María Torres

2.7k total citations
40 papers, 761 citations indexed

About

María Torres is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, María Torres has authored 40 papers receiving a total of 761 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 18 papers in Molecular Biology and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in María Torres's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Chromatin Dynamics (5 papers) and Genetic Associations and Epidemiology (5 papers). María Torres is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Chromatin Dynamics (5 papers) and Genetic Associations and Epidemiology (5 papers). María Torres collaborates with scholars based in Spain, Saudi Arabia and United States. María Torres's co-authors include Ángel Carracedo, Pablo Lapunzina, Christopher Phillips, Alicia Delicado, Peter M. Schneider, M.V. Lareu, A. Freire-Aradas, M. A. Mori, Ana Mosquera‐Miguel and I. López Pajares and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

María Torres

38 papers receiving 734 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María Torres Spain 16 411 383 105 65 47 40 761
Luísa Mota‐Vieira Portugal 16 254 0.6× 301 0.8× 69 0.7× 57 0.9× 32 0.7× 63 883
D.S. Rath United States 15 694 1.7× 601 1.6× 51 0.5× 51 0.8× 40 0.9× 31 1.2k
Marie Legendre France 23 583 1.4× 741 1.9× 97 0.9× 143 2.2× 104 2.2× 82 1.6k
Maria Luisa Giovannucci Uzielli Italy 13 316 0.8× 287 0.7× 49 0.5× 37 0.6× 54 1.1× 26 546
R Pallotta Italy 11 369 0.9× 633 1.7× 88 0.8× 83 1.3× 67 1.4× 30 914
Roberto Lala Italy 18 333 0.8× 585 1.5× 74 0.7× 153 2.4× 28 0.6× 33 1.2k
Michał Witt Poland 25 671 1.6× 690 1.8× 158 1.5× 112 1.7× 46 1.0× 87 1.7k
Luciani R. Carvalho Brazil 17 409 1.0× 486 1.3× 75 0.7× 116 1.8× 15 0.3× 52 1.0k
Ana Elisa C. Billerbeck Brazil 23 747 1.8× 1.1k 2.8× 67 0.6× 108 1.7× 21 0.4× 53 1.5k
Alla G. Reddy India 17 730 1.8× 486 1.3× 41 0.4× 34 0.5× 13 0.3× 29 1.2k

Countries citing papers authored by María Torres

Since Specialization
Citations

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

Fields of papers citing papers by María Torres

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Torres

This figure shows the co-authorship network connecting the top 25 collaborators of María Torres. A scholar is included among the top collaborators of María Torres 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 María Torres. María Torres 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.
2.
Gago-Domínguez, Manuela, Manuel Calaza, María A. Bermúdez, et al.. (2021). LIPG endothelial lipase and breast cancer risk by subtypes. Scientific Reports. 11(1). 10436–10436. 2 indexed citations
3.
Lorenzo-González, María, Alberto Ruano‐Raviña, María Torres‐Durán, et al.. (2019). Residential radon, genetic polymorphisms in DNA damage and repair-related. Lung Cancer. 135. 10–15. 22 indexed citations
4.
Agra, Rosa M., Manuela Gago-Domínguez, Beatriz Paradela‐Dobarro, et al.. (2019). Obesity-Related Genetic Determinants of Heart Failure Prognosis. Cardiovascular Drugs and Therapy. 33(4). 415–424. 5 indexed citations
5.
Freire-Aradas, A., Christopher Phillips, Ana Mosquera‐Miguel, et al.. (2016). Development of a methylation marker set for forensic age estimation using analysis of public methylation data and the Agena Bioscience EpiTYPER system. Forensic Science International Genetics. 24. 65–74. 118 indexed citations
6.
Alcalde, Mireia, Óscar Campuzano, Catarina Allegue, et al.. (2014). Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications. International Journal of Legal Medicine. 129(1). 1–10. 15 indexed citations
7.
Delicado, Alicia, Luís Fernández, María Torres, et al.. (2014). Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrier. BMC Medical Genetics. 15(1). 116–116. 3 indexed citations
8.
Teruel, Beatríz Marcheco, Esteban J. Parra, Antonio Salas, et al.. (2014). Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers. PLoS Genetics. 10(7). e1004488–e1004488. 50 indexed citations
9.
Phillips, Christopher, Walther Parson, Carla Santos, et al.. (2014). Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set. Forensic Science International Genetics. 11. 13–25. 101 indexed citations
10.
Vallespín, Elena, María Palomares‐Bralo, M. A. Mori, et al.. (2013). Customized high resolution CGH‐array for clinical diagnosis reveals additional genomic imbalances in previous well‐defined pathological samples. American Journal of Medical Genetics Part A. 161(8). 1950–1960. 27 indexed citations
11.
Maside, Xulio, J. Llovo, Xabier Bello, et al.. (2013). High-throughput genotyping assay for the large-scale genetic characterization ofCryptosporidiumparasites from human and bovine samples. Parasitology. 141(4). 491–500. 8 indexed citations
12.
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
13.
Brión, Marı́a, Inés Quintela, Beatriz Sobrino, et al.. (2010). New technologies in the genetic approach to sudden cardiac death in the young. Forensic Science International. 203(1-3). 15–24. 17 indexed citations
14.
Palomares‐Bralo, María, Alicia Delicado, Pablo Lapunzina, et al.. (2008). Direct tandem duplication in chromosome 19q characterized by array CGH. European Journal of Medical Genetics. 51(3). 257–263. 9 indexed citations
15.
Ortega‐Gutiérrez, Silvia, Alicia Delicado, María Ángeles Mori, et al.. (2006). The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population. American Journal of Medical Genetics Part A. 140A(24). 2832–2833. 9 indexed citations
16.
Pajares, I. López, Olaya Villa, Marta Salido, et al.. (2006). Euchromatic variant 16p+. Implications in prenatal diagnosis. Prenatal Diagnosis. 26(6). 535–538. 15 indexed citations
17.
Martín, José Manuel Somoza, Abel Garcı́a Garcı́a, Francisco Barros, et al.. (2005). Gene Expression Profile in Oral Squamous Cell Carcinoma: A Pilot Study. Journal of Oral and Maxillofacial Surgery. 63(6). 786–792. 13 indexed citations
18.
Lapunzina, Pablo, et al.. (2004). Macrocephaly‐cutis marmorata telangiectatica congenita: Report of six new patients and a review. American Journal of Medical Genetics Part A. 130A(1). 45–51. 61 indexed citations
19.
Vega, Ana, Josema Torres, María Torres, et al.. (2003). A Novel Loss-of-Function Mutation (N48K) in the PTEN Gene in a Spanish Patient with Cowden Disease. Journal of Investigative Dermatology. 121(6). 1356–1359. 16 indexed citations
20.
Satre, Véronique, Nicole Monnier, Carmen Ayuso, et al.. (1999). Characterization of a Germline Mosaicism in Families with Lowe Syndrome, and Identification of Seven Novel Mutations in the OCRL1 Gene. The American Journal of Human Genetics. 65(1). 68–76. 42 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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