| Year |
Citation |
Score |
| 2022 |
Burns AM, Farinelli-Scharly M, Hugues-Ascery S, Sanchez-Mut JV, Santoni G, Gräff J. The HDAC inhibitor CI-994 acts as a molecular memory aid by facilitating synaptic and intracellular communication after learning. Proceedings of the National Academy of Sciences of the United States of America. 119: e2116797119. PMID 35613054 DOI: 10.1073/pnas.2116797119 |
0.606 |
|
| 2020 |
Sohrabi F, Jahani Y, Sanchez-Mut JV, Mohammadi E, Barzegar Z, Li X, Glauser L, Gräff J, Hamidi SM. Membrane activity detection in cultured cells using phase-sensitive plasmonics. Optics Express. 28: 36643-36655. PMID 33379754 DOI: 10.1364/OE.399713 |
0.569 |
|
| 2020 |
Sanchez-Mut JV, Glauser L, Monk D, Gräff J. Comprehensive analysis of PM20D1 QTL in Alzheimer's disease. Clinical Epigenetics. 12: 20. PMID 32014019 DOI: 10.1186/S13148-020-0814-Y |
0.683 |
|
| 2019 |
Delacrétaz A, Glatard A, Dubath C, Gholam-Rezaee M, Sanchez-Mut JV, Gräff J, von Gunten A, Conus P, Eap CB. Psychotropic drug-induced genetic-epigenetic modulation of CRTC1 gene is associated with early weight gain in a prospective study of psychiatric patients. Clinical Epigenetics. 11: 198. PMID 31878957 DOI: 10.1186/S13148-019-0792-0 |
0.643 |
|
| 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 |
0.46 |
|
| 2018 |
Ruiz de Garibay G, Herranz C, Llorente A, Boni J, Serra-Musach J, Mateo F, Aguilar H, Gómez-Baldó L, Petit A, Vidal A, Climent F, Hernández-Losa J, Cordero Á, González-Suárez E, Sánchez-Mut JV, et al. Correction: Lymphangioleiomyomatosis Biomarkers Linked to Lung Metastatic Potential and Cell Stemness. Plos One. 13: e0207586. PMID 30419005 DOI: 10.1371/Journal.Pone.0207586 |
0.378 |
|
| 2018 |
Bacq A, Astori S, Gebara E, Tang W, Silva BA, Sanchez-Mut J, Grosse J, Guillot de Suduiraut I, Zanoletti O, Maclachlan C, Knott GW, Gräff J, Sandi C. Amygdala GluN2B-NMDAR dysfunction is critical in abnormal aggression of neurodevelopmental origin induced by St8sia2 deficiency. Molecular Psychiatry. PMID 30089788 DOI: 10.1038/S41380-018-0132-3 |
0.638 |
|
| 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 |
0.7 |
|
| 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 |
0.626 |
|
| 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 |
0.721 |
|
| 2016 |
Mateo F, Arenas EJ, Aguilar H, Serra-Musach J, de Garibay GR, Boni J, Maicas M, Du S, Iorio F, Herranz-Ors C, Islam A, Prado X, Llorente A, Petit A, Vidal A, et al. Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition. Oncogene. PMID 27991928 DOI: 10.1038/Onc.2016.427 |
0.434 |
|
| 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 |
0.566 |
|
| 2016 |
Nuñez O, Román A, Johnson SR, Inoue Y, Hirose M, Casanova Á, de Garibay GR, Herranz C, Bueno-Moreno G, Boni J, Mateo F, Petit A, Climent F, Soler T, Vidal A, et al. Study of breast cancer incidence in patients of lymphangioleiomyomatosis. Breast Cancer Research and Treatment. PMID 26951504 DOI: 10.1007/S10549-016-3737-8 |
0.395 |
|
| 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 |
0.559 |
|
| 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 |
0.757 |
|
| 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 |
0.695 |
|
| 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 |
0.712 |
|
| 2015 |
Ruiz de Garibay G, Herranz C, Llorente A, Boni J, Serra-Musach J, Mateo F, Aguilar H, Gómez-Baldó L, Petit A, Vidal A, Climent F, Hernández-Losa J, Cordero Á, González-Suárez E, Sánchez-Mut JV, et al. Lymphangioleiomyomatosis Biomarkers Linked to Lung Metastatic Potential and Cell Stemness. Plos One. 10: e0132546. PMID 26167915 DOI: 10.1371/Journal.Pone.0132546 |
0.449 |
|
| 2014 |
Carmona FJ, Davalos V, Vidal E, Gomez A, Heyn H, Hashimoto Y, Vizoso M, Martinez-Cardus A, Sayols S, Ferreira HJ, Sánchez-Mut JV, Morán S, Margelí M, Castella E, Berdasco M, et al. A comprehensive DNA methylation profile of epithelial-to-mesenchymal transition. Cancer Research. 74: 5608-19. PMID 25106427 DOI: 10.1158/0008-5472.Can-13-3659 |
0.533 |
|
| 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 |
0.562 |
|
| 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 |
0.571 |
|
| 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 |
0.552 |
|
| 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 |
0.602 |
|
| 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 |
0.545 |
|
| 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 |
0.577 |
|
| 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 |
0.501 |
|
| 2012 |
Rubio A, Sánchez-Mut JV, García E, Velasquez ZD, Oliver J, Esteller M, Avila J. Epigenetic control of somatostatin and cortistatin expression by β amyloid peptide Journal of Neuroscience Research. 90: 13-20. PMID 21922516 DOI: 10.1002/Jnr.22731 |
0.454 |
|
| 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 |
0.57 |
|
| 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 |
0.598 |
|
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