Sonia Clavero

500 total citations
15 papers, 351 citations indexed

About

Sonia Clavero is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Sonia Clavero has authored 15 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Pediatrics, Perinatology and Child Health and 7 papers in Clinical Biochemistry. Recurrent topics in Sonia Clavero's work include Porphyrin Metabolism and Disorders (8 papers), Neonatal Health and Biochemistry (7 papers) and Metabolism and Genetic Disorders (7 papers). Sonia Clavero is often cited by papers focused on Porphyrin Metabolism and Disorders (8 papers), Neonatal Health and Biochemistry (7 papers) and Metabolism and Genetic Disorders (7 papers). Sonia Clavero collaborates with scholars based in United States, Spain and Switzerland. Sonia Clavero's co-authors include Magdalena Ugarte, Lourdes R. Desviat, Celia Pérez‐Cerdá, Belén Pérez, Pilar Rodríguez‐Pombo, David F. Bishop, Robert J. Desnick, Rosa Navarrete, Mark E. Haskins and Urs Giger and has published in prestigious journals such as Blood, Human Molecular Genetics and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

Sonia Clavero

15 papers receiving 348 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sonia Clavero United States 12 286 165 59 55 55 15 351
Megumi Tsuji Japan 9 111 0.4× 72 0.4× 16 0.3× 34 0.6× 58 1.1× 25 285
Anne Chun‐Hui Tsai United States 10 126 0.4× 52 0.3× 58 1.0× 47 0.9× 117 2.1× 22 295
Junko Muroi Japan 12 228 0.8× 168 1.0× 26 0.4× 79 1.4× 172 3.1× 19 439
Jun Akanuma Japan 9 233 0.8× 142 0.9× 56 0.9× 18 0.3× 58 1.1× 14 335
Izelle Smuts South Africa 12 273 1.0× 192 1.2× 12 0.2× 17 0.3× 66 1.2× 25 354
Bregje Jaeger Netherlands 9 80 0.3× 95 0.6× 57 1.0× 26 0.5× 16 0.3× 22 216
Claudia Soler‐Alfonso United States 12 197 0.7× 129 0.8× 55 0.9× 33 0.6× 135 2.5× 21 333
Kristin Lindstrom United States 9 126 0.4× 64 0.4× 31 0.5× 21 0.4× 35 0.6× 19 241
María del Mar O’Callaghan Spain 10 147 0.5× 57 0.3× 66 1.1× 20 0.4× 47 0.9× 11 343
Mara Lúcia Schmitz Ferreira Santos Brazil 8 101 0.4× 57 0.3× 28 0.5× 25 0.5× 23 0.4× 37 276

Countries citing papers authored by Sonia Clavero

Since Specialization
Citations

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

Fields of papers citing papers by Sonia Clavero

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Clavero

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

All Works

15 of 15 papers shown
1.
Yasuda, Makiko, Angelika Erwin, Lawrence U. Liu, et al.. (2015). Liver Transplantation for Acute Intermittent Porphyria: Biochemical and Pathologic Studies of the Explanted Liver. Molecular Medicine. 21(1). 487–495. 44 indexed citations
2.
Clavero, Sonia, Yuri Ahuja, David F. Bishop, et al.. (2013). Diagnosis of feline acute intermittent porphyria presenting with erythrodontia requires molecular analyses. The Veterinary Journal. 198(3). 720–722. 3 indexed citations
3.
Bishop, David F., Sonia Clavero, Narla Mohandas, & Robert J. Desnick. (2011). Congenital Erythropoietic Porphyria: Characterization of Murine Models of the Severe Common (C73R/C73R) and Later-Onset Genotypes. Molecular Medicine. 17(7-8). 748–756. 8 indexed citations
4.
Clavero, Sonia, David F. Bishop, Urs Giger, Mark E. Haskins, & Robert J. Desnick. (2010). Feline Congenital Erythropoietic Porphyria: Two Homozygous UROS Missense Mutations Cause the Enzyme Deficiency and Porphyrin Accumulation. Molecular Medicine. 16(9-10). 381–388. 14 indexed citations
5.
Hasanoğlu, Alev, Manisha Balwani, Fatih Süheyl Ezgü, et al.. (2010). Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R. Journal of Inherited Metabolic Disease. 34(1). 225–231. 19 indexed citations
6.
Clavero, Sonia & David F. Bishop. (2010). . Molecular Medicine. 16(9-10). 1–1. 3 indexed citations
7.
Clavero, Sonia, David F. Bishop, Mark E. Haskins, et al.. (2009). Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutations. Human Molecular Genetics. 19(4). 584–596. 21 indexed citations
8.
Bishop, David F., Xiaoye Schneider‐Yin, Sonia Clavero, et al.. (2009). Congenital erythropoietic porphyria: a novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcripts. Blood. 115(5). 1062–1069. 11 indexed citations
9.
Desviat, Lourdes R., Sonia Clavero, Celia Pérez‐Cerdá, et al.. (2006). New splicing mutations in propionic acidemia. Journal of Human Genetics. 51(11). 992–997. 16 indexed citations
10.
Desviat, Lourdes R., Belén Pérez, Celia Pérez‐Cerdá, et al.. (2004). Propionic acidemia: mutation update and functional and structural effects of the variant alleles. Molecular Genetics and Metabolism. 83(1-2). 28–37. 69 indexed citations
11.
Clavero, Sonia, et al.. (2004). Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypes. Human Genetics. 115(3). 239–47. 15 indexed citations
12.
Pérez‐Cerdá, Celia, Sonia Clavero, Belén Pérez, et al.. (2003). Functional analysis of PCCB mutations causing propionic acidemia based on expression studies in deficient human skin fibroblasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1638(1). 43–49. 26 indexed citations
13.
Pérez, Belén, Lourdes R. Desviat, Pilar Rodríguez‐Pombo, et al.. (2003). Propionic acidemia: identification of twenty-four novel mutations in Europe and North America. Molecular Genetics and Metabolism. 78(1). 59–67. 50 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.
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

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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