Rachel Lough
- Molecular Biology
- Organic Chemistry
- Computational Theory and Mathematics top 10%
- Physical and Theoretical Chemistry top 10%
- Immunology
- Co-authors
- Francis BurrowsKaren LundgrenAdeela KamalGregg TimonyDavid J. BuschMarcus F. BoehmKevin HongSrinivas Rao Kasibhatla
- Topics
- Heat shock proteins research (9 papers)Computational Drug Discovery Methods (4 papers)Protein Structure and Dynamics (2 papers)
- Partner nations
- United StatesUnited KingdomIreland
In The Last Decade
Rachel Lough
9 papers receiving 386 citations
Peers
Comparison fields: 5 of 58
- Molecular Biology 308
- Organic Chemistry 95
- Computational Theory and Mathematics 71
- Physical and Theoretical Chemistry 49
- Immunology 49
Countries citing papers authored by Rachel Lough
This map shows the geographic impact of Rachel Lough'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 Rachel Lough with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Lough more than expected).
Fields of papers citing papers by Rachel Lough
This network shows the impact of papers produced by Rachel Lough. 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 Rachel Lough. The network helps show where Rachel Lough may publish in the future.
Co-authorship network of co-authors of Rachel Lough
This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Lough. A scholar is included among the top collaborators of Rachel Lough 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 Rachel Lough. Rachel Lough is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 62 | |
| 2 | BIIB021 is a small molecule inhibitor of the heat shock protein, Hsp90, that shows potent anti-tumor activity in preclinical models | 3 |
| 3 | Synthetic Hsp90 inhibitors are active against 17-AAG-resistant tumor lines | 1 |
| 4 | 95 | |
| 5 | CNF2024 - The first clinical stage synthetic oral Hsp90 inhibitor | 1 |
| 6 | 95 | |
| 7 | 32 | |
| 8 | 50 | |
| 9 | 68 |
About Rachel Lough
Rachel Lough is a scholar working on Computational Theory and Mathematics, Small Animals and Molecular Biology, having authored 9 papers that have together received 407 indexed citations. Recurring topics across this work include Heat shock proteins research (9 papers), Computational Drug Discovery Methods (4 papers) and Protein Structure and Dynamics (2 papers). The work is most often cited by research in Toxicology (22 citations), Physical and Theoretical Chemistry (49 citations) and Computational Theory and Mathematics (71 citations). Rachel Lough has collaborated with scholars based in United States, United Kingdom and Ireland. Frequent co-authors include Francis Burrows, Karen Lundgren, Adeela Kamal, Gregg Timony, David J. Busch, Marcus F. Boehm, Kevin Hong, Srinivas Rao Kasibhatla, Lin Zhang and John Sensintaffar. Their work appears in journals such as Cancer Research, Journal of Medicinal Chemistry and International Journal of Cancer.
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.