Aída Ormazábal

2.7k total citations
86 papers, 1.8k citations indexed

About

Aída Ormazábal is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Aída Ormazábal has authored 86 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Clinical Biochemistry, 39 papers in Molecular Biology and 21 papers in Biochemistry. Recurrent topics in Aída Ormazábal's work include Metabolism and Genetic Disorders (60 papers), Amino Acid Enzymes and Metabolism (21 papers) and Mitochondrial Function and Pathology (17 papers). Aída Ormazábal is often cited by papers focused on Metabolism and Genetic Disorders (60 papers), Amino Acid Enzymes and Metabolism (21 papers) and Mitochondrial Function and Pathology (17 papers). Aída Ormazábal collaborates with scholars based in Spain, United States and Greece. Aída Ormazábal's co-authors include Rafael Artuch, Àngels García‐Cazorla, Mercedes Serrano, Belén Pérez‐Dueñas, Jaume Campistol, Julio Montoya, Cristina Sierra, María Antònia Vilaseca, Emilio Fernández‐Álvarez and Paz Briones and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Aída Ormazábal

84 papers receiving 1.8k citations

Peers

Countries citing papers authored by Aída Ormazábal

Since Specialization

Citations

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

Fields of papers citing papers by Aída Ormazábal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aída Ormazábal

This figure shows the co-authorship network connecting the top 25 collaborators of Aída Ormazábal. A scholar is included among the top collaborators of Aída Ormazábal 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 Aída Ormazábal. Aída Ormazábal 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	A simple, sensitive and high-throughput assay using UPLC-MS/MS for the quantification of plasma methylmalonic acid to detect and monitor genetic and acquired methylmalonic acidurias 2024 ·Microchemical Journal ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mario De La Rosa, (unknown), (unknown), (unknown), Aída Ormazábal, (unknown), Judit García‐Villoria, (unknown)	0
2	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
3	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
4	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
5	Effect of Special Low-Protein Foods Consumption in the Dietary Pattern and Biochemical Profile of Patients with Inborn Errors of Protein Metabolism: Application of a Database of Special Low-Protein Foods 2023 ·Nutrients ·(unknown), (unknown), (unknown), Rafaël Llorach, (unknown), Ángeles García‐Cazorla, Aída Ormazábal, Mireia Urpí-Sardà	3
6	Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns 2021 ·Orphanet Journal of Rare Diseases ·(unknown), José Antonio Arranz, Aída Ormazábal, Mireia del Toro, Ángeles García‐Cazorla, Aleix Navarro‐Sastre, Rosa María López, (unknown), (unknown), (unknown), (unknown), (unknown), José Luis Marı́n, (unknown), Rafael Artuch, Frederic Tort, Laura Gort, (unknown), Judit García‐Villoria, Antònia Ribes	22
7	Cerebrospinal fluid neopterin as a biomarker of neuroinflammatory diseases 2020 ·Scientific Reports ·Marta Molero-Luís, Dídac Casas‐Alba, Gabriela Orellana, Aída Ormazábal, Cristina Sierra, (unknown), (unknown), Jesús Velasco, Cristian Launes, Daniel Cuadras, Belén Pérez‐Dueñas, Iolanda Jordán, Francisco José Cambra Lasaosa, Juan Darío Ortigoza‐Escobar, Carmen Muñoz‐Almagro, Àngels García‐Cazorla, Thaís Armangué, Rafael Artuch	32
8	Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism 2019 ·Scientific Reports ·(unknown), (unknown), (unknown), (unknown), Elisenda Cortès‐Saladelafont, Federico Ramos, (unknown), (unknown), (unknown), (unknown), María L. Couce, Cristina Sierra, Aída Ormazábal, (unknown), Rafael Artuch, Judith Armstrong, Soledad Alcántara, Àngels García‐Cazorla	6
9	Effect of blood contamination of cerebrospinal fluid on amino acids, biogenic amines, pterins and vitamins 2019 ·Fluids and Barriers of the CNS ·(unknown), Mercedes Casado, Cristina Sierra, (unknown), Laura Martí‐Sánchez, (unknown), Guerau Fernández, Àngels García‐Cazorla, Aída Ormazábal, Marta Molero-Luís, Rafael Artuch	10
10	White matter microstructural damage in early treated phenylketonuric patients 2018 ·Orphanet Journal of Rare Diseases ·(unknown), Mónica Rebollo, Pablo Ripollés, Rosa Gassió, Aída Ormazábal, Cristina Sierra, (unknown), Rafael Artuch, Jaume Campistol	20
11	A targeted metabolomic procedure for amino acid analysis in different biological specimens by ultra-high-performance liquid chromatography–tandem mass spectrometry 2018 ·Metabolomics ·Mercedes Casado, Cristina Sierra, (unknown), Rafael Artuch, Aída Ormazábal	30
12	Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome 2014 ·Orphanet Journal of Rare Diseases ·Pilar Quijada‐Fraile, Mar O’Callaghan, Elena Martín‐Hernández, Raquel Montero, Àngels García‐Cazorla, Ana Martı́nez de Aragón, Jordi Muchart, Ignacio Málaga, (unknown), (unknown), Cristina Jou, Julio Montoya, Sonia Emperador, Eduardo Ruiz‐Pesini, Joaquı́n Arenas, Miguel A. Martı́n, Aída Ormazábal, Mercè Pineda, María Teresa García‐Silva, Rafael Artuch	31
13	cblE-Type Homocystinuria Presenting with Features of Haemolytic-Uremic Syndrome in the Newborn Period 2012 ·JIMD Reports ·Daniel Palanca Arias, Àngels García‐Cazorla, (unknown), Cristina Jou, V. Cusí, Mariona Suñol, (unknown), Belén Pérez, Aída Ormazábal, Brian Fowler, Rafael Artuch	6
14	Cerebrospinal Fluid Neopterin and Cryopyrin-Associated Periodic Syndrome 2009 ·Pediatric Neurology ·Mercedes Serrano, Aída Ormazábal, Jordi Antón, Juan I. Aróstegui, (unknown)	7
15	Dopa-responsive infantile hypokinetic rigid syndrome due to dominant guanosine triphosphate cyclohydrolase 1 deficiency 2007 ·Journal of the Neurological Sciences ·Eduardo López‐Laso, (unknown), María Elena Mateos, Juan Luís Pérez-Navero, (unknown), (unknown), Aída Ormazábal, Rafael Artuch	11
16	Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome 2007 ·Neuropediatrics ·V. Ramaekers, J.M. Sequeira, Rafael Artuch, Nenad Blau, Teresa Temudo, Aída Ormazábal, M. Pineda, (unknown), Filip Roelens, Franco Laccone, E. Quadros	49
17	A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: Clinical, biochemical and genetic analysis 2007 ·Molecular Genetics and Metabolism ·Marta Ribasès, Mercedes Serrano, Emilio Fernández‐Álvarez, (unknown), Aída Ormazábal, Àngels García‐Cazorla, Belén Pérez‐Dueñas, Jaume Campistol, Rafael Artuch, Bru Cormand	16
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	Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency 2005 ·Prenatal Diagnosis ·Lisbeth Birk Møller, Anne Romstad, (unknown), (unknown), Aída Ormazábal, Merçè Pineda, Nenad Blau, Flemming Güttler, Rafael Artuch	13
20	HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins 2004 ·Journal of Neuroscience Methods ·Aída Ormazábal, Àngels García‐Cazorla, Yolanda Fernández, Emilio Fernández‐Álvarez, Jaume Campistol, Rafael Artuch	91

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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