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| 0 | -- | 0 | Philippe E. Thomas, Roman Klinger, Laura Inés Furlong, Martin Hofmann-Apitius, Christoph M. Friedrich. Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers |
| 0 | -- | 0 | Emidio Capriotti, Russ B. Altman. Improving the prediction of disease-related variants using protein three-dimensional structure |
| 0 | -- | 0 | José M. G. Izarzugaza, Lisa E. M. Hopcroft, Anja Baresic, Christine A. Orengo, Andrew C. R. Martin, Alfonso Valencia. Characterization of pathogenic germline mutations in human Protein Kinases |
| 0 | -- | 0 | Jeroen F. J. Laros, André Blavier, Johan T. den Dunnen, Peter E. M. Taschner. A formalized description of the standard human variant nomenclature in Extended Backus-Naur Form |
| 0 | -- | 0 | Alexandre Riazanov, Jonas Laurila Bergman, Christopher J. O. Baker. Deploying mutation impact text-mining software with the SADI Semantic Web Services framework |