Mauricio Sáez

598 total citations
17 papers, 413 citations indexed

About

Mauricio Sáez is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Mauricio Sáez has authored 17 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Cognitive Neuroscience. Recurrent topics in Mauricio Sáez's work include Genetics and Neurodevelopmental Disorders (7 papers), Epigenetics and DNA Methylation (6 papers) and Autism Spectrum Disorder Research (5 papers). Mauricio Sáez is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Epigenetics and DNA Methylation (6 papers) and Autism Spectrum Disorder Research (5 papers). Mauricio Sáez collaborates with scholars based in Chile, Spain and United States. Mauricio Sáez's co-authors include Juan I. Young, Matías Alvarez-Saavedra, Bredford Kerr, Huda Y. Zoghbi, Dori Huertas, Manel Esteller, Dongcheul Kang, Maria Merino, Julián Sanz‐Ortega and Seth M. Steinberg and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Mauricio Sáez

15 papers receiving 409 citations

Peers

Mauricio Sáez
Kirill Makedonski Israel
Paolo Petazzi Spain
James C. McGann United States
Julie Krosting United States
Shelley Jacobs Australia
Thijs van der Vaart Netherlands
Karolina Szczęsna Spain
Pierre Cacciagli France
Jéssica Molina United States
Eva Rossier Germany
Kirill Makedonski Israel
Mauricio Sáez
Citations per year, relative to Mauricio Sáez Mauricio Sáez (= 1×) peers Kirill Makedonski

Countries citing papers authored by Mauricio Sáez

Since Specialization
Citations

This map shows the geographic impact of Mauricio Sáez's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mauricio Sáez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mauricio Sáez more than expected).

Fields of papers citing papers by Mauricio Sáez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mauricio Sáez. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mauricio Sáez. The network helps show where Mauricio Sáez may publish in the future.

Co-authorship network of co-authors of Mauricio Sáez

This figure shows the co-authorship network connecting the top 25 collaborators of Mauricio Sáez. A scholar is included among the top collaborators of Mauricio Sáez based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mauricio Sáez. Mauricio Sáez is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Riquelme, Erick, et al.. (2025). Neuroprotective and gut health benefits of Ugni molinae in preclinical Huntington's disease models. Experimental Neurology. 393. 115406–115406.
2.
Pérez, Pablo Ernesto, Alberto J. M. Martín, Fabio Mammano, et al.. (2025). Connexin46 in the nucleus of cancer cells: a possible role as transcription modulator. Cell Communication and Signaling. 23(1). 153–153. 1 indexed citations
3.
4.
Pollastri, Gianluca, et al.. (2024). Understanding relationships between epigenetic marks and their application to robust assignment of chromatin states. Briefings in Bioinformatics. 26(1). 1 indexed citations
5.
Sánchez, Mario, et al.. (2023). Transcriptional and Histone Acetylation Changes Associated with CRE Elements Expose Key Factors Governing the Regulatory Circuit in the Early Stage of Huntington’s Disease Models. International Journal of Molecular Sciences. 24(13). 10848–10848. 5 indexed citations
6.
Sáez, Mauricio, et al.. (2023). Unraveling patient heterogeneity in complex diseases through individualized co-expression networks: a perspective. Frontiers in Genetics. 14. 1209416–1209416. 2 indexed citations
7.
Pollastri, Gianluca, et al.. (2023). Benefiting from the intrinsic role of epigenetics to predict patterns of CTCF binding. Computational and Structural Biotechnology Journal. 21. 3024–3031.
8.
Pinto, Mauricio P., Charlotte Hill, Carolina Sánchez‐Rodríguez, et al.. (2022). Differentially Expressed Genes and Signaling Pathways Potentially Involved in Primary Resistance to Chemo-Immunotherapy in Advanced-Stage Gastric Cancer Patients. International Journal of Molecular Sciences. 24(1). 1–1. 9 indexed citations
9.
Szczęsna, Karolina, Laura M. Roa, Carmen Casal, et al.. (2018). Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice. Cell Reports. 23(6). 1665–1677. 42 indexed citations
10.
Vidal, Enrique, Silvia M. Vidal, Mauricio Sáez, et al.. (2016). Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. Human Genetics. 135(12). 1343–1354. 48 indexed citations
11.
Aguilar, Rodrigo, Fernando J. Bustos, Mauricio Sáez, et al.. (2016). Polycomb PRC2 complex mediates epigenetic silencing of a critical osteogenic master regulator in the hippocampus. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859(8). 1043–1055. 16 indexed citations
12.
Paz, Alexia Martínez de, José V. Sánchez‐Mut, Paolo Petazzi, et al.. (2015). Circadian Cycle-Dependent MeCP2 and Brain Chromatin Changes. PLoS ONE. 10(4). e0123693–e0123693. 26 indexed citations
13.
Szczęsna, Karolina, Paolo Petazzi, Marta Soler, et al.. (2014). Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor. Neuropsychopharmacology. 39(12). 2846–2856. 25 indexed citations
14.
Kerr, Bredford, et al.. (2011). Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes. European Journal of Human Genetics. 20(1). 69–76. 44 indexed citations
15.
Kerr, Bredford, et al.. (2008). Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice. Human Molecular Genetics. 17(12). 1707–1717. 59 indexed citations
16.
Alvarez-Saavedra, Matías, Mauricio Sáez, Dongcheul Kang, Huda Y. Zoghbi, & Juan I. Young. (2007). Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis. Human Molecular Genetics. 16(19). 2315–2325. 55 indexed citations
17.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026