Nuria Muelas

2.6k total citations
50 papers, 922 citations indexed

About

Nuria Muelas is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Nuria Muelas has authored 50 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Nuria Muelas's work include Muscle Physiology and Disorders (13 papers), Genetic Neurodegenerative Diseases (10 papers) and Hereditary Neurological Disorders (9 papers). Nuria Muelas is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Genetic Neurodegenerative Diseases (10 papers) and Hereditary Neurological Disorders (9 papers). Nuria Muelas collaborates with scholars based in Spain, Germany and Finland. Nuria Muelas's co-authors include Juan J. Vílchez, Teresa Sevilla, Carmen Espinós, Luís Bataller, María José Chumillas, Francesc Palau, Rafael Sivera, Dolores Martínez‐Rubio, Juan F. Vázquez‐Costa and Inmaculada Azorı́n and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Nuria Muelas

46 papers receiving 913 citations

Peers

Nuria Muelas

CMN

NEURO

GENET

CCM

Michito Namekawa Japan

Andoni Urtizberea France

Carmen Paradas Spain

Isabelle Nelson France

J. He China

Yasushi Oya Japan

Ralitza H. Gavrilova United States

Edoardo Malfatti France

David S. Lynch United Kingdom

Cristina Sancricca Italy

Michito Namekawa Japan

Nuria Muelas

488 ×1.2

500 ×1.4

CMN

236 ×0.9

NEURO

112 ×0.7

GENET

39 ×0.3

CCM

Citations per year, relative to Nuria Muelas Nuria Muelas (= 1×) peers Michito Namekawa

Countries citing papers authored by Nuria Muelas

Since Specialization

Citations

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

Fields of papers citing papers by Nuria Muelas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nuria Muelas

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

All Works

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20 of 20 papers shown

Vázquez‐Costa, Juan F., et al.. (2026). Muscle MRI Contributes to the Differential Diagnosis Between Distal Myopathies and Distal Hereditary Motor Neuropathies. European Journal of Neurology. 33(1). e70456–e70456.

Liquori, Alessandro, Elisa González‐Romero, Rafael P. Vázquez‐Manrique, et al.. (2024). Deletion of exons 45 to 55 in the DMD gene: from the therapeutic perspective to the in vitro model. Skeletal Muscle. 14(1). 21–21. 1 indexed citations

Ceballos, Francisco C., Pablo Serrano‐Lorenzo, Laura Bermejo‐Guerrero, et al.. (2024). Clinical and Genetic Analysis of Patients With TK2 Deficiency. Neurology Genetics. 10(2). e200138–e200138. 4 indexed citations

Azorı́n, Inmaculada, Pilar Martí, Nuria Muelas, et al.. (2024). Insights into phenotypic variability caused by GARS1 pathogenic variants. European Journal of Neurology. 31(10). e16416–e16416. 4 indexed citations

Vázquez‐Costa, Juan F., Mónica Povedano, S. Kapetanovic García, et al.. (2022). Nusinersen in adult patients with 5q spinal muscular atrophy: A multicenter observational cohorts' study. European Journal of Neurology. 29(11). 3337–3346. 20 indexed citations

Vázquez‐Costa, Juan F., Mónica Povedano, S. Kapetanovic García, et al.. (2022). Validation of motor and functional scales for the evaluation of adult patients with 5q spinal muscular atrophy. European Journal of Neurology. 29(12). 3666–3675. 26 indexed citations

Domínguez‐González, Cristina, Laura Bermejo‐Guerrero, Germán Morís, et al.. (2022). Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study. Neuromuscular Disorders. 32(9). 728–735. 5 indexed citations

Domínguez‐González, Cristina, Roberto Fernández‐Torrón, U. Moore, et al.. (2022). Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis. Journal of Neurology. 269(7). 3550–3562. 9 indexed citations

Díez‐Fuertes, Francisco, María Rosa López‐Huertas, Javier García‐Pérez, et al.. (2022). Transcriptomic Evidence of the Immune Response Activation in Individuals With Limb Girdle Muscular Dystrophy Dominant 2 (LGMDD2) Contributes to Resistance to HIV-1 Infection. Frontiers in Cell and Developmental Biology. 10. 839813–839813. 2 indexed citations

10.

Bermejo‐Guerrero, Laura, Pablo Serrano‐Lorenzo, Alberto Blázquez, et al.. (2021). Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations. Journal of Clinical Medicine. 11(1). 22–22. 6 indexed citations

11.

Sivera, Rafael, Vincenzo Lupo, Marina Frasquet, et al.. (2021). Charcot–Marie–Tooth disease due to MORC2 mutations in Spain. European Journal of Neurology. 28(9). 3001–3011. 10 indexed citations

12.

Martínez‐Torres, Irene, Juan F. Vázquez‐Costa, Nuria Muelas, et al.. (2021). Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations. Journal of the Neurological Sciences. 429. 118062–118062. 3 indexed citations

13.

Bermejo‐Guerrero, Laura, et al.. (2020). Persistent asymptomatic or mild symptomatic hyperCKemia due to mutations in ANO5: the mildest end of the anoctaminopathies spectrum. Journal of Neurology. 267(9). 2546–2555. 9 indexed citations

14.

Blázquez, Alberto, Pablo Serrano‐Lorenzo, Gerardo Gutiérrez‐Gutiérrez, et al.. (2020). Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia. Journal of Medical Genetics. 57(9). 643–646. 20 indexed citations

15.

Martí, Pilar, et al.. (2020). HNRNPDL-related limb girdle muscular dystrophy in a Spanish family with scapulo-peroneal phenotype, the first family in Europe. Journal of the Neurological Sciences. 414. 116875–116875. 3 indexed citations

16.

Benito, Daniel Natera‐de, Nuria Muelas, A. Nascimento, et al.. (2016). Phenotypic heterogeneity in two large Roma families with a congenital myasthenic syndrome due to CHRNE 1267delG mutation. A long-term follow-up. Neuromuscular Disorders. 26(11). 789–795. 17 indexed citations

17.

Gutiérrez‐Rivas, Eduardo, Juan Bautista, Juan J. Vílchez, et al.. (2015). Dried Blood Spot for Screening for Late-Onset Pompe Disease: A Spanish Cohort. Journal of Neuromuscular Diseases. 2(s1). S42–S42. 2 indexed citations

18.

Gutiérrez‐Rivas, Eduardo, J. Bautista, Juan J. Vílchez, et al.. (2015). Targeted screening for the detection of Pompe disease in patients with unclassified limb-girdle muscular dystrophy or asymptomatic hyperCKemia using dried blood: A Spanish cohort. Neuromuscular Disorders. 25(7). 548–553. 43 indexed citations

19.

Sevilla, Teresa, Vincenzo Lupo, Dolores Martínez‐Rubio, et al.. (2015). Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease. Brain. 139(1). 62–72. 58 indexed citations

20.

Chaouch, Amina, Juliane S. Müller, Velina Guergueltcheva, et al.. (2011). A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome. Journal of Neurology. 259(3). 474–481. 50 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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