Celia Pérez‐Cerdá

4.6k total citations
119 papers, 2.5k citations indexed

About

Celia Pérez‐Cerdá is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Celia Pérez‐Cerdá has authored 119 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 75 papers in Clinical Biochemistry and 20 papers in Rheumatology. Recurrent topics in Celia Pérez‐Cerdá's work include Metabolism and Genetic Disorders (75 papers), Mitochondrial Function and Pathology (30 papers) and Biochemical and Molecular Research (29 papers). Celia Pérez‐Cerdá is often cited by papers focused on Metabolism and Genetic Disorders (75 papers), Mitochondrial Function and Pathology (30 papers) and Biochemical and Molecular Research (29 papers). Celia Pérez‐Cerdá collaborates with scholars based in Spain, United States and Netherlands. Celia Pérez‐Cerdá's co-authors include Magdalena Ugarte, Belén Pérez, Lourdes R. Desviat, B. Merinero, Pilar Rodríguez‐Pombo, Eva Richard, Sonia Clavero, Alejandra Gámez, Rosa Navarrete and Ana Vega and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PEDIATRICS.

In The Last Decade

Celia Pérez‐Cerdá

119 papers receiving 2.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Celia Pérez‐Cerdá Spain 30 1.8k 1.3k 412 346 325 119 2.5k
Belén Pérez Spain 35 2.6k 1.4× 2.0k 1.5× 618 1.5× 613 1.8× 412 1.3× 160 3.5k
Lourdes R. Desviat Spain 36 2.7k 1.5× 2.1k 1.6× 567 1.4× 729 2.1× 415 1.3× 154 3.7k
Paula J. Waters Canada 24 1.2k 0.7× 1.1k 0.9× 456 1.1× 402 1.2× 340 1.0× 75 2.0k
Kuniaki Narisawa Japan 31 1.4k 0.8× 944 0.7× 347 0.8× 650 1.9× 304 0.9× 97 2.5k
Stephanie Grünewald United Kingdom 28 1.4k 0.8× 558 0.4× 516 1.3× 251 0.7× 354 1.1× 85 2.1k
Ewa Pronicka Poland 26 1.2k 0.6× 553 0.4× 201 0.5× 172 0.5× 326 1.0× 114 2.0k
Terttu Suormala Switzerland 30 1.5k 0.8× 1.3k 1.0× 207 0.5× 1.1k 3.1× 203 0.6× 81 2.7k
G. T. N. Besley United Kingdom 26 948 0.5× 510 0.4× 904 2.2× 254 0.7× 195 0.6× 87 1.9k
Federica Deodato Italy 23 801 0.4× 608 0.5× 640 1.6× 404 1.2× 144 0.4× 55 1.7k
R A Gravel Canada 33 1.9k 1.1× 580 0.4× 1.1k 2.6× 682 2.0× 292 0.9× 54 3.3k

Countries citing papers authored by Celia Pérez‐Cerdá

Since Specialization
Citations

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

Fields of papers citing papers by Celia Pérez‐Cerdá

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celia Pérez‐Cerdá

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

All Works

20 of 20 papers shown
1.
Yuste‐Checa, Patricia, Lourdes R. Desviat, Magdalena Ugarte, et al.. (2020). Proteostasis regulators as potential rescuers of PMM2 activity. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(7). 165777–165777. 14 indexed citations
2.
López‐Márquez, Arístides, Rosa Navarrete, Celia Pérez‐Cerdá, et al.. (2019). Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene. Stem Cell Research. 38. 101469–101469. 5 indexed citations
3.
Navarrete, Rosa, Eva Richard, Magdalena Ugarte, et al.. (2018). Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations. Molecular Genetics and Metabolism. 125(3). 266–275. 16 indexed citations
4.
Ruiz‐Sala, Pedro, et al.. (2017). Urine oligosaccharide tests for the diagnosis of oligosaccharidoses. Reviews in Analytical Chemistry. 36(3). 6 indexed citations
5.
Merinero, B., Patricia Alcaide, Elena Martín‐Hernández, et al.. (2017). Four Years’ Experience in the Diagnosis of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in Infants Detected in Three Spanish Newborn Screening Centers. JIMD Reports. 39. 63–74. 22 indexed citations
6.
Martínez‐Monseny, Antonio Federico, Jordi Muchart, Daniel Cuadras, et al.. (2017). Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2‐CDG). Journal of Inherited Metabolic Disease. 40(5). 709–713. 15 indexed citations
7.
Coughlin, Curtis R., Michael A. Swanson, Kathryn E. Kronquist, et al.. (2016). The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. Genetics in Medicine. 19(1). 104–111. 56 indexed citations
8.
Couce, María L., Luis Aldámiz‐Echevarría, Amaya Bélanger-Quintana, et al.. (2016). Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia. Journal of Human Genetics. 62(3). 355–360. 14 indexed citations
9.
Ruiz‐Sala, Pedro, et al.. (2013). Determination of urinary alpha-aminoadipic semialdehyde by LC–MS/MS in patients with congenital metabolic diseases. Journal of Chromatography B. 944. 141–143. 9 indexed citations
10.
Houtkooper, Riekelt H., Marjolein Turkenburg, Bwee Tien Poll‐The, et al.. (2009). The enigmatic role of tafazzin in cardiolipin metabolism. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1788(10). 2003–2014. 124 indexed citations
11.
Vega, Ana, Celia Pérez‐Cerdá, Lourdes R. Desviat, et al.. (2009). Functional analysis of three splicing mutations identified in the PMM2 gene: Toward a new therapy for congenital disorder of glycosylation type Ia. Human Mutation. 30(5). 795–803. 44 indexed citations
12.
Pérez‐Cerdá, Celia, et al.. (2008). Congenital Disorder of Glycosylation type Ia: antisense therapeutics for an intronic variation causing exonization of an intronic sequence. European Journal of Human Genetics. 16. 431. 1 indexed citations
13.
Pérez‐Cerdá, Celia, Judit García‐Villoria, Rob Ofman, et al.. (2005). 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase (MHBD) Deficiency: An X-linked Inborn Error of Isoleucine Metabolism that May Mimic a Mitochondrial Disease. Pediatric Research. 58(3). 488–491. 44 indexed citations
14.
Clavero, Sonia, M. Ángeles Martínez‐García, Belén Pérez, et al.. (2002). Functional characterization of PCCA mutations causing propionic acidemia. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1588(2). 119–125. 34 indexed citations
15.
Fukao, Toshiyuki, Haruki Nakamura, Kozue Nakamura, et al.. (2002). Characterization of Six Mutations in Five Spanish Patients with Mitochondrial Acetoacetyl-CoA Thiolase Deficiency: Effects of Amino Acid Substitutions on Tertiary Structure. Molecular Genetics and Metabolism. 75(3). 235–243. 23 indexed citations
16.
Wolf, Barry, Kevin P. Jensen, Mübeccel Demirkol, et al.. (2002). Seventeen novel mutations that cause profound biotinidase deficiency. Molecular Genetics and Metabolism. 77(1-2). 108–111. 31 indexed citations
17.
Muro, Silvia, Belén Pérez, Lourdes R. Desviat, et al.. (2001). Effect of PCCB Gene Mutations on the Heteromeric and Homomeric Assembly of Propionyl-CoA Carboxylase. Molecular Genetics and Metabolism. 74(4). 476–483. 18 indexed citations
18.
Gallardo, M. Esther, Lourdes R. Desviat, José Manuel Rodríguez Rodríguez, et al.. (2001). The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism. The American Journal of Human Genetics. 68(2). 334–346. 62 indexed citations
19.
Hoenicka, Janet, Pilar Rodríguez‐Pombo, Celia Pérez‐Cerdá, et al.. (1998). New frequent mutation in the PCCB gene in Spanish propionic acidemia patients. Human Mutation. 11(S1). S234–S236. 11 indexed citations
20.
Merinero, B., et al.. (1988). Acidosis láctica neonatal debida a deficiencia aislada de piruvato carboxilasa. Anales de Pediatría. 29(1). 57–60. 2 indexed citations

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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