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Whole genome sequencing in pharmacogenomics.
Katsila T, Patrinos GP. Katsila T, et al. Among authors: patrinos gp. Front Pharmacol. 2015 Mar 26;6:61. doi: 10.3389/fphar.2015.00061. eCollection 2015. Front Pharmacol. 2015. PMID: 25859217 Free PMC article.
Success stories in genomic medicine from resource-limited countries.
Mitropoulos K, Al Jaibeji H, Forero DA, Laissue P, Wonkam A, Lopez-Correa C, Mohamed Z, Chantratita W, Lee MT, Llerena A, Brand A, Ali BR, Patrinos GP. Mitropoulos K, et al. Among authors: patrinos gp. Hum Genomics. 2015 Jun 18;9(1):11. doi: 10.1186/s40246-015-0033-3. Hum Genomics. 2015. PMID: 26081768 Free PMC article.
Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients.
Chalikiopoulou C, Tavianatou AG, Sgourou A, Kourakli A, Kelepouri D, Chrysanthakopoulou M, Kanelaki VK, Mourdoukoutas E, Siamoglou S, John A, Symeonidis A, Ali BR, Katsila T, Papachatzopoulou A, Patrinos GP. Chalikiopoulou C, et al. Among authors: patrinos gp. Pharmacogenomics. 2016 Mar;17(4):393-403. doi: 10.2217/pgs.16.1. Epub 2016 Feb 19. Pharmacogenomics. 2016. PMID: 26895070
Pharmacometabolomics Informs Viromics toward Precision Medicine.
Balasopoulou A, Patrinos GP, Katsila T. Balasopoulou A, et al. Among authors: patrinos gp. Front Pharmacol. 2016 Oct 27;7:411. doi: 10.3389/fphar.2016.00411. eCollection 2016. Front Pharmacol. 2016. PMID: 27833560 Free PMC article.
Novel genetic risk variants for pediatric celiac disease.
Balasopoulou A, Stanković B, Panagiotara A, Nikčevic G, Peters BA, John A, Mendrinou E, Stratopoulos A, Legaki AI, Stathakopoulou V, Tsolia A, Govaris N, Govari S, Zagoriti Z, Poulas K, Kanariou M, Constantinidou N, Krini M, Spanou K, Radlovic N, Ali BR, Borg J, Drmanac R, Chrousos G, Pavlovic S, Roma E, Zukic B, Patrinos GP, Katsila T. Balasopoulou A, et al. Among authors: patrinos gp. Hum Genomics. 2016 Oct 24;10(1):34. doi: 10.1186/s40246-016-0091-1. Hum Genomics. 2016. PMID: 27836013 Free PMC article.
Key Pharmacogenomic Considerations for Sickle Cell Disease Patients.
Kolliopoulou A, Stratopoulos A, Siamoglou S, Sgourou A, Ali BR, Papachatzopoulou A, Katsila T, Patrinos GP. Kolliopoulou A, et al. Among authors: patrinos gp. OMICS. 2017 Jun;21(6):314-322. doi: 10.1089/omi.2017.0058. Epub 2017 May 9. OMICS. 2017. PMID: 28486096
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients.
Chondrou V, Kolovos P, Sgourou A, Kourakli A, Pavlidaki A, Kastrinou V, John A, Symeonidis A, Ali BR, Papachatzopoulou A, Katsila T, Patrinos GP. Chondrou V, et al. Among authors: patrinos gp. Hum Genomics. 2017 Oct 23;11(1):24. doi: 10.1186/s40246-017-0120-8. Hum Genomics. 2017. PMID: 29061162 Free PMC article.
336 results