Gregory B. Craven

613 total citations
17 papers, 397 citations indexed

About

Gregory B. Craven is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Gregory B. Craven has authored 17 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Organic Chemistry and 3 papers in Oncology. Recurrent topics in Gregory B. Craven's work include Click Chemistry and Applications (8 papers), Chemical Synthesis and Analysis (6 papers) and Protein Degradation and Inhibitors (3 papers). Gregory B. Craven is often cited by papers focused on Click Chemistry and Applications (8 papers), Chemical Synthesis and Analysis (6 papers) and Protein Degradation and Inhibitors (3 papers). Gregory B. Craven collaborates with scholars based in United Kingdom, United States and Italy. Gregory B. Craven's co-authors include Alan Armstrong, Jack Taunton, Christopher R. Jones, Dominic P. Affron, Adolfo Cuesta, Rhodri M. L. Morgan, Sotiris Amillis, Edward W. Tate, Emmanuel Mikros and Yilmaz Alguel and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Gregory B. Craven

17 papers receiving 395 citations

Peers

Countries citing papers authored by Gregory B. Craven

Since Specialization

Citations

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

Fields of papers citing papers by Gregory B. Craven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory B. Craven. 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 Gregory B. Craven. The network helps show where Gregory B. Craven may publish in the future.

Co-authorship network of co-authors of Gregory B. Craven

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	The structure of KRAS ^G12C bound to divarasib highlights features of potent switch-II pocket engagement 2024 ·Small GTPases ·(unknown), Gregory B. Craven, Kevan M. Shokat	2
2	Mutant-selective AKT inhibition through lysine targeting and neo-zinc chelation 2024 ·Nature ·Gregory B. Craven, Hang Chu, Jessica D. Sun, Jordan D. Carelli, (unknown), (unknown), Ying Chen, Xiaolei Ma, Subhamoy Das, (unknown), (unknown), Kaiping Yang, Steeve Reisberg, Peter A. Thompson, J. Russell Lipford, Jack Taunton	9
3	Aminomethyl Salicylaldehydes Lock onto a Surface Lysine by Forming an Extended Intramolecular Hydrogen Bond Network 2024 ·Journal of the American Chemical Society ·(unknown), Gregory B. Craven, (unknown), (unknown), Jack Taunton	6
4	Direct mapping of ligandable tyrosines and lysines in cells with chiral sulfonyl fluoride probes 2023 ·Nature Chemistry ·Ying Chen, Gregory B. Craven, Roarke A. Kamber, Adolfo Cuesta, (unknown), Yurii S. Moroz, Michael C. Bassik, Jack Taunton	41
5	Acrylamide fragment inhibitors that induce unprecedented conformational distortions in enterovirus 71 3C and SARS-CoV-2 main protease 2022 ·Acta Pharmaceutica Sinica B ·Bo Qin, Gregory B. Craven, Pengjiao Hou, (unknown), (unknown), Emma S. Child, Rhodri M. L. Morgan, Wenchao Niu, Lina Zhao, Alan Armstrong, David J. Mann, Sheng Cui	7
6	CRISPR-based oligo recombineering prioritizes apicomplexan cysteines for drug discovery 2022 ·Nature Microbiology ·(unknown), Marko Storch, (unknown), (unknown), Fábio K. Tamaki, (unknown), (unknown), (unknown), Natalie Wiedemar, Gregory B. Craven, Beatriz Baragaña, Susan Wyllie, Jake Baum, Geoff Baldwin, Eranthie Weerapana, Edward W. Tate, Matthew A. Child	14
7	Unexpected structures formed by the kinase RET C634R mutant extracellular domain suggest potential oncogenic mechanisms in MEN2A 2022 ·Journal of Biological Chemistry ·(unknown), Orquídea Ribeiro, Outi Haapanen, Gregory B. Craven, Vivek Sharma, Stephen P. Muench, Adrian Goldman	1
8	Reversible lysine-targeted probes reveal residence time-based kinase selectivity 2022 ·Nature Chemical Biology ·Tangpo Yang, Adolfo Cuesta, Xiaobo Wan, Gregory B. Craven, Brad Hirakawa, (unknown), (unknown), John C. Kath, John D. Lapek, Sherry Niessen, Alma L. Burlingame, Jordan D. Carelli, Jack Taunton	63
9	Identification of the first structurally validated covalent ligands of the small GTPase RAB27A 2021 ·RSC Medicinal Chemistry ·(unknown), Thomas Lanyon‐Hogg, (unknown), Gregory B. Craven, (unknown), Elena De Vita, (unknown), Inmaculada Pérez‐Dorado, (unknown), (unknown), Rhodri M. L. Morgan, (unknown), Jim C. Norman, Alan Armstrong, David J. Mann, Ernesto Cota, Edward W. Tate	9
10	Synthesis and Configurational Assignment of Vinyl Sulfoximines and Sulfonimidamides 2021 ·The Journal of Organic Chemistry ·Gregory B. Craven, Edward L. Briggs, (unknown), (unknown), (unknown), Dominic P. Affron, (unknown), (unknown), (unknown), Renzo Luisi, James A. Bull, Alan Armstrong	20
11	Quantitative Irreversible Tethering (qIT) for Target-directed Covalent Fragment Screening 2020 ·BIO-PROTOCOL ·Gregory B. Craven, David J. Mann, Alan Armstrong	1
12	Multiparameter Kinetic Analysis for Covalent Fragment Optimization by Using Quantitative Irreversible Tethering (qIT) 2020 ·ChemBioChem ·Gregory B. Craven, Dominic P. Affron, (unknown), (unknown), (unknown), Chun‐Ting Liu, Rhodri M. L. Morgan, Alan Armstrong, (unknown)	16
13	Intramolecular hydride transfer onto arynes: redox-neutral and transition metal-free C(sp³)–H functionalization of amines 2018 ·Chemical Science ·(unknown), (unknown), Gregory B. Craven, Christopher R. Jones	44
14	High‐Throughput Kinetic Analysis for Target‐Directed Covalent Ligand Discovery 2018 ·Angewandte Chemie International Edition ·Gregory B. Craven, Dominic P. Affron, (unknown), (unknown), Joe G. Greener, Rhodri M. L. Morgan, Edward W. Tate, Alan Armstrong, (unknown)	56
15	Vinyl sulfonamide synthesis for irreversible tethering via a novel α-selenoether protection strategy 2018 ·MedChemComm ·Gregory B. Craven, Dominic P. Affron, (unknown), (unknown), Alan Armstrong	4
16	High‐Throughput Kinetic Analysis for Target‐Directed Covalent Ligand Discovery 2018 ·Angewandte Chemie ·Gregory B. Craven, Dominic P. Affron, (unknown), (unknown), Joe G. Greener, Rhodri M. L. Morgan, Edward W. Tate, Alan Armstrong, (unknown)	6
17	Structure of eukaryotic purine/H+ symporter UapA suggests a role for homodimerization in transport activity 2016 ·Nature Communications ·Yilmaz Alguel, Sotiris Amillis, James Leung, George Lambrinidis, Stefano Capaldi, (unknown), Gregory B. Craven, So Iwata, Alan Armstrong, Emmanuel Mikros, George Diallinas, Alexander D. Cameron, Bernadette Byrne	98

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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