Mitchell Hull

5.4k total citations · 2 hit papers
26 papers, 3.2k citations indexed

About

Mitchell Hull is a scholar working on Molecular Biology, Infectious Diseases and Cell Biology. According to data from OpenAlex, Mitchell Hull has authored 26 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Infectious Diseases and 5 papers in Cell Biology. Recurrent topics in Mitchell Hull's work include Ubiquitin and proteasome pathways (4 papers), Protein Degradation and Inhibitors (4 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Mitchell Hull is often cited by papers focused on Ubiquitin and proteasome pathways (4 papers), Protein Degradation and Inhibitors (4 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Mitchell Hull collaborates with scholars based in United States, France and United Kingdom. Mitchell Hull's co-authors include R. Marc Learned, Makoto Makishima, Kevin D. Lustig, Bei Shan, David J. Mangelsdorf, Joyce J. Repa, Hua Tu, Peter Coward, Jürgen M. Lehmann and Emily Chen and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Mitchell Hull

25 papers receiving 3.1k citations

Hit Papers

Identification of a Nuclear Receptor for Bile Acids 1999 2026 2008 2017 1999 2020 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitchell Hull United States 14 1.6k 1.3k 1.0k 637 427 26 3.2k
Claudio D’Amore Italy 29 854 0.5× 918 0.7× 482 0.5× 455 0.7× 307 0.7× 72 2.4k
María J. Monte Spain 36 2.1k 1.3× 1.1k 0.9× 1.2k 1.1× 814 1.3× 167 0.4× 115 3.8k
Gyan Chandra United States 8 1.8k 1.1× 898 0.7× 1.1k 1.0× 594 0.9× 340 0.8× 8 2.6k
Maria Chiara Monti Italy 32 702 0.4× 1.1k 0.9× 413 0.4× 444 0.7× 253 0.6× 134 2.7k
María A. Serrano Spain 33 1.6k 1.0× 825 0.7× 797 0.8× 427 0.7× 87 0.2× 103 3.1k
Rocı́o I.R. Macı́as Spain 39 2.4k 1.5× 1.3k 1.0× 1.4k 1.3× 581 0.9× 82 0.2× 143 4.3k
Genta Kakiyama United States 26 640 0.4× 1.3k 1.0× 607 0.6× 969 1.5× 89 0.2× 64 2.4k
Nicholas Murgolo United States 30 787 0.5× 1.8k 1.4× 1.5k 1.4× 476 0.7× 299 0.7× 64 4.3k
Valentina Sepe Italy 26 713 0.4× 638 0.5× 367 0.4× 318 0.5× 178 0.4× 72 1.9k
Péter Krajcsi Hungary 32 1.7k 1.0× 1.3k 1.0× 283 0.3× 246 0.4× 695 1.6× 92 3.2k

Countries citing papers authored by Mitchell Hull

Since Specialization
Citations

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

Fields of papers citing papers by Mitchell Hull

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitchell Hull

This figure shows the co-authorship network connecting the top 25 collaborators of Mitchell Hull. A scholar is included among the top collaborators of Mitchell Hull 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 Mitchell Hull. Mitchell Hull 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.
Smith, Emery, Meredith E. Davis-Gardner, Rubén D. Garcia-Ordoñez, et al.. (2023). High throughput screening for drugs that inhibit 3C-like protease in SARS-CoV-2. SLAS DISCOVERY. 28(3). 95–101. 13 indexed citations
2.
Tärning, Joel, Aurélie Fricot, Pablo Gamallo, et al.. (2023). Safe drugs with high potential to block malaria transmission revealed by a spleen-mimetic screening. Nature Communications. 14(1). 1951–1951. 7 indexed citations
3.
Chen, Emily, et al.. (2023). A covalent inhibitor of the YAP–TEAD transcriptional complex identified by high-throughput screening. RSC Chemical Biology. 4(11). 894–905. 3 indexed citations
4.
Grzelak, Edyta M., et al.. (2023). Pharmacological inhibition of CLK2 activates YAP by promoting alternative splicing of AMOTL2. eLife. 12. 1 indexed citations
5.
Tran, Tuan Anh, Siying Zhu, Seung‐Hyuk Choi, et al.. (2021). A small molecule UPR modulator for diabetes identified by high throughput screening. Acta Pharmaceutica Sinica B. 11(12). 3983–3993. 11 indexed citations
6.
Kitamura, Seiya, Natalia Milosevich, Joshua N. Asiaban, et al.. (2021). Chemical Inhibition of ENL/AF9 YEATS Domains in Acute Leukemia. ACS Central Science. 7(5). 815–830. 63 indexed citations
7.
Shalhout, Sophia Z., Pengyu Yang, Edyta M. Grzelak, et al.. (2021). YAP-dependent proliferation by a small molecule targeting annexin A2. Nature Chemical Biology. 17(7). 767–775. 44 indexed citations
8.
Kitamura, Seiya, Qinheng Zheng, Jordan L. Woehl, et al.. (2020). Sulfur(VI) Fluoride Exchange (SuFEx)-Enabled High-Throughput Medicinal Chemistry. Journal of the American Chemical Society. 142(25). 10899–10904. 152 indexed citations breakdown →
9.
Rice, Christopher A., Beatrice L. Colon, Emily Chen, Mitchell Hull, & Dennis E. Kyle. (2020). Discovery of repurposing drug candidates for the treatment of diseases caused by pathogenic free-living amoebae. PLoS neglected tropical diseases. 14(9). e0008353–e0008353. 45 indexed citations
10.
Smith, Emery, Meredith E. Davis-Gardner, Rubén D. Garcia-Ordoñez, et al.. (2020). High-Throughput Screening for Drugs That Inhibit Papain-Like Protease in SARS-CoV-2. SLAS DISCOVERY. 25(10). 1152–1161. 38 indexed citations
11.
Wall, Gina, Emily Chen, Mitchell Hull, & José L. López-Ribot. (2020). Screening the CALIBR ReFRAME Library in Search for Inhibitors of Candida auris Biofilm Formation. Frontiers in Cellular and Infection Microbiology. 10. 597931–597931. 11 indexed citations
12.
Kim, Yu-Jin, Beatrice Cubitt, Emily Chen, et al.. (2019). The ReFRAME library as a comprehensive drug repurposing library to identify mammarenavirus inhibitors. Antiviral Research. 169. 104558–104558. 25 indexed citations
13.
Xu, Zhengren, Shiming Fang, Malina A. Bakowski, et al.. (2019). Discovery of Kirromycins with Anti-Wolbachia Activity from Streptomyces sp. CB00686. ACS Chemical Biology. 14(6). 1174–1182. 6 indexed citations
14.
Janes, Jeff, Emily Chen, Nicole H. Rogers, et al.. (2018). The ReFRAME library as a comprehensive drug repurposing library and its application to the treatment of cryptosporidiosis. Proceedings of the National Academy of Sciences. 115(42). 10750–10755. 125 indexed citations
15.
Choi, Seung Hyuk, Sang Jun Lee, Mitchell Hull, et al.. (2017). Targeted Disruption of Myc–Max Oncoprotein Complex by a Small Molecule. ACS Chemical Biology. 12(11). 2715–2719. 52 indexed citations
16.
Lee, Sang Jun, Huafei Zou, Elizabeth Chao, et al.. (2017). A Novel Role for RARα Agonists as Apolipoprotein CIII Inhibitors Identified from High Throughput Screening. Scientific Reports. 7(1). 5824–5824. 12 indexed citations
17.
Mietton, Flore, Elena Ferri, Danièle Maubon, et al.. (2017). Selective BET bromodomain inhibition as an antifungal therapeutic strategy. Nature Communications. 8(1). 15482–15482. 35 indexed citations
18.
Liu, Tao, Yi Yan, Ying Wang, et al.. (2014). Rational Design of CXCR4 Specific Antibodies with Elongated CDRs. Journal of the American Chemical Society. 136(30). 10557–10560. 31 indexed citations
19.
Rines, Daniel R., Buu P. Tu, Loren Miraglia, et al.. (2006). High‐Content Screening of Functional Genomic Libraries. Methods in enzymology on CD-ROM/Methods in enzymology. 414. 530–565. 16 indexed citations
20.
Makishima, Makoto, Joyce J. Repa, Hua Tu, et al.. (1999). Identification of a Nuclear Receptor for Bile Acids. Science. 284(5418). 1362–1365. 2206 indexed citations breakdown →

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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