Ángela Arias

1.2k total citations
31 papers, 673 citations indexed

About

Ángela Arias is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, Ángela Arias has authored 31 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 13 papers in Cell Biology. Recurrent topics in Ángela Arias's work include Metabolism and Genetic Disorders (15 papers), Muscle metabolism and nutrition (11 papers) and Biochemical Acid Research Studies (5 papers). Ángela Arias is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Muscle metabolism and nutrition (11 papers) and Biochemical Acid Research Studies (5 papers). Ángela Arias collaborates with scholars based in Spain, Netherlands and Austria. Ángela Arias's co-authors include Antònia Ribes, Judit García‐Villoria, Rafael Artuch, Paz Briones, Gajja S. Salomons, Pilar Rodríguez‐Pombo, María Josep Coll, Laura Gort, Leslie Matalonga and Marta Vilaseca and has published in prestigious journals such as Nature Communications, Brain and International Journal of Molecular Sciences.

In The Last Decade

Ángela Arias

29 papers receiving 667 citations

Peers

Countries citing papers authored by Ángela Arias

Since Specialization

Citations

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

Fields of papers citing papers by Ángela Arias

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ángela Arias

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Cerebrospinal amino acid profiling in a large cohort of neuropediatric patients with epilepsy 2025 ·Neurobiology of Disease ·(unknown), (unknown), Aída Ormazábal, Mercedes Casado, Ángela Arias, (unknown), (unknown), Alexandre Perera-Lluna, Àngels García‐Cazorla, Carmen Fons, Rafael Artuch	1
2	Exploring Plasma Coenzyme Q10 Status in Paediatric Dyslipidaemia 2024 ·Antioxidants ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ángela Arias, (unknown), Dèlia Yubero, Mireia Tondo, Carlos Santos‐Ocaña, (unknown), Rafael Artuch	1
3	Structure and mechanisms of transport of human Asc1/CD98hc amino acid transporter 2024 ·Nature Communications ·(unknown), (unknown), Paola Bartoccioni, (unknown), Ángela Arias, Suwipa Saen‐oon, Camille Stephan‐Otto Attolini, Rafael Artuch, Lucía Díaz, Vı́ctor Guallar, Ekaitz Errasti‐Murugarren, Manuel Palacı́n, Óscar Llorca	7
4	Targeted ultra performance liquid chromatography tandem mass spectrometry procedures for the diagnosis of inborn errors of metabolism: validation through ERNDIM external quality assessment schemes 2024 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·(unknown), Ángela Arias, Pedro Ruiz‐Sala, Judit García‐Villoria, Rachel S. Carling, Jörgen Bierau, George J. G. Ruijter, Mercedes Casado, Aída Ormazábal, Rafael Artuch	0
5	Cerebrospinal Fluid Homovanillic and 5-Hydroxyindoleacetic Acids in a Large Pediatric Population; Establishment of Reference Intervals and Impact of Disease and Medication 2024 ·Clinical Chemistry ·(unknown), Aída Ormazábal, Mercedes Casado, Ángela Arias, (unknown), (unknown), (unknown), Francesc García Cuyàs, A. Nascimento, C. Ortez, Daniel Natera‐de Benito, Thaís Armangué, (unknown), Natalia Juliá‐Palacios, Alejandra Darling, Juan Darío Ortigoza‐Escobar, Carmen Fons, Àngels García‐Cazorla, Alexandre Perera-Lluna, Rafael Artuch	3
6	Exploring the Contribution of the Transporter AGT1/rBAT in Cystinuria Progression: Insights from Mouse Models and a Retrospective Cohort Study 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), (unknown), Laura González, (unknown), (unknown), (unknown), Ángela Arias, Rafael Artuch, Miguel López de Heredia, (unknown), (unknown), (unknown), Ekaitz Errasti‐Murugarren, Virginia Nunes	0
7	Fibroblast phenylalanine concentration as a surrogate biomarker of cellular number 2023 ·Journal of Chromatography B ·(unknown), Ángela Arias, Montserrat Ruíz, Aurora Pujol, Glòria Garrabou, (unknown), Roser Urreizti, (unknown), (unknown), Cristina Jou, Mercedes Casado, Aída Ormazábal, Rafael Artuch	3
8	Lysosomal Acid Lipase Deficiency in 23 Spanish Patients: High Frequency of the Novel c.966+2T>G Mutation in Wolman Disease 2017 ·JIMD Reports ·(unknown), (unknown), (unknown), Ángela Arias, Laura Gort	9
9	Treatment of genetic defects of thiamine transport and metabolism 2016 ·Expert Review of Neurotherapeutics ·Juan Darío Ortigoza‐Escobar, Marta Molero-Luís, Ángela Arias, Laura Martí‐Sánchez, Pilar Rodríguez‐Pombo, Rafael Artuch, Belén Pérez‐Dueñas	30
10	Effect of Readthrough Treatment in Fibroblasts of Patients Affected by Lysosomal Diseases Caused by Premature Termination Codons 2015 ·Neurotherapeutics ·Leslie Matalonga, Ángela Arias, Frederic Tort, (unknown), Judit García‐Villoria, María Josep Coll, Laura Gort, Antònia Ribes	18
11	Free-thiamine is a potential biomarker of thiamine transporter-2 deficiency: a treatable cause of Leigh syndrome 2015 ·Brain ·Juan Darío Ortigoza‐Escobar, Marta Molero-Luís, Ángela Arias, Alfonso Oyarzábal, Niklas Darín, Mercedes Serrano, Àngels García‐Cazorla, Mireia Tondo, María Isabel Hernández, Judit García‐Villoria, Mercedes Casado, Laura Gort, Johannes A. Mayr, Pilar Rodríguez‐Pombo, Antònia Ribes, Rafael Artuch, Belén Pérez‐Dueñas	48
12	A leaky splicing mutation in NFU1 is associated with a particular biochemical phenotype. Consequences for the diagnosis 2015 ·Mitochondrion ·(unknown), Juan Narbona, (unknown), Leslie Matalonga, Mireia del Toro, José Antonio Arranz, E. Riudor, Àngels García‐Cazorla, Cristina Jou, Mar O’Callaghan, Mercè Pineda, Raquel Montero, Ángela Arias, Judit García‐Villoria, Charlotte L. Alston, Robert W. Taylor, Paz Briones, Antònia Ribes, Frederic Tort	15
13	Analysis of coenzyme Q10 in lymphocytes by HPLC–MS/MS 2012 ·Journal of Chromatography B ·Ángela Arias, Judit García‐Villoria, Ana I. Rojo, (unknown), P. Briones, Antònia Ribes	17
14	Improvement of the cystine measurement in granulocytes by liquid chromatograhy-tandem mass spectrometry 2012 ·Clinical Biochemistry ·Judit García‐Villoria, José María Hernández Pérez, Ángela Arias, Antònia Ribes	14
15	Defining the pathogenicity of creatine deficiency syndrome 2010 ·Human Mutation ·Patricia Alcaide, B. Merinero, Pedro Ruiz‐Sala, Eva Richard, Rosa Navarrete, Ángela Arias, Antònia Ribes, Rafael Artuch, Jaume Campistol, Magdalena Ugarte, Pilar Rodríguez‐Pombo	27
16	Deficiencia cerebral de creatina: primeros pacientes españoles con mutaciones en el gen GAMT 2009 ·Medicina Clínica ·(unknown), Carmen Fons, Ángela Arias, Pilar Rodríguez‐Pombo, B. Merinero, Patricia Alcaide, Antoni Capdevila, Antònia Ribes, (unknown), Jesús Manuel Eirís Puñal, Pilar Póo, Emilio Fernández‐Álvarez, Jaume Campistol, Rafael Artuch	7
17	Response to creatine analogs in fibroblasts and patients with creatine transporter deficiency 2009 ·Molecular Genetics and Metabolism ·Carmen Fons, Ángela Arias, Ángel Pérez Sempere, Pilar Póo, M. Pineda, Albert Mas, Anna López‐Sala, Judit García‐Villoria, Marta Vilaseca, (unknown), (unknown), Rafael Artuch, Josep M. Campistol, Antònia Ribes	20
18	Creatine transporter deficiency: Prevalence among patients with mental retardation and pitfalls in metabolite screening 2007 ·Clinical Biochemistry ·Ángela Arias, (unknown), Carmen Fons, (unknown), 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	51
19	Methods for the diagnosis of creatine deficiency syndromes: A comparative study 2006 ·Journal of Neuroscience Methods ·Ángela Arias, Aída Ormazábal, Juan Antonio Moreno, (unknown), María Antònia Vilaseca, Judit García‐Villoria, Teresa Pàmpols, Paz Briones, Rafael Artuch, Antònia Ribes	28
20	Guanidinoacetate and creatine/creatinine levels in controls and patients with urea cycle defects 2004 ·Molecular Genetics and Metabolism ·Ángela Arias, Judit García‐Villoria, Antònia Ribes	38

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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