Ana Cuesta

615 total citations
10 papers, 439 citations indexed

About

Ana Cuesta is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Ana Cuesta has authored 10 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 3 papers in Cell Biology. Recurrent topics in Ana Cuesta's work include Hereditary Neurological Disorders (4 papers), Skin and Cellular Biology Research (2 papers) and Neurological diseases and metabolism (2 papers). Ana Cuesta is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Skin and Cellular Biology Research (2 papers) and Neurological diseases and metabolism (2 papers). Ana Cuesta collaborates with scholars based in Spain, France and Cuba. Ana Cuesta's co-authors include Francesc Palau, Laia Pedrola, Juan J. Vílchez, Teresa Sevilla, Javier Garcı́a-Planells, María José Chumillas, F. Mayordomo, Ignacio Marı́n, Éric Leguern and Vincent Timmerman and has published in prestigious journals such as Nature Genetics, Neurology and Journal of Clinical Pathology.

In The Last Decade

Ana Cuesta

10 papers receiving 426 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ana Cuesta Spain	6	373	162	153	110	61	10	439
Sonia Nouioua Algeria	11	298 0.8×	164 1.0×	124 0.8×	105 1.0×	136 2.2×	18	441
Alessandro Geroldi Italy	13	285 0.8×	214 1.3×	94 0.6×	134 1.2×	90 1.5×	30	461
Alleene V. Strickland United States	7	256 0.7×	185 1.1×	113 0.7×	101 0.9×	105 1.7×	7	417
Estelle Arnaud Switzerland	7	194 0.5×	227 1.4×	63 0.4×	58 0.5×	73 1.2×	7	381
Simona Capponi Italy	12	222 0.6×	211 1.3×	74 0.5×	92 0.8×	76 1.2×	16	405
Kishin Koh Japan	11	194 0.5×	136 0.8×	99 0.6×	72 0.7×	51 0.8×	38	295
Helle Høyer Norway	8	243 0.7×	97 0.6×	105 0.7×	96 0.9×	50 0.8×	17	329
Alexander P. Drew Australia	10	148 0.4×	152 0.9×	84 0.5×	35 0.3×	45 0.7×	15	303
Maria Schabhüttl Austria	9	202 0.5×	162 1.0×	101 0.7×	51 0.5×	132 2.2×	9	382
Menelaos Pipis United Kingdom	7	214 0.6×	90 0.6×	79 0.5×	74 0.7×	41 0.7×	10	289

Countries citing papers authored by Ana Cuesta

Since Specialization

Citations

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

Fields of papers citing papers by Ana Cuesta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ana Cuesta

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

All Works

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10 of 10 papers shown

Verdú‐Amorós, Jaime, et al.. (2021). Kutane und systemische Veränderungen mit Ähnlichkeiten zum Omenn‐Syndrom bei heterozygoter Mutation im RAG2‐Gen. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 19(6). 906–908. 1 indexed citations

Martín, J.M., et al.. (2020). Depressed indurated plaque with elastorrhexis as a distinctive lesion in Buschke‐Ollendorff syndrome. Pediatric Dermatology. 37(2). 385–387. 1 indexed citations

Martín, J.M., et al.. (2018). Two-year-old girl with tuberous xanthomas. Journal of Clinical Pathology. 71(10). 860–862. 2 indexed citations

Martín, Vicente, et al.. (2015). Incidencia hospitalaria, tendencia y distribución municipal del cáncer de próstata en el área de salud de León (1996-2010). Revista Española de Salud Pública. 89(6). 575–583. 2 indexed citations

Arpa, Javier, Ana Cuesta, A Cruz-Martı́nez, et al.. (2009). Clinical features and genetic analysis of a Spanish family with spinocerebellar ataxia 6. Acta Neurologica Scandinavica. 99(1). 43–47. 13 indexed citations

Claramunt, Reyes, Teresa Sevilla, Vincenzo Lupo, et al.. (2007). The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot–Marie–Tooth disease type 4. Clinical Genetics. 71(4). 343–349. 34 indexed citations

Palau, Francesc, Ana Cuesta, & Laia Pedrola. (2002). Avances en la genética molecular de las neuropatías hereditarias. Revista de Neurología. 35(3). 246–246. 5 indexed citations

Nelis, Eva, Sevim Erdem‐Özdamar, Peter Van den Bergh, et al.. (2002). Mutations in GDAP1. Neurology. 59(12). 1865–1872. 110 indexed citations

Cuesta, Ana, Laia Pedrola, Teresa Sevilla, et al.. (2001). The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease. Nature Genetics. 30(1). 22–25. 262 indexed citations

10.

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

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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