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Emmanouil Viennas
Researcher at University of Patras
Publications - 31
Citations - 573
Emmanouil Viennas is an academic researcher from University of Patras. The author has contributed to research in topics: Population & Mobile device. The author has an hindex of 9, co-authored 30 publications receiving 513 citations. Previous affiliations of Emmanouil Viennas include RMIT University & American Hotel & Lodging Educational Institute.
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Journal ArticleDOI
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Belinda Giardine,Joseph Borg,Emmanouil Viennas,Cristiana Pavlidis,Kamran Moradkhani,Philippe Joly,Marina Bartsakoulia,Cathy Riemer,Webb Miller,Giannis Tzimas,Henri Wajcman,Ross C. Hardison,George P. Patrinos +12 more
TL;DR: These updates significantly enriched the database content and querying potential, enhanced the database profile and data quality and broadened the inter-relation of HbVar with other databases, which should increase the already high impact of this resource to the globin and genetic database community.
Journal ArticleDOI
Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase.
Marianthi Georgitsi,Emmanouil Viennas,Vassiliki Gkantouna,Elena Christodoulopoulou,Zoi Zagoriti,Christina Tafrali,Fotios Ntellos,Olga Giannakopoulou,Athanassia Boulakou,Panagiota Vlahopoulou,Eva Kyriacou,John Tsaknakis,A. Tsakalidis,Konstantinos Poulas,Giannis Tzimas,George P. Patrinos +15 more
TL;DR: FINDbase-PGx is a comprehensive database, which, unlike other pharmacogenomic knowledgebases, fulfills the much needed requirement to systematically document pharmacogenome allelic frequencies in various populations and ethnic groups worldwide.
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Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies
Petros Papadopoulos,Emmanouil Viennas,Vassiliki Gkantouna,Cristiana Pavlidis,Marina Bartsakoulia,Zafeiria-Marina Ioannou,Ilham Ratbi,Abdelaziz Sefiani,John Tsaknakis,Konstantinos Poulas,Giannis Tzimas,George P. Patrinos +11 more
TL;DR: In addition to the regular data content updates, significant developments in FINDbase are reported, related to data visualization and querying, data submission, interrelation with other resources and a new module for genetic disease summaries.
Journal ArticleDOI
FINDbase: a worldwide database for genetic variation allele frequencies updated
Marianthi Georgitsi,Emmanouil Viennas,Dimitris Antoniou,Vassiliki Gkantouna,Sjozef van Baal,Emanuel F. Petricoin,Konstantinos Poulas,Giannis Tzimas,George P. Patrinos +8 more
TL;DR: Frequency of INherited Disorders database (FIND base) records frequencies of causative genetic variations worldwide, and reports the establishment of the first database journal, by affiliating FINDbase with Human Genomics and Proteomics, a new open-access scientific journal.
Journal ArticleDOI
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Emmanouil Viennas,Angeliki Komianou,Clint Mizzi,Clint Mizzi,Maja Stojiljkovic,Christina Mitropoulou,Juha Muilu,Mauno Vihinen,Panagiota Grypioti,Styliani Papadaki,Cristiana Pavlidis,Branka Zukic,Theodora Katsila,Peter J. van der Spek,Sonja Pavlovic,Giannis Tzimas,George P. Patrinos,George P. Patrinos +17 more
TL;DR: FINDbase as discussed by the authors is a comprehensive data repository that records the prevalence of clinically relevant genomic variants in various populations worldwide, such as pathogenic variants leading mostly to monogenic disorders and pharmacogenomics biomarkers.