Pilar Camaño

2.2k total citations · 1 hit paper
22 papers, 1.3k citations indexed

About

Pilar Camaño is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Pilar Camaño has authored 22 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in Pilar Camaño's work include Muscle Physiology and Disorders (8 papers), RNA modifications and cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Pilar Camaño is often cited by papers focused on Muscle Physiology and Disorders (8 papers), RNA modifications and cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Pilar Camaño collaborates with scholars based in Spain, United States and Netherlands. Pilar Camaño's co-authors include Sabrina Sacconi, Silvère M. van der Maarel, Richard J.L.F. Lemmers, Rabi Tawil, Rune R. Frants, Stephen J. Tapscott, Patrick J. van der Vliet, George W. Padberg, Daniel G. Miller and Johannes G. Dauwerse and has published in prestigious journals such as Science, Journal of Clinical Oncology and Neurology.

In The Last Decade

Pilar Camaño

21 papers receiving 1.3k citations

Hit Papers

A Unifying Genetic Model for Facioscapulohumeral Muscular... 2010 2026 2015 2020 2010 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
    2010 528 citations Richard J.L.F. Lemmers, Patrick J. van der Vliet et al. Science profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pilar Camaño Spain 11 1.1k 254 227 192 183 22 1.3k
Rabah Ben Yaou France 23 1.8k 1.7× 562 2.2× 223 1.0× 29 0.2× 173 0.9× 66 2.1k
Pagon Ra United States 6 450 0.4× 57 0.2× 70 0.3× 59 0.3× 82 0.4× 291 791
P. Gallano Spain 20 1.0k 1.0× 261 1.0× 261 1.1× 18 0.1× 213 1.2× 65 1.4k
Francesco Chemello Italy 18 1.2k 1.1× 246 1.0× 87 0.4× 21 0.1× 96 0.5× 34 1.4k
Ana Lía Taratuto Argentina 19 402 0.4× 155 0.6× 278 1.2× 18 0.1× 189 1.0× 42 1.1k
Xiomara Q. Rosales United States 10 533 0.5× 164 0.6× 124 0.5× 22 0.1× 81 0.4× 17 653
Valérie Drouin‐Garraud France 16 492 0.5× 169 0.7× 141 0.6× 27 0.1× 49 0.3× 32 875
Heasoo Koo South Korea 18 316 0.3× 90 0.4× 78 0.3× 28 0.1× 291 1.6× 54 875
Adolf Pou Spain 13 374 0.4× 73 0.3× 136 0.6× 25 0.1× 89 0.5× 14 638
Kohei Hamanaka Japan 14 453 0.4× 65 0.3× 115 0.5× 22 0.1× 132 0.7× 49 908

Countries citing papers authored by Pilar Camaño

Since Specialization
Citations

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

Fields of papers citing papers by Pilar Camaño

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pilar Camaño

This figure shows the co-authorship network connecting the top 25 collaborators of Pilar Camaño. A scholar is included among the top collaborators of Pilar Camaño 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 Pilar Camaño. Pilar Camaño 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.
2.
González‐Sánchez, Marta, Fernando Benito Bartolomé, Desireé Antequera, et al.. (2020). Decreased salivary lactoferrin levels are specific to Alzheimer's disease. EBioMedicine. 57. 102834–102834. 79 indexed citations
3.
González‐Sánchez, Marta, Fernando Benito Bartolomé, Desireé Antequera, et al.. (2020). Decreased salivary lactoferrin levels are specific to Alzheimer’s disease. Alzheimer s & Dementia. 16(S4). 2 indexed citations
4.
5.
Lopez, Gabriel, et al.. (2018). Complementary and integrative medicine use for individuals seeking conventional medical oncology care in Chile: Prevalence and patient characteristics.. Journal of Clinical Oncology. 36(34_suppl). 110–110. 1 indexed citations
6.
Boogaard, Marlinde L. van den, Pilar Camaño, Patrick J. van der Vliet, et al.. (2015). Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2. European Journal of Human Genetics. 24(1). 78–85. 21 indexed citations
7.
Lemmers, Richard J.L.F., Pilar Camaño, Patrick J. van der Vliet, et al.. (2014). G.O.4. Neuromuscular Disorders. 24(9-10). 793–793. 1 indexed citations
8.
Paradas, Carmen, Pilar Camaño, David Otaegui, et al.. (2013). Longitudinal Clinical Follow-up of a Large Family With the R357P Twinkle Mutation. JAMA Neurology. 70(11). 1425–1425. 3 indexed citations
9.
Kinter, Jochen, Jürgen Hench, Stephan Frank, et al.. (2012). Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular Disorders. 23(2). 149–154. 10 indexed citations
10.
Sacconi, Sabrina, Pilar Camaño, Jessica C. de Greef, et al.. (2011). Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity. Journal of Medical Genetics. 49(1). 41–46. 43 indexed citations
11.
Lemmers, Richard J.L.F., Patrick J. van der Vliet, Rinse Klooster, et al.. (2010). A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy. Science. 329(5999). 1650–1653. 528 indexed citations breakdown →
12.
Greef, Jessica C. de, Richard J.L.F. Lemmers, Pilar Camaño, et al.. (2010). Clinical features of facioscapulohumeral muscular dystrophy 2. Neurology. 75(17). 1548–1554. 117 indexed citations
13.
Stojkovic, Tanya, Pascale Richard, Adolfo López de Munaín, et al.. (2009). Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia. Neuromuscular Disorders. 19(5). 316–323. 66 indexed citations
14.
León, Montserrat, Eva Andrés, Martín Laclaustra, et al.. (2008). Comparison of Cardiovascular Risk Factors in Young Spanish Men Between the 1980s and After the Year 2000. Data From the AGEMZA Study. Revista Española de Cardiología (English Edition). 61(12). 1260–1266. 7 indexed citations
15.
Sistiaga, Andone, Pilar Camaño, David Otaegui, et al.. (2008). Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defect. Genes Brain & Behavior. 8(1). 53–59. 5 indexed citations
16.
Quinzii, Catarina M., Tuan Vu, K. Christopher Min, et al.. (2008). X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1. The American Journal of Human Genetics. 82(1). 208–213. 74 indexed citations
17.
Ehrlich, Melanie, et al.. (2006). Hybridization analysis of D4Z4 repeat arrays linked to FSHD. Chromosoma. 116(2). 107–116. 22 indexed citations
18.
Otaegui, David, Amets Sáenz, Pilar Camaño, et al.. (2006). CD24 V/V is an allele associated with the risk of developing multiple sclerosis in the Spanish population. Multiple Sclerosis Journal. 12(4). 511–514. 36 indexed citations
19.
Salviati, Leonardo, Sabrina Sacconi, Michelangelo Mancuso, et al.. (2002). Mitochondrial DNA depletion and dGK gene mutations. Annals of Neurology. 52(3). 311–317. 132 indexed citations
20.
Mancuso, Michelangelo, Leonardo Salviati, Sabrina Sacconi, et al.. (2002). Mitochondrial DNA depletion. Neurology. 59(8). 1197–1202. 124 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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