Rafael Muley

460 total citations
11 papers, 336 citations indexed

About

Rafael Muley is a scholar working on Molecular Biology, Nephrology and Clinical Biochemistry. According to data from OpenAlex, Rafael Muley has authored 11 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Nephrology and 2 papers in Clinical Biochemistry. Recurrent topics in Rafael Muley's work include Mitochondrial Function and Pathology (3 papers), Ion Transport and Channel Regulation (3 papers) and Metabolism and Genetic Disorders (2 papers). Rafael Muley is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Ion Transport and Channel Regulation (3 papers) and Metabolism and Genetic Disorders (2 papers). Rafael Muley collaborates with scholars based in Spain and Uruguay. Rafael Muley's co-authors include Joaquı́n Arenas, Carmen Bustos, Jesús Egido, Yolanda Campos, Eva González, Miguel A. Martı́n, Elena Martín‐Hernández, Julia Vara, M.T. García‐Silva and Ana Cabello and has published in prestigious journals such as PLoS ONE, Clinical Journal of the American Society of Nephrology and Nephrology Dialysis Transplantation.

In The Last Decade

Rafael Muley

11 papers receiving 324 citations

Peers

Rafael Muley

NEPHR

PFM

RHEUM

María Elena Rodríguez‐García Spain

T Matsuo Japan

Takamitsu Saigusa United States

Yujing Shu Japan

Corinne E. Metzger United States

A Hayward United Kingdom

Kathleen Heilig United States

Ilona Visapää Finland

Marie-Helena Docherty United Kingdom

N. Yevdokimova Ukraine

María Elena Rodríguez‐García Spain

Rafael Muley

133 ×0.8

126 ×1.0

NEPHR

27 ×0.3

48 ×1.1

PFM

20 ×0.5

RHEUM

Citations per year, relative to Rafael Muley Rafael Muley (= 1×) peers María Elena Rodríguez‐García

Countries citing papers authored by Rafael Muley

Since Specialization

Citations

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

Fields of papers citing papers by Rafael Muley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rafael Muley

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

All Works

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11 of 11 papers shown

Rivera, Henry, Elena Martín‐Hernández, Aitor Delmiro, et al.. (2013). A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome. BMC Nephrology. 14(1). 195–195. 29 indexed citations

Claverie-Martı́n, Félix, Víctor Manuel García Nieto, C Loris, et al.. (2013). Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis. PLoS ONE. 8(1). e53151–e53151. 40 indexed citations

Claverie-Martı́n, Félix, Víctor Manuel García Nieto, C Loris, et al.. (2013). Correction: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis. PLoS ONE. 8(10). 3 indexed citations

Claverie-Martı́n, Félix, Víctor Manuel García Nieto, Gema Ariceta, et al.. (2013). Dent's disease: Identification of seven new pathogenic mutations in the CLCN5 gene.. PubMed. 2(3). 133–40. 4 indexed citations

Santos, Fernando, Gema Ariceta, Julia Vara, et al.. (2010). Improvement in Growth After 1 Year of Growth Hormone Therapy in Well-Nourished Infants with Growth Retardation Secondary to Chronic Renal Failure. Clinical Journal of the American Society of Nephrology. 5(7). 1190–1197. 27 indexed citations

Martín‐Hernández, Elena, M.T. García‐Silva, Julia Vara, et al.. (2005). Renal pathology in children with mitochondrial diseases. Pediatric Nephrology. 20(9). 1299–1305. 80 indexed citations

Bustos, Carmen, Eva González‐Roca, S. Gonzalez-Cuadrado, et al.. (1996). Urinary excretion of platelet-activating factor in human and experimental nephrosis. Nephrology Dialysis Transplantation. 11(2). 282–286. 9 indexed citations

Campos, Yolanda, et al.. (1995). Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome. Pediatric Neurology. 13(1). 69–72. 39 indexed citations

Gómez‐Reino, Juan J., et al.. (1995). MENSTRUAL DISORDERS IN GIRLS WITH SYSTEMIC LUPUS ERYTHEMATOSUS TREATED WITH CYCLOPHOSPHAMIDE. Lara D. Veeken. 34(8). 737–741. 23 indexed citations

10.

Bustos, Carmen, et al.. (1994). Increase of tumour necrosis factor α synthesis and gene expression in peripheral blood mononuclear cells of children with idiopathic nephrotic syndrome. European Journal of Clinical Investigation. 24(12). 799–805. 72 indexed citations

11.

López, Francisco Cabrera, et al.. (1993). Pyelic benign fibroepithelial polyp in childhood: a case report.. PubMed. 28(7). 948–9. 10 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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