Rafael Artuch

11.4k total citations
291 papers, 6.9k citations indexed

About

Rafael Artuch is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Rafael Artuch has authored 291 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 166 papers in Molecular Biology, 138 papers in Clinical Biochemistry and 52 papers in Biochemistry. Recurrent topics in Rafael Artuch's work include Metabolism and Genetic Disorders (137 papers), Mitochondrial Function and Pathology (80 papers) and Folate and B Vitamins Research (42 papers). Rafael Artuch is often cited by papers focused on Metabolism and Genetic Disorders (137 papers), Mitochondrial Function and Pathology (80 papers) and Folate and B Vitamins Research (42 papers). Rafael Artuch collaborates with scholars based in Spain, United States and United Kingdom. Rafael Artuch's co-authors include Aída Ormazábal, Jaume Campistol, Àngels García‐Cazorla, Belén Pérez‐Dueñas, Raquel Montero, María Antònia Vilaseca, Paz Briones, Mercedes Serrano, Marta Vilaseca and Mercè Pineda and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Rafael Artuch

285 papers receiving 6.8k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Rafael Artuch 3.7k 2.5k 1.2k 1.1k 906 291 6.9k
Joaquı́n Arenas 4.7k 1.3× 1.9k 0.8× 1.6k 1.4× 1.5k 1.4× 335 0.4× 307 8.9k
Rita Horváth 7.1k 1.9× 3.2k 1.3× 473 0.4× 884 0.8× 372 0.4× 280 9.4k
Leonardo Salviati 6.7k 1.8× 1.3k 0.5× 376 0.3× 2.1k 1.9× 982 1.1× 162 9.5k
Fernando Scaglia 4.8k 1.3× 3.0k 1.2× 495 0.4× 1.0k 0.9× 505 0.6× 168 7.1k
Shamima Rahman 4.7k 1.3× 2.8k 1.1× 319 0.3× 561 0.5× 533 0.6× 160 6.3k
Vincenzo Leuzzi 3.3k 0.9× 3.1k 1.2× 646 0.5× 1.6k 1.5× 498 0.5× 221 6.0k
Gerard T. Berry 3.1k 0.8× 3.3k 1.3× 716 0.6× 1.1k 1.1× 947 1.0× 213 7.1k
S. DiMauro 12.7k 3.5× 8.0k 3.1× 1.9k 1.5× 1.5k 1.4× 794 0.9× 237 15.9k
Bwee Tien Poll‐The 6.0k 1.6× 2.8k 1.1× 711 0.6× 1.8k 1.7× 1.0k 1.1× 225 8.6k
Ronald G. Haller 3.2k 0.9× 1.4k 0.6× 1.6k 1.3× 1.5k 1.4× 303 0.3× 135 6.3k

Countries citing papers authored by Rafael Artuch

Since Specialization
Citations

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

Fields of papers citing papers by Rafael Artuch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rafael Artuch

This figure shows the co-authorship network connecting the top 25 collaborators of Rafael Artuch. A scholar is included among the top collaborators of Rafael Artuch 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 Rafael Artuch. Rafael Artuch 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.
Guitart‐Mampel, Mariona, Francesc Josep García‐García, Ester Tobías, et al.. (2024). Metabolic, Mitochondrial, and Inflammatory Effects of Efavirenz, Emtricitabine, and Tenofovir Disoproxil Fumarate in Asymptomatic Antiretroviral-Naïve People with HIV. International Journal of Molecular Sciences. 25(15). 8418–8418.
2.
Bartoccioni, Paola, Ángela Arias, Suwipa Saen‐oon, et al.. (2024). Structure and mechanisms of transport of human Asc1/CD98hc amino acid transporter. Nature Communications. 15(1). 2986–2986. 7 indexed citations
3.
Arias, Ángela, et al.. (2024). Exploring Plasma Coenzyme Q10 Status in Paediatric Dyslipidaemia. Antioxidants. 13(8). 966–966. 1 indexed citations
4.
Mariñó, Zoe, Célia Bádenas, Jesús Quintero, et al.. (2023). Benefits of using exchangeable copper and the ratio of exchangeable copper in a real‐world cohort of patients with Wilson disease. Journal of Inherited Metabolic Disease. 46(5). 982–991. 11 indexed citations
5.
González, Laura, Ángela Arias, Rafael Artuch, et al.. (2023). Exploring the Contribution of the Transporter AGT1/rBAT in Cystinuria Progression: Insights from Mouse Models and a Retrospective Cohort Study. International Journal of Molecular Sciences. 24(24). 17140–17140.
6.
Tobías, Ester, Francesc Josep García‐García, Mariona Guitart‐Mampel, et al.. (2023). Unravelling inclusion body myositis using a patient‐derived fibroblast model. Journal of Cachexia Sarcopenia and Muscle. 14(2). 964–977. 6 indexed citations
7.
Jurado, Susana, Glòria Garrabou, Mariona Guitart‐Mampel, et al.. (2023). CRISPR/Cas9‐based functional genomics strategy to decipher the pathogenicity of genetic variants in inherited metabolic disorders. Journal of Inherited Metabolic Disease. 46(6). 1029–1042. 1 indexed citations
8.
Fernández‐Carasa, Irene, Carles Calatayud, Meritxell Pons‐Espinal, et al.. (2023). iPSC ‐based modeling of THD recapitulates disease phenotypes and reveals neuronal malformation. EMBO Molecular Medicine. 15(3). e15847–e15847. 8 indexed citations
9.
Engelke, Udo F. H., Jean‐Baptiste Roullet, Sanne Broekman, et al.. (2023). Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective. Journal of Inherited Metabolic Disease. 47(3). 417–430. 3 indexed citations
10.
Yubero, Dèlia, Fátima Leal, María L. Couce, et al.. (2022). The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1 . Clinical Genetics. 102(1). 40–55. 6 indexed citations
11.
Juliá‐Palacios, Natalia, Elisenda Cortès‐Saladelafont, Javier Aparicio, et al.. (2022). Monoamine neurotransmitters in early epileptic encephalopathies: New insights into pathophysiology and therapy. Developmental Medicine & Child Neurology. 64(7). 915–923. 7 indexed citations
12.
Serrano, Mercedes, Juan A. G. Ranea, Pedro Seoane, et al.. (2022). Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2. Journal of Medical Genetics. 60(4). 406–415. 5 indexed citations
13.
Arranz, José Antonio, Aída Ormazábal, Mireia del Toro, et al.. (2021). Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns. Orphanet Journal of Rare Diseases. 16(1). 195–195. 22 indexed citations
14.
Bellusci, Marcello, et al.. (2021). The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call. Genes. 12(10). 1590–1590. 8 indexed citations
15.
Montero, Raquel, Anna Codina, Cristina Jou, et al.. (2020). Coenzyme Q10 Treatment Monitoring in Different Human Biological Samples. Antioxidants. 9(10). 979–979. 14 indexed citations
16.
Pope, Simon, Rafael Artuch, Simon Heales, & Shamima Rahman. (2019). Cerebral folate deficiency: Analytical tests and differential diagnosis. Journal of Inherited Metabolic Disease. 42(4). 655–672. 53 indexed citations
17.
Castellanos, Aida, et al.. (2019). Role of zebrafish ClC‐K/barttin channels in apical kidney chloride reabsorption. The Journal of Physiology. 597(15). 3969–3983. 9 indexed citations
18.
Cortès‐Saladelafont, Elisenda, Federico Ramos, María L. Couce, et al.. (2019). Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism. Scientific Reports. 9(1). 9128–9128. 6 indexed citations
19.
Ruiz‐Sala, Pedro, et al.. (2017). Urine oligosaccharide tests for the diagnosis of oligosaccharidoses. Reviews in Analytical Chemistry. 36(3). 6 indexed citations
20.
Fernández‐Ayala, Daniel J.M., Sandra Jiménez-Gancedo, María V. Cascajo, et al.. (2013). Survival transcriptome in the coenzyme Q 10 deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q 10 deficiencies. BMJ Open. 3(3). e002524–e002524. 16 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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