Editha Andres

492 total citations
20 papers, 393 citations indexed

About

Editha Andres is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Editha Andres has authored 20 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Editha Andres's work include RNA modifications and cancer (5 papers), Genetic Associations and Epidemiology (4 papers) and Congenital heart defects research (3 papers). Editha Andres is often cited by papers focused on RNA modifications and cancer (5 papers), Genetic Associations and Epidemiology (4 papers) and Congenital heart defects research (3 papers). Editha Andres collaborates with scholars based in Saudi Arabia, Australia and France. Editha Andres's co-authors include Nduna Dzimiri, Zohair Al‐Halees, Brian F. Meyer, Maie Alshahid, Salma M. Wakil, Dilek Çolak, Namik Kaya, Batoul Baz, Nejat Mazhar and Asma I. Tahir and has published in prestigious journals such as PLoS ONE, The FASEB Journal and Gene.

In The Last Decade

Editha Andres

19 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Editha Andres Saudi Arabia 10 237 141 70 45 39 20 393
John H. Cleator United States 9 207 0.9× 159 1.1× 30 0.4× 60 1.3× 43 1.1× 19 503
Ali R. Keramati United States 11 182 0.8× 190 1.3× 89 1.3× 72 1.6× 15 0.4× 18 506
John Dixon United Kingdom 8 180 0.8× 122 0.9× 87 1.2× 43 1.0× 41 1.1× 11 508
Yujing Dang United States 13 282 1.2× 55 0.4× 142 2.0× 26 0.6× 16 0.4× 16 441
Isbaal Ramos Spain 8 253 1.1× 193 1.4× 17 0.2× 53 1.2× 21 0.5× 11 470
Stephen Archacki United States 13 291 1.2× 83 0.6× 58 0.8× 45 1.0× 25 0.6× 20 487
Chunyan Luo China 11 149 0.6× 79 0.6× 39 0.6× 29 0.6× 11 0.3× 17 271
Yuichi Koide Japan 12 266 1.1× 210 1.5× 22 0.3× 26 0.6× 40 1.0× 13 522
Kazuwa Nakao Japan 6 141 0.6× 243 1.7× 33 0.5× 46 1.0× 23 0.6× 7 398
Rodolfo Battista Italy 4 204 0.9× 72 0.5× 50 0.7× 54 1.2× 10 0.3× 6 378

Countries citing papers authored by Editha Andres

Since Specialization
Citations

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

Fields of papers citing papers by Editha Andres

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Editha Andres

This figure shows the co-authorship network connecting the top 25 collaborators of Editha Andres. A scholar is included among the top collaborators of Editha Andres 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 Editha Andres. Editha Andres 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.
Fusella, M., Editha Andres, Lisa Milan, et al.. (2024). Results of 2023 survey on the use of synthetic computed tomography for magnetic resonance Imaging-only radiotherapy: Current status and future steps. Physics and Imaging in Radiation Oncology. 32. 100652–100652. 2 indexed citations
2.
Sun, Roger, Marvin Lerousseau, Alexandre Carré, et al.. (2021). Intelligence artificielle en radiothérapie : radiomique, pathomique, et prédiction de la survie et de la réponse aux traitements. Cancer/Radiothérapie. 25(6-7). 630–637. 5 indexed citations
3.
Andres, Editha, Lucas Fidon, Maria Vakalopoulou, et al.. (2019). PO-1002 Pseudo Computed Tomography generation using 3D deep learning – Application to brain radiotherapy. Radiotherapy and Oncology. 133. S553–S553. 1 indexed citations
4.
Dasouki, Majed, Salma M. Wakil, Olfat Al‐Harazi, et al.. (2019). New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia. OMICS A Journal of Integrative Biology. 24(1). 16–28. 6 indexed citations
5.
Çolak, Dilek, Ayodele Alaiya, Namik Kaya, et al.. (2016). Integrated Left Ventricular Global Transcriptome and Proteome Profiling in Human End-Stage Dilated Cardiomyopathy. PLoS ONE. 11(10). e0162669–e0162669. 43 indexed citations
6.
Wakil, Salma M., Ramesh Ram, Munish Mehta, et al.. (2016). Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs. Data in Brief. 7. 172–176.
7.
Wakil, Salma M., Ramesh Ram, Munish Mehta, et al.. (2015). A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. Atherosclerosis. 245. 62–70. 55 indexed citations
8.
Wakil, Salma M., Editha Andres, Batoul Baz, et al.. (2015). The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs. Disease Markers. 2015. 1–8. 9 indexed citations
9.
Wakil, Salma M., Asma I. Tahir, Batoul Baz, et al.. (2014). A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits. Gene. 544(2). 152–158. 33 indexed citations
10.
Wakil, Salma M., Asma I. Tahir, Batoul Baz, et al.. (2014). A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24. Disease Markers. 2014. 1–10. 17 indexed citations
11.
Tahir, Asma I., Editha Andres, Nejat Mazhar, et al.. (2013). The 3′-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits. BMC Medical Genetics. 14(1). 127–127. 6 indexed citations
12.
Tahir, Asma I., Editha Andres, Nejat Mazhar, et al.. (2013). Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population. BMC Cardiovascular Disorders. 13(1). 17–17. 23 indexed citations
13.
Alshahid, Maie, Salma M. Wakil, Editha Andres, et al.. (2013). New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3. Human Genomics. 7(1). 15–15. 16 indexed citations
14.
Wakil, Salma M., Asma I. Tahir, Nada Al Tassan, et al.. (2013). A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders. Human Genomics. 7(1). 11 indexed citations
15.
Andres, Editha, et al.. (2013). The HNF1a is a susceptibility gene for myocardial infarction and dyslipidaemia. The FASEB Journal. 27(S1). 2 indexed citations
16.
Andres, Editha, et al.. (2011). The AGT is a susceptibility gene for coronary artery disease. The FASEB Journal. 25(S1). 2 indexed citations
17.
Çolak, Dilek, et al.. (2009). Left ventricular global transcriptional profiling in human end-stage dilated cardiomyopathy. Genomics. 94(1). 20–31. 45 indexed citations
18.
Khalak, Hanif, Editha Andres, Maie Alshahid, et al.. (2009). A study of the role of the myocyte-specific enhancer factor-2A gene in coronary artery disease. Atherosclerosis. 209(1). 152–154. 22 indexed citations
19.
Dzimiri, Nduna, et al.. (2006). Differential regulation of cardiomyocyte death/survival signalling in human dilated cardiomyopathy. The FASEB Journal. 20(4). 1 indexed citations
20.
Dzimiri, Nduna, et al.. (2004). Differential functional expression of human myocardial G protein receptor kinases in left ventricular cardiac diseases. European Journal of Pharmacology. 489(3). 167–177. 94 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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