Antònia Ribes

7.0k citations

174 papers · 4.2k · h-index 39

Impact in

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
Biochemistry top 0.5%
- Biochemical Acid Research Studies
- Amino Acid Enzymes and Metabolism

Papers in

Molecular Biology 115
- Biochemical and Molecular Research 47
- Mitochondrial Function and Pathology 46
- RNA modifications and cancer 13
Clinical Biochemistry 110
- Metabolism and Genetic Disorders 110

Co-authors: Judit García‐Villoria (55 shared papers)Frederic Tort (27 shared papers)Ángela Arias (22 shared papers)Rafael Artuch (30 shared papers)B. Merinero (13 shared papers)Paz Briones (21 shared papers)E. Christensen (7 shared papers)Johannes A. Mayr (4 shared papers)
Journals: Journal of Inherited Metabolic Disease (48 papers)Molecular Genetics and Metabolism (14 papers)Clinical Biochemistry (5 papers)Human Mutation (5 papers)Pediatric Neurology (5 papers)
Partner nations: Spain United States Netherlands

In The Last Decade

Antònia Ribes

168 papers receiving 4.1k citations

Peers

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-authors

The 25 scholars most cited alongside Antònia Ribes, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Antònia Ribes Line = papers co-authored together Antònia Ribes links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 174 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Lipoic acid biosynthesis defects Journal of Inherited Metabolic Disease ·Johannes A. Mayr, René G. Feichtinger, Frederic Tort, Antònia Ribes, Wolfgang Sperl	2014	202
2	Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct Pediatric Research ·Christiane Busquets, B. Merinero, Ernst Christensen, Josep Lluis Gelpí, Jaume Campistol, Merçè Pineda, Emilio Fernández‐Álvarez, J M Prats, Ana Sans, Rosa Arteaga, M Martí, Jaime Campos, Mercedes Martínez‐Pardo, A Martínez-Bermejo, J Vaquerizo, Modesto Orozco, Magdalena Ugarte, María Josep Coll, Antònia Ribes	2000	108
3	Correlation of genotype and phenotype in glutaryl‐CoA dehydrogenase deficiency Journal of Inherited Metabolic Disease ·E. Christensen, Antònia Ribes, B. Merinero, Johannes Zschocke	2004	105
4	Ethylmalonic Aciduria Is Associated with an Amino Acid Variant of Short Chain Acyl-Coenzyme A Dehydrogenase Pediatric Research ·Morten J. Corydon, N. Gregersen, W. Lehnert, Antònia Ribes, Piero Rinaldo, Stanislav Kmoch, E. Christensen, Thomas J. Kristensen, Brage Storstein Andresen, Peter Bross, Vibeke Winter, G Martı́nez, Søren Neve, Thomas G. Jensen, Lars Bolund, Steen Kølvraa	1996	86
5	Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines Journal of Inherited Metabolic Disease ·Martina Huemer, Viktor Kožich, Piero Rinaldo, Matthias R. Baumgartner, B. Merinero, Elisabetta Pasquini, Antònia Ribes, Henk J. Blom	2015	85
6	Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation Journal of the Neurological Sciences ·Rafael Artuch, Gloria Brea‐Calvo, Paz Briones, Asunción Aracil, Marta Ferrer Galván, Carmen Espinós, Jordi Corral, Vı́ctor Volpini, Antònia Ribes, Antoni L. Andreu, Francesc Palau, José A. Sánchez‐Alcázar, Plácido Navas, Mercè Pineda	2006	82
7	The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level Human Genetics ·Christina B. Pedersen, Steen Kølvraa, Agnete Kølvraa, Vibeke Stenbroen, Margrethe Kjeldsen, Regina Ensenauer, Ingrid Tein, Dietrich Matern, Piero Rinaldo, Christine Vianey‐Saban, Antònia Ribes, W. Lehnert, Ernst Christensen, Thomas J. Corydon, Brage Storstein Andresen, Søren Vang, Lars Bolund, Jerry Vockley, Peter Bross, Niels Gregersen	2008	81
8	Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC) Human Mutation ·Eva Richard, Ana Jorge‐Finnigan, Judit García‐Villoria, B. Merinero, Lourdes R. Desviat, Laura Gort, Paz Briones, Fátima Leal, Celia Pérez‐Cerdá, Antònia Ribes, Magdalena Ugarte, Belén Pérez, (unknown)	2009	74
9	β-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities Human Molecular Genetics ·André B. P. Kuilenburg, Rutger Meinsma, Eva Beke, Birgit Assmann, Antònia Ribes, Isabel Lorente, Rebekka Busch, Ertan Mayatepek, N. G. G. M. Abeling, Arno van Cruchten, A. E. M. Stroomer, Henk van Lenthe, Lida Zoetekouw, Willem Kulik, Georg F. Hoffmann, Thomas Voït, Ron A. Wevers, Frank Rutsch, Albert H. Gennip	2004	71
10	Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds Human Molecular Genetics ·Gustavo Tiscórnia, Erika Lorenzo-Vivas, Leslie Matalonga, Ina Berniakovich, (unknown), Cristina Eguizábal, Laura Gort, Federico Gonzãlez, Carmen Ortiz Mellet, José M. Garcı́a Fernández, Antònia Ribes, Anna Veiga, Juan Carlos Izpisúa Belmonte	2012	70
11	X‐Linked creatine transporter deficiency in two patients with severe mental retardation and autism Journal of Inherited Metabolic Disease ·P. Póo‐Argüelles, Ángela Arias, Marta Vilaseca, Antònia Ribes, Rafael Artuch, Anna Sans-Fitó, (unknown), C. Jakobs, Gajja S. Salomons	2006	66
12	Mutations in the lipoyltransferaseLIPT1gene cause a fatal disease associated with a specific lipoylation defect of the 2-ketoacid dehydrogenase complexes Human Molecular Genetics ·Frederic Tort, Xènia Ferrer-Cortés, Marta Thió, Aleix Navarro‐Sastre, Leslie Matalonga, Ester Quintana, Núria Bujan, Ángela Arias, Judit García‐Villoria, Cécile Acquaviva, Christine Vianey‐Saban, Rafael Artuch, Àngels García‐Cazorla, Paz Briones, Antònia Ribes	2013	65
13	The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism The American Journal of Human Genetics ·M. Esther Gallardo, Lourdes R. Desviat, José Manuel Rodríguez Rodríguez, Jorge Esparza-Gordillo, Celia Pérez‐Cerdá, Belén Pérez, Pilar Rodríguez‐Pombo, Olga Criado‐García, Raúl Sanz, D. Holmes Morton, K. Michael Gibson, Thuy Le, Antònia Ribes, Santiago Rodrı́guez de Córdoba, Magdalena Ugarte, Miguel Á. Peñalva	2001	64
14	Molecular and functional analysis ofSLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency Human Mutation ·Vito Iacobazzi, Federica Invernizzi, Silvia Baratta, Roser Pons, Wendy K. Chung, Barbara Garavaglia, Carlo Dionisi‐Vici, Antònia Ribes, Rossella Parini, Maria Dolores Huertas, S. Roldán, Graziantonio Lauria, Ferdinando Palmieri, Franco Taroni	2004	63
15	Creatine transporter deficiency: Prevalence among patients with mental retardation and pitfalls in metabolite screening Clinical Biochemistry ·Ángela Arias, Marc Corbella, Carmen Fons, Ángela Sempere, Judit García‐Villoria, Aída Ormazábal, Pilar Póo, Mercè Pineda, María Antònia Vilaseca, Jaume Campistol, Paz Briones, Teresa Pàmpols, Gajja S. Salomons, Antònia Ribes, Rafael Artuch	2007	58
16	A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA Pediatric Research ·Kay Tanaka, Niels Gregersen, Antònia Ribes, Julie Kim, Steen Kølvraa, Vibeke Winter, Hans Eiberg, Gemma Martínez, Thomas Deufel, Barbara Leifert, René Santer, Baudouin Francois, Ewa Pronicka, Aranka László, Stanislav Kmoch, Ivo Kremensky, Luba Kalaydjicva, İ Özalp, Michinori Ito	1997	57
17	Potential relationship between genotype and clinical outcome in propionic acidaemia patients European Journal of Human Genetics ·Celia Pérez‐Cerdá, B. Merinero, Pilar Rodríguez‐Pombo, Belén Pérez, Lourdes R. Desviat, Silvia Muro, Eva Richard, MJ García, Jon A. Gangoiti, (unknown), Patricia Sanz, P. Briones, Antònia Ribes, Mercedes Martínez‐Pardo, Josep M. Campistol, M. Pérez, R. Lama, M. Luisa Murga, T Lema-Garrett, Alfonso Verdú, Magdalena Ugarte	2000	56
18	Cholestane-3β,5α,6β-triol: high levels in Niemann-Pick type C, cerebrotendinous xanthomatosis, and lysosomal acid lipase deficiency Journal of Lipid Research ·Sonia Pajares, Ángela Arias, Judit García‐Villoria, Judit Macías‐Vidal, Emilio Ros, Javier de las Heras, M. Girós, María Josep Coll, Antònia Ribes	2015	56
19	Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2) European Journal of Paediatric Neurology ·Emmanuel Scalais, Ronit Chafai, Rudy Van Coster, L. Bindl, C. Nuttin, Chryssa Panagiotaraki, Sara Seneca, Willy Lissens, Antònia Ribes, Caroline Geers, Joél Smet, Linda De Meırleır	2013	56
20	A new fatal case of pyridox(am)ine 5′-phosphate oxidase (PNPO) deficiency Molecular Genetics and Metabolism ·Ángeles Ruiz, Judit García‐Villoria, Aída Ormazábal, Johannes Zschocke, Miquel Fiol, Aleix Navarro‐Sastre, Rafael Artuch, María Antònia Vilaseca, Antònia Ribes	2007	54

About Antònia Ribes

Antònia Ribes is a scholar working on Molecular Biology, Clinical Biochemistry, Physiology, Biochemistry and Cell Biology, having authored 174 papers that have together received 4.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (110 papers), Biochemical and Molecular Research (47 papers), Mitochondrial Function and Pathology (46 papers), Muscle metabolism and nutrition (13 papers), Neonatal Health and Biochemistry (13 papers), Folate and B Vitamins Research (13 papers), RNA modifications and cancer (13 papers) and Amino Acid Enzymes and Metabolism (12 papers). The work is most often cited by research in Clinical Biochemistry (2.2k citations), Biochemistry (603 citations), Rheumatology (516 citations), Molecular Biology (2.4k citations) and Cell Biology (442 citations). Antònia Ribes has collaborated with scholars based in Spain, United States and Netherlands. Frequent co-authors include Judit García‐Villoria, Frederic Tort, Ángela Arias, Rafael Artuch, B. Merinero, Paz Briones, E. Christensen, Johannes A. Mayr, P. Briones and Wolfgang Sperl. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Clinical Biochemistry, Human Mutation and Pediatric Neurology.

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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