Mairead Young

593 total citations
8 papers, 399 citations indexed

About

Mairead Young is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Mairead Young has authored 8 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Organic Chemistry and 3 papers in Pharmacology. Recurrent topics in Mairead Young's work include Microbial Natural Products and Biosynthesis (2 papers), PI3K/AKT/mTOR signaling in cancer (2 papers) and Click Chemistry and Applications (1 paper). Mairead Young is often cited by papers focused on Microbial Natural Products and Biosynthesis (2 papers), PI3K/AKT/mTOR signaling in cancer (2 papers) and Click Chemistry and Applications (1 paper). Mairead Young collaborates with scholars based in United States and China. Mairead Young's co-authors include Judy Lucas, Mark Tischler, Carolyn Discafani, Minu Dutia, Karen Miller, Fei Ye, Biqi Wu, Jennifer M. Weber, Diane H. Boschelli and Jay Gibbons and has published in prestigious journals such as Journal of Medicinal Chemistry, Journal of Natural Products and Organic Process Research & Development.

In The Last Decade

Mairead Young

8 papers receiving 386 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mairead Young United States 8 239 148 86 79 59 8 399
Naoki Teno Japan 15 218 0.9× 133 0.9× 156 1.8× 72 0.9× 19 0.3× 52 561
Jonathan L. Doty United States 8 315 1.3× 172 1.2× 78 0.9× 17 0.2× 60 1.0× 11 563
Stephanos Ioannidis United States 13 181 0.8× 125 0.8× 123 1.4× 42 0.5× 12 0.2× 20 370
Ian Bruce United Kingdom 8 390 1.6× 244 1.6× 49 0.6× 21 0.3× 27 0.5× 10 614
Laura Capolongo Italy 15 378 1.6× 171 1.2× 199 2.3× 107 1.4× 39 0.7× 34 599
Christophe Henry France 12 160 0.7× 100 0.7× 158 1.8× 54 0.7× 18 0.3× 25 459
Grace E. Munie United States 14 212 0.9× 95 0.6× 204 2.4× 43 0.5× 30 0.5× 17 478
Masaki Gouda Japan 9 235 1.0× 49 0.3× 85 1.0× 37 0.5× 13 0.2× 11 385
Stephen C. Yabut United States 10 210 0.9× 205 1.4× 37 0.4× 50 0.6× 20 0.3× 14 417
Cyrille Kuhn United States 13 245 1.0× 135 0.9× 128 1.5× 25 0.3× 16 0.3× 15 456

Countries citing papers authored by Mairead Young

Since Specialization
Citations

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

Fields of papers citing papers by Mairead Young

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mairead Young

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

All Works

8 of 8 papers shown
1.
Liu, Hongbo, Bradley Haltli, Xidong Feng, et al.. (2009). Rapid Cloning and Heterologous Expression of the Meridamycin Biosynthetic Gene Cluster Using a Versatile Escherichia coli−Streptomyces Artificial Chromosome Vector, pSBAC. Journal of Natural Products. 72(3). 389–395. 51 indexed citations
2.
Ayral‐Kaloustian, Semiramis, Jianxin Gu, Judy Lucas, et al.. (2009). Hybrid Inhibitors of Phosphatidylinositol 3-Kinase (PI3K) and the Mammalian Target of Rapamycin (mTOR): Design, Synthesis, and Superior Antitumor Activity of Novel Wortmannin−Rapamycin Conjugates. Journal of Medicinal Chemistry. 53(1). 452–459. 42 indexed citations
3.
Koehn, Frank E., Donald R. Kirsch, Xidong Feng, Jeffrey E. Janso, & Mairead Young. (2008). A Cell Wall-Active Lipopeptide from the Fungus Pochonia bulbillosa. Journal of Natural Products. 71(12). 2045–2048. 7 indexed citations
4.
Zask, Arie, Joshua A. Kaplan, Lourdes Toral‐Barza, et al.. (2008). Synthesis and Structure–Activity Relationships of Ring-Opened 17-Hydroxywortmannins: Potent Phosphoinositide 3-Kinase Inhibitors with Improved Properties and Anticancer Efficacy. Journal of Medicinal Chemistry. 51(5). 1319–1323. 30 indexed citations
5.
Nikitenko, Antonia A., Deborah A. Evrard, Annmarie L. Sabb, et al.. (2007). First Scale-Up: Problems and Resolutions on the Synthesis of WAY-253752, a Novel, Dual-Acting SSRI/5HT1A Antagonist. Organic Process Research & Development. 12(1). 76–80. 22 indexed citations
6.
Kerns, Edward H., Li Di, Jonathan A. Gross, et al.. (2005). Integrity Profiling of High Throughput Screening Hits Using LC-MS and Related Techniques. Combinatorial Chemistry & High Throughput Screening. 8(6). 459–466. 8 indexed citations
7.
Boschelli, Diane H., Fei Ye, Yanong D. Wang, et al.. (2001). Optimization of 4-Phenylamino-3-quinolinecarbonitriles as Potent Inhibitors of Src Kinase Activity. Journal of Medicinal Chemistry. 44(23). 3965–3977. 179 indexed citations
8.
Patel, Dinesh V., Eric M. Gordon, Robert J. Schmidt, et al.. (1995). Phosphinyl Acid-Based Bisubstrate Analog Inhibitors of Farnesyl Protein Transferase. Journal of Medicinal Chemistry. 38(3). 435–442. 60 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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