George P. Patrinos

Orcid: 0000-0002-0519-7776

According to our database1, George P. Patrinos authored at least 16 papers between 2004 and 2022.

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

Timeline

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Links

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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
Ten simple rules for international short-term research stays.
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

Enabling pharmacogenomic services: Informatics and computational discovery aspects.
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

A set of novel mining tools for efficient biological knowledge discovery.
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
VarioML framework for comprehensive variation data representation and exchange.
BMC Bioinform., 2012

Genome-Based Population Clustering: Nuggets of Truth Buried in a Pile of Numbers?
Proceedings of the Artificial Intelligence Applications and Innovations, 2012

2011
FINDbase: a worldwide database for genetic variation allele frequencies updated.
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


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