Bernat del Olmo

643 total citations
18 papers, 229 citations indexed

About

Bernat del Olmo is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Bernat del Olmo has authored 18 papers receiving a total of 229 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Bernat del Olmo's work include Cardiac electrophysiology and arrhythmias (11 papers), Cardiovascular Effects of Exercise (8 papers) and RNA and protein synthesis mechanisms (5 papers). Bernat del Olmo is often cited by papers focused on Cardiac electrophysiology and arrhythmias (11 papers), Cardiovascular Effects of Exercise (8 papers) and RNA and protein synthesis mechanisms (5 papers). Bernat del Olmo collaborates with scholars based in Spain, Italy and United States. Bernat del Olmo's co-authors include Mónica Coll, Óscar Campuzano, Anna Iglesias, Ramón Brugada, Jesús Matés, Ferran Picó, Alexandra Pérez‐Serra, Antonio Oliva, Pasquale Striano and Marta Puigmulé and has published in prestigious journals such as PLoS ONE, The FASEB Journal and International Journal of Molecular Sciences.

In The Last Decade

Bernat del Olmo

18 papers receiving 227 citations

Peers

Bernat del Olmo

CCM

PMH

CMN

GENET

Jesús Matés Spain

Ferran Picó Spain

Nishtha Joshi United States

Roberta Paravidino Italy

Vandana Shashi United States

Sinéad B. Heavin Australia

Barbara Podestà Italy

Melanie Bonner United States

Jennifer D. Kunic United States

Jesús Matés Spain

Bernat del Olmo

260 ×1.8

CCM

177 ×1.5

50 ×1.0

PMH

48 ×1.4

CMN

47 ×1.6

GENET

Citations per year, relative to Bernat del Olmo Bernat del Olmo (= 1×) peers Jesús Matés

Countries citing papers authored by Bernat del Olmo

Since Specialization

Citations

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

Fields of papers citing papers by Bernat del Olmo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernat del Olmo. 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 Bernat del Olmo. The network helps show where Bernat del Olmo may publish in the future.

Co-authorship network of co-authors of Bernat del Olmo

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

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Bosch‐Barrera, Joaquim, Mel·lina Pinsach‐Abuin, Bernat del Olmo, et al.. (2025). The STAT3/TIMP1 inhibitor silibinin overcomes secondary immunoresistance to pembrolizumab in brain metastases from METex14 skipping mutated non-small cell lung cancer: a case report. Frontiers in Medicine. 12. 1612327–1612327. 1 indexed citations

Toro, Rocío, Anna Iglesias, Anna Fernández-Falgueras, et al.. (2024). Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy. International Journal of Molecular Sciences. 25(7). 3807–3807. 2 indexed citations

Coll, Mónica, Anna Fernández-Falgueras, Anna Iglesias, et al.. (2022). Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples. International Journal of Molecular Sciences. 23(20). 12640–12640. 1 indexed citations

Alcalde, Mireia, Coloma Tirón, Anna Fernández-Falgueras, et al.. (2022). Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations. Forensic Science International Genetics. 58. 102688–102688. 2 indexed citations

Coll, Mónica, Anna Fernández-Falgueras, Coloma Tirón, et al.. (2022). Post-mortem toxicology analysis in a young sudden cardiac death cohort. Forensic Science International Genetics. 59. 102723–102723. 5 indexed citations

Carbó, Anna, Jordi Rubió‐Casadevall, Montse Puigdemont, et al.. (2022). Epidemiology and Molecular Profile of Mucosal Melanoma: A Population-Based Study in Southern Europe. Cancers. 14(3). 780–780. 11 indexed citations

Pinsach‐Abuin, Mel·lina, Bernat del Olmo, Jesús Matés, et al.. (2021). Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants. Cell Reports Medicine. 2(4). 100250–100250. 4 indexed citations

Campuzano, Óscar, Georgia Sarquella‐Brugada, Anna Fernández-Falgueras, et al.. (2019). Genetic interpretation and clinical translation of minor genes related to Brugada syndrome. Human Mutation. 40(6). 749–764. 29 indexed citations

Campuzano, Óscar, Anna Fernández-Falgueras, Georgia Sarquella‐Brugada, et al.. (2019). Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants. Journal of Clinical Medicine. 8(7). 1035–1035. 26 indexed citations

10.

Coll, Mónica, Pasquale Striano, Carles Ferrer‐Costa, et al.. (2017). Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP. PLoS ONE. 12(12). e0189618–e0189618. 34 indexed citations

11.

D’Ovidio, Cristian, Enrica Rosato, Bernat del Olmo, et al.. (2017). Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications. Forensic Science Medicine and Pathology. 13(2). 217–225. 5 indexed citations

12.

Campuzano, Óscar, Ana María Cameán Fernández, Irene Mademont‐Soler, et al.. (2017). Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis. Sports Medicine. 47(10). 2101–2115. 13 indexed citations

13.

Coll, Mónica, Alexandra Pérez‐Serra, Jesús Matés, et al.. (2017). Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death. Biology. 7(1). 3–3. 29 indexed citations

14.

Campuzano, Óscar, Irene Mademont‐Soler, Mónica Coll, et al.. (2017). Genetic analysis in post-mortem samples with micro-ischemic alterations. Forensic Science International. 271. 120–125. 1 indexed citations

15.

Mademont‐Soler, Irene, Mel·lina Pinsach‐Abuin, Helena Riuró, et al.. (2016). Large Genomic Imbalances in Brugada Syndrome. PLoS ONE. 11(9). e0163514–e0163514. 16 indexed citations

16.

Campuzano, Óscar, Georgia Sarquella‐Brugada, Sergi César, et al.. (2016). A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia. Forensic Science International. 270. 173–177. 2 indexed citations

17.

Pinsach‐Abuin, Mel·lina, Jesús Matés, Bernat del Olmo, et al.. (2016). Regulome‐Seq: Searching for Single Nucleotide Variants (SNVs) Associated with Disease Beyond Protein‐Coding Regions. The FASEB Journal. 30(S1). 1 indexed citations

18.

Coll, Mónica, Catarina Allegue, Sara Partemi, et al.. (2015). Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing. International Journal of Legal Medicine. 130(2). 331–339. 47 indexed citations

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.

Explore authors with similar magnitude of impact