Ascensión Giménez

498 total citations
14 papers, 363 citations indexed

About

Ascensión Giménez is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ascensión Giménez has authored 14 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Ophthalmology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ascensión Giménez's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (3 papers). Ascensión Giménez is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (3 papers). Ascensión Giménez collaborates with scholars based in Spain and United States. Ascensión Giménez's co-authors include Carmen Ayuso, Almudena Ávila‐Fernández, Rosa Riveiro-Álvarez, Blanca Garcı́a-Sandoval, Diego Cantalapiedra, Fiona Blanco‐Kelly, Jana Aguirre-Lambán, Elena Vallespín, Robert Wilke and M J Trujillo-Tiebas and has published in prestigious journals such as Ophthalmology, Investigative Ophthalmology & Visual Science and Human Genetics.

In The Last Decade

Ascensión Giménez

13 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ascensión Giménez Spain	9	335	183	64	53	44	14	363
María Isabel López-Molina Spain	12	287 0.9×	130 0.7×	70 1.1×	45 0.8×	45 1.0×	18	351
T. P. Dryja United States	7	320 1.0×	147 0.8×	57 0.9×	78 1.5×	41 0.9×	10	371
Maigi Külm United States	6	297 0.9×	183 1.0×	39 0.6×	45 0.8×	55 1.3×	7	349
F.P.M. Cremers Netherlands	8	377 1.1×	243 1.3×	83 1.3×	44 0.8×	26 0.6×	10	443
Jennifer A. Halder United States	6	334 1.0×	103 0.6×	89 1.4×	41 0.8×	119 2.7×	6	415
Waldo Herrera United States	6	405 1.2×	235 1.3×	39 0.6×	112 2.1×	55 1.3×	7	446
María González‐del Pozo Spain	13	408 1.2×	179 1.0×	123 1.9×	41 0.8×	16 0.4×	21	461
T.J.R. van de Pol Netherlands	8	195 0.6×	95 0.5×	55 0.9×	35 0.7×	17 0.4×	11	243
Shreyasi Choudhury United States	11	328 1.0×	130 0.7×	87 1.4×	80 1.5×	11 0.3×	13	376
René Goliath South Africa	8	257 0.8×	48 0.3×	48 0.8×	47 0.9×	32 0.7×	12	313

Countries citing papers authored by Ascensión Giménez

Since Specialization

Citations

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

Fields of papers citing papers by Ascensión Giménez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ascensión Giménez

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

All Works

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14 of 14 papers shown

José, Patrícia, Fiona Blanco‐Kelly, Marta Cortón, et al.. (2014). Prevalence of Rhodopsin mutations in autosomal dominant Retinitis Pigmentosa in Spain: clinical and analytical review in 200 families. Acta Ophthalmologica. 93(1). e38–44. 33 indexed citations

Blanco‐Kelly, Fiona, Teresa Jaijo, Elena Aller, et al.. (2014). Clinical Aspects of Usher Syndrome and theUSH2AGene in a Cohort of 433 Patients. JAMA Ophthalmology. 133(2). 157–157. 56 indexed citations

Riveiro-Álvarez, Rosa, Jana Zernant, Jana Aguirre-Lambán, et al.. (2013). Outcome of ABCA4 Disease-Associated Alleles in Autosomal Recessive Retinal Dystrophies. Ophthalmology. 120(11). 2332–2337. 61 indexed citations

Blanco‐Kelly, Fiona, Maria García‐Hoyos, Marta Cortón, et al.. (2012). Genotyping microarray: mutation screening in Spanish families with autosomal dominant retinitis pigmentosa.. PubMed. 18. 1478–83. 30 indexed citations

García‐Hoyos, Maria, Berta Almoguera, Diego Cantalapiedra, et al.. (2011). Mutation analysis at codon 838 of the Guanylate Cyclase 2D gene in Spanish families with autosomal dominant cone, cone-rod, and macular dystrophies.. PubMed. 17. 1103–9. 17 indexed citations

Riveiro-Álvarez, Rosa, Ascensión Giménez, M J Trujillo-Tiebas, et al.. (2008). Gene symbol: RS1. Disease: Retinoschisis, X linked juvenile.. PubMed. 123(3). 307–551. 1 indexed citations

Ávila‐Fernández, Almudena, Rosa Riveiro-Álvarez, Elena Vallespín, et al.. (2008). CERKLMutations and Associated Phenotypes in Seven Spanish Families with Autosomal Recessive Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 49(6). 2709–2709. 36 indexed citations

Riveiro-Álvarez, Rosa, Elena Vallespín, Robert Wilke, et al.. (2008). Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa.. PubMed. 14. 262–7. 19 indexed citations

Vallespín, Elena, Diego Cantalapiedra, Rosa Riveiro-Álvarez, et al.. (2007). Mutation Screening of 299 Spanish Families with Retinal Dystrophies by Leber Congenital Amaurosis Genotyping Microarray. Investigative Ophthalmology & Visual Science. 48(12). 5653–5653. 75 indexed citations

10.

Riveiro-Álvarez, Rosa, et al.. (2006). Gene symbol: NDP. Disease: Norrie disease.. PubMed. 119(3). 308–308. 1 indexed citations

11.

Trujillo-Tiebas, M J, et al.. (2005). Novel human pathological mutations. Human Genetics. 118(3-4). 534–538.

12.

Trujillo, M.J., Blanca Garcı́a-Sandoval, Isabel Lorda‐Sánchez, et al.. (2000). Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family. Ophthalmic Genetics. 21(4). 251–256. 1 indexed citations

13.

Lorda‐Sánchez, Isabel, Raúl Sanz, M.J. Trujillo, et al.. (2000). Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation. Ophthalmic Genetics. 21(3). 185–189. 29 indexed citations

14.

Lorda‐Sánchez, Isabel, M.J. Trujillo, Ascensión Giménez, et al.. (1999). Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs. Ophthalmic Genetics. 20(2). 127–131. 4 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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