Inés Quintela

6.4k total citations
29 papers, 492 citations indexed

About

Inés Quintela is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Inés Quintela has authored 29 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Inés Quintela's work include Genomic variations and chromosomal abnormalities (12 papers), Genetic Associations and Epidemiology (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Inés Quintela is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genetic Associations and Epidemiology (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Inés Quintela collaborates with scholars based in Spain, Saudi Arabia and United Kingdom. Inés Quintela's co-authors include Ángel Carracedo, Isabel Rodríguez‐Moldes, Ramón Anadón, Agustı́n González, Jesús M. López, Pilar Molíst, Francisco Barros, Jesús Manuel Eirís Puñal, Manuel Castro‐Gago and Peter Donnelly and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Inés Quintela

29 papers receiving 474 citations

Peers

Inés Quintela
Aparna Prasad United States
Gloria L. Fawcett United States
Michal Bronstein Israel
Hashem Shahin Palestinian Territory
Ann Foley United States
Alexis Rea United States
Susan Zeesman Canada
A. Gulhan Ercan‐Sencicek United States
Shaheen Khan United States
Claire Bacon Germany
Aparna Prasad United States
Inés Quintela
Citations per year, relative to Inés Quintela Inés Quintela (= 1×) peers Aparna Prasad

Countries citing papers authored by Inés Quintela

Since Specialization
Citations

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

Fields of papers citing papers by Inés Quintela

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inés Quintela

This figure shows the co-authorship network connecting the top 25 collaborators of Inés Quintela. A scholar is included among the top collaborators of Inés Quintela 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 Inés Quintela. Inés Quintela 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.
Ruano‐Raviña, Alberto, Silvia Diz‐de Almeida, Raquel Cruz, et al.. (2023). A Genome-Wide Association Study of Small Cell Lung Cancer. Archivos de Bronconeumología. 59(10). 645–650. 3 indexed citations
2.
Bycroft, Clare, Ceres Fernández–Rozadilla, Clara Ruíz-Ponte, et al.. (2019). Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula. Nature Communications. 10(1). 551–551. 50 indexed citations
3.
Albuquerque, David, et al.. (2018). The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability. Journal of Human Genetics. 64(3). 221–231. 6 indexed citations
4.
Quintela, Inés, et al.. (2018). Assessment of genotyping tools applied in genetic susceptibility studies of periodontal disease: A systematic review. Archives of Oral Biology. 92. 38–50. 12 indexed citations
5.
Quintela, Inés, Jesús Manuel Eirís Puñal, Carmen Gómez‐Lado, et al.. (2017). Copy number variation analysis of patients with intellectual disability from North-West Spain. Gene. 626. 189–199. 16 indexed citations
6.
Álvarez‐Mora, María Isabel, Rosa Calvo, Irene Madrigal, et al.. (2016). Comprehensive molecular testing in patients with high functioning autism spectrum disorder. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 784-785. 46–52. 22 indexed citations
7.
Costas, Javier, Noa Carrera, Pino Alonso, et al.. (2016). Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Translational Psychiatry. 6(3). e768–e768. 45 indexed citations
8.
García‐Etxebarria, Koldo, María Alma Bracho, Tomàs Pumarola, et al.. (2015). No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. PLoS ONE. 10(9). e0135983–e0135983. 18 indexed citations
9.
Hernandéz-Ferrer, Carles, et al.. (2015). affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling. BMC Bioinformatics. 16(1). 167–167. 3 indexed citations
10.
Quintela, Inés, Francisco Barros, Ramón Manuel Lago‐Lestón, et al.. (2015). A maternally inherited 16p13.11‐p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features. American Journal of Medical Genetics Part A. 167(6). 1315–1322. 16 indexed citations
11.
12.
Gómez‐Lado, Carmen, et al.. (2013). Microdeleción 2q23.1 y hallazgos sindrómicos. Revista de Neurología. 57(9). 430–430. 1 indexed citations
13.
Lareu, M.V., Manuel García‐Magariños, Christopher Phillips, et al.. (2011). Analysis of a claimed distant relationship in a deficient pedigree using high density SNP data. Forensic Science International Genetics. 6(3). 350–353. 21 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.
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
16.
Salas, Antonio, Ana Vega, María Torres, et al.. (2005). High-density screening of the Zbtb7gene in breast cancer patients. Breast Cancer Research. 7(S2). 1 indexed citations
17.
Salas, Antonio, Ana Vega, Christopher Phillips, et al.. (2005). ZBTB7 HapMap in a worldwide population study. Breast Cancer Research. 7(S2). 1 indexed citations
18.
Anadón, Ramón, Isabel Rodríguez‐Moldes, Gregory P. Evangelatos, et al.. (2001). Differential expression of thymosins β4 and β10 during rat cerebellum postnatal development. Brain Research. 894(2). 255–265. 35 indexed citations
19.
Moreno, Luís A., et al.. (2001). Postprandial Triglyceridemia in Obese and Non-obese Adolescents. Importance of Body Composition and Fat Distribution. Journal of Pediatric Endocrinology and Metabolism. 14(2). 193–202. 16 indexed citations
20.
Anadón, Ramón, Pilar Molíst, Isabel Rodríguez‐Moldes, et al.. (2000). Distribution of choline acetyltransferase immunoreactivity in the brain of an elasmobranch, the lesser spotted dogfish (Scyliorhinus canicula). The Journal of Comparative Neurology. 420(2). 139–170. 118 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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