Félix Prieto

1.1k total citations
40 papers, 869 citations indexed

About

Félix Prieto is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Félix Prieto has authored 40 papers receiving a total of 869 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 15 papers in Hematology and 12 papers in Genetics. Recurrent topics in Félix Prieto's work include Acute Myeloid Leukemia Research (14 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetic Neurodegenerative Diseases (5 papers). Félix Prieto is often cited by papers focused on Acute Myeloid Leukemia Research (14 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetic Neurodegenerative Diseases (5 papers). Félix Prieto collaborates with scholars based in Spain, Germany and United States. Félix Prieto's co-authors include Francesc Palau, Lourdes Badı́a, Francisco Martı́nez, Juan J. Vílchez, S Bort, Magdalena Beneyto, Teresa Sevilla, Christine Van Broeckhoven, Eva Nelis and José M. Millán and has published in prestigious journals such as Circulation, Blood and Human Molecular Genetics.

In The Last Decade

Félix Prieto

40 papers receiving 850 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Félix Prieto Spain 16 369 223 151 151 148 40 869
John Wolff United States 18 481 1.3× 411 1.8× 101 0.7× 137 0.9× 81 0.5× 23 844
Thalia Antoniadi Greece 16 327 0.9× 217 1.0× 89 0.6× 155 1.0× 145 1.0× 28 850
Sherryl A. Taylor Canada 16 455 1.2× 318 1.4× 131 0.9× 137 0.9× 45 0.3× 35 768
Michael Lindenbaum Canada 10 1.3k 3.5× 378 1.7× 55 0.4× 166 1.1× 55 0.4× 11 1.6k
Magdalena Beneyto Spain 18 738 2.0× 64 0.3× 51 0.3× 140 0.9× 116 0.8× 48 965
Güney Bademci United States 19 582 1.6× 91 0.4× 25 0.2× 331 2.2× 166 1.1× 63 1.1k
Muriel Bozon France 19 407 1.1× 564 2.5× 51 0.3× 97 0.6× 33 0.2× 36 1.1k
TB Shows United States 8 652 1.8× 220 1.0× 80 0.5× 103 0.7× 28 0.2× 11 963
Hélène Bruyèrè Canada 17 462 1.3× 77 0.3× 306 2.0× 401 2.7× 18 0.1× 44 1.0k
Josselyne Salaün France 18 521 1.4× 307 1.4× 149 1.0× 255 1.7× 53 0.4× 34 1.5k

Countries citing papers authored by Félix Prieto

Since Specialization
Citations

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

Fields of papers citing papers by Félix Prieto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Félix Prieto

This figure shows the co-authorship network connecting the top 25 collaborators of Félix Prieto. A scholar is included among the top collaborators of Félix Prieto 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 Félix Prieto. Félix Prieto 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.
Martínez‐Garay, Isabel, Miguel Tomás Vila, Silvestre Oltra, et al.. (2006). A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. European Journal of Human Genetics. 15(1). 29–34. 28 indexed citations
2.
Barragán, Eva, et al.. (2006). Molecular detection of Spanish δβ-thalassemia associated with β-thalassemia identified during prenatal diagnosis. Clinica Chimica Acta. 368(1-2). 195–198. 2 indexed citations
3.
Sánchez‐Sánchez, Francisco, Carmen Ramírez‐Castillejo, Daniel Weekes, et al.. (2006). Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma. Human Mutation. 28(2). 159–167. 31 indexed citations
4.
Andreu, Núria, et al.. (2003). Identification and characterization of a novel splice-site mutation in a patient with Wiskott-Aldrich syndrome. Journal of Human Genetics. 48(11). 590–593. 3 indexed citations
5.
Rodríguez-Ballesteros, Montserrat, Francisco Castillo, Yolanda Martín, et al.. (2003). Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF). Human Mutation. 22(6). 451–456. 155 indexed citations
6.
Collado, Rosa, et al.. (1999). Chromosome 11 Abnormalities in Myelodysplastic Syndromes. Cancer Genetics and Cytogenetics. 114(1). 58–61. 19 indexed citations
7.
Orellana, Carmen, Francisco Martı́nez, Victoria Castel, et al.. (1998). Pediatric Brain Tumors: Loss of Heterozygosity at 17p and TP53 Gene Mutations. Cancer Genetics and Cytogenetics. 102(2). 93–99. 24 indexed citations
8.
9.
Monrós, Eugènia, et al.. (1996). A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus. Human Genetics. 97(6). 824–828. 9 indexed citations
10.
Beneyto, Magdalena, José M. Millán, Marina De Marco, et al.. (1996). Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP). Ophthalmic Genetics. 17(1). 29–33. 1 indexed citations
11.
Martı́nez, Francisco, Andreas Gal, Francesc Palau, & Félix Prieto. (1995). Localization of a gene for X‐linked nonspecific mental retardation (MRX24) in Xp22.2–p22.3. American Journal of Medical Genetics. 55(3). 387–390. 17 indexed citations
12.
Moltó, María Dolores, Juan J. Vílchez, Massimo Pandolfo, et al.. (1994). Mapping of Friedreich's AtaxiaLocus by Identification ofRecombination Events in PatientsHomozygous by Descent. European Journal of Human Genetics. 2(4). 291–299. 8 indexed citations
13.
Millán, José M., Moritz Meins, Magdalena Beneyto, et al.. (1994). Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa. Human Mutation. 3(3). 321–323. 29 indexed citations
14.
Badı́a, Lourdes, et al.. (1993). Translocation (12;14)(q13;q32) in myelodysplastic syndrome. Cancer Genetics and Cytogenetics. 65(1). 76–78. 3 indexed citations
15.
Palau, Francesc, Ann Löfgren, Peter De Jonghe, et al.. (1993). Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Human Molecular Genetics. 2(12). 2031–2035. 102 indexed citations
16.
Martı́nez, Francisco, Lourdes Badı́a, & Félix Prieto. (1992). A fragile X family with high penetrance in females: risk heterogeneity?. Clinical Genetics. 42(1). 22–26. 5 indexed citations
17.
Verdeguer, Amparo, et al.. (1992). Acute nonlymphoblastic leukemia in children treated for acute lymphoblastic leukemia with an intensive regimen including teniposide. Medical and Pediatric Oncology. 20(1). 48–52. 10 indexed citations
18.
Prieto, Félix, et al.. (1991). Gene localization in a family with X‐linked syndromal mental retardation (Prieto syndrome). American Journal of Medical Genetics. 38(2-3). 234–239. 15 indexed citations
19.
Palau, Francesc, et al.. (1991). Chromosome 5 abnormalities in acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 52(2). 173–179. 6 indexed citations
20.
Prieto, Félix, et al.. (1990). 11q23 abnormalities in children with acute nonlymphocytic leukemia (M4–M5). Cancer Genetics and Cytogenetics. 45(1). 1–11. 37 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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