Àngels García‐Cazorla

6.6k total citations
137 papers, 2.5k citations indexed

About

Àngels García‐Cazorla is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Àngels García‐Cazorla has authored 137 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 74 papers in Clinical Biochemistry and 37 papers in Genetics. Recurrent topics in Àngels García‐Cazorla's work include Metabolism and Genetic Disorders (74 papers), Mitochondrial Function and Pathology (38 papers) and Genetics and Neurodevelopmental Disorders (33 papers). Àngels García‐Cazorla is often cited by papers focused on Metabolism and Genetic Disorders (74 papers), Mitochondrial Function and Pathology (38 papers) and Genetics and Neurodevelopmental Disorders (33 papers). Àngels García‐Cazorla collaborates with scholars based in Spain, United States and Germany. Àngels García‐Cazorla's co-authors include Rafael Artuch, Aída Ormazábal, Jean‐Marie Saudubray, Belén Pérez‐Dueñas, Jaume Campistol, Mercedes Serrano, Antònia Ribes, Marta Molero-Luís, Emilio Fernández‐Álvarez and Julio Montoya and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Brain.

In The Last Decade

Àngels García‐Cazorla

136 papers receiving 2.5k citations

Peers

Countries citing papers authored by Àngels García‐Cazorla

Since Specialization

Citations

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

Fields of papers citing papers by Àngels García‐Cazorla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Àngels García‐Cazorla. 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 Àngels García‐Cazorla. The network helps show where Àngels García‐Cazorla may publish in the future.

Co-authorship network of co-authors of Àngels García‐Cazorla

This figure shows the co-authorship network connecting the top 25 collaborators of Àngels García‐Cazorla. A scholar is included among the top collaborators of Àngels García‐Cazorla 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 Àngels García‐Cazorla. Àngels García‐Cazorla 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	The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolism 2025 ·Molecular Genetics and Metabolism ·Itay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, (unknown), (unknown), Onur Afacan, Àngels García‐Cazorla, Natalia Juliá‐Palacios, Thomas Opladen, Oya Kuseyri Hübschmann, Kathrin Jeltsch, (unknown), (unknown), Alexander Rotenberg, Melissa Tsuboyama, Jean‐Baptiste Roullet, Phillip L. Pearl	2
2	Development and Preliminary Validation of a Parkinsonism‐Dystonia Scale for Infants and Young Children 2025 ·Movement Disorders ·Roser Pons, Toni S. Pearson, Belén Pérez‐Dueñas, Àngels García‐Cazorla, Manju A. Kurian, (unknown), Vasiliki Zouvelou, (unknown), (unknown), (unknown), Alejandra Darling, María del Mar O’Callaghan, (unknown), Dora Steel, (unknown), María João Forjaz, Carmen Rodríguez‐Blázquez	1
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	Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency 2023 ·Developmental Medicine & Child Neurology ·Itay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, Àngels García‐Cazorla, Melissa Tsuboyama, (unknown), Alexander Rotenberg, Jean‐Baptiste Roullet, Phillip L. Pearl	11
5	Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity 2023 ·Journal of Clinical Investigation ·Laura Planas‐Serra, Nathalie Launay, Leire Goicoechea, Bénédicte Héron, Cristina Jou, Natalia Juliá‐Palacios, Montserrat Ruíz, Stéphane Fourcade, Carlos Casasnovas, Carolina de la Torre, A. Gélot, María Marsal, Pablo Loza‐Álvarez, Àngels García‐Cazorla, (unknown), Isidró Ferrer, Manuel Portero-Otı́n, Estela Área-Gómez, Aurora Pujol	24
6	iPSC ‐based modeling of THD recapitulates disease phenotypes and reveals neuronal malformation 2023 ·EMBO Molecular Medicine ·(unknown), Irene Fernández‐Carasa, Carles Calatayud, (unknown), Meritxell Pons‐Espinal, (unknown), Leticia Campa, Francesc Artigas, Analı́a Bortolozzi, Rosario Domingo‐Jiménez, (unknown), Mercè Pineda, Rafael Artuch, Ángel Raya, Àngels García‐Cazorla, Antonella Consiglio	8
7	The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1 2022 ·Clinical Genetics ·(unknown), Dèlia Yubero, Fátima Leal, María L. Couce, (unknown), Eduardo López‐Laso, Àngels García‐Cazorla, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Magdalena Ugarte, Rafael Artuch, Belén Pérez	6
8	Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders 2022 ·Neuroradiology ·(unknown), Christian Stephan‐Otto, Elisenda Cortès‐Saladelafont, Natalia Juliá Palacios, (unknown), (unknown), Rosario Domingo‐Jiménez, (unknown), Miguel Tomás Vila, Kathrin Jeltsch, Oya Kuseyri Hübschmann, Thomas Opladen, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Àngels García‐Cazorla	2
9	Monoamine neurotransmitters in early epileptic encephalopathies: New insights into pathophysiology and therapy 2022 ·Developmental Medicine & Child Neurology ·Natalia Juliá‐Palacios, (unknown), (unknown), Elisenda Cortès‐Saladelafont, Javier Aparicio, Daniel Cuadras, Gabriella Horváth, Carmen Fons, Rafael Artuch, Àngels García‐Cazorla, (unknown)	7
10	Cognitive stimulation has potential for brain activation in individuals with Rett syndrome 2021 ·Journal of Intellectual Disability Research ·(unknown), (unknown), Alejandro Bachiller, (unknown), Joan Francesc Alonso, Anna López‐Sala, Judith Armstrong, (unknown), M. Pineda, Miguel Ángel Mañanas, Sergio Romero, Àngels García‐Cazorla	8
11	U-IMD: the first Unified European registry for inherited metabolic diseases 2021 ·Orphanet Journal of Rare Diseases ·Thomas Opladen, Florian Gleich, Viktor Kožich, Maurizio Scarpa, Diego Martinelli, Franz Schaefer, Kathrin Jeltsch, Natalia Juliá‐Palacios, Àngels García‐Cazorla, Carlo Dionisi‐Vici, Stefan Kölker	16
12	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
13	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
14	Inborn Errors of Metabolism Overview 2018 ·Pediatric Clinics of North America ·Jean‐Marie Saudubray, Àngels García‐Cazorla	106
15	The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders 2016 ·Molecular Genetics and Metabolism Reports ·Thomas Opladen, Elisenda Cortès‐Saladelafont, Mario Mastrangelo, Gabriella Horváth, Roser Pons, Eduardo López‐Laso, Joaquín Alejandro Fernández‐Ramos, Tomáš Honzík, Toni S. Pearson, Jennifer Friedman, Sabine Scholl‐Bürgi, Tessa Wassenberg, Sabine Jung‐Klawitter, Oya Kuseyri Hübschmann, Kathrin Jeltsch, Manju A. Kurian, Àngels García‐Cazorla	39
16	Behavioural and emotional problems, intellectual impairment and health‐related quality of life in patients with organic acidurias and urea cycle disorders 2015 ·Journal of Inherited Metabolic Disease ·(unknown), Stefan Kölker, (unknown), Ivo Barić, J Zeman, Matthias R. Baumgartner, Chris Mühlhausen, Àngels García‐Cazorla, Florian Gleich, Gisela Haege, Peter Burgard	27
17	Mutation loads in different tissues from six pathogenic mtDNA point mutations 2015 ·Mitochondrion ·(unknown), Sonia Emperador, Mercè Pineda, Ester López‐Gallardo, Raquel Montero, Dèlia Yubero, Cristina Jou, C. Jimenez‐Mallebrera, A. Nascimento, Isidró Ferrer, Àngels García‐Cazorla, Eduardo Ruiz‐Pesini, Julio Montoya, Rafael Artuch	11
18	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
19	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
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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