Celsa Quinteiro

746 total citations
20 papers, 521 citations indexed

About

Celsa Quinteiro is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Celsa Quinteiro has authored 20 papers receiving a total of 521 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Endocrinology, Diabetes and Metabolism, 7 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Celsa Quinteiro's work include Growth Hormone and Insulin-like Growth Factors (8 papers), Sexual Differentiation and Disorders (6 papers) and Alcohol Consumption and Health Effects (4 papers). Celsa Quinteiro is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (8 papers), Sexual Differentiation and Disorders (6 papers) and Alcohol Consumption and Health Effects (4 papers). Celsa Quinteiro collaborates with scholars based in Spain, Portugal and Germany. Celsa Quinteiro's co-authors include Lourdes Loidi, Fernando Domı́nguez, Silvia Parajes, Arturo González‐Quintela, J. Campos Franco, Francisco Gudé, Francisco C. Ceballos, Gonzalo Álvarez, Ignacio Bernabéu and Luis‐Fernando Perez and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Clinical Chemistry.

In The Last Decade

Celsa Quinteiro

19 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Celsa Quinteiro Spain 13 247 213 160 65 64 20 521
Mouna Mnif Tunisia 16 277 1.1× 315 1.5× 176 1.1× 95 1.5× 56 0.9× 84 680
Shelly G. Smith United States 14 101 0.4× 181 0.8× 236 1.5× 43 0.7× 55 0.9× 16 553
Paula Scaglia Argentina 10 378 1.5× 162 0.8× 236 1.5× 37 0.6× 18 0.3× 27 471
Stefano Borgato Italy 11 279 1.1× 310 1.5× 244 1.5× 34 0.5× 33 0.5× 18 837
Mariarosaria Lang‐Muritano Switzerland 14 337 1.4× 366 1.7× 375 2.3× 176 2.7× 27 0.4× 35 756
Ans van den Ouweland Netherlands 18 107 0.4× 305 1.4× 315 2.0× 71 1.1× 116 1.8× 20 1.4k
Péter Gergics Hungary 14 257 1.0× 209 1.0× 134 0.8× 90 1.4× 54 0.8× 29 501
S Gough United Kingdom 9 190 0.8× 132 0.6× 198 1.2× 79 1.2× 27 0.4× 16 512
Cornelia M. Spies Germany 13 143 0.6× 155 0.7× 123 0.8× 27 0.4× 31 0.5× 17 597
Ricardo Gracía Spain 11 183 0.7× 277 1.3× 241 1.5× 50 0.8× 13 0.2× 17 461

Countries citing papers authored by Celsa Quinteiro

Since Specialization
Citations

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

Fields of papers citing papers by Celsa Quinteiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celsa Quinteiro

This figure shows the co-authorship network connecting the top 25 collaborators of Celsa Quinteiro. A scholar is included among the top collaborators of Celsa Quinteiro 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 Celsa Quinteiro. Celsa Quinteiro 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.
Ramos‐Leví, Ana M., Mónica Marazuela, Celsa Quinteiro, et al.. (2014). Analysis of IGF(CA)19 and IGFBP3-202A/C gene polymorphisms in patients with acromegaly: association with clinical presentation and response to treatments. European Journal of Endocrinology. 172(2). 115–122. 12 indexed citations
2.
3.
Quinteiro, Celsa, Jesús Barreiro, Mónica Marazuela, et al.. (2011). Pituitary Stalk Dysgenesis-Induced Hypopituitarism in Adult Patients: Prevalence, Evolution of Hormone Dysfunction and Genetic Analysis. Neuroendocrinology. 93(3). 181–188. 37 indexed citations
4.
García‐Barchino, María J., Sara Labiano, Mikhail Shugay, et al.. (2011). LIF, a Novel STAT5-Regulated Gene, Is Aberrantly Expressed in Myeloproliferative Neoplasms. Genes & Cancer. 2(5). 593–596. 9 indexed citations
5.
Bernabéu, Ignacio, Mónica Marazuela, Tomás Lúcas, et al.. (2010). Pegvisomant-Induced Liver Injury Is Related to the UGT1A1*28 Polymorphism of Gilbert’s Syndrome. The Journal of Clinical Endocrinology & Metabolism. 95(5). 2147–2154. 37 indexed citations
6.
Parajes, Silvia, Arturo González‐Quintela, J. Campos Franco, et al.. (2010). Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant. BMC Genetics. 11(1). 110–110. 22 indexed citations
7.
Bernabéu, Ignacio, Cristina Álvarez‐Escolá, Celsa Quinteiro, et al.. (2009). The Exon 3-Deleted Growth Hormone Receptor Is Associated with Better Response to Pegvisomant Therapy in Acromegaly. The Journal of Clinical Endocrinology & Metabolism. 95(1). 222–229. 48 indexed citations
8.
Álvarez, Gonzalo, Francisco C. Ceballos, & Celsa Quinteiro. (2009). The Role of Inbreeding in the Extinction of a European Royal Dynasty. PLoS ONE. 4(4). e5174–e5174. 47 indexed citations
9.
Parajes, Silvia, Celsa Quinteiro, Fernando Domı́nguez, & Lourdes Loidi. (2008). High Frequency of Copy Number Variations and Sequence Variants at CYP21A2 Locus: Implication for the Genetic Diagnosis of 21-Hydroxylase Deficiency. PLoS ONE. 3(5). e2138–e2138. 62 indexed citations
10.
Loidi, Lourdes, Vivek Dhir, Silvia Parajes, et al.. (2008). Functional characterization of threeCYP21A2sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system. Human Mutation. 30(2). E443–E450. 15 indexed citations
11.
González‐Quintela, Arturo, J. Campos Franco, Lourdes Loidi, et al.. (2008). Serum TNF-α levels in relation to alcohol consumption and common TNF gene polymorphisms. Alcohol. 42(6). 513–518. 55 indexed citations
12.
Franco, J. Campos, Francisco Gudé, Celsa Quinteiro, Carmen Vidal, & Arturo González‐Quintela. (2006). Gene by Environment Interaction: The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Modifies the Effect of Alcohol Consumption on Serum IgE Levels. Alcoholism Clinical and Experimental Research. 30(1). 7–14. 18 indexed citations
13.
Loidi, Lourdes, Celsa Quinteiro, Silvia Parajes, et al.. (2006). High variability in CYP21A2 mutated alleles in Spanish 21‐hydroxylase deficiency patients, six novel mutations and a founder effect. Clinical Endocrinology. 64(3). 330–336. 45 indexed citations
14.
Franco, J. Campos, Arturo González‐Quintela, Celsa Quinteiro, et al.. (2005). The −159C/T Polymorphism in the Promoter Region of the CD14 Gene Is Associated With Advanced Liver Disease and Higher Serum Levels of Acute‐Phase Proteins in Heavy Drinkers. Alcoholism Clinical and Experimental Research. 29(7). 1206–1213. 35 indexed citations
15.
Loidi, Lourdes, Lidia Castro-Feijóo, Jesús Barreiro, et al.. (2005). Kallmann's Syndrome with a Novel Missense Mutation in the KALI Gene that Modifies the Major Cell Adhesion Site of the Anosmin-1 Protein. Journal of Pediatric Endocrinology and Metabolism. 18(6). 545–8. 6 indexed citations
16.
Castro-Feijóo, Lidia, et al.. (2004). Tratamiento combinado con análogos de GnRH y GH. Anales de Pediatría. 60. 15–23. 1 indexed citations
17.
18.
Castro-Feijóo, Lidia, R. Peinó, Mary Lage, et al.. (2004). Therapeutic optimization of growth hormone deficiency in children and adolescents.. PubMed. 17 Suppl 3. 401–10. 2 indexed citations
19.
Quinteiro, Celsa, Lidia Castro-Feijóo, Lourdes Loidi, et al.. (2002). Novel Mutation Involving the Translation Initiation Codon of the Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism. 15(7). 1041–5. 15 indexed citations
20.
Rodrı́guez-Segade, Santiago, et al.. (1996). High serum IgA concentrations in patients with diabetes mellitus: agewise distribution and relation to chronic complications. Clinical Chemistry. 42(7). 1064–1067. 38 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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