F Salamanca

906 total citations
60 papers, 709 citations indexed

About

F Salamanca is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, F Salamanca has authored 60 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 20 papers in Genetics and 7 papers in Plant Science. Recurrent topics in F Salamanca's work include Genomic variations and chromosomal abnormalities (8 papers), Muscle Physiology and Disorders (7 papers) and Chromosomal and Genetic Variations (6 papers). F Salamanca is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Muscle Physiology and Disorders (7 papers) and Chromosomal and Genetic Variations (6 papers). F Salamanca collaborates with scholars based in Mexico, United States and Guatemala. F Salamanca's co-authors include S Armendares, Ramón Mauricio Coral‐Vázquez, S Frenk, Haydeé Rosas‐Vargas, Diego Arenas, R Lisker, Rosario Tapia, R Kretschmer, Patricia Ostrosky‐Wegman and Alejandro Campos and has published in prestigious journals such as Nature, Biochemical and Biophysical Research Communications and Journal of Medical Genetics.

In The Last Decade

F Salamanca

59 papers receiving 662 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 Salamanca Mexico 15 287 285 111 89 74 60 709
Éva Oláh Hungary 19 187 0.7× 358 1.3× 31 0.3× 75 0.8× 88 1.2× 85 1.1k
Kiran Kucheria India 17 585 2.0× 633 2.2× 131 1.2× 169 1.9× 36 0.5× 67 1.1k
Marte K. Viken Norway 20 343 1.2× 339 1.2× 110 1.0× 28 0.3× 37 0.5× 50 1.3k
Dilek Aktaş Türkiye 17 455 1.6× 423 1.5× 70 0.6× 104 1.2× 42 0.6× 68 873
Yung-Ming Lin Taiwan 17 345 1.2× 449 1.6× 62 0.6× 28 0.3× 118 1.6× 46 1.0k
Audrey Lynn United States 17 430 1.5× 852 3.0× 329 3.0× 120 1.3× 60 0.8× 22 1.3k
Alfred Rademaker United States 12 153 0.5× 137 0.5× 88 0.8× 82 0.9× 92 1.2× 17 560
Gita Akots United States 12 363 1.3× 405 1.4× 62 0.6× 51 0.6× 29 0.4× 14 839
Rajiva Raman India 21 525 1.8× 543 1.9× 163 1.5× 252 2.8× 37 0.5× 85 1.2k
C D Boehm United States 15 459 1.6× 537 1.9× 39 0.4× 184 2.1× 39 0.5× 18 1.5k

Countries citing papers authored by F Salamanca

Since Specialization
Citations

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

Fields of papers citing papers by F Salamanca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Salamanca

This figure shows the co-authorship network connecting the top 25 collaborators of F Salamanca. A scholar is included among the top collaborators of F Salamanca 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 Salamanca. F Salamanca 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.
Salamanca, F, et al.. (2010). Estudio de la estructura genética de una comunidad nahua del centro de Veracruz. 12(1). 1 indexed citations
2.
Rodríguez‐Cruz, Maricela, et al.. (2007). pRB detection as a common event in human retinoblastomas: An immunohistochemical study. Acta Histochemica. 110(2). 109–116. 2 indexed citations
3.
Peñaloza‐Espinosa, Rosenda I., Diego Arenas‐Aranda, Ricardo M. Cerda‐Flores, et al.. (2007). Characterization of mtDNA Haplogroups in 14 Mexican Indigenous Populations. Human Biology. 79(3). 313–320. 23 indexed citations
4.
Delgado-Olguı́n, Paul, J. Manuel Hernández‐Hernández, F Salamanca, Félix Recillas‐Targa, & Ramón Mauricio Coral‐Vázquez. (2007). Identification of two E-boxes that negatively modulate the activity of MyoD on the alpha-sarcoglycan core promoter. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1779(1). 74–80. 5 indexed citations
5.
Delgado-Olguı́n, Paul, Félix Recillas‐Targa, Haydeé Rosas‐Vargas, F Salamanca, & Ramón Mauricio Coral‐Vázquez. (2006). Partial characterization of the mouse α-sarcoglycan promoter and its responsiveness to MyoD. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1759(5). 240–246. 7 indexed citations
6.
Mayani, Héctor, et al.. (2006). In vitro leukemic cell differentiation and WT1 gene expression. Leukemia Research. 31(3). 395–397. 2 indexed citations
7.
García-Hernández, Normand, F Salamanca, Horacio Astudillo‐de la Vega, et al.. (2005). A molecular analysis by gene expression profiling reveals Bik/NBK overexpression in sporadic breast tumor samples of Mexican females. BMC Cancer. 5(1). 93–93. 19 indexed citations
8.
Valladares, Adán, F Salamanca, Eduardo Madrigal‐Santillán, & Diego Arenas. (2004). Identification of chromosomal changes with comparative genomic hybridization in sporadic breast cancer in Mexican women. Cancer Genetics and Cytogenetics. 152(2). 163–166. 8 indexed citations
9.
Coral‐Vázquez, Ramón Mauricio, et al.. (2003). Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin α-2 gene. Journal of Human Genetics. 48(2). 91–95. 6 indexed citations
10.
Salcedo, Mauricio, et al.. (2002). Identification of novel mutations in the RB1 gene in Mexican patients with retinoblastoma. Cancer Genetics and Cytogenetics. 138(1). 27–31. 10 indexed citations
11.
Bendesky, Andrés, et al.. (2002). Role of P53 functionality in the genotoxicity of metronidazole and its hydroxy metabolite. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 501(1-2). 57–67. 25 indexed citations
12.
Cervantes, Alicia, Marisol López, Mónica Aguinaga‐Ríos, et al.. (2001). PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype. Clinical Genetics. 60(5). 385–392. 6 indexed citations
13.
Arenas, Diego, Bulmaro Cisneros, F Salamanca, et al.. (1996). Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.. PubMed. 27(2). 151–6. 2 indexed citations
14.
Garcı́a-Carrancá, Alejandro, et al.. (1995). Frequency of haplotypes in the beta globin gene cluster in a selected sample of the mexican population. American Journal of Human Biology. 7(1). 45–49. 11 indexed citations
15.
Palma, Vincenzo, et al.. (1993). Methods for the analysis of cellular kinetics in PHA-stimulated blood lymphocytes using BrdU incorporation. A comparative study. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 286(2). 267–273. 10 indexed citations
16.
Salamanca, F, et al.. (1985). Diploid‐tetraploid mosaicism in a malformed boy. Clinical Genetics. 27(2). 183–186. 15 indexed citations
17.
Salamanca, F, et al.. (1983). Clinical use of "somatometric profiles" and the effect of polygenic inheritance for stature in patients with bone dysplasias.. PubMed. 35(3). 231–5. 3 indexed citations
18.
Campos, Alejandro, et al.. (1975). Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 18(1). 45–9. 19 indexed citations
19.
Armendares, S, et al.. (1975). The 12p trisomy syndrome.. PubMed. 18(2). 89–94. 22 indexed citations
20.
Armendares, S, et al.. (1971). An extra small metacentric autosome in a mentally retarded boy with multiple malformations.. Journal of Medical Genetics. 8(3). 378–380. 7 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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