E, Lapunzina P, Soejima H, et al. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment. Genome Research. 24: 554-69. PMID 24402520 DOI: 10.1101/gr.164913.113  0.44
2013 Sanchez-Mut JV, Aso E, Panayotis N, Lott I, Dierssen M, Rabano A, Urdinguio RG, Fernandez AF, Astudillo A, Martin-Subero JI, Balint B, Fraga MF, Gomez A, Gurnot C, Roux JC, et al. DNA methylation map of mouse and human brain identifies target genes in Alzheimer's disease. Brain : a Journal of Neurology. 136: 3018-27. PMID 24030951 DOI: 10.1093/brain/awt237  0.44
2012 Heyn H, Li N, Ferreira HJ, Moran S, Pisano DG, Gomez A, Diez J, Sanchez-Mut JV, Setien F, Carmona FJ, Puca AA, Sayols S, Pujana MA, Serra-Musach J, Iglesias-Platas I, et al. Distinct DNA methylomes of newborns and centenarians. Proceedings of the National Academy of Sciences of the United States of America. 109: 10522-7. PMID 22689993 DOI: 10.1073/pnas.1120658109  0.44
2012 Heyn H, Vidal E, Sayols S, Sanchez-Mut JV, Moran S, Medina I, Sandoval J, Simó-Riudalbas L, Szczesna K, Huertas D, Gatto S, Matarazzo MR, Dopazo J, Esteller M. Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient. Epigenetics : Official Journal of the Dna Methylation Society. 7: 542-50. PMID 22595875 DOI: 10.4161/epi.20523  0.44
2012 Sanchez-Mut JV, Huertas D, Esteller M. Aberrant epigenetic landscape in intellectual disability Progress in Brain Research. 197: 53-71. PMID 22541288 DOI: 10.1016/B978-0-444-54299-1.00004-2  0.44
2012 Fernandez AF, Assenov Y, Martin-Subero JI, Balint B, Siebert R, Taniguchi H, Yamamoto H, Hidalgo M, Tan AC, Galm O, Ferrer I, Sanchez-Cespedes M, Villanueva A, Carmona J, Sanchez-Mut JV, et al. A DNA methylation fingerprint of 1628 human samples. Genome Research. 22: 407-19. PMID 21613409 DOI: 10.1101/gr.119867.110  0.44
2009 Urdinguio RG, Sanchez-Mut JV, Esteller M. Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies. The Lancet. Neurology. 8: 1056-72. PMID 19833297 DOI: 10.1016/S1474-4422(09)70262-5  0.36
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