Jon Andoni Urtizberea

4.3k total citations · 1 hit paper
50 papers, 2.4k citations indexed

About

Jon Andoni Urtizberea is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jon Andoni Urtizberea has authored 50 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 17 papers in Genetics and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jon Andoni Urtizberea's work include Muscle Physiology and Disorders (18 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Cardiomyopathy and Myosin Studies (9 papers). Jon Andoni Urtizberea is often cited by papers focused on Muscle Physiology and Disorders (18 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Cardiomyopathy and Myosin Studies (9 papers). Jon Andoni Urtizberea collaborates with scholars based in France, United States and Spain. Jon Andoni Urtizberea's co-authors include J. M. Connor, George Feldman, Frederick S. Kaplan, Eileen M. Shore, Roger Smith, Martine LeMerrer, James T. Triffitt, Tae‐Joon Cho, David L. Glaser and Rolf Morhart and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Brain.

In The Last Decade

Jon Andoni Urtizberea

47 papers receiving 2.3k citations

Hit Papers

A recurrent mutation in the BMP type I receptor ACVR1 cau... 2006 2026 2012 2019 2006 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
    2006 866 citations Eileen M. Shore, Meiqi Xu et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jon Andoni Urtizberea France 17 1.5k 755 546 498 466 50 2.4k
Hideyuki Beppu United States 23 1.8k 1.2× 179 0.2× 198 0.4× 251 0.5× 869 1.9× 29 2.7k
Teerin Liewluck United States 23 788 0.5× 170 0.2× 409 0.7× 237 0.5× 286 0.6× 120 1.9k
Nicolas Chassaing France 25 1.1k 0.8× 175 0.2× 211 0.4× 130 0.3× 151 0.3× 83 2.1k
O. Dubourg France 33 985 0.7× 559 0.7× 385 0.7× 354 0.7× 160 0.3× 70 3.0k
Sigrid Tinschert Germany 31 1.3k 0.9× 596 0.8× 133 0.2× 42 0.1× 431 0.9× 94 3.1k
Marja Nissinen Finland 14 1.2k 0.8× 128 0.2× 148 0.3× 75 0.2× 129 0.3× 19 2.2k
Ernie M.H.F. Bongers Netherlands 30 1.4k 1.0× 131 0.2× 156 0.3× 76 0.2× 469 1.0× 56 2.4k
Marco Di Duca Italy 20 925 0.6× 162 0.2× 155 0.3× 34 0.1× 327 0.7× 49 1.8k
Yuichi Kawagashira Japan 23 665 0.5× 270 0.4× 158 0.3× 48 0.1× 149 0.3× 62 1.7k
Michael N. Wosczyna United States 9 844 0.6× 371 0.5× 328 0.6× 56 0.1× 148 0.3× 12 1.3k

Countries citing papers authored by Jon Andoni Urtizberea

Since Specialization
Citations

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

Fields of papers citing papers by Jon Andoni Urtizberea

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jon Andoni Urtizberea. 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 Jon Andoni Urtizberea. The network helps show where Jon Andoni Urtizberea may publish in the future.

Co-authorship network of co-authors of Jon Andoni Urtizberea

This figure shows the co-authorship network connecting the top 25 collaborators of Jon Andoni Urtizberea. A scholar is included among the top collaborators of Jon Andoni Urtizberea 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 Jon Andoni Urtizberea. Jon Andoni Urtizberea 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.
Grimaldi‐Bensouda, Lamiae, Céline Tard, Pascale Saugier-Véber, et al.. (2025). REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in France. Journal of Neuromuscular Diseases. 12(6). 793–803.
2.
Skrypnyk, Cristina, Nathalie Da Silva, Jon Andoni Urtizberea, et al.. (2021). A novel bi‐allelic loss‐of‐function mutation in STIM1 expands the phenotype of STIM1 ‐related diseases. Clinical Genetics. 100(1). 84–89. 5 indexed citations
3.
Nouioua, Sonia, et al.. (2021). Un cas de myasthénie congénitale des ceintures résolu grâce à une collaboration tripartite. médecine/sciences. 37. 50–52. 1 indexed citations
4.
Helman, Guy, Suvasini Sharma, Joanna Crawford, et al.. (2019). Leukoencephalopathy due to variants in GFPT1- associated congenital myasthenic syndrome. Neurology. 92(6). e587–e593. 9 indexed citations
5.
Savarese, Marco, Johanna Palmio, Juan José Poza, et al.. (2019). Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations. Annals of Neurology. 85(6). 899–906. 26 indexed citations
6.
Urtizberea, Jon Andoni, et al.. (2019). Quand tous les chemins mènent à l’Afrique…. médecine/sciences. 35. 15–17. 1 indexed citations
7.
Urtizberea, Jon Andoni, et al.. (2018). Combien de patients atteints de SMA en France ?. médecine/sciences. 34. 32–34. 2 indexed citations
8.
Ferreiro, Ana & Jon Andoni Urtizberea. (2017). Pathologies musculaires liées à la titine. médecine/sciences. 33. 16–26. 3 indexed citations
9.
Modrego, Pedro J., et al.. (2016). Une cause inhabituelle d’hyperCKémie. médecine/sciences. 32. 12–13. 1 indexed citations
10.
Gorokhova, Svetlana, Anthony Béhin, Jon Andoni Urtizberea, et al.. (2015). Novel Pathogenic Variants in a French Cohort Widen the Mutational Spectrum of GNE Myopathy. Journal of Neuromuscular Diseases. 2(2). 131–136. 8 indexed citations
11.
Urtizberea, Jon Andoni. (2012). Iranian neurological events: The second Iranian congress of neuromuscular disorders.. PubMed. 11(3). 125–6.
12.
Blandin, Gaëlle, Christophe Béroud, Véronique Labelle, et al.. (2011). UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene. Human Mutation. 33(3). E2317–E2331. 36 indexed citations
13.
Nguyen, Karine, Guillaume Bassez, Martin Krahn, et al.. (2007). Phenotypic Study in 40 Patients With Dysferlin Gene Mutations. Archives of Neurology. 64(8). 1176–1176. 184 indexed citations
14.
Carmignac, Virginie, Mustafa A. Salih, Susana Quijano‐Roy, et al.. (2007). C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy. Annals of Neurology. 61(4). 340–351. 156 indexed citations
15.
Cuisset, Jean‐Marie, C.A. Maurage, J. F. Pellissier, et al.. (2006). ‘Cap myopathy’: Case report of a family. Neuromuscular Disorders. 16(4). 277–281. 11 indexed citations
16.
Shore, Eileen M., Meiqi Xu, George Feldman, et al.. (2006). A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics. 38(5). 525–527. 866 indexed citations breakdown →
17.
Laurent‐Vannier, A., et al.. (2002). Quoi de neuf en rééducation neurologique infantile ?. Archives de Pédiatrie. 9(1). 70–77. 1 indexed citations
18.
Pelin, Katarina, Kati Donner, Caroline A. Sewry, et al.. (1999). Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. Proceedings of the National Academy of Sciences. 96(5). 2305–2310. 252 indexed citations
19.
Lasa, Adriana, Fédérica Piccolo, Marc Jeanpierre, et al.. (1998). Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the γ-sarcoglycan gene. European Journal of Human Genetics. 6(4). 396–399. 15 indexed citations
20.
Dinçer, Pervin, France Leturcq, Isabelle Richard, et al.. (1997). A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Annals of Neurology. 42(2). 222–229. 87 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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