Fernanda Borges

Orcid: 0000-0003-1050-2402

According to our database1, Fernanda Borges authored at least 9 papers between 2007 and 2019.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of five.

Timeline

Legend:

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Bibliography

2019
CompScore: Boosting Structure-Based Virtual Screening Performance by Incorporating Docking Scoring Function Components into Consensus Scoring.
J. Chem. Inf. Model., 2019

2015
Harmonization of QSAR Best Practices and Molecular Docking Provides an Efficient Virtual Screening Tool for Discovering New G-Quadruplex Ligands.
J. Chem. Inf. Model., 2015

2013
Classifier Ensemble Based on Feature Selection and Diversity Measures for Predicting the Affinity of A<sub>2B</sub> Adenosine Receptor Antagonists.
J. Chem. Inf. Model., 2013

2011
Two New Parameters Based on Distances in a Receiver Operating Characteristic Chart for the Selection of Classification Models.
J. Chem. Inf. Model., 2011

Jointly Handling Potency and Toxicity of Antimicrobial Peptidomimetics by Simple Rules from Desirability Theory and Chemoinformatics.
J. Chem. Inf. Model., 2011

2010
Unified QSAR & network-based computational chemistry approach to antimicrobials. II. Multiple distance and triadic census analysis of antiparasitic drugs complex networks.
J. Comput. Chem., 2010

2008
Desirability-based multiobjective optimization for global QSAR studies: Application to the design of novel NSAIDs with improved analgesic, antiinflammatory, and ulcerogenic profiles.
J. Comput. Chem., 2008

2007
Computational chemistry development of a unified free energy Markov model for the distribution of 1300 chemicals to 38 different environmental or biological systems.
J. Comput. Chem., 2007

Computational chemistry approach for the early detection of drug-induced idiosyncratic liver toxicity.
J. Comput. Chem., 2007


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