Javier Santoyo‐López

6.3k total citations
30 papers, 2.3k citations indexed

About

Javier Santoyo‐López is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Javier Santoyo‐López has authored 30 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Javier Santoyo‐López's work include RNA and protein synthesis mechanisms (5 papers), RNA Research and Splicing (5 papers) and RNA regulation and disease (4 papers). Javier Santoyo‐López is often cited by papers focused on RNA and protein synthesis mechanisms (5 papers), RNA Research and Splicing (5 papers) and RNA regulation and disease (4 papers). Javier Santoyo‐López collaborates with scholars based in Spain, United Kingdom and Switzerland. Javier Santoyo‐López's co-authors include César de Haro, Raúl Méndez, Joaquı́n Dopazo, Juan José Berlanga, David Montaner, Ignacio Medina, Ana Conesa, Peter Ghazal, Emma Shanks and Caleb J. Kennedy and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Javier Santoyo‐López

30 papers receiving 2.3k citations

Peers

Countries citing papers authored by Javier Santoyo‐López

Since Specialization

Citations

This map shows the geographic impact of Javier Santoyo‐López'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 Javier Santoyo‐López with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Javier Santoyo‐López more than expected).

Fields of papers citing papers by Javier Santoyo‐López

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Javier Santoyo‐López. 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 Javier Santoyo‐López. The network helps show where Javier Santoyo‐López may publish in the future.

Co-authorship network of co-authors of Javier Santoyo‐López

This figure shows the co-authorship network connecting the top 25 collaborators of Javier Santoyo‐López. A scholar is included among the top collaborators of Javier Santoyo‐López 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 Javier Santoyo‐López. Javier Santoyo‐López is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia 2024 ·Pediatric Pulmonology ·(unknown), Sophie Marion de Procé, José Luis Campos, Alison Meynert, Mihail Halachev, Joseph A. Marsh, Robert A. Hirst, Chris O’Callaghan, Amelia Shoemark, (unknown), (unknown), Javier Santoyo‐López, Jennie Murray, Kenneth Macleod, Don S. Urquhart, Stefan Unger, Timothy J. Aitman, Pleasantine Mill	3
2	Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome 2023 ·Journal of Medical Genetics ·Anthony M. Vandersteen, Ruwan Weerakkody, David Parry, (unknown), (unknown), Jana Vandrovcová, Rebecca Darlay, Javier Santoyo‐López, Alison Meynert, (unknown), Hanadi Kazkaz, Rodney Grahame, (unknown), (unknown), Neeti Ghali, Angela F. Brady, F M Pope, Fleur S. van Dijk, Heather J. Cordell, Timothy J. Aitman	7
3	Selective miRNA inhibition in CD8+ cytotoxic T lymphocytes enhances HIV-1 specific cytotoxic responses 2022 ·Frontiers in Immunology ·Nadia Madrid-Elena, Sergio Serrano‐Villar, Carolina Gutiérrez, Beatriz Sastre, Matías Morin, (unknown), (unknown), Javier Santoyo‐López, María Rosa López‐Huertas, Elena Moreno, Laura García‐Bermejo, Miguel A. Moreno‐Pelayo, Santiago Moreno	5
4	An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort 2019 ·Scientific Reports ·Shona M. Kerr, Lucija Klarić, Mihail Halachev, Caroline Hayward, Thibaud Boutin, Alison Meynert, Colin A. Semple, (unknown), Heikki Swan, Javier Santoyo‐López, Véronique Vitart, Chris Haley, John Dean, Zosia Miedzybrodzka, Timothy J. Aitman, James F. Wilson	16
5	Selective miRNA Modulation Fails to Activate HIV Replication in In Vitro Latency Models 2019 ·Molecular Therapy — Nucleic Acids ·María Rosa López‐Huertas, Matías Morin, Nadia Madrid-Elena, Carolina Gutiérrez, (unknown), Javier Santoyo‐López, Francisco Sanz‐Rodríguez, Miguel A. Moreno‐Pelayo, Laura García‐Bermejo, Santiago Moreno	8
6	A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer 2018 ·The American Journal of Human Genetics ·D. Gareth Evans, Elke M. van Veen, Helen Byers, Andrew J. Wallace, Jamie M. Ellingford, Glenda M. Beaman, Javier Santoyo‐López, Timothy J. Aitman, Diana Eccles, Fiona Lalloo, Miriam J. Smith, William G. Newman	57
7	Mutational landscape of a chemically-induced mouse model of liver cancer 2018 ·Journal of Hepatology ·Frances Connor, Tim F. Rayner, Sarah J. Aitken, Christine Feig, Margus Lukk, Javier Santoyo‐López, Duncan T. Odom	98
8	Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq) 2016 ·Nature Communications ·Julien Lagarde, Barbara Uszczyńska-Ratajczak, Javier Santoyo‐López, José M. González, Electra Tapanari, Jonathan M. Mudge, Charles A. Steward, Laurens Wilming, Andrea Tanzer, Cédric Howald, Jacqueline Chrast, Alicia Vela‐Boza, Antonio Rueda, (unknown), Joaquı́n Dopazo, Alexandre Reymond, Roderic Guigó, Jennifer Harrow	58
9	PAX4 preserves endoplasmic reticulum integrity preventing beta cell degeneration in a mouse model of type 1 diabetes mellitus 2016 ·Diabetologia ·José Manuel Mellado‐Gil, (unknown), Alejandro Martín‐Montalvo, Ana I. Álvarez‐Mercado, Esther Fuente-Martín, Nadia Cobo‐Vuilleumier, Petra I. Lorenzo, (unknown), (unknown), Livia López–Noriega, Javier Pérez-Florido, Javier Santoyo‐López, (unknown), Paolo Meda, Bernhard O. Boehm, Iván Quesada, Benoit R. Gauthier	34
10	poRe: an R package for the visualization and analysis of nanopore sequencing data 2014 ·Bioinformatics ·Mick Watson, Marian Thomson, Judith Risse, Richard Talbot, Javier Santoyo‐López, Karim Gharbi, Mark Blaxter	55
11	The role of the interactome in the maintenance of deleterious variability in human populations 2014 ·Molecular Systems Biology ·Luz García‐Alonso, Jorge Jiménez, José Carbonell‐Caballero, Alicia Vela‐Boza, Javier Santoyo‐López, Guillermo Antiñolo, Joaquı́n Dopazo	23
12	ngsCAT: a tool to assess the efficiency of targeted enrichment sequencing 2014 ·Bioinformatics ·(unknown), Javier Pérez-Florido, Antonio Rueda, Joaquı́n Dopazo, Javier Santoyo‐López	7
13	Extensive Translatome Remodeling during ER Stress Response in Mammalian Cells 2012 ·PLoS ONE ·Iván Ventoso, А. В. Кочетов, David Montaner, Joaquı́n Dopazo, Javier Santoyo‐López	29
14	Mutation Screening of Multiple Genes in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa by Targeted Resequencing 2011 ·PLoS ONE ·María González‐del Pozo, Salud Borrego, Isabel Barragán, (unknown), Javier Santoyo‐López, Nerea Matamala, Belén Naranjo, Joaquı́n Dopazo, Guillermo Antiñolo	36
15	Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa 2010 ·Human Mutation ·Isabel Barragán, Salud Borrego, (unknown), María González‐del Pozo, Javier Santoyo‐López, Carmen Ayuso, Montserrat Baiget, José M. Millán, Marcela Mena, (unknown), Isabelle Audo, Christina Zeitz, Karin W. Littink, Joaquı́n Dopazo, (unknown), Guillermo Antiñolo	71
16	Initial Genomics of the Human Nucleolus 2010 ·PLoS Genetics ·Attila Németh, Ana Conesa, Javier Santoyo‐López, Ignacio Medina, David Montaner, Bálint Péterfia, Irina Solovei, Thomas Cremer, Joaquı́n Dopazo, Gernot Längst	284
17	Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling 2010 ·Nucleic Acids Research ·Ignacio Medina, José Carbonell‐Caballero, (unknown), Sara C. Madeira, (unknown), Ana Conesa, (unknown), Alberto Pascual-Montano, Rubén Nogales‐Cadenas, Javier Santoyo‐López, Francisco García‐García, (unknown), David Montaner, Joaquı́n Dopazo	266
18	Statistical methods for analysis of high-throughput RNA interference screens 2009 ·Nature Methods ·Amanda Birmingham, Laura M. Selfors, Thorsten Forster, David M. Wrobel, Caleb J. Kennedy, Emma Shanks, Javier Santoyo‐López, Dara J. Dunican, Aideen Long, Dermot Kelleher, (unknown), Roderick L. Beijersbergen, Peter Ghazal, Caroline E. Shamu	439
19	Using Gene Ontology on genome-scale studies to find significant associations of biologically relevant terms to group of genes 2003 ·Fátima Al‐Shahrour, Javier Herrero, Álvaro Mateos, Javier Santoyo‐López, Ramón Díaz‐Uriarte, Joaquı́n Dopazo	2
20	Characterization of a mammalian homolog of the GCN2 eukaryotic initiation factor 2α kinase 1999 ·European Journal of Biochemistry ·Juan José Berlanga, Javier Santoyo‐López, César de Haro	216

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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