Daniel Natera‐de Benito

1.8k total citations
59 papers, 399 citations indexed

About

Daniel Natera‐de Benito is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Daniel Natera‐de Benito has authored 59 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 20 papers in Genetics and 13 papers in Genetics. Recurrent topics in Daniel Natera‐de Benito's work include Muscle Physiology and Disorders (19 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Cardiomyopathy and Myosin Studies (9 papers). Daniel Natera‐de Benito is often cited by papers focused on Muscle Physiology and Disorders (19 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Cardiomyopathy and Myosin Studies (9 papers). Daniel Natera‐de Benito collaborates with scholars based in Spain, United Kingdom and United States. Daniel Natera‐de Benito's co-authors include C. Ortez, A. Nascimento, J. Expósito, Laura Carrera‐García, J. Colomer, C. Jimenez‐Mallebrera, Nuria Muelas, Janet Hoenicka, Hanns Lochmüller and Angela Abicht and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Daniel Natera‐de Benito

48 papers receiving 389 citations

Peers

Daniel Natera‐de Benito
H. Jacobus Gilhuis Netherlands
Nizar Chahin United States
Sarina Meinen Switzerland
Daigo Miyazaki Japan
Stefan Nicolau United States
Sanna Huovinen Finland
Gina O’Grady New Zealand
Grace McMacken United Kingdom
Maryam Sedghi Iran
Jochen Schäfer Germany
H. Jacobus Gilhuis Netherlands
Daniel Natera‐de Benito
Citations per year, relative to Daniel Natera‐de Benito Daniel Natera‐de Benito (= 1×) peers H. Jacobus Gilhuis

Countries citing papers authored by Daniel Natera‐de Benito

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Natera‐de Benito

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Natera‐de Benito. 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 Daniel Natera‐de Benito. The network helps show where Daniel Natera‐de Benito may publish in the future.

Co-authorship network of co-authors of Daniel Natera‐de Benito

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Natera‐de Benito. A scholar is included among the top collaborators of Daniel Natera‐de Benito 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 Daniel Natera‐de Benito. Daniel Natera‐de Benito 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.
Romo, Lucía, Emily O’Heir, Juliette Nectoux, et al.. (2025). 490PA recurrent non-coding 3’UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy. Neuromuscular Disorders. 53. 105786–105786.
2.
Camacho, Ana, C. Ortez, Laura Carrera‐García, et al.. (2024). Epilepsy in Duchenne and Becker muscular dystrophies. Annals of Clinical and Translational Neurology. 11(6). 1456–1464.
3.
Simón, Rogelio, Daniel Natera‐de Benito, Jair Tenorio, et al.. (2024). A Novel Missense Variant in the NKX2-1 Homeodomain Prevents Transcriptional Rescue by TAZ. Thyroid. 34(7). 942–948.
4.
Ormazábal, Aída, Mercedes Casado, Ángela Arias, et al.. (2024). Cerebrospinal Fluid Homovanillic and 5-Hydroxyindoleacetic Acids in a Large Pediatric Population; Establishment of Reference Intervals and Impact of Disease and Medication. Clinical Chemistry. 70(12). 1443–1451. 3 indexed citations
5.
Cao, Xinyu, Spyridoula Karamanou, Aleyde Van Eynde, et al.. (2024). SDS22 coordinates the assembly of holoenzymes from nascent protein phosphatase-1. Nature Communications. 15(1). 5359–5359. 3 indexed citations
6.
Benito, Daniel Natera‐de, Carla Garcia‐Cabau, Cristina Jou, et al.. (2023). Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of Clinical and Translational Neurology. 10(3). 408–425. 7 indexed citations
7.
Codina, Anna, Mónica Roldán, Daniel Natera‐de Benito, et al.. (2023). Innovative Computerized Dystrophin Quantification Method Based on Spectral Confocal Microscopy. International Journal of Molecular Sciences. 24(7). 6358–6358.
8.
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
9.
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
10.
Domínguez‐González, Cristina, Aurelio Hernández‐Laín, Ana Camacho, et al.. (2022). Genetic diagnosis of Duchenne and Becker muscular dystrophy through mRNA analysis: new splicing events. Journal of Medical Genetics. 60(6). 615–619. 12 indexed citations
11.
Almendrote, Míriam, Daniel Natera‐de Benito, A. Nascimento, et al.. (2022). An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation. Biomedicines. 10(6). 1372–1372. 4 indexed citations
12.
López‐Márquez, Arístides, Matías Morin, Daniel Natera‐de Benito, et al.. (2022). CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts. International Journal of Molecular Sciences. 23(8). 4410–4410. 15 indexed citations
13.
Carrera‐García, Laura, Jordi Muchart, Juan José Lázaro, et al.. (2021). Pediatric SMA patients with complex spinal anatomy: Implementation and evaluation of a decision-tree algorithm for administration of nusinersen. European Journal of Paediatric Neurology. 31. 92–101. 10 indexed citations
14.
Benito, Daniel Natera‐de, C. Ortez, Cristina Jou, et al.. (2020). The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort. Pediatric Neurology. 115. 50–65. 13 indexed citations
15.
16.
Milev, Miroslav P., Daniela Stanga, Anne Schänzer, et al.. (2019). Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein. Scientific Reports. 9(1). 14036–14036. 9 indexed citations
17.
Frongia, A., Daniel Natera‐de Benito, C. Ortez, et al.. (2019). Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II. Neuromuscular Disorders. 29(7). 517–524. 16 indexed citations
18.
Benito, Daniel Natera‐de, María Ángeles Mori, María Palomares‐Bralo, et al.. (2018). The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. European Journal of Medical Genetics. 61(7). 393–398. 12 indexed citations
19.
Pisón, Javier López, et al.. (2016). Genetic testing among Spanish pediatric neurologists: Knowledge, attitudes and practices. European Journal of Medical Genetics. 60(2). 124–129. 13 indexed citations
20.
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

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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