Ana I. Corao

635 total citations
25 papers, 478 citations indexed

About

Ana I. Corao is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ana I. Corao has authored 25 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ana I. Corao's work include Mitochondrial Function and Pathology (7 papers), Alzheimer's disease research and treatments (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Ana I. Corao is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Alzheimer's disease research and treatments (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Ana I. Corao collaborates with scholars based in Spain, United States and Germany. Ana I. Corao's co-authors include Victoria Álvarez, Eliécer Coto, Marta Díaz, Lorena de Mena, Germán Morís, Manuel Menéndez‐González, René Ribacoba, Belén Alonso, Lucía Cardo and Carlos Salvador and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain Research and Biochemical and Biophysical Research Communications.

In The Last Decade

Ana I. Corao

24 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ana I. Corao Spain 14 282 117 87 61 58 25 478
Marc D’Hooghe Belgium 12 337 1.2× 95 0.8× 45 0.5× 29 0.5× 65 1.1× 18 580
Hendrik Rosewich Germany 18 567 2.0× 71 0.6× 95 1.1× 76 1.2× 26 0.4× 34 857
Laura Cassina Italy 11 515 1.8× 163 1.4× 135 1.6× 26 0.4× 90 1.6× 21 804
Michela Ripolone Italy 13 349 1.2× 121 1.0× 72 0.8× 18 0.3× 15 0.3× 40 526
Rosa Ferrando-Miguel Austria 9 254 0.9× 64 0.5× 100 1.1× 24 0.4× 25 0.4× 12 420
María Bjarnadóttir Sweden 8 156 0.6× 95 0.8× 28 0.3× 63 1.0× 21 0.4× 9 462
Francesca Mastropasqua Italy 11 549 1.9× 27 0.2× 77 0.9× 136 2.2× 39 0.7× 15 693
Katharina Heim Germany 7 135 0.5× 53 0.5× 90 1.0× 33 0.5× 53 0.9× 8 300
Melody Chao United Kingdom 11 301 1.1× 85 0.7× 41 0.5× 30 0.5× 93 1.6× 18 763
Yoshio Morimatsu Japan 15 391 1.4× 181 1.5× 102 1.2× 24 0.4× 59 1.0× 28 605

Countries citing papers authored by Ana I. Corao

Since Specialization
Citations

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

Fields of papers citing papers by Ana I. Corao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ana I. Corao. 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 Ana I. Corao. The network helps show where Ana I. Corao may publish in the future.

Co-authorship network of co-authors of Ana I. Corao

This figure shows the co-authorship network connecting the top 25 collaborators of Ana I. Corao. A scholar is included among the top collaborators of Ana I. Corao 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 Ana I. Corao. Ana I. Corao 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.
Coto, Eliécer, Juan Manuel López Gómez, Beatriz Tavira, et al.. (2013). A Common <b><i>APOE</i></b> Polymorphism Is an Independent Risk Factor for Reduced Glomerular Filtration Rate in the Spanish RENASTUR Cohort. Cardiorenal Medicine. 3(2). 113–119. 9 indexed citations
2.
3.
Coto, Eliécer, Julián R. Reguero, Juan Gómez, et al.. (2012). Resequencing the Whole MYH7 Gene (Including the Intronic, Promoter, and 3′ UTR Sequences) in Hypertrophic Cardiomyopathy. Journal of Molecular Diagnostics. 14(5). 518–524. 17 indexed citations
4.
Eirís, Noemí, Jorge Santos‐Juanes, Pablo Coto‐Segura, et al.. (2012). Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes. Cytokine. 60(1). 27–29. 17 indexed citations
5.
Mena, Lorena de, Lluı́s Samaranch, Eliécer Coto, et al.. (2012). Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease. Journal of Molecular Neuroscience. 50(2). 264–269. 10 indexed citations
6.
Coto‐Segura, Pablo, Jorge Santos‐Juanes, Juan Gómez, et al.. (2011). Common European Mitochondrial Haplogroups in the Risk for Psoriasis and Psoriatic Arthritis. Genetic Testing and Molecular Biomarkers. 16(6). 621–623. 9 indexed citations
7.
Coto, Eliécer, Julián R. Reguero, Marı́a Martı́n, et al.. (2011). DNA Variation in myoMIRs of the 1, 133, and 208 Families in Hypertrophic Cardiomyopathy. SHILAP Revista de lepidopterología. 1(1). e12–e12.
8.
Cardo, Lucía, Eliécer Coto, Lorena de Mena, et al.. (2011). A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease. Journal of Molecular Neuroscience. 47(3). 425–430. 39 indexed citations
9.
Miar, Ana, Victoria Álvarez, Ana I. Corao, et al.. (2011). Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease. Brain Research. 1383. 252–256. 15 indexed citations
10.
Sánchez-Ferrero, Elena, Eliécer Coto, Ana I. Corao, et al.. (2011). Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. Journal of Neurology. 259(2). 246–250. 4 indexed citations
11.
Mena, Lorena de, Lucía Cardo, Eliécer Coto, et al.. (2010). FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients. Neuroscience Letters. 479(1). 22–25. 39 indexed citations
12.
Álvarez, Victoria, Marı́a Martı́n, Marta Díaz, et al.. (2010). Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H. Mitochondrion. 11(1). 176–181. 34 indexed citations
13.
Coto, Eliécer, María G. Castro, Ana I. Corao, et al.. (2009). Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy. American Journal of Medical Genetics Part A. 149A(2). 286–289. 4 indexed citations
14.
Coto‐Segura, Pablo, Eliécer Coto, Victoria Álvarez, et al.. (2009). Apolipoprotein ε4 allele is associated with psoriasis severity. Archives of Dermatological Research. 302(2). 145–149. 16 indexed citations
15.
Coto, Eliécer, Gabriel de Arriba, Mónica Garcı́a-Castro, et al.. (2009). Clinical and Analytical Findings in Gitelman’s Syndrome Associated with Homozygosity for the c.1925 G>A SLC12A3 Mutation. American Journal of Nephrology. 30(3). 218–221. 5 indexed citations
16.
Álvarez, Victoria, Ana I. Corao, Cristina Alonso‐Montes, et al.. (2008). Mitochondrial Transcription Factor A (TFAM) Gene Variation and Risk of Late-Onset Alzheimer's Disease. Journal of Alzheimer s Disease. 13(3). 275–280. 26 indexed citations
17.
Álvarez, Victoria, Pelayo González, Ana I. Corao, et al.. (2008). The Sp1/Egr1-tandem Repeat Polymorphism in the 5-Lipoxygenase Gene Promoter is not Associated With Late Onset Alzheimer Disease. Alzheimer Disease & Associated Disorders. 22(2). 177–180. 9 indexed citations
18.
Álvarez, Victoria, Ana I. Corao, Elena Sánchez-Ferrero, et al.. (2008). Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease. Neuroscience Letters. 432(1). 79–82. 27 indexed citations
19.
González, Pelayo, Victoria Álvarez, Manuel Menéndez‐González, et al.. (2006). Myocyte enhancing factor-2A in Alzheimer's disease: Genetic analysis and association with MEF2A-polymorphisms. Neuroscience Letters. 411(1). 47–51. 15 indexed citations
20.
Castro, María G., Cecilia Huerta, Julián R. Reguero, et al.. (2005). Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy. International Journal of Cardiology. 112(2). 202–206. 49 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marc D’Hooghe Breakdown of academic impact, for papers by Hendrik Rosewich Breakdown of academic impact, for papers by Laura Cassina Breakdown of academic impact, for papers by Michela Ripolone Breakdown of academic impact, for papers by Rosa Ferrando-Miguel Breakdown of academic impact, for papers by María Bjarnadóttir Breakdown of academic impact, for papers by Francesca Mastropasqua Breakdown of academic impact, for papers by Katharina Heim Breakdown of academic impact, for papers by Melody Chao Breakdown of academic impact, for papers by Yoshio Morimatsu
Rankless by CCL
2026