Georgia Corner

2.2k total citations
25 papers, 1.8k citations indexed

About

Georgia Corner is a scholar working on Oncology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Georgia Corner has authored 25 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Oncology, 15 papers in Molecular Biology and 13 papers in Pathology and Forensic Medicine. Recurrent topics in Georgia Corner's work include Genetic factors in colorectal cancer (13 papers), Cancer-related Molecular Pathways (5 papers) and Colorectal Cancer Treatments and Studies (4 papers). Georgia Corner is often cited by papers focused on Genetic factors in colorectal cancer (13 papers), Cancer-related Molecular Pathways (5 papers) and Colorectal Cancer Treatments and Studies (4 papers). Georgia Corner collaborates with scholars based in United States, Australia and Finland. Georgia Corner's co-authors include Leonard H. Augenlicht, John M. Mariadason, Diego Arango, Courtney Nicholas, Maria Aranes, Andrew J. Wilson, Martin Lesser, Wancai Yang, Qiuhu Shi and Anna Velcich and has published in prestigious journals such as Journal of Biological Chemistry, Gastroenterology and Cancer Research.

In The Last Decade

Georgia Corner

25 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georgia Corner United States 20 1.1k 703 347 290 252 25 1.8k
C Paraskeva United Kingdom 17 1.0k 1.0× 606 0.9× 292 0.8× 378 1.3× 346 1.4× 21 1.9k
Qihan Dong Australia 29 1.4k 1.3× 631 0.9× 190 0.5× 405 1.4× 191 0.8× 83 2.5k
Barbara G. Heerdt United States 23 1.3k 1.2× 571 0.8× 270 0.8× 381 1.3× 258 1.0× 36 2.1k
Munna L. Agarwal United States 26 1.7k 1.6× 1.1k 1.6× 353 1.0× 417 1.4× 140 0.6× 38 2.7k
Yoshihiro Sowa Japan 30 2.9k 2.7× 968 1.4× 212 0.6× 440 1.5× 210 0.8× 88 3.7k
Sébastien Cagnol Canada 15 1.5k 1.4× 489 0.7× 198 0.6× 305 1.1× 107 0.4× 17 2.3k
Francesca Tosetti Italy 23 1.1k 1.0× 502 0.7× 137 0.4× 339 1.2× 119 0.5× 48 2.0k
Ladislav Anděra Czechia 29 1.9k 1.7× 778 1.1× 190 0.5× 435 1.5× 117 0.5× 79 2.7k
Parthasarathy Chandrakesan United States 27 715 0.7× 680 1.0× 120 0.3× 301 1.0× 102 0.4× 56 1.6k

Countries citing papers authored by Georgia Corner

Since Specialization
Citations

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

Fields of papers citing papers by Georgia Corner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georgia Corner

This figure shows the co-authorship network connecting the top 25 collaborators of Georgia Corner. A scholar is included among the top collaborators of Georgia Corner 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 Georgia Corner. Georgia Corner 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
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Lee, Sze Ting, Hong Ji, David W. Greening, et al.. (2013). Global protein profiling reveals anti-EGFR monoclonal antibody 806-modulated proteins in A431 tumor xenografts. Growth Factors. 31(5). 154–164. 3 indexed citations
4.
Arango, Diego, Sheren Al-Obaidi, David S. Williams, et al.. (2012). Villin Expression Is Frequently Lost in Poorly Differentiated Colon Cancer. American Journal Of Pathology. 180(4). 1509–1521. 26 indexed citations
5.
Wilson, Andrew J., Anderly C. Chüeh, Lars Tögel, et al.. (2010). Apoptotic Sensitivity of Colon Cancer Cells to Histone Deacetylase Inhibitors Is Mediated by an Sp1/Sp3-Activated Transcriptional Program Involving Immediate-Early Gene Induction. Cancer Research. 70(2). 609–620. 96 indexed citations
6.
Wang, Donghai, Rossanna C. Pezo, Georgia Corner, et al.. (2010). Altered Dynamics of Intestinal Cell Maturation in Apc1638N/+ Mice. Cancer Research. 70(13). 5348–5357. 10 indexed citations
7.
Corner, Georgia, D. Chang, Niall C. Tebbutt, et al.. (2009). Gene expression profiling of primary and metastatic colon cancers identifies a reduced proliferative rate in metastatic tumors. Clinical & Experimental Metastasis. 27(1). 1–9. 23 indexed citations
8.
Yang, Kan, Naoto Kurihara, Kunhua Fan, et al.. (2008). Dietary Induction of Colonic Tumors in a Mouse Model of Sporadic Colon Cancer. Cancer Research. 68(19). 7803–7810. 85 indexed citations
9.
Laguinge, Luciana M., Raed Samara, Wenge Wang, et al.. (2008). DR5 Receptor Mediates Anoikis in Human Colorectal Carcinoma Cell Lines. Cancer Research. 68(3). 909–917. 40 indexed citations
10.
Chance, Mark R., Courtney Nicholas, Naseem Ahmed, et al.. (2008). Proteomic changes during intestinal cell maturation in vivo. Journal of Proteomics. 71(5). 530–546. 48 indexed citations
11.
Mariadason, John M., Courtney Nicholas, Min Zhuang, et al.. (2005). Gene expression profiling of intestinal epithelial cell maturation along the crypt-villus axis. Gastroenterology. 128(4). 1081–1088. 163 indexed citations
12.
Arango, Diego, Andrew J. Wilson, Qiuhu Shi, et al.. (2004). Molecular mechanisms of action and prediction of response to oxaliplatin in colorectal cancer cells. British Journal of Cancer. 91(11). 1931–1946. 216 indexed citations
13.
Velcich, Anna, Georgia Corner, Dharam Paul, et al.. (2004). Quantitative rather than qualitative differences in gene expression predominate in intestinal cell maturation along distinct cell lineages. Experimental Cell Research. 304(1). 28–39. 15 indexed citations
14.
Augenlicht, Leonard H., Anna Velcich, Lidija Klampfer, et al.. (2003). Application of Gene Expression Profiling to Colon Cell Maturation, Transformation and Chemoprevention. Journal of Nutrition. 133(7). 2410S–2416S. 15 indexed citations
15.
Klampfer, Lidija, Jie Huang, Georgia Corner, et al.. (2003). Oncogenic Ki-Ras Inhibits the Expression of Interferon-responsive Genes through Inhibition of STAT1 and STAT2 Expression. Journal of Biological Chemistry. 278(47). 46278–46287. 60 indexed citations
16.
Arango, Diego, John M. Mariadason, Andrew J. Wilson, et al.. (2003). c-Myc overexpression sensitises colon cancer cells to camptothecin-induced apoptosis. British Journal of Cancer. 89(9). 1757–1765. 71 indexed citations
17.
Mariadason, John M., Diego Arango, Georgia Corner, et al.. (2002). A gene expression profile that defines colon cell maturation in vitro.. PubMed. 62(16). 4791–804. 112 indexed citations
18.
Yang, Wancai, Anna Velcich, John M. Mariadason, et al.. (2001). p21(WAF1/cip1) is an important determinant of intestinal cell response to sulindac in vitro and in vivo.. PubMed. 61(16). 6297–302. 39 indexed citations
19.
Velcich, Anna, et al.. (1999). Altered phenotype of HT29 colonic adenocarcinoma cells following expression of the DCC gene. Oncogene. 18(16). 2599–2606. 29 indexed citations
20.
Augenlicht, Leonard H., et al.. (1996). Evidence for genomic instability in human colonic aberrant crypt foci.. PubMed. 12(8). 1767–72. 51 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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