Publikationen in Zusammenarbeit mit Forschern von Instituto de Salud Carlos III (26)

2024

  1. Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome

    Clinical Epigenetics, Vol. 16, Núm. 1

2023

  1. A human genome editing–based MLL::AF4 ALL model recapitulates key cellular and molecular leukemogenic features

    Blood, Vol. 142, Núm. 20, pp. 1752-1756

  2. The TINCR ubiquitin-like microprotein is a tumor suppressor in squamous cell carcinoma

    Nature Communications, Vol. 14, Núm. 1

2022

  1. Blood DNA Methylation Patterns in Older Adults With Evolving Dementia

    The journals of gerontology. Series A, Biological sciences and medical sciences, Vol. 77, Núm. 9, pp. 1743-1749

  2. MATERNAL OBESITY AND GESTATIONAL DIABETES ARE ASSOCIATED WITH DNA METHYLATION ALTERATIONS IN THE OFFSPRING THROUGHOUT THE FIRST YEAR OF LIFE

    Journal of hypertension, Vol. 40, pp. e53

  3. Pdx1 Is Transcriptionally Regulated by EGR-1 during Nitric Oxide-Induced Endoderm Differentiation of Mouse Embryonic Stem Cells

    International Journal of Molecular Sciences, Vol. 23, Núm. 7

2021

  1. Conservation of Aging and Cancer Epigenetic Signatures across Human and Mouse

    Molecular Biology and Evolution, Vol. 38, Núm. 8, pp. 3415-3435

  2. Integrative methylome-transcriptome analysis unravels cancer cell vulnerabilities in infant MLLrearranged B cell acute lymphoblastic leukemia

    Journal of Clinical Investigation, Vol. 131, Núm. 13

2019

  1. Chromatin regulation by Histone H4 acetylation at Lysine 16 during cell death and differentiation in the myeloid compartment

    Nucleic Acids Research, Vol. 47, Núm. 10, pp. 5016-5037

  2. Longitudinal genome-wide DNA methylation analysis uncovers persistent early-life DNA methylation changes

    Journal of Translational Medicine, Vol. 17, Núm. 1

  3. Natural history and cell of origin of TCF3-ZNF384 and PTPN11 mutations in monozygotic twins with concordant BCP-ALL

    Blood

2018

  1. Epigenome-wide analysis reveals specific DNA hypermethylation of T cells during human hematopoietic differentiation

    Epigenomics, Vol. 10, Núm. 7, pp. 903-924

  2. Loss of 5hmC identifies a new type of aberrant DNA hypermethylation in glioma

    Human Molecular Genetics, Vol. 27, Núm. 17, pp. 3046-3059

2017

  1. DNA methylation changes in human lung epithelia cells exposed to multi-walled carbon nanotubes

    Nanotoxicology, Vol. 11, Núm. 7, pp. 857-870

  2. Generation and characterization of a human iPSC cell line expressing inducible Cas9 in the “safe harbor” AAVS1 locus

    Stem Cell Research, Vol. 21, pp. 137-140

2016

  1. Age-associated hydroxymethylation in human bone-marrow mesenchymal stem cells

    Journal of Translational Medicine, Vol. 14, Núm. 1

  2. Clinical and molecular analyses of Beckwith–Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques

    American Journal of Medical Genetics, Part A, Vol. 170, Núm. 10, pp. 2740-2749

  3. Differentiation of mouse embryonic stem cells toward functional pancreatic β-cell surrogates through epigenetic regulation of Pdx1 by nitric oxide

    Cell Transplantation, Vol. 25, Núm. 10, pp. 1879-1892

  4. Longitudinal study of DNA methylation during the first 5 years of life

    Journal of Translational Medicine, Vol. 14, Núm. 1

2015

  1. DNA methylation patterns in newborns exposed to tobacco in utero

    Journal of Translational Medicine, Vol. 13, Núm. 1