George Stavrides

1.4k total citations
6 papers, 489 citations indexed

About

George Stavrides is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, George Stavrides has authored 6 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Surgery. Recurrent topics in George Stavrides's work include Acute Myeloid Leukemia Research (1 paper), RNA modifications and cancer (1 paper) and Genetic Associations and Epidemiology (1 paper). George Stavrides is often cited by papers focused on Acute Myeloid Leukemia Research (1 paper), RNA modifications and cancer (1 paper) and Genetic Associations and Epidemiology (1 paper). George Stavrides collaborates with scholars based in United Kingdom, Greece and Australia. George Stavrides's co-authors include David Bentley, Panos Deloukas, Pamela Whittaker, Philip J. Mason, Annemarie Poustka, G. Shashidhar Pai, T. Vulliamy, S. W. Knight, Nina S. Heiss and G.G. Lestringant and has published in prestigious journals such as Oncogene, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

George Stavrides

6 papers receiving 476 citations

Peers

George Stavrides
Keqin Zheng Canada
Swanand Hardikar United States
NP Anagnou United States
Sparkes Rs United States
Santina Acuto Italy
KarinE. Buckton United Kingdom
Skye C McIver United States
G. Bourrouillou France
P Colombiès France
Steven Schonberg United States
Keqin Zheng Canada
George Stavrides
Citations per year, relative to George Stavrides George Stavrides (= 1×) peers Keqin Zheng

Countries citing papers authored by George Stavrides

Since Specialization
Citations

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

Fields of papers citing papers by George Stavrides

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of George Stavrides

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

All Works

6 of 6 papers shown
1.
Voudris, Vassilis, Andrew T.L. Ong, Patrick W. Serruys, et al.. (2006). Sex differences and their impact on clinical outcome after percutaneous or surgical revascularisation: a report from the Arterial Revascularisation Therapies Study (ARTS).. PubMed. 2(2). 175–80. 4 indexed citations
2.
Patsalis, Philippos C., Nicos Skordis, Carolina Sismani, et al.. (2005). Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y‐chromosome instability. American Journal of Medical Genetics Part A. 135A(2). 145–149. 42 indexed citations
3.
Ke, Xiayi, Sarah Hunt, William Tapper, et al.. (2004). The impact of SNP density on fine-scale patterns of linkage disequilibrium. Human Molecular Genetics. 13(6). 577–588. 141 indexed citations
4.
Bench, Anthony J., Elisabeth P. Nacheva, Lisa French, et al.. (2000). Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. Oncogene. 19(34). 3902–3913. 112 indexed citations
5.
Knight, S. W., Nina S. Heiss, T. Vulliamy, et al.. (1999). X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene. The American Journal of Human Genetics. 65(1). 50–58. 187 indexed citations
6.

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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