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Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey.
Genomics. 2012 Aug;100(2):93-101. doi: 10.1016/j.ygeno.2012.05.009. Epub 2012 May 30.
Genomics. 2012.
PMID: 22659238
Free article.
Introducing dAUTObase: a first step towards the global scale geoepidemiology of autoimmune syndromes and diseases.
Gkantouna VA, Kambouris ME, Viennas ES, Ioannou ZM, Paraskevas M, Lagoumintzis G, Zagoriti Z, Patrinos GP, Tzimas GE, Poulas K.
Gkantouna VA, et al. Among authors: viennas es.
Bioinformatics. 2015 Feb 15;31(4):581-6. doi: 10.1093/bioinformatics/btu690. Epub 2014 Oct 20.
Bioinformatics. 2015.
PMID: 25332376
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FINDbase: a worldwide database for genetic variation allele frequencies updated.
Georgitsi M, Viennas E, Antoniou DI, Gkantouna V, van Baal S, Petricoin EF 3rd, Poulas K, Tzimas G, Patrinos GP.
Georgitsi M, et al. Among authors: viennas e.
Nucleic Acids Res. 2011 Jan;39(Database issue):D926-32. doi: 10.1093/nar/gkq1236. Epub 2010 Nov 27.
Nucleic Acids Res. 2011.
PMID: 21113021
Free PMC article.
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Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase.
Georgitsi M, Viennas E, Gkantouna V, Christodoulopoulou E, Zagoriti Z, Tafrali C, Ntellos F, Giannakopoulou O, Boulakou A, Vlahopoulou P, Kyriacou E, Tsaknakis J, Tsakalidis A, Poulas K, Tzimas G, Patrinos GP.
Georgitsi M, et al. Among authors: viennas e.
Pharmacogenomics. 2011 Jan;12(1):49-58. doi: 10.2217/pgs.10.169.
Pharmacogenomics. 2011.
PMID: 21174622
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Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Papadopoulos P, Viennas E, Gkantouna V, Pavlidis C, Bartsakoulia M, Ioannou ZM, Ratbi I, Sefiani A, Tsaknakis J, Poulas K, Tzimas G, Patrinos GP.
Papadopoulos P, et al. Among authors: viennas e.
Nucleic Acids Res. 2014 Jan;42(Database issue):D1020-6. doi: 10.1093/nar/gkt1125. Epub 2013 Nov 14.
Nucleic Acids Res. 2014.
PMID: 24234438
Free PMC article.
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DruGeVar: an online resource triangulating drugs with genes and genomic biomarkers for clinical pharmacogenomics.
Dalabira E, Viennas E, Daki E, Komianou A, Bartsakoulia M, Poulas K, Katsila T, Tzimas G, Patrinos GP.
Dalabira E, et al. Among authors: viennas e.
Public Health Genomics. 2014;17(5-6):265-71. doi: 10.1159/000365895. Epub 2014 Sep 9.
Public Health Genomics. 2014.
PMID: 25228099
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Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Viennas E, Komianou A, Mizzi C, Stojiljkovic M, Mitropoulou C, Muilu J, Vihinen M, Grypioti P, Papadaki S, Pavlidis C, Zukic B, Katsila T, van der Spek PJ, Pavlovic S, Tzimas G, Patrinos GP.
Viennas E, et al.
Nucleic Acids Res. 2017 Jan 4;45(D1):D846-D853. doi: 10.1093/nar/gkw949. Epub 2016 Oct 18.
Nucleic Acids Res. 2017.
PMID: 27924022
Free PMC article.
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Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Giardine B, Borg J, Viennas E, Pavlidis C, Moradkhani K, Joly P, Bartsakoulia M, Riemer C, Miller W, Tzimas G, Wajcman H, Hardison RC, Patrinos GP.
Giardine B, et al. Among authors: viennas e.
Nucleic Acids Res. 2014 Jan;42(Database issue):D1063-9. doi: 10.1093/nar/gkt911. Epub 2013 Oct 16.
Nucleic Acids Res. 2014.
PMID: 24137000
Free PMC article.
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