Fernando Santos

531 total citations
13 papers, 325 citations indexed

About

Fernando Santos is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Fernando Santos has authored 13 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Organic Chemistry. Recurrent topics in Fernando Santos's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Fernando Santos is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Fernando Santos collaborates with scholars based in Spain, Brazil and Australia. Fernando Santos's co-authors include Sixto García‐Miñáur, Pablo Lapunzina, Julián Nevado, Víctor Martínez‐Glez, María Palomares‐Bralo, Luís Fernández, Jair Tenorio, Pedro Arias, Elena Vallespín and María Torres and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and European Journal of Human Genetics.

In The Last Decade

Fernando Santos

12 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fernando Santos Spain	9	228	193	84	30	23	13	325
Koen Devriendt Belgium	9	137 0.6×	205 1.1×	61 0.7×	19 0.6×	17 0.7×	13	290
Kristen L. Sund United States	9	171 0.8×	193 1.0×	56 0.7×	43 1.4×	31 1.3×	15	326
Barbara Delle Chiaie Belgium	7	251 1.1×	195 1.0×	136 1.6×	48 1.6×	30 1.3×	10	423
Jostein Westvik Norway	9	172 0.8×	246 1.3×	35 0.4×	37 1.2×	31 1.3×	14	364
Maria Paola Recalcati Italy	11	240 1.1×	191 1.0×	89 1.1×	16 0.5×	25 1.1×	21	378
Amal Hashem Saudi Arabia	9	138 0.6×	236 1.2×	46 0.5×	16 0.5×	21 0.9×	11	354
Jacquelyn Roberson United States	10	223 1.0×	151 0.8×	50 0.6×	43 1.4×	28 1.2×	18	341
Lorraine Gaunt United Kingdom	10	249 1.1×	146 0.8×	108 1.3×	20 0.7×	17 0.7×	16	368
Julie Scuffins United States	5	215 0.9×	123 0.6×	126 1.5×	13 0.4×	18 0.8×	10	348
Carla S. D’Angelo Brazil	10	229 1.0×	156 0.8×	42 0.5×	17 0.6×	30 1.3×	15	302

Countries citing papers authored by Fernando Santos

Since Specialization

Citations

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

Fields of papers citing papers by Fernando Santos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Santos

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Santos. A scholar is included among the top collaborators of Fernando Santos 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 Fernando Santos. Fernando Santos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

García‐Santiago, Fe Amalia, Víctor Martínez‐Glez, Fernando Santos, et al.. (2015). Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization. American Journal of Medical Genetics Part A. 167(5). 1018–1025. 21 indexed citations

Nevado, Julián, María Palomares‐Bralo, Elena Vallespín, et al.. (2014). New microdeletion and microduplication syndromes: a comprehensive review. Genetics and Molecular Biology. 37(1 suppl 1). 210–219. 65 indexed citations

Paumard‐Hernández, Beatriz, Eva Barroso, Sara Benito‐Sanz, et al.. (2014). Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants. European Journal of Human Genetics. 23(7). 907–914. 41 indexed citations

Tenorio, Jair, Pedro Arias, Víctor Martínez‐Glez, et al.. (2014). Simpson-Golabi-Behmel syndrome types I and II. Orphanet Journal of Rare Diseases. 9(1). 138–138. 68 indexed citations

Vallespín, Elena, María Palomares‐Bralo, M. A. Mori, et al.. (2013). Customized high resolution CGH‐array for clinical diagnosis reveals additional genomic imbalances in previous well‐defined pathological samples. American Journal of Medical Genetics Part A. 161(8). 1950–1960. 27 indexed citations

Amiñoso, Cinthia, Elena Vallespín, Luís Fernández, et al.. (2013). Identification of the first deletion–insertion involving the complete structure of GAA gene and part of CCDC40 gene mediated by an Alu element. Gene. 519(1). 169–172. 6 indexed citations

Rodríguez‐Revenga, Laia, Elena Vallespín, Irene Madrigal, et al.. (2013). A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability. Gene. 521(1). 82–86. 16 indexed citations

Aza‐Carmona, Miriam, Eva Barroso, Damián Heine‐Suñer, et al.. (2011). Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia. European Journal of Human Genetics. 19(12). 1218–1225. 8 indexed citations

Fernández, Luís, Julián Nevado, Fernando Santos, et al.. (2009). A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review. BMC Medical Genetics. 10(1). 48–48. 54 indexed citations

10.

Flores, Carlos A., Víctor Manuel García Nieto, Encarna Guillén‐Navarro, et al.. (2007). A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent’s disease. Journal of Human Genetics. 52(3). 255–261. 11 indexed citations

11.

Santos, Fernando, et al.. (2004). Conduta anestésica em balneoterapia de pacientes queimados: avaliação prospectiva de 2852 procedimentos. SHILAP Revista de lepidopterología. 54(2). 229–238. 1 indexed citations

12.

Santos, Fernando, et al.. (2004). Conduta Anestésica em Balneoterapia de Pacientes Queimados: Avaliação Prospectiva de 2852 Procedimentos * Anesthetic Procedure for Balneotherapy of Burned Patients: Prospective Evaluation of 2852 Cases.

13.

Martínez‐Díaz, M. Victoria, Javier de Mendoza, Fernando Santos, & Tomás Torres⊗. (1994). Preparation and enantiomeric purity determination of new chiral C2 building blocks based on the 4-amino-1,2,4-triazole unit. Tetrahedron Asymmetry. 5(7). 1291–1296. 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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