George P. Patrinos
Orcid: 0000-0002-0519-7776
According to our database1,
George P. Patrinos
authored at least 16 papers
between 2004 and 2022.
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Bibliography
2022
A formalization of one of the main claims of "Cost-effectiveness analysis of pharmacogenomics-guided clopidogrel treatment in Spanish patients undergoing percutaneous coronary intervention" by Fragoulakis et al. 20191.
Data Sci., 2022
2021
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Nucleic Acids Res., 2021
2017
PLoS Comput. Biol., 2017
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Nucleic Acids Res., 2017
2015
Introducing dAUTObase: a first step towards the global scale geoepidemiology of autoimmune syndromes and diseases.
Bioinform., 2015
Proceedings of the 15th IEEE International Conference on Bioinformatics and Bioengineering, 2015
2014
Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Nucleic Acids Res., 2014
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Nucleic Acids Res., 2014
Artif. Intell. Rev., 2014
Information technology meets pharmacogenomics: Design specifications of an integrated personalized pharmacogenomics information system.
Proceedings of IEEE-EMBS International Conference on Biomedical and Health Informatics, 2014
2012
BMC Bioinform., 2012
Proceedings of the Artificial Intelligence Applications and Innovations, 2012
2011
Nucleic Acids Res., 2011
2008
Development of a universal, flexible and freely available database management system for gene-centered data collection, curation and display of DNA variation.
Proceedings of the 8th IEEE International Conference on Bioinformatics and Bioengineering, 2008
2007
FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.
Nucleic Acids Res., 2007
2004
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.
Nucleic Acids Res., 2004