Eloy Rivas

1.8k total citations
74 papers, 835 citations indexed

About

Eloy Rivas is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Eloy Rivas has authored 74 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Eloy Rivas's work include Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Cardiomyopathy and Myosin Studies (6 papers). Eloy Rivas is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Cardiomyopathy and Myosin Studies (6 papers). Eloy Rivas collaborates with scholars based in Spain, Australia and United States. Eloy Rivas's co-authors include Juan Carlos Burgos, Juan Carlos García-Prada, Francisco Santamaría, José A. Sánchez‐Alcázar, Mario de la Mata, Juan Garrido‐Maraver, Manuel Oropesa-Ávila, Sandra L. Jackson, David Cotán and Manuel de Miguel and has published in prestigious journals such as Renewable and Sustainable Energy Reviews, PLoS ONE and Brain.

In The Last Decade

Eloy Rivas

66 papers receiving 816 citations

Peers

Eloy Rivas

EEE

EPIDE

PHYSI

CMN

Lili Huang China

Yi Cheng China

Takashi Ueta Japan

Daquan Liu China

Gao Wang China

Xiaogang Hou United States

Yixuan Wang China

Quanwei Wang China

Haifeng Wei China

Lili Huang China

Eloy Rivas

199 ×0.5

47 ×0.3

EEE

35 ×0.3

EPIDE

37 ×0.4

PHYSI

102 ×1.1

CMN

Citations per year, relative to Eloy Rivas Eloy Rivas (= 1×) peers Lili Huang

Countries citing papers authored by Eloy Rivas

Since Specialization

Citations

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

Fields of papers citing papers by Eloy Rivas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eloy Rivas

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

Rivas, Eloy, et al.. (2024). Redefining periodic paralysis with CACNA1S mutation in a Spanish cohort. Neurología. 40(7). 630–640.

Mavillard, Fabiola, Emilia Servián‐Morilla, I. Rojas-Marcos, et al.. (2023). Ablation of the carboxy-terminal end of MAMDC2 causes a distinct muscular dystrophy. Brain. 146(12). 5235–5248. 4 indexed citations

Blanco, Patricia, et al.. (2023). Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant. Neuromuscular Disorders. 33(7). 557–561. 3 indexed citations

Rivas, Eloy, et al.. (2023). Lessons learned from a sporadic FUSopathy in a young man: a case report. BMC Neurology. 23(1). 55–55. 1 indexed citations

Sánchez, Sandra Cebada, María del Mar Arroyo Jiménez, Mónica Muñoz, et al.. (2023). Study of the human hippocampal formation: a method for histological and magnetic resonance correlation in perinatal cases. Brain Imaging and Behavior. 17(4). 403–413. 1 indexed citations

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

Servián‐Morilla, Emilia, Eloy Rivas, Fathimath Faiz, et al.. (2022). A KLHL40 3’ UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism. Human Molecular Genetics. 32(7). 1127–1136. 7 indexed citations

Suárez‐Calvet, Xavier, Jorge Alonso‐Pérez, Noemí de Luna, et al.. (2022). BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients. American Journal Of Pathology. 192(8). 1151–1166. 4 indexed citations

Mavillard, Fabiola, Emilia Servián‐Morilla, Eloy Rivas, Carmen Paradas, & Macarena Cabrera‐Serrano. (2021). Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy. Clinical Genetics. 100(1). 106–110. 1 indexed citations

10.

Henrich, Kai‐Oliver, Konstantin Okonechnikov, Eloy Rivas, et al.. (2020). Identification of VRK1 as a New Neuroblastoma Tumor Progression Marker Regulating Cell Proliferation. Cancers. 12(11). 3465–3465. 14 indexed citations

11.

Marcos, Ana T., D. Amorós, Beatriz Muñoz Cabello, et al.. (2020). A novel dominant mutation in CRYAB gene leading to a severe phenotype with childhood onset. Molecular Genetics & Genomic Medicine. 8(8). e1290–e1290. 11 indexed citations

12.

Fernández‐Torres, Rut, Mercedes Villar-Navarro, Eloy Rivas, et al.. (2020). Lacosamide intake during pregnancy increases the incidence of foetal malformations and symptoms associated with schizophrenia in the offspring of mice. Scientific Reports. 10(1). 7615–7615. 11 indexed citations

13.

Mavillard, Fabiola, Marcos Madruga‐Garrido, Eloy Rivas, et al.. (2019). NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay. Annals of Clinical and Translational Neurology. 6(11). 2328–2333. 1 indexed citations

14.

Cabrera‐Serrano, Macarena, Emilia Servián‐Morilla, Eloy Rivas, et al.. (2018). A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain. Neuromuscular Disorders. 28(10). 828–836. 7 indexed citations

15.

Rivas, Eloy, et al.. (2018). Preparation of Demand Response Management: Case Study. 1–6. 5 indexed citations

16.

Velásquez, Carlos, et al.. (2016). Endoscopic Histologic Mapping of a Mixed Germ Pineal Tumor. World Neurosurgery. 95. 625.e1–625.e5. 2 indexed citations

17.

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

18.

Rivero-Garvía, Mónica, et al.. (2012). Primary Cerebral Radiotherapy-Induced Rhabdomyosarcoma: Treatment with Intraoperative Carmustine Implants. Pediatric Hematology and Oncology. 30(1). 30–32. 6 indexed citations

19.

García‐Díaz, Lutgardo, et al.. (2011). Hemimegalencephaly: Prenatal Diagnosis and Outcome. Fetal Diagnosis and Therapy. 30(3). 234–238. 12 indexed citations

20.

Rivas, Eloy, et al.. (2002). Angiofibroma extranasofaríngeo: Aportación de un nuevo caso y revisión bibliográfica. Acta Otorrinolaringológica Española. 53(4). 297–301. 4 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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