Christopher Korch

3.7k total citations · 1 hit paper
52 papers, 3.0k citations indexed

About

Christopher Korch is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Christopher Korch has authored 52 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 14 papers in Oncology and 10 papers in Genetics. Recurrent topics in Christopher Korch's work include Fungal and yeast genetics research (10 papers), Cancer-related Molecular Pathways (6 papers) and Epigenetics and DNA Methylation (6 papers). Christopher Korch is often cited by papers focused on Fungal and yeast genetics research (10 papers), Cancer-related Molecular Pathways (6 papers) and Epigenetics and DNA Methylation (6 papers). Christopher Korch collaborates with scholars based in United States, Sweden and Australia. Christopher Korch's co-authors include Adrie van Bokhoven, Gary J. Miller, Per Hagblom, Marileila Varella‐Garcia, M. Scott Lucia, Heidi L. Miller, Rebecca E. Schweppe, Widya Johannes, Steven K. Nordeen and Andeŕs S. Byström and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Christopher Korch

52 papers receiving 3.0k citations

Hit Papers

Molecular characterization of human prostate carcinoma ce... 2003 2026 2010 2018 2003 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Korch United States 28 1.9k 795 503 445 442 52 3.0k
Marc Navre United States 31 1.9k 1.0× 1.3k 1.7× 1.0k 2.1× 369 0.8× 217 0.5× 49 3.8k
José M. Silva Spain 30 2.6k 1.3× 744 0.9× 756 1.5× 103 0.2× 138 0.3× 55 3.8k
Hidetoshi Sumimoto Japan 28 1.7k 0.9× 1.1k 1.4× 253 0.5× 196 0.4× 191 0.4× 55 3.1k
D. Joshua Liao United States 27 1.6k 0.8× 640 0.8× 663 1.3× 80 0.2× 168 0.4× 111 2.6k
Robin Humphreys United States 29 1.5k 0.8× 903 1.1× 367 0.7× 89 0.2× 147 0.3× 55 2.2k
C. Hanski Germany 34 2.2k 1.1× 1.1k 1.4× 262 0.5× 111 0.2× 184 0.4× 89 3.7k
Luke A. Selth Australia 31 1.9k 1.0× 456 0.6× 1.2k 2.3× 149 0.3× 977 2.2× 81 3.0k
Gregory S. Buzard United States 26 1.4k 0.7× 624 0.8× 677 1.3× 57 0.1× 463 1.0× 54 2.6k
Hsiang‐Fu Kung Hong Kong 38 3.4k 1.7× 866 1.1× 1.4k 2.8× 104 0.2× 204 0.5× 80 4.6k
Yingqiu Xie Kazakhstan 27 1.1k 0.6× 505 0.6× 300 0.6× 105 0.2× 399 0.9× 80 2.0k

Countries citing papers authored by Christopher Korch

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Korch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Korch

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Korch. A scholar is included among the top collaborators of Christopher Korch 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 Christopher Korch. Christopher Korch 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.
Landa, Iñigo, Nikita Pozdeyev, Christopher Korch, et al.. (2019). Comprehensive Genetic Characterization of Human Thyroid Cancer Cell Lines: A Validated Panel for Preclinical Studies. Clinical Cancer Research. 25(10). 3141–3151. 130 indexed citations
2.
Schweppe, Rebecca E., Nikita Pozdeyev, Laura A. Pike, et al.. (2019). Establishment and Characterization of Four Novel Thyroid Cancer Cell Lines and PDX Models Expressing the RET/PTC1 Rearrangement, BRAFV600E, or RASQ61R as Drivers. Molecular Cancer Research. 17(5). 1036–1048. 12 indexed citations
3.
Vaughan, Liwen, Wolfgang Glänzel, Christopher Korch, & Amanda Capes‐Davis. (2017). Widespread Use of Misidentified Cell Line KB (HeLa): Incorrect Attribution and Its Impact Revealed through Mining the Scientific Literature. Cancer Research. 77(11). 2784–2788. 50 indexed citations
4.
Nasarre, Patrick, Robert M. Gemmill, Vincent Potiron, et al.. (2013). Neuropilin-2 Is Upregulated in Lung Cancer Cells during TGF-β1–Induced Epithelial–Mesenchymal Transition. Cancer Research. 73(23). 7111–7121. 55 indexed citations
5.
Baturin, Dmitry, et al.. (2013). Inhibition of Wee1 Sensitizes Cancer Cells to Antimetabolite Chemotherapeutics In Vitro and In Vivo , Independent of p53 Functionality. Molecular Cancer Therapeutics. 12(12). 2675–2684. 106 indexed citations
6.
Handschy, Anne V., et al.. (2013). Transcription Factor Ets1 Cooperates with Estrogen Receptor α to Stimulate Estradiol-Dependent Growth in Breast Cancer Cells and Tumors. PLoS ONE. 8(7). e68815–e68815. 19 indexed citations
7.
Dong, Xiaoyun, et al.. (2012). RAP1GAP inhibits cytoskeletal remodeling and motility in thyroid cancer cells. Endocrine Related Cancer. 19(4). 575–588. 18 indexed citations
8.
Bozkaya, Giray, Peyda Korhan, Esra Erdal, et al.. (2012). Cooperative interaction of MUC1 with the HGF/c-Met pathway during hepatocarcinogenesis. Molecular Cancer. 11(1). 64–64. 62 indexed citations
9.
Korch, Christopher, Monique A. Spillman, Twila A. Jackson, et al.. (2012). DNA profiling analysis of endometrial and ovarian cell lines reveals misidentification, redundancy and contamination. Gynecologic Oncology. 127(1). 241–248. 209 indexed citations
10.
Pitts, Todd M., Aik Choon Tan, Gillian N. Kulikowski, et al.. (2010). Development of an Integrated Genomic Classifier for a Novel Agent in Colorectal Cancer: Approach to Individualized Therapy in Early Development. Clinical Cancer Research. 16(12). 3193–3204. 56 indexed citations
11.
Wittenburg, Luke A., et al.. (2010). The histone deacetylase inhibitor valproic acid sensitizes human and canine osteosarcoma to doxorubicin. Cancer Chemotherapy and Pharmacology. 67(1). 83–92. 55 indexed citations
12.
Schweppe, Rebecca E., Joshua Klopper, Christopher Korch, et al.. (2008). Deoxyribonucleic Acid Profiling Analysis of 40 Human Thyroid Cancer Cell Lines Reveals Cross-Contamination Resulting in Cell Line Redundancy and Misidentification. The Journal of Clinical Endocrinology & Metabolism. 93(11). 4331–4341. 490 indexed citations
13.
Naeem, Rizwan, et al.. (2007). A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma. Genes Chromosomes and Cancer. 46(9). 805–812. 27 indexed citations
14.
Gemmill, Robert M., Ming Zhou, Luciano J. Costa, et al.. (2005). Synergistic growth inhibition by Iressa and Rapamycin is modulated by VHL mutations in renal cell carcinoma. British Journal of Cancer. 92(12). 2266–2277. 44 indexed citations
15.
Bokhoven, Adrie van, Marileila Varella‐Garcia, Christopher Korch, et al.. (2003). Molecular characterization of human prostate carcinoma cell lines. The Prostate. 57(3). 205–225. 513 indexed citations breakdown →
16.
Bokhoven, Adrie van, Marileila Varella‐Garcia, Christopher Korch, Daphne Hessels, & Gary J. Miller. (2001). Widely used prostate carcinoma cell lines share common origins. The Prostate. 47(1). 36–51. 68 indexed citations
17.
Korch, Christopher & Harry A. Drabkin. (1999). Improved DNA Sequencing Accuracy and Detection of Heterozygous Alleles Using Manganese Citrate and Different Fluorescent Dye Terminators. Genome Research. 9(6). 588–595. 14 indexed citations
18.
Korch, Christopher, et al.. (1997). Cloning Heterologous Genes: Problems and Approaches. Fungal Genetics and Biology. 21(3). 292–301. 7 indexed citations
19.
Byström, Andeŕs S., et al.. (1993). The general amivno acid control regulates MET4, which encodes a methionine‐pathway‐specific transcriptional activator of Saccharomyces cerevisiae. Molecular Microbiology. 9(1). 221–223. 3 indexed citations
20.
Byström, Andeŕs S., et al.. (1993). The general amino acid control regulates MET4, which encodes a methionine‐pathway‐specific transcriptional activator of Saccharomyces cerevisiae. Molecular Microbiology. 7(2). 215–228. 35 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

Rankless by CCL
2026