Antonio Pérez Aytés

1.9k total citations
45 papers, 795 citations indexed

About

Antonio Pérez Aytés is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Antonio Pérez Aytés has authored 45 papers receiving a total of 795 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Antonio Pérez Aytés's work include Genetic Syndromes and Imprinting (5 papers), Galectins and Cancer Biology (5 papers) and Connective tissue disorders research (5 papers). Antonio Pérez Aytés is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Galectins and Cancer Biology (5 papers) and Connective tissue disorders research (5 papers). Antonio Pérez Aytés collaborates with scholars based in Spain, United States and United Kingdom. Antonio Pérez Aytés's co-authors include Máximo Vento, Virginia Bosó, Ana da Silva Lédo, John C. Carey, Purificación Marín Reina, Eva Romá, José Luís Poveda, Pilar Sáenz, Eulalia Valencia and Judith A. Goodship and has published in prestigious journals such as Nature Genetics, PLoS ONE and PEDIATRICS.

In The Last Decade

Antonio Pérez Aytés

44 papers receiving 765 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antonio Pérez Aytés Spain 15 369 341 147 126 111 45 795
Yangzhu Du United States 13 611 1.7× 366 1.1× 76 0.5× 55 0.4× 54 0.5× 20 979
Giorgio Adriano Paskulin Brazil 17 351 1.0× 344 1.0× 195 1.3× 88 0.7× 190 1.7× 89 899
Sixto García‐Miñáur Spain 20 603 1.6× 609 1.8× 174 1.2× 49 0.4× 236 2.1× 57 1.2k
Anwar Baban Italy 20 621 1.7× 313 0.9× 262 1.8× 52 0.4× 78 0.7× 76 1.2k
Tahsin Yakut Türkiye 15 315 0.9× 191 0.6× 77 0.5× 117 0.9× 174 1.6× 78 762
Christine Oley United Kingdom 13 572 1.6× 431 1.3× 76 0.5× 62 0.5× 192 1.7× 21 954
P Malet France 15 336 0.9× 214 0.6× 72 0.5× 142 1.1× 119 1.1× 65 768
Silvana Guerneri Italy 17 357 1.0× 406 1.2× 110 0.7× 76 0.6× 344 3.1× 50 902
Sevilhan Artan Türkiye 18 308 0.8× 187 0.5× 81 0.6× 48 0.4× 104 0.9× 84 760
Michel Bahuau France 19 278 0.8× 297 0.9× 217 1.5× 30 0.2× 98 0.9× 38 1.1k

Countries citing papers authored by Antonio Pérez Aytés

Since Specialization
Citations

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

Fields of papers citing papers by Antonio Pérez Aytés

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Antonio Pérez Aytés. 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 Antonio Pérez Aytés. The network helps show where Antonio Pérez Aytés may publish in the future.

Co-authorship network of co-authors of Antonio Pérez Aytés

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Pérez Aytés. A scholar is included among the top collaborators of Antonio Pérez Aytés 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 Antonio Pérez Aytés. Antonio Pérez Aytés 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.
Aytés, Antonio Pérez, et al.. (2022). [Genomic newborn screening. Perspective from the Ethics Commission of the Spanish Society for Human Genetics. Part II: Ethical, legal and social issues (ELSIs) of the introduction of next generation sequencing technologies in a public health newborn screening program.]. PubMed. 96. 1 indexed citations
2.
Aytés, Antonio Pérez, et al.. (2021). Medio siglo de cribado neonatal en España: Evolución de los aspectos éticos, legales y sociales (AELS). Parte II, marco legal. Revista Española de Salud Pública. 95(95). 15. 1 indexed citations
3.
Reina, Purificación Marín, et al.. (2019). Mixed Phenotype of Langer–Giedion's and Cornelia de Lange's Syndromes in an 8q23.3-q24.1 Microdeletion without TRPS1 Deletion. Journal of Pediatric Genetics. 9(1). 53–57. 1 indexed citations
4.
Aytés, Antonio Pérez, et al.. (2019). Pruebas genéticas de venta directa a los consumidores. Perspectiva de la Comisión de Ética de la Asociación Española de Genética Humana. Medicina Clínica. 153(1). 35–40. 2 indexed citations
5.
Martı́nez, Francisco, Purificación Marín Reina, Antonio Pérez Aytés, et al.. (2015). Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes. Pediatric Research. 78(5). 533–539. 28 indexed citations
6.
Reina, Purificación Marín, et al.. (2015). Silver‐Rusell syndrome caused by epigenetic alteration in a child conceived by intrauterine insemination from donor sperm. American Journal of Medical Genetics Part A. 167(11). 2861–2864. 1 indexed citations
7.
Reina, Purificación Marín, et al.. (2014). Postnatal development of fetuses with a single umbilical artery: differences between malformed and non-malformed infants. World Journal of Pediatrics. 11(1). 61–66. 7 indexed citations
8.
Carcavilla, Atilano, Sixto García‐Miñáur, Antonio Pérez Aytés, et al.. (2014). Síndrome cardiofaciocutáneo, un trastorno relacionado con el síndrome de Noonan: hallazgos clínicos y moleculares en 11 pacientes. Medicina Clínica. 144(2). 67–72. 3 indexed citations
9.
Caparrós‐Martín, José A., Eulalia Valencia, María Pacheco, et al.. (2012). The ciliary Evc/Evc2 complex interacts with Smo and controls Hedgehog pathway activity in chondrocytes by regulating Sufu/Gli3 dissociation and Gli3 trafficking in primary cilia. Human Molecular Genetics. 22(1). 124–139. 84 indexed citations
10.
Vergult, Sarah, A. Jeannette M. Hoogeboom, Emilia K. Bijlsma, et al.. (2012). Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients. Genetics in Medicine. 15(3). 195–202. 22 indexed citations
11.
Ezquieta, Begoña, José L. Santomé, Atilano Carcavilla, et al.. (2012). Alterations in RAS-MAPK Genes in 200 Spanish Patients With Noonan and Other Neuro-Cardio-Facio-Cutaneous Syndromes. Genotype and Cardiopathy. Revista Española de Cardiología (English Edition). 65(5). 447–455. 21 indexed citations
12.
Ezquieta, Begoña, José L. Santomé, Atilano Carcavilla, et al.. (2012). Alteraciones de los genes de la vía RAS-MAPK en 200 pacientes españoles con síndrome de Noonan y otros síndromes neurocardiofaciocutáneos. Genotipo y cardiopatía. Revista Española de Cardiología. 65(5). 447–455. 24 indexed citations
13.
Sukalo, Maja, Marie-Claude Addor, Han G. Brunner, et al.. (2011). Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome. PLoS ONE. 6(9). e24925–e24925. 39 indexed citations
14.
Adam, Margaret P, Louanne Hudgins, John C. Carey, et al.. (2008). Preaxial hallucal polydactyly as a marker for diabetic embryopathy. Birth Defects Research Part A Clinical and Molecular Teratology. 85(1). 13–19. 16 indexed citations
15.
Aytés, Antonio Pérez, et al.. (2002). [Schwartz-Jampel syndrome type 2 versus Stüve-Wiedemann syndrome].. PubMed. 56(5). 473–4. 2 indexed citations
16.
Dios, Javier González de & Antonio Pérez Aytés. (1999). GENETICA Y DISMORFOLOGIA EN EL CONTEXTO DE LAS SUBESPECIALIDADES PEDIATRICAS. Anales de Pediatría. 51(3). 222–229. 2 indexed citations
17.
Aytés, Antonio Pérez, et al.. (1999). Macrocefalia-cutis marmorata telangiectásica congénita: Un nuevo caso de una entidad recientemente reconocida. Anales de Pediatría. 51(4). 399–401. 3 indexed citations
18.
Aytés, Antonio Pérez, et al.. (1995). Non‐immunological hydrops fetalis and intrapericardial teratoma: Case report and review. Prenatal Diagnosis. 15(9). 859–863. 27 indexed citations
19.
Aytés, Antonio Pérez, et al.. (1993). Síndrome de Fraser, agenesia renal y ascitis fetal. Anales de Pediatría. 39(2). 163–166. 2 indexed citations
20.
Aytés, Antonio Pérez, et al.. (1978). [Salmonella infection in children. Epidemiological and clinical considerations (author's transl)].. PubMed. 11(5). 373–82. 2 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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