Ivonne Jericó

1.8k total citations
35 papers, 632 citations indexed

About

Ivonne Jericó is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ivonne Jericó has authored 35 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Neurology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ivonne Jericó's work include Amyotrophic Lateral Sclerosis Research (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Epigenetics and DNA Methylation (5 papers). Ivonne Jericó is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Epigenetics and DNA Methylation (5 papers). Ivonne Jericó collaborates with scholars based in Spain, France and United States. Ivonne Jericó's co-authors include Maite Mendióroz, Miren Roldán, Teresa Ayuso, María Elena Erro, Idoia Blanco‐Luquin, Miguel Pocovı́, Elena H. Martínez‐Lapiscina, María Victoria Zelaya, Marta Artieda and Fernando Civeira and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Ivonne Jericó

34 papers receiving 624 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ivonne Jericó Spain 14 338 211 100 100 65 35 632
Jay P. Ross Canada 15 226 0.7× 241 1.1× 111 1.1× 97 1.0× 74 1.1× 39 653
Anita Y. Bahar Australia 11 160 0.5× 162 0.8× 211 2.1× 74 0.7× 121 1.9× 13 763
Chantal Watrin France 11 223 0.7× 124 0.6× 80 0.8× 56 0.6× 112 1.7× 16 555
Erpo Tian China 15 465 1.4× 116 0.5× 97 1.0× 75 0.8× 135 2.1× 26 868
Aubrey C. Chan United States 10 405 1.2× 407 1.9× 154 1.5× 50 0.5× 57 0.9× 18 1.1k
Daniel F. Brown United States 14 171 0.5× 190 0.9× 98 1.0× 230 2.3× 61 0.9× 28 727
Masayoshi Tada Japan 11 299 0.9× 209 1.0× 174 1.7× 86 0.9× 157 2.4× 29 598
Chris McKinnon United Kingdom 11 457 1.4× 188 0.9× 244 2.4× 111 1.1× 133 2.0× 17 873
Guida Landouré Mali 13 304 0.9× 87 0.4× 204 2.0× 59 0.6× 87 1.3× 54 715
Mohtashem Samsam United States 8 212 0.6× 90 0.4× 214 2.1× 52 0.5× 77 1.2× 14 515

Countries citing papers authored by Ivonne Jericó

Since Specialization
Citations

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

Fields of papers citing papers by Ivonne Jericó

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivonne Jericó

This figure shows the co-authorship network connecting the top 25 collaborators of Ivonne Jericó. A scholar is included among the top collaborators of Ivonne Jericó 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 Ivonne Jericó. Ivonne Jericó 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.
Blanco‐Luquin, Idoia, Agustín F. Fernández, Amaya Urdánoz‐Casado, et al.. (2025). Advancing Personalized Medicine in Alzheimer’s Disease: Liquid Biopsy Epigenomics Unveil APOE ε4-Linked Methylation Signatures. International Journal of Molecular Sciences. 26(7). 3419–3419. 2 indexed citations
2.
Iruzubieta, Pablo, Solange Kapetanovic, Aurelio Hernández‐Laín, et al.. (2025). A founder variant in the RYR1 gene is associated with hyperCKemia, myalgia and muscle cramps. European Journal of Neurology. 32(1). e16471–e16471. 1 indexed citations
3.
Sivera, Rafael, Ana L. Pelayo‐Negro, Ivonne Jericó, et al.. (2024). Expanding the Clinical Spectrum of DRP2 -Associated Charcot-Marie-Tooth Disease. Neurology. 102(7). e209174–e209174. 2 indexed citations
4.
Jericó, Ivonne, Idoia Blanco‐Luquin, Miren Roldán, et al.. (2023). Profiling TREM2 expression in amyotrophic lateral sclerosis. Brain Behavior and Immunity. 109. 117–126. 21 indexed citations
5.
Gordoa, Javier Sánchez‐Ruiz de, Iván Méndez-López, Miren Roldán, et al.. (2023). Association of Blood-Based DNA Methylation Markers With Late-Onset Alzheimer Disease. Neurology. 101(23). e2434–e2447. 9 indexed citations
6.
Blanco‐Luquin, Idoia, et al.. (2023). Exploring the Disease-Associated Microglia State in Amyotrophic Lateral Sclerosis. Biomedicines. 11(11). 2994–2994. 10 indexed citations
7.
Urdánoz‐Casado, Amaya, Miren Roldán, Javier Sánchez‐Ruiz de Gordoa, et al.. (2023). Liquid Biopsy in Alzheimer’s Disease Patients Reveals Epigenetic Changes in the PRLHR Gene. Cells. 12(23). 2679–2679. 9 indexed citations
8.
Jericó, Ivonne, et al.. (2021). Clinical features and incidence trends of amyotrophic lateral sclerosis in Navarre, Spain, 2007–2018: a population-based study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 22(5-6). 401–409. 10 indexed citations
9.
Jericó, Ivonne, et al.. (2020). Transcultural adaptation and validation of the Spanish-language version of ACTIVLIM in adults with inherited myopathies using the Rasch model. SHILAP Revista de lepidopterología. 36(7). 514–524. 1 indexed citations
10.
Cabada, T., et al.. (2020). Longitudinal study in patients with myotonic dystrophy type 1: correlation of brain MRI abnormalities with cognitive performances. Neuroradiology. 63(7). 1019–1029. 13 indexed citations
11.
Montoya, Julio, Sonia Emperador, Eduardo Ruiz‐Pesini, et al.. (2019). A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues. Mitochondrion. 50. 14–18. 7 indexed citations
12.
Vicente, Esther, et al.. (2019). Epidemiological study and genetic characterization of inherited muscle diseases in a northern Spanish region. Orphanet Journal of Rare Diseases. 14(1). 276–276. 24 indexed citations
13.
Altuna, Miren, Amaya Urdánoz‐Casado, Javier Sánchez‐Ruiz de Gordoa, et al.. (2019). DNA methylation signature of human hippocampus in Alzheimer’s disease is linked to neurogenesis. Clinical Epigenetics. 11(1). 91–91. 79 indexed citations
14.
Mendióroz, Maite, et al.. (2018). Liquid biopsy: a new source of candidate biomarkers in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 5(6). 763–768. 15 indexed citations
15.
Galbete, Arkaitz, Miren Roldán, Pilar Irún, et al.. (2018). Evaluation of Chitotriosidase and CC-Chemokine Ligand 18 as Biomarkers of Microglia Activation in Amyotrophic Lateral Sclerosis. Neurodegenerative Diseases. 18(4). 208–215. 13 indexed citations
16.
Cabada, T., et al.. (2017). Brain Involvement in Myotonic Dystrophy Type 1: A Morphometric and Diffusion Tensor Imaging Study with Neuropsychological Correlation. Archives of Clinical Neuropsychology. 32(4). 401–412. 35 indexed citations
17.
López‐Gallardo, Ester, Sonia Emperador, Abelardo Solano, et al.. (2014). Expanding the clinical phenotypes of MT-ATP6 mutations. Human Molecular Genetics. 23(23). 6191–6200. 32 indexed citations
18.
Martínez‐Lapiscina, Elena H., María Elena Erro, Teresa Ayuso, & Ivonne Jericó. (2012). Myasthenia gravis: Sleep quality, quality of life, and disease severity. Muscle & Nerve. 46(2). 174–180. 52 indexed citations
19.
Artieda, Marta, Ana Cenarro, A.L. García-Otín, et al.. (2008). Association and Linkage Disequilibrium Analyses of APOE Polymorphisms in Atherosclerosis. Disease Markers. 24(2). 65–72. 6 indexed citations
20.
Jericó, Ivonne, et al.. (1997). [Miller-Fisher syndrome associated with toxoplasmosis].. PubMed. 12(4). 172–4. 1 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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