F. Prieto

826 total citations
35 papers, 503 citations indexed

About

F. Prieto is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, F. Prieto has authored 35 papers receiving a total of 503 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in F. Prieto's work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Genetic Neurodegenerative Diseases (6 papers). F. Prieto is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Genetic Neurodegenerative Diseases (6 papers). F. Prieto collaborates with scholars based in Spain, United States and Denmark. F. Prieto's co-authors include Lourdes Badı́a, Francesc Palau, Francisco Martı́nez, María Dolores Moltó, Eugènia Monrós, Juan J. Vílchez, Joaquı́n Cañizares, R. de Frutos, José Blanca and Magdalena Beneyto and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

F. Prieto

34 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F. Prieto Spain 13 297 203 150 82 69 35 503
Linda Meredith United Kingdom 10 347 1.2× 198 1.0× 115 0.8× 22 0.3× 99 1.4× 15 595
Juan Cota United States 6 198 0.7× 74 0.4× 148 1.0× 28 0.3× 10 0.1× 8 384
Grant Sutherland Australia 12 287 1.0× 312 1.5× 39 0.3× 17 0.2× 42 0.6× 26 535
Peter B. Jacky United States 11 274 0.9× 421 2.1× 28 0.2× 49 0.6× 48 0.7× 23 594
M. Chery France 12 281 0.9× 284 1.4× 44 0.3× 16 0.2× 58 0.8× 26 466
Edmond G. Lemire Canada 14 240 0.8× 202 1.0× 28 0.2× 15 0.2× 27 0.4× 42 616
van Ommen Gj Netherlands 4 327 1.1× 134 0.7× 51 0.3× 41 0.5× 13 0.2× 5 445
Ali Hellani Saudi Arabia 14 286 1.0× 333 1.6× 43 0.3× 41 0.5× 46 0.7× 39 787
M. G. Daker United Kingdom 13 225 0.8× 333 1.6× 18 0.1× 22 0.3× 113 1.6× 28 538
Christina Galonska United States 7 791 2.7× 140 0.7× 37 0.2× 12 0.1× 45 0.7× 9 841

Countries citing papers authored by F. Prieto

Since Specialization
Citations

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

Fields of papers citing papers by F. Prieto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Prieto

This figure shows the co-authorship network connecting the top 25 collaborators of F. Prieto. A scholar is included among the top collaborators of F. 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 F. Prieto. F. 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.
Orellana, Carmen, Lourdes Badı́a, Francisco Martı́nez, et al.. (2006). Recombinant X chromosome in a prenatal diagnosis. Cytogenetic and Genome Research. 112(3-4). 337–340. 3 indexed citations
2.
Prieto, F., et al.. (2004). Applying formal concepts analysis to the construction and evolution of domain frameworks. 1. 139–148. 1 indexed citations
3.
Martínez‐Garay, Isabel, Silvestre Oltra, Carmen Orellana, et al.. (2003). Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin–Lowry syndrome. Clinical Genetics. 64(6). 491–496. 21 indexed citations
4.
Orellana, Carmen, et al.. (2001). Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features. Clinical Genetics. 60(3). 206–211. 9 indexed citations
5.
Marfany, Gemma, et al.. (1999). Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR. Journal of Medical Genetics. 36(9). 694–699. 16 indexed citations
6.
Garcı́a-Planells, Javier, Ana Cuesta, Juan J. Vílchez, et al.. (1999). Genetics of the SCA6 gene in a large family segregating an autosomal dominant “pure” cerebellar ataxia. Journal of Medical Genetics. 36(2). 148–151. 9 indexed citations
7.
Monrós, Eugènia, María Dolores Moltó, Francisco Martı́nez, et al.. (1997). Phenotype Correlation and Intergenerational Dynamics of the Friedreich Ataxia GAA Trinucleotide Repeat. The American Journal of Human Genetics. 61(1). 101–110. 131 indexed citations
8.
Monrós, Eugènia, Joaquı́n Cañizares, María Dolores Moltó, et al.. (1996). Evidence for a Common Origin ofMost Friedreich AtaxiaChromosomes in the SpanishPopulation. European Journal of Human Genetics. 4(4). 191–198. 10 indexed citations
9.
Silla, José María Peiró, et al.. (1996). El trabajo como fenomeno psicosocial. Data Archiving and Networked Services (DANS). 15–33. 9 indexed citations
10.
Descals, Francisco José Palací, et al.. (1995). Las definiciones del trabajo en jóvenes durante sus primeros años de empleo. 11–23. 1 indexed citations
11.
Monrós, Eugènia, et al.. (1995). Prenatal diagnosis of friedreich ataxia: Improved accuracy by using new genetic flanking markers. Prenatal Diagnosis. 15(6). 551–554. 8 indexed citations
12.
Nájera, Carmén, José M. Millán, Magdalena Beneyto, & F. Prieto. (1995). Epidemiology of retinitis pigmentosa in the valencian community (Spain). Genetic Epidemiology. 12(1). 37–46. 24 indexed citations
13.
Bartsch, Oliver, Michael B. Petersen, Hanne Poulsen, et al.. (1993). Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome. Human Genetics. 92(2). 127–32. 19 indexed citations
14.
Prieto, F., et al.. (1989). Nucleolus organizer regions (NORs) inserted in 6q15. Human Genetics. 81(3). 289–90. 10 indexed citations
15.
Prieto, F., et al.. (1987). X‐linked dysmorphic syndrome with mental retardation. Clinical Genetics. 32(5). 326–334. 18 indexed citations
16.
Prieto, F., et al.. (1980). Two reciprocal translocations t(9p+;13q?) and t(13q?;21q+). Human Genetics. 54(1). 7–11. 12 indexed citations
17.
Prieto, F., et al.. (1978). [Twenty-six chromosomes hypodiploidy in acute lymphoblastic leukaemia (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 23(4). 484–8. 12 indexed citations
18.
Prieto, F., et al.. (1978). [Trysomy of chromosome 1 long arms plus chromosome 9 inversion in leukaemic cells (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 23(1). 64–8. 4 indexed citations
19.
Prieto, F., et al.. (1977). [Chromosomal heteromorphism in patients with chronic lymphocytic leukaemia (author's transl)].. PubMed. 22(5B). 807–13. 3 indexed citations
20.
Prieto, F., et al.. (1976). [Chromosome abnormalities in refractory anaemia with partial myeloblastosis (author's transl)].. PubMed. 21(3B). 701–12. 6 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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