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Expert Opinion on Drug Discovery|March 14, 2013
Design of chemical libraries for screeningHugo O Villar, Mark R HansenCurrent Topics in Medicinal Chemistry|September 28, 2007
Computational techniques in fragment based drug discoveryHugo O Villar, Mark R HansenCurrent Opinion in Drug Discovery & Development|April 28, 2009
Mining and visualizing the chemical content of large databasesHugo O Villar, Mark R HansenJournal of Chemical Information and Modeling|October 9, 2013
Development of an informatics platform for therapeutic protein and peptide analyticsMark R Hansen, Hugo O Villar, Eric FeyfantCurrent Computer-Aided Drug Design|February 4, 2021
Molecular Diversity Assessment using ChemotypesHugo O Villar, Raghav Mandayan, Mark R HansenCurrent Opinion in Chemical Biology|August 4, 2004
Using NMR for ligand discovery and optimizationHugo O Villar, Jiangli Yan, Mark R HansenJournal of Medicinal Chemistry|October 14, 2005
Ring systems in mutagenicity databasesRichard Kho, Jason A Hodges, Mark R Hansen, et al.Journal of Proteome Research|December 25, 2003
Genome-wide profile of oxidoreductases in viruses, prokaryotes, and eukaryotesRichard Kho, Joseph V Newman, Richard M Jack, et al.Proteins|February 11, 2003
A path from primary protein sequence to ligand recognitionRichard Kho, Brian L Baker, Joseph V Newman, et al.Drug Discovery Today|January 28, 2003
Chemoproteomics as a basis for post-genomic drug discoveryPaul Beroza, Hugo O Villar, Michael M Wick, et al.Pageof 2