Marı́a Brión

4.7k total citations
90 papers, 2.1k citations indexed

About

Marı́a Brión is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marı́a Brión has authored 90 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 35 papers in Molecular Biology and 32 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marı́a Brión's work include Forensic and Genetic Research (38 papers), Cardiac electrophysiology and arrhythmias (20 papers) and Genetic diversity and population structure (19 papers). Marı́a Brión is often cited by papers focused on Forensic and Genetic Research (38 papers), Cardiac electrophysiology and arrhythmias (20 papers) and Genetic diversity and population structure (19 papers). Marı́a Brión collaborates with scholars based in Spain, Portugal and United Kingdom. Marı́a Brión's co-authors include Ángel Carracedo, Beatriz Sobrino, Alejandro Blanco‐Verea, M.V. Lareu, Anna González‐Neira, Catarina Allegue, Antonio Salas, Leonor Gusmão, L. Concheiro and M. S. Rodrìguez-Calvo and has published in prestigious journals such as PLoS ONE, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Marı́a Brión

87 papers receiving 2.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marı́a Brión Spain 27 1.1k 869 468 200 154 90 2.1k
Beatriz Sobrino Spain 22 906 0.8× 777 0.9× 121 0.3× 45 0.2× 162 1.1× 46 1.8k
María Cerezo Spain 13 1.1k 1.0× 917 1.1× 49 0.1× 15 0.1× 127 0.8× 19 1.8k
Analabha Basu India 19 483 0.4× 332 0.4× 37 0.1× 91 0.5× 90 0.6× 52 1.2k
Barbara Simionati Italy 16 274 0.2× 741 0.9× 481 1.0× 16 0.1× 43 0.3× 22 1.5k
М. И. Воевода Russia 18 742 0.7× 587 0.7× 329 0.7× 11 0.1× 113 0.7× 277 2.5k
Héctor Rangel‐Villalobos Mexico 26 914 0.8× 586 0.7× 70 0.1× 8 0.0× 120 0.8× 134 2.0k
Aisha Mohyuddin Pakistan 18 909 0.8× 548 0.6× 59 0.1× 21 0.1× 265 1.7× 32 1.6k
Sebastian Schönherr Austria 17 884 0.8× 768 0.9× 41 0.1× 19 0.1× 321 2.1× 54 1.7k
Antonel Olckers South Africa 15 913 0.8× 781 0.9× 152 0.3× 9 0.0× 222 1.4× 28 1.8k
Hansi Weißensteiner Austria 15 848 0.8× 835 1.0× 27 0.1× 20 0.1× 330 2.1× 40 1.6k

Countries citing papers authored by Marı́a Brión

Since Specialization
Citations

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

Fields of papers citing papers by Marı́a Brión

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marı́a Brión

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

All Works

20 of 20 papers shown
1.
Blanco‐Verea, Alejandro, Ángel Carracedo, & Marı́a Brión. (2024). Retos de la genética en el diagnóstico de la muerte súbita de origen cardiaco. Interés para la medicina legal y forense. Medicina Clínica. 164(3). e1–e7. 1 indexed citations
2.
Grassi, Simone, Marı́a Brión, Rocío Toro, et al.. (2023). Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death. Frontiers in Medicine. 10. 1118585–1118585. 33 indexed citations
3.
Cruz, Raquel, Alejandro Blanco‐Verea, Isabel Moscoso, et al.. (2022). Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome. PLoS ONE. 17(3). e0263469–e0263469. 5 indexed citations
4.
Grassi, Simone, Óscar Campuzano, Mónica Coll, et al.. (2020). Genetic variants of uncertain significance: How to match scientific rigour and standard of proof in sudden cardiac death?. Legal Medicine. 45. 101712–101712. 26 indexed citations
5.
Blanco‐Verea, Alejandro, Helena Riuró, Óscar Dı́az-Castro, et al.. (2019). Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation. Forensic Science International Genetics. 43. 102159–102159. 1 indexed citations
6.
Ramos‐Luis, Eva, Alejandro Blanco‐Verea, Constanze Nieß, et al.. (2018). Sudden unexpected death in the young — Value of massive parallel sequencing in postmortem genetic analyses. Forensic Science International. 293. 70–76. 12 indexed citations
7.
Brión, Marı́a, et al.. (2015). Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young. Forensic Science International Genetics. 18. 160–170. 29 indexed citations
8.
Suárez‐Rama, Jose Javier, Manuel Arrojo, Beatriz Sobrino, et al.. (2015). Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility. Journal of Psychiatric Research. 66-67. 38–44. 14 indexed citations
9.
Blanco‐Verea, Alejandro, et al.. (2015). Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood. Archives of Disease in Childhood. 100(10). 952–956. 22 indexed citations
10.
Allegue, Catarina, Mónica Coll, Jesús Matés, et al.. (2015). Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PLoS ONE. 10(7). e0133037–e0133037. 42 indexed citations
11.
Ussa, Fernando, Itziar Fernández, Marı́a Brión, et al.. (2015). Association between SNPs of Metalloproteinases and Prostaglandin F2α Receptor Genes and Latanoprost Response in Open-Angle Glaucoma. Ophthalmology. 122(5). 1040–1048.e4. 30 indexed citations
12.
Silbiger, Vivian Nogueira, André Ducati Luchessi, Rosário Dominguez Crespo Hirata, et al.. (2013). Novel genes detected by transcriptional profiling from whole-blood cells in patients with early onset of acute coronary syndrome. Clinica Chimica Acta. 421. 184–190. 46 indexed citations
13.
Brión, Marı́a, Catarina Allegue, Alejandro Blanco‐Verea, et al.. (2010). Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy.. PubMed. 40(3). 285–9. 5 indexed citations
14.
Allegue, Catarina, Paula Sánchez‐Diz, María Torres, et al.. (2010). A new approach to long QT syndrome mutation detection by Sequenom MassARRAY® system. Electrophoresis. 31(10). 1648–1655. 11 indexed citations
15.
Blanco‐Verea, Alejandro, et al.. (2009). Y-chromosome lineages in native South American population. Forensic Science International Genetics. 4(3). 187–193. 21 indexed citations
16.
Capelli, Cristian, Francesca Brisighelli, Francesca Scarnicci, et al.. (2007). Phylogenetic evidence for multiple independent duplication events at the DYS19 locus. Forensic Science International Genetics. 1(3-4). 287–290. 7 indexed citations
17.
Sánchez, Juan José Martínez, Marı́a Brión, Walther Parson, et al.. (2004). Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications. Forensic Science International. 140(2-3). 241–250. 24 indexed citations
18.
Brión, Marı́a. (2004). Y Chromosome SNP Analysis Using the Single-Base Extension: A Hierarchical Multiplex Design. Humana Press eBooks. 297. 229–242. 7 indexed citations
19.
Brión, Marı́a, Beatriz Sobrino, Alejandro Blanco‐Verea, M.V. Lareu, & Ángel Carracedo. (2004). Hierarchical analysis of 30 Y-chromosome SNPs in European populations. International Journal of Legal Medicine. 119(1). 10–15. 86 indexed citations
20.
Dupuy, B.M., Rune Andreassen, Thore Egeland, et al.. (2001). Y-chromosome variation in a Norwegian population sample. Forensic Science International. 117(3). 163–173. 25 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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