Eva Ramos‐Luis

783 total citations
15 papers, 199 citations indexed

About

Eva Ramos‐Luis is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Eva Ramos‐Luis has authored 15 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Cardiology and Cardiovascular Medicine and 7 papers in Molecular Biology. Recurrent topics in Eva Ramos‐Luis's work include Forensic and Genetic Research (7 papers), Cardiac electrophysiology and arrhythmias (6 papers) and Ion channel regulation and function (3 papers). Eva Ramos‐Luis is often cited by papers focused on Forensic and Genetic Research (7 papers), Cardiac electrophysiology and arrhythmias (6 papers) and Ion channel regulation and function (3 papers). Eva Ramos‐Luis collaborates with scholars based in Spain, France and Italy. Eva Ramos‐Luis's co-authors include Ãngel Carracedo, Marı́a Brión, Alejandro Blanco‐Verea, Beatriz Sobrino, Peter M. Schneider, E. Musgrave-Brown, Rixun Fang, Christopher Phillips, Manohar R. Furtado and C. Harrison and has published in prestigious journals such as PLoS ONE, Molecular Biology and Evolution and Electrophoresis.

In The Last Decade

Eva Ramos‐Luis

14 papers receiving 196 citations

Peers

Eva Ramos‐Luis

GENET

CCM

ECOLO

ARCHE

Takeshi Takeyasu Japan

Makiko Uno Japan

Stephen Cutie United States

Denilce R. Sumita Brazil

James Go United States

Omid Paknia Germany

Domena Tu Canada

Kaiyin Zhong Netherlands

R. K. Kumawat India

Petra Kaiser Germany

Takeshi Takeyasu Japan

Eva Ramos‐Luis

71 ×0.6

GENET

219 ×2.1

9 ×0.2

CCM

6 ×0.3

ECOLO

7 ×0.5

ARCHE

Citations per year, relative to Eva Ramos‐Luis Eva Ramos‐Luis (= 1×) peers Takeshi Takeyasu

Countries citing papers authored by Eva Ramos‐Luis

Since Specialization

Citations

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

Fields of papers citing papers by Eva Ramos‐Luis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eva Ramos‐Luis. 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 Eva Ramos‐Luis. The network helps show where Eva Ramos‐Luis may publish in the future.

Co-authorship network of co-authors of Eva Ramos‐Luis

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

All Works

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15 of 15 papers shown

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

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

Ramos‐Luis, Eva, et al.. (2020). The place of metropolitan France in the European genomic landscape. Human Genetics. 139(8). 1091–1105. 2 indexed citations

Blanco‐Verea, Alejandro, Juan Ansede‐Bermejo, Eva Ramos‐Luis, et al.. (2019). Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths. Forensic Science International Genetics. 42. 203–212. 8 indexed citations

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

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.

Blanco‐Verea, Alejandro, Eva Ramos‐Luis, Javier García‐Seara, et al.. (2018). Una nueva delección de calsequestrina 2 que causa taquicardia ventricular polimórfica catecolaminérgica y muerte súbita cardiaca. Revista Española de Cardiología. 72(8). 681–683. 1 indexed citations

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

Ramos‐Luis, Eva, Alejandro Blanco‐Verea, Marı́a Brión, et al.. (2014). Y-chromosomal DNA analysis in French male lineages. Forensic Science International Genetics. 9. 162–168. 14 indexed citations

10.

Brión, Marı́a, Alejandro Blanco‐Verea, Beatriz Sobrino, et al.. (2014). Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders. Electrophoresis. 35(21-22). 3111–3116. 25 indexed citations

11.

Martínez‐Cruz, Begoña, Christine Harmant, Daniel E. Platt, et al.. (2012). Evidence of Pre-Roman Tribal Genetic Structure in Basques from Uniparentally Inherited Markers. Molecular Biology and Evolution. 29(9). 2211–2222. 31 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, Marı́a Brión, Eva Ramos‐Luis, M.V. Lareu, & Ãngel Carracedo. (2008). Forensic validation and implementation of Y-chromosome SNP multiplexes. Forensic science international. Genetics supplement series. 1(1). 181–183. 3 indexed citations

14.

Phillips, Christopher, Rixun Fang, David Ballard, et al.. (2007). Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel. Forensic Science International Genetics. 1(2). 180–185. 74 indexed citations

15.

Ãlvarez-Iglesias, Vanesa, Antonio Salas, María Cerezo, et al.. (2006). Genotyping coding region mtDNA SNPs for Asian and Native American haplogroup assignation. International Congress Series. 1288. 4–6. 3 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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