James P. Edwards - Concepedia

Author

James P. Edwards

Also Known As

Edwards, J. P., Edwards, James P., J P Edwards, J. EDWARDS, J. Edwards, J. P. EDWARDS, J. P. Edwards, J.P. EDWARDS, J.P. Edwards, James Edwards

203

Publications

Citations

H-Index

115

Concepts

All Affiliations

Johnson & Johnson (United States)Janssen (United States)Ligand Pharmaceuticals (United States)Janssen (Belgium)University of Illinois Urbana-Champaign

About

James P. Edwards is an author at Johnson & Johnson (United States) specializing in pharmacology, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	45	1.8K
2	Natural Sciences	20	30	1.3K
3	Engineering	14	14	982
4	Allergy	4	4	450
5	Health Sciences	1	1	55

James P. Edwards

Publications

4.7K

Citations

H-Index

Page 1

	Year	Citations
Polygonal Eyewalls, Asymmetric Eye Contraction, and Potential Vorticity Mixing in Hurricanes Wayne H. Schubert, Michael T. Montgomery, Richard K. Taft, Journal of the Atmospheric Sciences	1999	417
A Potent and Selective Histamine H4 Receptor Antagonist with Anti-Inflammatory Properties Robin L. Thurmond, Pragnya J. Desai, Paul J. Dunford, Journal of Pharmacology and Experimental Therapeutics	2004	349
Histamine H<sub>4</sub> receptor mediates eosinophil chemotaxis with cell shape change and adhesion molecule upregulation Ping Ling, Karen Ngo, Steven Nguyen, British Journal of Pharmacology Allergy MedicineMast Cell DisorderImmunologyMast Cell DegranulationEosinophilic Disorder	2004	263
Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes Scott E. Denmark, Robert A. Stavenger, Anne‐Marie Faucher, The Journal of Organic Chemistry Inorganic ChemistryChemical EngineeringEngineeringAlkene MetathesisCoordination Complex	1997	241
A comparison of (chloromethyl)- and (iodomethyl)zinc cyclopropanation reagents Scott E. Denmark, James P. Edwards The Journal of Organic Chemistry HalogenationInorganic ChemistryEngineeringHeterocyclicChemical Analysis	1991	226
The First Potent and Selective Non-Imidazole Human Histamine H<sub>4</sub>Receptor Antagonists Jill A. Jablonowski, Cheryl A. Grice, Wenying Chai, Journal of Medicinal Chemistry Pharmaceutical ScienceDrug TargetPotential LeadPharmacotherapyChemical Biology	2003	195
Preparation of Chiral Bisoxazolines: Observations on the Effect of Substituents Scott E. Denmark, Noriyuki Nakajima, O. J.‐C. NICAISE, The Journal of Organic Chemistry Molecular SciencesChemical MeasurementChemical AnalysisSubstituentsscott E. DenmarkAltmetric Attention Score	1995	151
Synthesis and Biological Activity of a Novel Series of Nonsteroidal, Peripherally Selective Androgen Receptor Antagonists Derived from 1,2-Dihydropyridono[5,6-<i>g</i>]quinolines Lawrence G. Hamann, Robert I. Higuchi, Lin Zhi, Journal of Medicinal Chemistry PharmacotherapyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryBiological Activity	1998	142
Preparation and Biological Evaluation of Indole, Benzimidazole, and Thienopyrrole Piperazine Carboxamides: Potent Human Histamine H<sub>4</sub>Antagonists Jennifer D. Venable, Hui Cai, Wenying Chai, Journal of Medicinal Chemistry Pharmaceutical SciencePharmacotherapyChemical BiologyPharmaceutical ChemistryMedicinal Chemistry	2005	107
Anti-Inflammatory Activity of a Potent, Selective Leukotriene A4 Hydrolase Inhibitor in Comparison with the 5-Lipoxygenase Inhibitor Zileuton Navin Rao, Paul J. Dunford, Xiaohua Xue, Journal of Pharmacology and Experimental Therapeutics	2007	90

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