Alejandro Blanco‐Verea

896 total citations
35 papers, 650 citations indexed

About

Alejandro Blanco‐Verea is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Alejandro Blanco‐Verea has authored 35 papers receiving a total of 650 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 16 papers in Molecular Biology and 16 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Alejandro Blanco‐Verea's work include Forensic and Genetic Research (17 papers), Cardiac electrophysiology and arrhythmias (13 papers) and Genetic diversity and population structure (9 papers). Alejandro Blanco‐Verea is often cited by papers focused on Forensic and Genetic Research (17 papers), Cardiac electrophysiology and arrhythmias (13 papers) and Genetic diversity and population structure (9 papers). Alejandro Blanco‐Verea collaborates with scholars based in Spain, United Kingdom and Italy. Alejandro Blanco‐Verea's co-authors include Ángel Carracedo, Marı́a Brión, M.V. Lareu, Beatriz Sobrino, Antonio Salas, M. Fondevila, Cristian Capelli, Eva Ramos‐Luis, Peter M. Schneider and Antonio Alonso and has published in prestigious journals such as PLoS ONE, Heart and Clinica Chimica Acta.

In The Last Decade

Alejandro Blanco‐Verea

33 papers receiving 640 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alejandro Blanco‐Verea Spain 15 430 246 142 57 39 35 650
K. Hiester United States 6 348 0.8× 160 0.7× 12 0.1× 22 0.4× 8 0.2× 6 544
C. Brandt-Casadevall Switzerland 10 187 0.4× 132 0.5× 16 0.1× 46 0.8× 14 0.4× 33 338
Usha Soundararajan United States 13 427 1.0× 277 1.1× 7 0.0× 32 0.6× 5 0.1× 14 584
Mauro Pesaresi Italy 11 250 0.6× 180 0.7× 28 0.2× 28 0.5× 4 0.1× 35 448
Peter de Barros Damgaard Denmark 4 85 0.2× 41 0.2× 7 0.0× 25 0.4× 26 0.7× 4 188
Carlo Sidore Italy 12 417 1.0× 309 1.3× 10 0.1× 12 0.2× 7 0.2× 24 671
Yaqun Guan China 11 239 0.6× 191 0.8× 21 0.1× 65 1.1× 1 0.0× 28 452
Eva Ramos‐Luis Spain 8 128 0.3× 103 0.4× 46 0.3× 15 0.3× 10 0.3× 15 199
Melisa Kiyamu United States 10 260 0.6× 84 0.3× 16 0.1× 2 0.0× 39 1.0× 16 350
Dennis Y. Wang United Kingdom 16 411 1.0× 452 1.8× 3 0.0× 41 0.7× 11 0.3× 20 778

Countries citing papers authored by Alejandro Blanco‐Verea

Since Specialization
Citations

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

Fields of papers citing papers by Alejandro Blanco‐Verea

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alejandro Blanco‐Verea. 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 Alejandro Blanco‐Verea. The network helps show where Alejandro Blanco‐Verea may publish in the future.

Co-authorship network of co-authors of Alejandro Blanco‐Verea

This figure shows the co-authorship network connecting the top 25 collaborators of Alejandro Blanco‐Verea. A scholar is included among the top collaborators of Alejandro Blanco‐Verea 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 Alejandro Blanco‐Verea. Alejandro Blanco‐Verea 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.
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
3.
Blanco‐Verea, Alejandro, Eva Ramos‐Luis, Beatriz Sobrino, et al.. (2022). Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing. Molecular Diagnosis & Therapy. 27(1). 105–113. 1 indexed citations
4.
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
5.
Blanco‐Verea, Alejandro, Eva Ramos‐Luis, Javier García‐Seara, et al.. (2018). A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death. Revista Española de Cardiología (English Edition). 72(8). 681–683.
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.
Ramos‐Luis, Eva, Esther Zorio, Pilar Molina, et al.. (2017). Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection. International Journal of Legal Medicine. 131(5). 1211–1219. 13 indexed citations
8.
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
9.
Blanco‐Verea, Alejandro, Gisela Teixidó‐Turà, Irene Valenzuela, et al.. (2014). Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease. Clinica Chimica Acta. 437. 88–92. 13 indexed citations
10.
Brisighelli, Francesca, Alejandro Blanco‐Verea, Ilaria Boschi, et al.. (2012). Patterns of Y-STR variation in Italy. Forensic Science International Genetics. 6(6). 834–839. 12 indexed citations
11.
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
12.
Ramos‐Luis, Eva, Alejandro Blanco‐Verea, Marı́a Brión, et al.. (2009). Phylogeography of French male lineages. Forensic science international. Genetics supplement series. 2(1). 439–441. 7 indexed citations
13.
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
14.
Blanco‐Verea, Alejandro, Marı́a Brión, Eva Ramos‐Luis, M.V. Lareu, & Ángel Carracedo. (2008). Forensic validation and implementation of Y-chromosome SNP multiplexes. Forensic science international. Genetics supplement series. 1(1). 181–183. 3 indexed citations
15.
Blanco‐Verea, Alejandro, et al.. (2008). The genetic male component of two South-Western Colombian populations. Forensic Science International Genetics. 3(2). e59–e61. 11 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.
Brión, Marı́a, Juan José Martínez Sánchez, C.R. Thacker, et al.. (2006). Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages. International Congress Series. 1288. 13–15. 5 indexed citations
18.
Brión, Marı́a, Juan J. Sánchez, C.R. Thacker, et al.. (2005). Introduction of an single nucleodite polymorphism‐based “Major Y‐chromosome haplogroup typing kit” suitable for predicting the geographical origin of male lineages. Electrophoresis. 26(23). 4411–4420. 65 indexed citations
19.
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
20.
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

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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