Ferran Picó

726 total citations
15 papers, 232 citations indexed

About

Ferran Picó is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Ferran Picó has authored 15 papers receiving a total of 232 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cardiology and Cardiovascular Medicine, 8 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Ferran Picó's work include Cardiac electrophysiology and arrhythmias (10 papers), Cardiomyopathy and Myosin Studies (6 papers) and Cardiovascular Effects of Exercise (6 papers). Ferran Picó is often cited by papers focused on Cardiac electrophysiology and arrhythmias (10 papers), Cardiomyopathy and Myosin Studies (6 papers) and Cardiovascular Effects of Exercise (6 papers). Ferran Picó collaborates with scholars based in Spain, Netherlands and Italy. Ferran Picó's co-authors include Óscar Campuzano, Anna Iglesias, Ramón Brugada, Alexandra Pérez‐Serra, Mónica Coll, Jesús Matés, Bernat del Olmo, Irene Mademont‐Soler, Georgia Sarquella‐Brugada and Josép Brugada and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Sports Medicine.

In The Last Decade

Ferran Picó

15 papers receiving 228 citations

Peers

Ferran Picó
Bernat del Olmo Spain
Jennifer D. Kunic United States
Gerard A. Marchal Netherlands
Yijun Tang China
Anna Fernández-Falgueras Spain
Michael S. Bohnen United States
Elliott H. Sherr United States
Jaakko T. Leinonen Finland
Roberta Paravidino Italy
Miriam Bloom United States
Bernat del Olmo Spain
Ferran Picó
Citations per year, relative to Ferran Picó Ferran Picó (= 1×) peers Bernat del Olmo

Countries citing papers authored by Ferran Picó

Since Specialization
Citations

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

Fields of papers citing papers by Ferran Picó

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ferran Picó. 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 Ferran Picó. The network helps show where Ferran Picó may publish in the future.

Co-authorship network of co-authors of Ferran Picó

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

All Works

15 of 15 papers shown
1.
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
2.
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
3.
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
4.
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
5.
Puigmulé, Marta, Mónica Coll, Alexandra Pérez‐Serra, et al.. (2021). High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP. Experimental Biology and Medicine. 247(3). 276–281. 2 indexed citations
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
Selga, Elisabet, Óscar Campuzano, Mel·lina Pinsach‐Abuin, et al.. (2015). Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. PLoS ONE. 10(7). e0132888–e0132888. 19 indexed citations
13.
Campuzano, Óscar, Irene Mademont‐Soler, Helena Riuró, et al.. (2015). Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death. International Journal of Molecular Sciences. 16(10). 25773–25787. 17 indexed citations
14.
Riuró, Helena, Óscar Campuzano, Paola Berne, et al.. (2014). Genetic analysis, in silico prediction, and family segregation in long QT syndrome. European Journal of Human Genetics. 23(1). 79–85. 17 indexed citations
15.
Selga, Elisabet, Pedro Beltrán-Álvarez, Alexandra Pérez‐Serra, et al.. (2013). A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome. PLoS ONE. 8(1). e53220–e53220. 20 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.

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2026