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Dori Huertas · SciRah

Researcher profile · Semantic Scholar

Dori Huertas

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Dori Huertas — researcher profile on SciRah

h-index: 16
Works: 17
Citations: 1,025

Most-cited papers

Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome
R. G. Urdinguio, A. Fernández, P. López-Nieva, S. Rossi +6 more
2010Epigenetics139 citations Open access
Semantic Scholar
Antitumor activity of a small-molecule inhibitor of the histone kinase Haspin
Dori Huertas, M. T. Soler, J. Moretó, A. Villanueva +11 more
2011Oncogene124 citations Open access
Semantic Scholar
Chromatin dynamics coupled to DNA repair
Dori Huertas, R. Sendra, P. Muñoz
2009Epigenetics96 citations Open access
Semantic Scholar
Lurbinectedin (PM01183), a New DNA Minor Groove Binder, Inhibits Growth of Orthotopic Primary Graft of Cisplatin-Resistant Epithelial Ovarian Cancer
A. Vidal, Clara Muñoz, M. Guillén, J. Moretó +20 more
2012Clinical Cancer Research94 citations Open access
Semantic Scholar
Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient
H. Heyn, E. Vidal, S. Sayols, J. Sanchez-Mut +10 more
2012Epigenetics82 citations Open access
Semantic Scholar
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype
Mario Lucariello, E. Vidal, S. Vidal, M. Sáez +8 more
2016Human Genetics74 citations Open access
Semantic Scholar
Dysregulation of the long non-coding RNA transcriptome in a Rett syndrome mouse model
P. Petazzi, J. Sandoval, Karolina Szczesna, Olga C. Jorge +5 more
2013RNA Biology74 citations Open access
Semantic Scholar
Comparative genome-wide DNA methylation analysis of colorectal tumor and matched normal tissues
F. Simmer, A. Brinkman, Y. Assenov, Filomena Matarese +10 more
2012Epigenetics74 citations Open access
Semantic Scholar
Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice.
Olga C. Jorge-Torres, Karolina Szczesna, Laura Roa, C. Casal +13 more
2018Cell Reports55 citations Open access
Semantic Scholar
Mutations in JMJD1C are involved in Rett syndrome and intellectual disability
M. Sáez, J. Fernández-Rodríguez, C. Moutinho, J. Sanchez-Mut +19 more
2015Genetics in Medicine49 citations Open access
Semantic Scholar
Expression of the human CFTR gene from episomal oriP-EBNA1-YACs in mouse cells.
Dori Huertas, Steve Howe, A. McGuigan, Clare Huxley
2000Human Molecular Genetics33 citations
Semantic Scholar
Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor
Karolina Szczesna, Olga de la Caridad, P. Petazzi, M. Soler +9 more
2014Neuropsychopharmacology29 citations Open access
Semantic Scholar
Circadian Cycle-Dependent MeCP2 and Brain Chromatin Changes
Alexia Martínez de Paz, J. Sanchez-Mut, M. Samitier-Martí, P. Petazzi +5 more
2015PLoS ONE28 citations Open access
Semantic Scholar
Aberrant epigenetic landscape in intellectual disability.
J. Sanchez-Mut, Dori Huertas, M. Esteller
2012Progress in Brain Research26 citations
Semantic Scholar
Generation and Characterization of Rat and Mouse Monoclonal Antibodies Specific for MeCP2 and Their Use in X-Inactivation Studies
K. Jost, Andrea Rottach, Manuela Milden, B. Bertulat +9 more
2011PLoS ONE24 citations Open access
Semantic Scholar
An increase in MECP2 dosage impairs neural tube formation.
P. Petazzi, N. Akizu, Alejandra García, C. Estarás +5 more
2014Neurobiology of Disease23 citations Open access
Semantic Scholar
Cancer Therapy : Preclinical Lurbinectedin ( PM 01183 ) , a New DNA Minor Groove Binder , Inhibits Growth of Orthotopic Primary Graft of Cisplatin-Resistant Epithelial Ovarian Cancer
A. Vidal, S. Puertas, Laura Padull, M. Berdiel-Acer +12 more
20120 citations
Semantic Scholar

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