Antònia Ribes

7.0k total citations
175 papers, 3.9k citations indexed

About

Antònia Ribes is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Antònia Ribes has authored 175 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Molecular Biology, 117 papers in Clinical Biochemistry and 26 papers in Biochemistry. Recurrent topics in Antònia Ribes's work include Metabolism and Genetic Disorders (117 papers), Biochemical and Molecular Research (52 papers) and Mitochondrial Function and Pathology (48 papers). Antònia Ribes is often cited by papers focused on Metabolism and Genetic Disorders (117 papers), Biochemical and Molecular Research (52 papers) and Mitochondrial Function and Pathology (48 papers). Antònia Ribes collaborates with scholars based in Spain, Netherlands and United States. Antònia Ribes's co-authors include Judit García‐Villoria, Frederic Tort, Ángela Arias, Rafael Artuch, B. Merinero, Paz Briones, E. Christensen, P. Briones, Johannes A. Mayr and Aleix Navarro‐Sastre and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Brain.

In The Last Decade

Antònia Ribes

171 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antònia Ribes Spain 38 2.5k 2.1k 610 586 558 175 3.9k
Magdalena Ugarte Spain 38 3.3k 1.3× 2.9k 1.4× 507 0.8× 753 1.3× 882 1.6× 218 4.7k
Barbara Plecko Austria 37 2.3k 0.9× 1.9k 0.9× 651 1.1× 984 1.7× 597 1.1× 138 4.6k
Graziella Uziel Italy 44 4.8k 1.9× 2.8k 1.3× 349 0.6× 702 1.2× 332 0.6× 121 6.1k
Pinar T. Ozand Saudi Arabia 34 2.2k 0.9× 1.9k 0.9× 383 0.6× 923 1.6× 375 0.7× 163 4.4k
Nancy Braverman Canada 35 4.6k 1.8× 1.4k 0.6× 496 0.8× 1.1k 1.9× 410 0.7× 113 6.0k
Lourdes R. Desviat Spain 36 2.7k 1.1× 2.1k 1.0× 278 0.5× 567 1.0× 729 1.3× 154 3.7k
Cary O. Harding United States 33 1.9k 0.8× 2.0k 1.0× 334 0.5× 1.1k 1.8× 416 0.7× 120 3.4k
Shamima Rahman United Kingdom 44 4.7k 1.9× 2.8k 1.3× 533 0.9× 561 1.0× 319 0.6× 160 6.3k
Yair Anikster Israel 36 1.9k 0.7× 977 0.5× 709 1.2× 553 0.9× 231 0.4× 132 4.2k
Maria Alice Donati Italy 31 2.5k 1.0× 1.4k 0.6× 177 0.3× 915 1.6× 475 0.9× 136 3.9k

Countries citing papers authored by Antònia Ribes

Since Specialization
Citations

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

Fields of papers citing papers by Antònia Ribes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antònia Ribes

This figure shows the co-authorship network connecting the top 25 collaborators of Antònia Ribes. A scholar is included among the top collaborators of Antònia Ribes 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 Antònia Ribes. Antònia Ribes 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.
Schröter, Julian, et al.. (2023). Exploring genotype–phenotype correlations in glutaric aciduria type 1. Journal of Inherited Metabolic Disease. 46(3). 371–390. 8 indexed citations
2.
Pané, Adriana, Pere Leyes, Pedro Moreno, et al.. (2023). Preparing Enteral Formulas for Adult Patients with Phenylketonuria: A Minor Necessity but Major Challenge—A Case Report. Journal of Clinical Medicine. 12(23). 7452–7452. 1 indexed citations
3.
Arrabal, Luisa, Laura Gort, Judit García‐Villoria, et al.. (2023). Functional Evidence of CCDC186 as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations. International Journal of Molecular Sciences. 24(15). 12319–12319.
4.
Jurado, Susana, Glòria Garrabou, Mariona Guitart‐Mampel, et al.. (2023). CRISPR/Cas9‐based functional genomics strategy to decipher the pathogenicity of genetic variants in inherited metabolic disorders. Journal of Inherited Metabolic Disease. 46(6). 1029–1042. 1 indexed citations
5.
Casaroli‐Marano, Ricardo P., Judit García‐Villoria, Vicente A. Yépez, et al.. (2022). Diagnostic Odyssey in an Adult Patient with Ophthalmologic Abnormalities and Hearing Loss: Contribution of RNA-Seq to the Diagnosis of a PEX1 Deficiency. International Journal of Molecular Sciences. 23(20). 12367–12367. 3 indexed citations
6.
Tort, Frederic, Laura Texidó, Cèlia Painous, et al.. (2022). Over-Mutated Mitochondrial, Lysosomal and TFEB-Regulated Genes in Parkinson’s Disease. Journal of Clinical Medicine. 11(6). 1749–1749. 4 indexed citations
7.
Arranz, José Antonio, Aída Ormazábal, Mireia del Toro, et al.. (2021). Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns. Orphanet Journal of Rare Diseases. 16(1). 195–195. 22 indexed citations
8.
Martín-Nalda, Andrea, Mónica Martínez‐Gallo, Marina García-Prat, et al.. (2021). Newborn Screening for SCID: Experience in Spain (Catalonia). International Journal of Neonatal Screening. 7(3). 46–46. 11 indexed citations
9.
García‐Silva, María Teresa, Luis Aldámiz‐Echevarría, Laura Gort, et al.. (2020). Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia. Mitochondrion. 55. 78–84. 4 indexed citations
10.
Garrabou, Glòria, et al.. (2020). Physiopathological Bases of the Disease Caused by HACE1 Mutations: Alterations in Autophagy, Mitophagy and Oxidative Stress Response. Journal of Clinical Medicine. 9(4). 913–913. 14 indexed citations
11.
Tort, Frederic, Ranjani Parthasarathy, Judit García‐Villoria, et al.. (2020). Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution. Molecular Genetics and Metabolism. 131(3). 349–357. 11 indexed citations
12.
Cardellach, Francesc & Antònia Ribes. (2018). Medicina interna y enfermedades raras. Transición niño-adulto. Arbor. 194(789). a460–a460. 1 indexed citations
13.
Ruíz, Miguel A., et al.. (2010). Homocistinuria y Acidemia Metilmalónica (CbIC) de evolución fatal en un recién nacido: a proposito de un caso. 25(3). 22–26. 1 indexed citations
14.
Fons, Carmen, Ángela Arias, Pilar Rodríguez‐Pombo, et al.. (2009). Deficiencia cerebral de creatina: primeros pacientes españoles con mutaciones en el gen GAMT. Medicina Clínica. 133(19). 745–749. 7 indexed citations
15.
Ribes, Antònia, Bernd A. Neubauer, Stanley H. Korman, et al.. (2005). L-2-hydroxyglutaric aciduria: novel mutations in the L-2-hydroxyglutarate dehydrogenase gene. Journal of Inherited Metabolic Disease. 28. 93–93. 1 indexed citations
16.
Invernizzi, Federica, Barbara Garavaglia, Antònia Ribes, et al.. (2000). Clinical and molecular heterogeneity in carnitine-acylcarnitine translocase deficiency.. Journal of Inherited Metabolic Disease. 23. 121. 6 indexed citations
17.
Benito, Javier, et al.. (2000). [Use of a hospital pediatric emergency department during the night].. PubMed. 52(4). 346–50. 1 indexed citations
18.
Martínez, Gemma, José-Raúl Garcı́a-Lozano, Antònia Ribes, et al.. (1998). High Risk of Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency among Gypsies. Pediatric Research. 44(1). 83–84. 9 indexed citations
19.
Marí, Ferrán García, et al.. (1994). Métodos de muestreo binomial y secuencial del trips de las flores Frankliniella occidentalis (Pergande) (Thysanoptera, Thripidae) y de antocóridos (Heteroptera, Anthocoridae) en fresón. Boletín de sanidad vegetal. Plagas. 20(3). 703–723. 5 indexed citations
20.
González-Zamora, José E., et al.. (1994). Control de trips en fresón: empleo de plantas de haba como refugio de poblaciones de antocóridos. Boletín de sanidad vegetal. Plagas. 20(1). 57–72. 5 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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