A. Nascimento

4.9k total citations
94 papers, 1.2k citations indexed

About

A. Nascimento is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, A. Nascimento has authored 94 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 23 papers in Genetics and 17 papers in Genetics. Recurrent topics in A. Nascimento's work include Muscle Physiology and Disorders (31 papers), Neurogenetic and Muscular Disorders Research (23 papers) and Mitochondrial Function and Pathology (16 papers). A. Nascimento is often cited by papers focused on Muscle Physiology and Disorders (31 papers), Neurogenetic and Muscular Disorders Research (23 papers) and Mitochondrial Function and Pathology (16 papers). A. Nascimento collaborates with scholars based in Spain, United Kingdom and United States. A. Nascimento's co-authors include C. Ortez, C. Jimenez‐Mallebrera, J. Colomer, Rafael Artuch, Julio Montoya, Cristina Jou, Daniel Natera‐de Benito, Jaume Colomer, P. Gallano and Paz Briones and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

A. Nascimento

79 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Nascimento Spain	20	757	232	190	184	171	94	1.2k
Göknur Haliloğlu Türkiye	23	922 1.2×	224 1.0×	210 1.1×	236 1.3×	183 1.1×	116	1.7k
Christine Barnérias France	20	704 0.9×	137 0.6×	139 0.7×	193 1.0×	156 0.9×	73	1.4k
Denise Cassandrini Italy	23	735 1.0×	222 1.0×	106 0.6×	132 0.7×	185 1.1×	62	1.3k
Jens Reimann Germany	22	845 1.1×	265 1.1×	192 1.0×	171 0.9×	296 1.7×	55	1.3k
Velina Guergueltcheva Bulgaria	23	899 1.2×	561 2.4×	408 2.1×	133 0.7×	308 1.8×	52	1.6k
Martine Tétreault Canada	26	1.4k 1.9×	348 1.5×	115 0.6×	91 0.5×	154 0.9×	67	2.0k
Jun Mitsui Japan	24	860 1.1×	480 2.1×	582 3.1×	214 1.2×	212 1.2×	115	1.7k
Ikuya Nonaka Japan	17	977 1.3×	228 1.0×	52 0.3×	124 0.7×	150 0.9×	31	1.2k
Anna Kamińska Poland	19	606 0.8×	189 0.8×	194 1.0×	101 0.5×	209 1.2×	94	1.3k
Beate Schlotter‐Weigel Germany	15	779 1.0×	338 1.5×	125 0.7×	110 0.6×	240 1.4×	24	1.3k

Countries citing papers authored by A. Nascimento

Since Specialization

Citations

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

Fields of papers citing papers by A. Nascimento

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Nascimento

This figure shows the co-authorship network connecting the top 25 collaborators of A. Nascimento. A scholar is included among the top collaborators of A. Nascimento 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 A. Nascimento. A. Nascimento 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

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.

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

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

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

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

Oskoui, Maryam, Nicolas Deconinck, Elena Mazzone, et al.. (2023). Sunfish parts 1 and 2: 4-year efficacy and safety data of risdiplam in types 2 and 3 spinal muscular atrophy (SMA). Journal of the Neurological Sciences. 455. 121096–121096. 2 indexed citations

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.

Crawford, Thomas O., et al.. (2023). P224 Effect of apitegromab on motor function at 36 months in patients with nonambulatory spinal muscular atrophy aged 2-12 years old. Neuromuscular Disorders. 33. S91–S91. 1 indexed citations

Stojkovic, Tanya, A. Nascimento, John Vissing, et al.. (2023). P424 Identify genetic modifiers controlling severity of collagen-6 related dystrophies (COL6-RD). Neuromuscular Disorders. 33. S158–S158.

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.

Carrera‐García, Laura, et al.. (2022). Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease. 6. 333–352. 5 indexed citations

13.

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

14.

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

15.

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

16.

Ortez, C., Cristina Jou, Marta Ramon‐Krauel, et al.. (2017). Differences in Adipose Tissue and Lean Mass Distribution in Patients with Collagen VI Related Myopathies Are Associated with Disease Severity and Physical Ability. Frontiers in Aging Neuroscience. 9. 268–268. 5 indexed citations

17.

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

18.

Ortez, C., et al.. (2014). Hypotonic male infant and MCT8 deficiency - a diagnosis to think about. BMC Pediatrics. 14(1). 252–252. 16 indexed citations

19.

Paco, Sonia, Susana G. Kalko, Cristina Jou, et al.. (2013). Gene Expression Profiling Identifies Molecular Pathways Associated with Collagen VI Deficiency and Provides Novel Therapeutic Targets. PLoS ONE. 8(10). e77430–e77430. 12 indexed citations

20.

Jimenez‐Mallebrera, C., Xavier Palomer, Valeria De Nigris, et al.. (2012). PGC-1α Induces Mitochondrial and Myokine Transcriptional Programs and Lipid Droplet and Glycogen Accumulation in Cultured Human Skeletal Muscle Cells. PLoS ONE. 7(1). e29985–e29985. 48 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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