Belén Pérez

5.5k total citations
160 papers, 3.5k citations indexed

About

Belén Pérez is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Belén Pérez has authored 160 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Molecular Biology, 104 papers in Clinical Biochemistry and 24 papers in Rheumatology. Recurrent topics in Belén Pérez's work include Metabolism and Genetic Disorders (104 papers), Mitochondrial Function and Pathology (54 papers) and Biochemical and Molecular Research (32 papers). Belén Pérez is often cited by papers focused on Metabolism and Genetic Disorders (104 papers), Mitochondrial Function and Pathology (54 papers) and Biochemical and Molecular Research (32 papers). Belén Pérez collaborates with scholars based in Spain, United States and Norway. Belén Pérez's co-authors include Lourdes R. Desviat, Magdalena Ugarte, Celia Pérez‐Cerdá, Alejandra Gámez, Eva Richard, Pilar Rodríguez‐Pombo, Aurora Martı́nez, Ángel L. Pey, Cristina Aguado and Sonia Clavero and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Belén Pérez

158 papers receiving 3.4k citations

Peers

Countries citing papers authored by Belén Pérez

Since Specialization

Citations

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

Fields of papers citing papers by Belén Pérez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Belén Pérez

This figure shows the co-authorship network connecting the top 25 collaborators of Belén Pérez. A scholar is included among the top collaborators of Belén Pérez 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 Belén Pérez. Belén Pérez 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	Integration of multi‐omics layers empowers precision diagnosis through unveiling pathogenic mechanisms on maple syrup urine disease 2024 ·Journal of Inherited Metabolic Disease ·Juan Ramón Tejedor, (unknown), Leonardo Beccari, (unknown), (unknown), (unknown), (unknown), Rocío G. Urdinguio, Magdalena Ugarte, Agustín F. Fernández, Pilar Rodríguez‐Pombo, Mario F. Fraga, Belén Pérez	2
2	Exploring miRNA–target gene pair detection in disease with coRmiT 2024 ·Briefings in Bioinformatics ·(unknown), James R. Perkins, (unknown), (unknown), (unknown), Mireia Moreno‐Estellés, (unknown), Fernando Bonet, Carlos Romá‐Mateo, Rocío Toro, Belén Pérez, Pascual Sanz, Matthias Kohl, (unknown), Pedro Seoane, Juan A. G. Ranea	1
3	PAH deficient pathology in humanized c.1066-11G>A phenylketonuria mice 2024 ·Human Molecular Genetics ·(unknown), Sara Picó, Arístides López‐Márquez, (unknown), (unknown), Mar Álvarez, Margarita Castro, Santiago Ramón‐Maiques, Belén Pérez, José J. Lucas, Eva Richard, Lourdes R. Desviat	1
4	An ETFDH-driven metabolon supports OXPHOS efficiency in skeletal muscle by regulating coenzyme Q homeostasis 2024 ·Nature Metabolism ·(unknown), (unknown), Gerardo Álvarez‐Rivera, (unknown), Pilar Rodríguez‐Pombo, Belén Pérez, Enrique Calvo, Alberto Paradela, David G. Míguez, Alejandro Cifuentes, José M. Cuezva, Laura Formentini	13
5	Dysregulated Cell Homeostasis and miRNAs in Human iPSC-Derived Cardiomyocytes from a Propionic Acidemia Patient with Cardiomyopathy 2023 ·International Journal of Molecular Sciences ·Mar Álvarez, Pedro Ruiz‐Sala, Belén Pérez, Lourdes R. Desviat, Eva Richard	6
6	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
7	Antisense Oligonucleotide Rescue of Deep-Intronic Variants Activating Pseudoexons in the 6-Pyruvoyl-Tetrahydropterin Synthase Gene 2022 ·Nucleic Acid Therapeutics ·(unknown), Fátima Leal, (unknown), Thomas Koed Doktor, (unknown), (unknown), Beat Thöny, Belén Pérez, Brage Storstein Andresen, Lourdes R. Desviat	11
8	Gene expression analysis method integration and co-expression module detection applied to rare glucide metabolism disorders using ExpHunterSuite 2021 ·Scientific Reports ·(unknown), (unknown), (unknown), Carlos Romá‐Mateo, Pascual Sanz, Belén Pérez, (unknown), Pedro Seoane, Juan A. G. Ranea, James R. Perkins	14
9	PMM2‐CDG caused by uniparental disomy: Case report and literature review 2020 ·JIMD Reports ·(unknown), George E. Tiller, Belén Pérez, (unknown), Susan A. Berry, Kyriakie Sarafoglou, Éva Morava	4
10	Metabolic Serendipities of Expanded Newborn Screening 2020 ·Genes ·Raquel Yahyaoui, Javier Blasco‐Alonso, (unknown), Carmen Benito, (unknown), Inmaculada González-Gallego, Pedro Ruiz‐Sala, Belén Pérez, Domingo González‐Lamuño	8
11	Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations 2018 ·Molecular Genetics and Metabolism ·(unknown), Rosa Navarrete, (unknown), Eva Richard, Magdalena Ugarte, Celia Pérez‐Cerdá, Belén Pérez, Alejandra Gámez, Lourdes R. Desviat	16
12	Four Years’ Experience in the Diagnosis of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in Infants Detected in Three Spanish Newborn Screening Centers 2017 ·JIMD Reports ·B. Merinero, Patricia Alcaide, Elena Martín‐Hernández, Ana Heloneida de Araújo Morais, (unknown), Pilar Quijada‐Fraile, Consuelo Pedrón‐Giner, Elena Dulín, Raquel Yahyaoui, (unknown), Amaya Bélanger-Quintana, Javier Blasco‐Alonso, Miguel L.F. Ruano, (unknown), (unknown), Fátima Leal, Magdalena Ugarte, Pedro Ruiz‐Sala, Belén Pérez, Celia Pérez‐Cerdá	22
13	Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia 2016 ·Journal of Human Genetics ·María L. Couce, Luis Aldámiz‐Echevarría, (unknown), (unknown), Amaya Bélanger-Quintana, Javier Blasco‐Alonso, (unknown), (unknown), Isidro Vitoria, (unknown), Rosa Navarrete, Ana Fernández‐Marmiesse, Belén Pérez, Celia Pérez‐Cerdá	14
14	Congenital Disorder of Glycosylation type Ia: antisense therapeutics for an intronic variation causing exonization of an intronic sequence 2008 ·European Journal of Human Genetics ·(unknown), Celia Pérez‐Cerdá, Gert Matthijs, Michael S. Adamowicz, Magdalena Ugarte, Belén Pérez	1
15	Spanish BH4-responsive phenylalanine hydroxylase-deficient patients: Evolution of seven patients on long-term treatment with tetrahydrobiopterin 2005 ·Molecular Genetics and Metabolism ·Amaya Bélanger‐Quintana, María José García, Margarita Castro, Lourdes R. Desviat, Belén Pérez, (unknown), Magdalena Ugarte, Mercedes Martínez‐Pardo	47
16	Functional characterization of PCCA mutations causing propionic acidemia 2002 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sonia Clavero, M. Ángeles Martínez‐García, Belén Pérez, Celia Pérez‐Cerdá, Magdalena Ugarte, Lourdes R. Desviat	34
17	Effect of PCCB Gene Mutations on the Heteromeric and Homomeric Assembly of Propionyl-CoA Carboxylase 2001 ·Molecular Genetics and Metabolism ·Silvia Muro, Belén Pérez, Lourdes R. Desviat, Pilar Rodríguez‐Pombo, Celia Pérez‐Cerdá, Sonia Clavero, Magdalena Ugarte	18
18	Mutation analysis of phenylketonuria in South Brazil 1996 ·Human Mutation ·Belén Pérez, Lourdes R. Desviat, (unknown), B J Schmidt, (unknown), Roberto Giugliani, Ricardo Flores Pires, Magdalena Ugarte	11
19	Molecular analysis of the phenylalanine hydroxylase gene in Mexican phenylketonuric patients. 1995 ·PubMed ·Humberto Nicolini, Christina M. Cruz, Beatríz Camarena, (unknown), Guadalupe Bilbao, (unknown), Antonia Velázquez, Belén Pérez, Lourdes R. Desviat, Magdalena Ugarte	3
20	Expression analysis of mutation P244L, which causes mild hyperphenylalaninemia 1995 ·Human Mutation ·Belén Pérez, Lourdes R. Desviat, Magdalena Ugarte	8

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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