Gloria Fraga

1.2k total citations
19 papers, 434 citations indexed

About

Gloria Fraga is a scholar working on Nephrology, Molecular Biology and Genetics. According to data from OpenAlex, Gloria Fraga has authored 19 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Nephrology, 8 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Gloria Fraga's work include Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (6 papers) and Genetic and Kidney Cyst Diseases (5 papers). Gloria Fraga is often cited by papers focused on Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (6 papers) and Genetic and Kidney Cyst Diseases (5 papers). Gloria Fraga collaborates with scholars based in Spain, United States and Palestinian Territory. Gloria Fraga's co-authors include Roser Torrá, Elisabet Ars, Gema Ariceta, José Ballarín, Gemma Bullich, A. Madrid, Juan Alberto Piñero‐Fernández, Albert Flotats, Esther Mena and Valle Camacho and has published in prestigious journals such as Kidney International, Annals of the Rheumatic Diseases and Nephrology Dialysis Transplantation.

In The Last Decade

Gloria Fraga

17 papers receiving 424 citations

Peers

Gloria Fraga
Whitney Besse United States
Hila Barak United States
Jane Striegel United States
Bliss Magella United States
M. van Weel Netherlands
Gloria Fraga
Citations per year, relative to Gloria Fraga Gloria Fraga (= 1×) peers Albertien M. van Eerde

Countries citing papers authored by Gloria Fraga

Since Specialization
Citations

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

Fields of papers citing papers by Gloria Fraga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gloria Fraga

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

All Works

19 of 19 papers shown
1.
Malouf, Jorge, Hye Sang Park, Gloria Fraga, et al.. (2025). Pediatric densitometry: is the Z score adjustment necessary in all cases?. Frontiers in Endocrinology. 16. 1587382–1587382. 1 indexed citations
2.
Cerdá, Dacia, Gloria Fraga, Mireia López-Corbeto, et al.. (2025). Risk factors associated with low bone mineral density and childhood osteoporosis in a population undergoing skeletal growth: a cross-sectional analytic study. Frontiers in Endocrinology. 16. 1587985–1587985.
3.
Fraga, Gloria, Marc Pybus, Miriam Aza‐Carmona, et al.. (2024). A Mild Presentation of X-Linked Hypophosphatemia Caused by a Non-Canonical Splice Site Variant in the PHEX Gene. Genes. 15(6). 679–679. 1 indexed citations
4.
Ariceta, Gema, Laure Collard, Saoussen Abroug, et al.. (2022). ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria. Pediatric Nephrology. 38(2). 403–415. 13 indexed citations
5.
Ars, Elisabet, Carmen Bernis, Gloria Fraga, et al.. (2022). Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Diseases. Review 2020. Nefrología (English Edition). 42(4). 367–389. 4 indexed citations
6.
Pybus, Marc, Gemma Bullich, Mónica Furlano, et al.. (2021). Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players. Nephrology Dialysis Transplantation. 37(4). 687–696. 47 indexed citations
7.
Santacana, Marı́a, A. Madrid, Gloria Fraga, et al.. (2021). CD44-negative parietal–epithelial cell staining in minimal change disease: association with clinical features, response to corticosteroids and kidney outcome. Clinical Kidney Journal. 15(3). 545–552. 2 indexed citations
8.
9.
Ariceta, Gema, Bradley P. Dixon, Seong Heon Kim, et al.. (2020). The long-acting C5 inhibitor, ravulizumab, is effective and safe in pediatric patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment. Kidney International. 100(1). 225–237. 58 indexed citations
10.
Cerdá, Dacia, Gloria Fraga, Susana Boronat, et al.. (2020). AB0997 IS HEIGHT ADJUSTMENT NECESSARY IN PEDIATRIC DENSITOMETRY IN ALL CHILDREN?. Annals of the Rheumatic Diseases. 79. 1791–1792. 1 indexed citations
12.
Bullich, Gemma, Iván Vargas, Patricia Ruíz, et al.. (2018). A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases. Kidney International. 94(2). 363–371. 86 indexed citations
13.
Bullich, Gemma, Iván Vargas, Daniel Trujillano, et al.. (2016). Contribution of the TTC21B gene to glomerular and cystic kidney diseases. Nephrology Dialysis Transplantation. 32(1). 151–156. 29 indexed citations
14.
Bullich, Gemma, Daniel Trujillano, Sheila Santín, et al.. (2014). Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity. European Journal of Human Genetics. 23(9). 1192–1199. 66 indexed citations
15.
Ars, Elisabet, C. Bernis, Gloria Fraga, et al.. (2014). Spanish guidelines for the management of autosomal dominant polycystic kidney disease. Nephrology Dialysis Transplantation. 29(suppl 4). iv95–iv105. 40 indexed citations
16.
Santín, Sheila, Gloria Fraga, Philip Ruiz, et al.. (2011). WT1 mutations may be a cause of severe renal failure due to nephroblastomatosis in Wilms’ tumor patients. Clinical Nephrology. 76(9). 244–248. 3 indexed citations
17.
Badell, Isabel, E. del Rı́o, Núria Pardo, et al.. (2007). Aplicación de la farmacogenética a la individualización terapéutica en la leucemia linfoblástica aguda: presentación de caso clínico. Anales de Pediatría. 66(4). 437–438.
18.
Camacho, Valle, et al.. (2004). DMSA study performed during febrile urinary tract infection: a predictor of patient outcome?. European Journal of Nuclear Medicine and Molecular Imaging. 31(6). 862–866. 60 indexed citations
19.
Pardo, Núria, Francesc Martí, Gloria Fraga, et al.. (1996). High-dose systemic interleukin-2 therapy in stage IV neuroblastoma for one year after autologous bone marrow transplantation: Pilot study. Medical and Pediatric Oncology. 27(6). 534–539. 16 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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