John D. Lawson
#93,913
Most Influential Person Now
British engineer and physicist
John D. Lawson 's AcademicInfluence.com Rankings
John D. Lawson engineering Degrees
Engineering
#8116
World Rank
#9592
Historical Rank
Applied Physics
#3583
World Rank
#3697
Historical Rank

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Physics Engineering
Why Is John D. Lawson Influential?
(Suggest an Edit or Addition)According to Wikipedia, John David Lawson FRS was a British engineer and physicist. Early life He was born in Coventry and educated at Wolverhampton Grammar School before going on to St John's College, Cambridge, to study for the short Mechanical Sciences degree, including a special wartime radio course. He graduated BA in 1943 and then joined the Telecommunications Research Establishment, Malvern, where he was assigned to work on microwave antenna design as part of the ongoing work on development of radar.
John D. Lawson 's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Intrinsically disordered protein. (2001) (1491)
- Intrinsic disorder in cell-signaling and cancer-associated proteins. (2002) (1111)
- Intrinsic Disorder and Protein Function (2002) (994)
- Intrinsic disorder and protein function. (2002) (728)
- Protein flexibility and intrinsic disorder (2004) (312)
- DisProt: a database of protein disorder (2005) (233)
- Molecular dynamics analysis of structural factors influencing back door pi release in myosin. (2004) (53)
- Fragment-Based Discovery of a Small Molecule Inhibitor of Bruton's Tyrosine Kinase. (2015) (48)
- Structural Model of the Regulatory Domain of Smooth Muscle Heavy Meromyosin* (2003) (30)
- A Back-to-Front Fragment-Based Drug Design Search Strategy Targeting the DFG-Out Pocket of Protein Tyrosine Kinases. (2012) (21)
- Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design-Part 2. (2016) (19)
- Fragment-based drug discovery of potent and selective MKK3/6 inhibitors. (2016) (18)
- Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design-Part 1. (2016) (14)
- Isolation of chloroform-resistant mutants of filamentous phage: localization in models of phage structure. (1999) (11)
- Identification of AHCY inhibitors using novel high-throughput mass spectrometry. (2017) (9)
- Structure-based optimization of 1H-imidazole-2-carboxamides as Axl kinase inhibitors utilizing a Mer mutant surrogate. (2017) (9)
- MET Tyrosine Kinase Inhibition Enhances the Antitumor Efficacy of an HGF Antibody (2017) (7)
- Design, synthesis and optimization of 7-substituted-pyrazolo[4,3-b]pyridine ALK5 (activin receptor-like kinase 5) inhibitors. (2017) (7)
- A novel restricted photoaffinity spin-labeled non-nucleoside ATP analogue as a covalently attached reporter group of the active site of Myosin subfragment 1. (2002) (5)
- Design, synthesis and optimization of novel Alk5 (activin-like kinase 5) inhibitors. (2016) (5)
- Approaches to Kinase Homology Modeling: Successes and Considerations for the Structural Kinome (2009) (2)
- Residence time and kinetic efficiency analysis of extracellular signal-regulated kinase 2 inhibitors. (2015) (2)
- Pyridinyl and merged pyridinyltriazolonderivater (2014) (0)
- Triazolone derivatives pyridinyl and pyridinyl condensed triazolone (2014) (0)
- Corrigendum to “Isolation of Chloroform-resistant Mutants of Filamentous Phage: Localization in Models of Phage Structure [J. Mol. Biol. (1999) 287, 449–457]” (2003) (0)
- PARP complexed with benzo[1,4]oxazin-3-one inhibitor (2013) (0)
- The crystal structure of human S-adenosylhomocysteine hydrolase (AHCY) bound to benzothiazole inhibitor (2017) (0)
- ALK-5 kinase inhibitor complex (2017) (0)
- The benefit of intrinsic disorder information in neural network prediction of calmodulin binding targets (2002) (0)
- Potent, Reversible MetAP2 Inhibitors via FBDD (2016) (0)
- Potent, Reversible MetAP2 Inhibitors via Fragment Based Drug Discovery (2016) (0)
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