Nancy Gélvez

696 total citations
23 papers, 245 citations indexed

About

Nancy Gélvez is a scholar working on Sensory Systems, Molecular Biology and Ophthalmology. According to data from OpenAlex, Nancy Gélvez has authored 23 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Sensory Systems, 7 papers in Molecular Biology and 4 papers in Ophthalmology. Recurrent topics in Nancy Gélvez's work include Hearing, Cochlea, Tinnitus, Genetics (11 papers), Retinal Diseases and Treatments (4 papers) and Retinal Development and Disorders (3 papers). Nancy Gélvez is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (11 papers), Retinal Diseases and Treatments (4 papers) and Retinal Development and Disorders (3 papers). Nancy Gélvez collaborates with scholars based in Colombia, United Kingdom and United States. Nancy Gélvez's co-authors include Genoveva Keyeux, Marta Lucía Tamayo, Dee Carter, Jaime E. Bernal, Iris Schrijver, Juan Rodriguez‐Paris, David X. Medina, M. A. Gil Olarte, Jaime L. Frías and Mariluz Gómez Rodríguez and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Atherosclerosis.

In The Last Decade

Nancy Gélvez

20 papers receiving 236 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy Gélvez Colombia 7 110 86 77 25 21 23 245
Yali Zhao China 10 197 1.8× 130 1.5× 92 1.2× 12 0.5× 26 1.2× 21 365
Clarke Fraser United Kingdom 4 181 1.6× 106 1.2× 53 0.7× 2 0.1× 33 1.6× 5 379
T. Elkan Miller Israel 9 164 1.5× 82 1.0× 130 1.7× 22 1.0× 22 444
Sarah E. Noon United States 10 226 2.1× 89 1.0× 37 0.5× 50 2.4× 15 373
Benjamin W. Kozyak United States 5 237 2.2× 136 1.6× 6 0.1× 18 0.7× 6 0.3× 13 387
Craig B. Stevens United States 11 183 1.7× 10 0.1× 65 0.8× 59 2.8× 15 358
Shoba Thirumangalathu United States 8 223 2.0× 64 0.7× 81 1.1× 16 0.8× 8 371
Prachi Kothiyal United States 7 171 1.6× 211 2.5× 28 0.4× 1 0.0× 9 0.4× 12 373
Regie Lyn P. Santos‐Cortez United States 9 150 1.4× 30 0.3× 110 1.4× 8 0.4× 31 278
Jelena S. Arnold United States 4 242 2.2× 70 0.8× 29 0.4× 12 0.6× 4 280

Countries citing papers authored by Nancy Gélvez

Since Specialization
Citations

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

Fields of papers citing papers by Nancy Gélvez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Gélvez

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy Gélvez. A scholar is included among the top collaborators of Nancy Gélvez 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 Nancy Gélvez. Nancy Gélvez 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.
Olarte, M. A. Gil, Nancy Gélvez, Manuela Villamar, et al.. (2024). Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases. Genes. 15(7). 951–951.
2.
Varela, Malena Daich, Patricio G. Schlottmann, A Francone, et al.. (2023). Clinical and Genetic Characterization of RDH12-Retinal Dystrophy in a South American Cohort. Ophthalmology Retina. 8(2). 163–173. 3 indexed citations
3.
Gélvez, Nancy, et al.. (2022). Caracterización fenotípica de la retinitis pigmentaria asociada a sordera. Biomédica. 42(Sp. 1). 130–143.
4.
Gélvez, Nancy, et al.. (2022). Epigenetic mechanisms and host factors impact ACE2 gene expression: Implications in COVID-19 susceptibility. Infection Genetics and Evolution. 104. 105357–105357. 14 indexed citations
5.
Gélvez, Nancy, et al.. (2021). Definición diagnóstica en una familia con malattia leventinese en Colombia. Biomédica. 41(3). 388–395. 1 indexed citations
6.
Gélvez, Nancy, et al.. (2019). Genetic association with intravitreal ranibizumab response for neovascular age-related macular degeneration in Hispanic population. Taiwan Journal of Ophthalmology. 9(4). 243–243. 5 indexed citations
7.
Olarte, M. A. Gil, Fernando Suárez‐Obando, Mary García-Acero, et al.. (2019). Detection of hearing loss in newborns: Definition of a screening strategy in Bogotá, Colombia. International Journal of Pediatric Otorhinolaryngology. 122. 76–81. 4 indexed citations
8.
Suárez‐Obando, Fernando, Nancy Gélvez, Juana Ángel, et al.. (2019). Risk factors associated with congenital defects that alter hearing or vision in children born in the city of Bogotá between 2002 and 2016. International Journal of Pediatric Otorhinolaryngology. 126. 109594–109594. 4 indexed citations
9.
Gélvez, Nancy, et al.. (2018). Mutational analysis of the LDLR gene in a cohort of Colombian families with familial hypercholesterolemia. Atherosclerosis. 277. 434–439. 3 indexed citations
10.
Gélvez, Nancy, et al.. (2016). Caracterización fenotípica y molecular de una familia colombiana con fenilcetonuria. Biomédica. 36(3). 390–396. 1 indexed citations
11.
Bernal, Jaime E., Mary García-Acero, Ignacio Zarante, et al.. (2014). Transient evoked oto-acoustic emission screening in newborns in Bogotá, Colombia: A retrospective study. International Journal of Pediatric Otorhinolaryngology. 78(10). 1752–1755. 3 indexed citations
12.
Gélvez, Nancy, et al.. (2014). Análisis Molecular de las Mutaciones 2299delG y C759F en Individuos Colombianos con Retinitis Pigmentosa e Hipoacusia Neurosensorial. SHILAP Revista de lepidopterología. 12(22). 131–141.
13.
Tamayo, Marta Lucía, et al.. (2013). The importance of fundus eye testing in rubella-induced deafness. International Journal of Pediatric Otorhinolaryngology. 77(9). 1536–1540. 5 indexed citations
14.
Rodriguez‐Paris, Juan, Marta Lucía Tamayo, Nancy Gélvez, & Iris Schrijver. (2011). Allele-Specific Impairment of GJB2 Expression by GJB6 Deletion del(GJB6-D13S1854). PLoS ONE. 6(6). e21665–e21665. 36 indexed citations
15.
Gélvez, Nancy, et al.. (2008). Deafness on the island of Providencia - Colombia: different etiology, different genetic counseling.. Repositorio Institucional (Pontificia Universidad Javeriana). 19(4). 403–12. 9 indexed citations
16.
Tamayo, Marta Lucía, M. A. Gil Olarte, Nancy Gélvez, et al.. (2008). Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: Results of a screening program. International Journal of Pediatric Otorhinolaryngology. 73(1). 97–101. 22 indexed citations
17.
Tamayo, Marta Lucía, et al.. (2008). Screening program for Waardenburg syndrome in Colombia: Clinical definition and phenotypic variability. American Journal of Medical Genetics Part A. 146A(8). 1026–1031. 33 indexed citations
18.
Gélvez, Nancy, et al.. (2003). Mitochondrial DNA Studies Show Asymmetrical Amerindian Admixture in Afro-Colombian and Mestizo Populations. Human Biology. 75(1). 13–30. 46 indexed citations
19.
Keyeux, Genoveva, et al.. (2002). Possible Migration Routes into South America Deduced from Mitochondrial DNA Studies in Colombian Amerindian Populations. Human Biology. 74(2). 211–233. 47 indexed citations
20.
Malagón, Nelcy Rodríguez, et al.. (2001). Estudio epidemiológico del Síndrome de Waardenburg en Colombia. SHILAP Revista de lepidopterología. 1 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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