Yolanda Campos

5.1k total citations
118 papers, 2.7k citations indexed

About

Yolanda Campos is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Yolanda Campos has authored 118 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Molecular Biology, 66 papers in Clinical Biochemistry and 22 papers in Rheumatology. Recurrent topics in Yolanda Campos's work include Mitochondrial Function and Pathology (78 papers), Metabolism and Genetic Disorders (66 papers) and ATP Synthase and ATPases Research (28 papers). Yolanda Campos is often cited by papers focused on Mitochondrial Function and Pathology (78 papers), Metabolism and Genetic Disorders (66 papers) and ATP Synthase and ATPases Research (28 papers). Yolanda Campos collaborates with scholars based in Spain, United States and Italy. Yolanda Campos's co-authors include Joaquı́n Arenas, Miguel A. Martı́n, Carlos Rubio-Terrés, Ana Cabello, Pilar del Hoyo, Rafael Garesse, Juan Bautista, Belén Bornstein, Yohei Kirino and Yu‐ichi Goto and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

In The Last Decade

Yolanda Campos

118 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yolanda Campos Spain 31 1.9k 1.1k 330 292 275 118 2.7k
Monica Sciacco Italy 29 2.2k 1.2× 1.1k 1.0× 497 1.5× 247 0.8× 127 0.5× 90 2.9k
Angela Pyle United Kingdom 36 2.6k 1.4× 881 0.8× 699 2.1× 322 1.1× 64 0.2× 90 3.4k
Majid Alfadhel Saudi Arabia 28 1.4k 0.7× 625 0.6× 144 0.4× 232 0.8× 254 0.9× 157 2.5k
Mary Kay Koenig United States 21 1.1k 0.6× 677 0.6× 167 0.5× 558 1.9× 93 0.3× 61 2.0k
Maria Alice Donati Italy 31 2.5k 1.3× 1.4k 1.2× 257 0.8× 915 3.1× 475 1.7× 136 3.9k
Marc Engelen Netherlands 28 1.9k 1.0× 832 0.8× 108 0.3× 662 2.3× 87 0.3× 97 2.6k
Tomáš Honzík Czechia 23 1.1k 0.6× 524 0.5× 83 0.3× 233 0.8× 217 0.8× 102 1.6k
Tuan Vu United States 27 1.2k 0.7× 757 0.7× 256 0.8× 213 0.7× 111 0.4× 92 2.4k
David Otaegui Spain 31 2.1k 1.1× 221 0.2× 251 0.8× 224 0.8× 157 0.6× 86 3.1k
Alex Agrotis Australia 35 1.2k 0.6× 325 0.3× 121 0.4× 311 1.1× 166 0.6× 62 3.3k

Countries citing papers authored by Yolanda Campos

Since Specialization
Citations

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

Fields of papers citing papers by Yolanda Campos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yolanda Campos

This figure shows the co-authorship network connecting the top 25 collaborators of Yolanda Campos. A scholar is included among the top collaborators of Yolanda Campos 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 Yolanda Campos. Yolanda Campos 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.
Campos, Yolanda, et al.. (2019). Vitamin B12 deficiency presenting as pseudo-thrombotic microangiopathy: a case report and literature review. SHILAP Revista de lepidopterología. 7 indexed citations
2.
3.
Martín‐Hernández, Elena, et al.. (2011). Clinical and cellular consequences of the mutation m.12300G>A in the mitochondrial tRNALeu(CUN) gene. Mitochondrion. 12(2). 288–293. 3 indexed citations
4.
Arpa, Javier, Yolanda Campos, A Cruz-Martı́nez, et al.. (2009). Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity. Acta Neurologica Scandinavica. 90(4). 281–284. 3 indexed citations
5.
Navarro, Susana, Pilar del Hoyo, Yolanda Campos, et al.. (2005). Increased mitochondrial respiratory chain enzyme activities correlate with minor extent of liver damage in mice suffering from erythropoietic protoporphyria. Experimental Dermatology. 14(1). 26–33. 9 indexed citations
6.
Cejudo, Pilar, Juan Bautista, Teodoro Montemayor, et al.. (2005). Exercise training in mitochondrial myopathy: A randomized controlled trial. Muscle & Nerve. 32(3). 342–350. 71 indexed citations
7.
Campos, Yolanda. (2003). Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes. Neuromuscular Disorders. 13(5). 416–420. 13 indexed citations
8.
Torroni, Antonio, Yolanda Campos, Chiara Rengo, et al.. (2003). Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation. The American Journal of Human Genetics. 72(4). 1005–1012. 47 indexed citations
9.
Aguilera, Isabel, et al.. (2001). Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease. Journal of the Neurological Sciences. 192(1-2). 81–84. 8 indexed citations
10.
Fernández‐Moreno, Miguel Ángel, Belén Bornstein, Yolanda Campos, Joaquı́n Arenas, & Rafael Garesse. (2000). The Pathogenic Role of Point Mutations Affecting the Translational Initiation Codon of Mitochondrial Genes. Molecular Genetics and Metabolism. 70(3). 238–240. 6 indexed citations
11.
Rubio-Terrés, Carlos, Miguel A. Martı́n, Yolanda Campos, Ana Cabello, & Joaquı́n Arenas. (2000). A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease. Neuromuscular Disorders. 10(2). 138–140. 10 indexed citations
12.
Campos, Yolanda, Miguel A. Martı́n, Pilar del Hoyo, et al.. (1998). Clinical heterogeneity associated with mitochondrial DNA depletion in muscle. Neuromuscular Disorders. 8(8). 568–573. 23 indexed citations
13.
Campos, Yolanda, et al.. (1997). Hallazgos oftalmológicos en pacientes con enfermedades mitocondriales. 7(2). 7. 1 indexed citations
14.
Campos, Yolanda, et al.. (1997). Bilateral Striatal Necrosis and MELAS Associated with a New T3308C Mutation in the Mitochondrial ND1 Gene. Biochemical and Biophysical Research Communications. 238(2). 323–325. 58 indexed citations
15.
Campos, Yolanda, et al.. (1996). Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNALeu(UUR) mutation of mitochondrial DNA. Muscle & Nerve. 19(2). 187–190. 37 indexed citations
16.
Campos, Yolanda, J. Bautista, Eduardo Gutiérrez‐Rivas, et al.. (1995). Clinical heterogeneity in two pedigrees with the 3243 bp tRNALeu(UUR)mutation of mitochondrial DNA. Acta Neurologica Scandinavica. 91(1). 62–65. 19 indexed citations
17.
18.
Castroviejo, Ignacio Pascual, et al.. (1994). [Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria].. PubMed. 9(7). 303–6. 1 indexed citations
19.
Campos, Yolanda, Juan Carlos Gómez‐Esteban, A. Cabello, & Joaquı́n Arenas. (1994). Genetic analysis of one family with myoclonic epilepsy and ragged-red fibers (MERRF). PubMed. 17(10). 1229–31. 3 indexed citations
20.
Campos, Yolanda, et al.. (1993). Plasma carnitine insufficiency and effectiveness of L‐carnitine therapy in patients with mitochondril myopathy. Muscle & Nerve. 16(2). 150–153. 72 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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