Raül Santamaría

766 total citations
13 papers, 323 citations indexed

About

Raül Santamaría is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Raül Santamaría has authored 13 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 6 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in Raül Santamaría's work include Lysosomal Storage Disorders Research (8 papers), Glycosylation and Glycoproteins Research (4 papers) and Cellular transport and secretion (4 papers). Raül Santamaría is often cited by papers focused on Lysosomal Storage Disorders Research (8 papers), Glycosylation and Glycoproteins Research (4 papers) and Cellular transport and secretion (4 papers). Raül Santamaría collaborates with scholars based in Spain, Greece and Argentina. Raül Santamaría's co-authors include Lluı̈sa Vilageliu, Daniel Grinberg, Amparo Chabás, Manoel Galvão Neto, Almino Ramos, Manoela Galvão, Anna Dı́az-Font, María Josep Coll, Clara Sá-Miranda and Laura Gort and has published in prestigious journals such as Journal of Lipid Research, Journal of the Neurological Sciences and Breast Cancer Research and Treatment.

In The Last Decade

Raül Santamaría

13 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raül Santamaría Spain 9 244 112 105 83 52 13 323
H. Ebrahim United Kingdom 7 192 0.8× 56 0.5× 34 0.3× 92 1.1× 101 1.9× 8 324
E. Mutel France 7 146 0.6× 23 0.2× 91 0.9× 165 2.0× 53 1.0× 7 369
Chuan‐Hong Kao Taiwan 7 204 0.8× 63 0.6× 17 0.2× 158 1.9× 103 2.0× 10 411
Han‐Wook Yoo South Korea 10 79 0.3× 44 0.4× 24 0.2× 113 1.4× 31 0.6× 16 253
Y Ikura Japan 4 106 0.4× 72 0.6× 60 0.6× 151 1.8× 44 0.8× 6 355
Isabelle Houberdon France 4 135 0.6× 17 0.2× 85 0.8× 151 1.8× 45 0.9× 4 320
Ferenc Szekeres Sweden 8 111 0.5× 50 0.4× 65 0.6× 184 2.2× 24 0.5× 14 328
Melis Köse Türkiye 8 59 0.2× 48 0.4× 23 0.2× 74 0.9× 22 0.4× 42 195
Charina M. Ramirez United States 8 371 1.5× 67 0.6× 84 0.8× 141 1.7× 65 1.3× 17 497
François Eyskens Belgium 8 153 0.6× 49 0.4× 8 0.1× 72 0.9× 54 1.0× 17 292

Countries citing papers authored by Raül Santamaría

Since Specialization
Citations

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

Fields of papers citing papers by Raül Santamaría

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raül Santamaría

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

All Works

13 of 13 papers shown
1.
2.
Quiles, Francisco, Mireia Menéndez, Eva Tornero, et al.. (2016). Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA. Breast Cancer Research and Treatment. 155(2). 253–260. 6 indexed citations
3.
López, Eva, et al.. (2015). Identification of two novel KIF5A mutations in hereditary spastic paraplegia associated with mild peripheral neuropathy. Journal of the Neurological Sciences. 358(1-2). 422–427. 15 indexed citations
4.
Ramos, Almino, et al.. (2008). Laparoscopic Duodenal–Jejunal Exclusion in the Treatment of Type 2 Diabetes Mellitus in Patients with BMI < 30 kg/m2 (LBMI). Obesity Surgery. 19(3). 307–312. 107 indexed citations
5.
Santamaría, Raül, Lluı̈sa Vilageliu, & Daniel Grinberg. (2008). SR proteins and the nonsense-mediated decay mechanism are involved in human GLB1 gene alternative splicing. BMC Research Notes. 1(1). 137–137. 5 indexed citations
6.
Santamaría, Raül, Helen Michelakakis, Marina Moraitou, et al.. (2008). Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H;H255Q] double mutant allele. Human Mutation. 29(6). E58–E67. 16 indexed citations
7.
Santamaría, Raül, Amparo Chabás, John W. Callahan, Daniel Grinberg, & Lluı̈sa Vilageliu. (2007). Expression and characterization of 14 GLB1 mutant alleles found in GM1-gangliosidosis and Morquio B patients. Journal of Lipid Research. 48(10). 2275–2282. 19 indexed citations
8.
Zafeiriou, Dimitrios, Euthymia Vargìami, Kyriaki Papadopoulou‐Legbelou, et al.. (2007). Serial magnetic resonance imaging and neurophysiological studies in multiple sulphatase deficiency. European Journal of Paediatric Neurology. 12(3). 190–194. 5 indexed citations
9.
Santamaría, Raül, Amparo Chabás, María Josep Coll, et al.. (2006). Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies. Human Mutation. 27(10). 1060–1060. 52 indexed citations
10.
Michelakakis, Helen, Marina Moraitou, Raül Santamaría, et al.. (2006). Homozygosity for the double D409H+H255Q allele in type II Gaucher disease. Journal of Inherited Metabolic Disease. 29(4). 591–591. 17 indexed citations
11.
Chabás, Amparo, Laura Gort, Anna Dı́az-Font, et al.. (2005). Perinatal lethal phenotype with generalized ichthyosis in a type 2 Gaucher disease patient with the [L444P;E326K]/P182L genotype: Effect of the E326K change in neonatal and classic forms of the disease. Blood Cells Molecules and Diseases. 35(2). 253–258. 31 indexed citations
12.
Dı́az-Font, Anna, Bru Cormand, Raül Santamaría, et al.. (2005). A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity. Human Genetics. 117(2-3). 275–277. 32 indexed citations
13.
Dı́az-Font, Anna, Raül Santamaría, Mónica Cozar, et al.. (2005). Clinical and mutational characterization of three patients with multiple sulfatase deficiency: Report of a new splicing mutation. Molecular Genetics and Metabolism. 86(1-2). 206–211. 14 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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