Patrinos GP - Search Results

1

Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.

Gravia A, Chondrou V, Sgourou A, Papantoni I, Borg J, Katsila T, Papachatzopoulou A, Patrinos GP. Gravia A, et al. Among authors: patrinos gp. Pharmacogenomics. 2014 Jul;15(10):1355-64. doi: 10.2217/pgs.14.101. Pharmacogenomics. 2014. PMID: 25155936 Review.

2

Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysis.

Papachatzopoulou A, Menounos PG, Kolonelou C, Patrinos GP. Papachatzopoulou A, et al. Among authors: patrinos gp. Am J Hematol. 2006 Feb;81(2):136-8. doi: 10.1002/ajh.20580. Am J Hematol. 2006. PMID: 16432873 Free article.

3

Increased gamma-globin gene expression in beta-thalassemia intermedia patients correlates with a mutation in 3'HS1.

Papachatzopoulou A, Kaimakis P, Pourfarzad F, Menounos PG, Evangelakou P, Kollia P, Grosveld FG, Patrinos GP. Papachatzopoulou A, et al. Among authors: patrinos gp. Am J Hematol. 2007 Nov;82(11):1005-9. doi: 10.1002/ajh.20979. Am J Hematol. 2007. PMID: 17654503 Free article.

4

Genetic recombination as a major cause of mutagenesis in the human globin gene clusters.

Borg J, Georgitsi M, Aleporou-Marinou V, Kollia P, Patrinos GP. Borg J, et al. Among authors: patrinos gp. Clin Biochem. 2009 Dec;42(18):1839-50. doi: 10.1016/j.clinbiochem.2009.07.014. Epub 2009 Jul 22. Clin Biochem. 2009. PMID: 19631200 Review.

5

Pharmacogenomics: paving the path to personalized medicine.

Patrinos GP, Innocenti F. Patrinos GP, et al. Pharmacogenomics. 2010 Feb;11(2):141-6. doi: 10.2217/pgs.09.174. Pharmacogenomics. 2010. PMID: 20136354

6

Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease.

Voutsinas GE, Stavrou EF, Karousos G, Dasoula A, Papachatzopoulou A, Syrrou M, Verkerk AJ, van der Spek P, Patrinos GP, Stöger R, Athanassiadou A. Voutsinas GE, et al. Among authors: patrinos gp. Hum Mutat. 2010 Jun;31(6):685-91. doi: 10.1002/humu.21248. Hum Mutat. 2010. PMID: 20340137

7

Genetic databases and their potential in pharmacogenomics.

Lagoumintzis G, Poulas K, Patrinos GP. Lagoumintzis G, et al. Among authors: patrinos gp. Curr Pharm Des. 2010;16(20):2224-31. doi: 10.2174/138161210791792804. Curr Pharm Des. 2010. PMID: 20459387 Review.

8

Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece.

Papachatzopoulou A, Kourakli A, Stavrou EF, Fragou E, Vantarakis A, Patrinos GP, Athanassiadou A. Papachatzopoulou A, et al. Among authors: patrinos gp. Hemoglobin. 2010;34(4):333-42. doi: 10.3109/03630269.2010.486354. Hemoglobin. 2010. PMID: 20642331

9

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.

Borg J, Papadopoulos P, Georgitsi M, Gutiérrez L, Grech G, Fanis P, Phylactides M, Verkerk AJ, van der Spek PJ, Scerri CA, Cassar W, Galdies R, van Ijcken W, Ozgür Z, Gillemans N, Hou J, Bugeja M, Grosveld FG, von Lindern M, Felice AE, Patrinos GP, Philipsen S. Borg J, et al. Among authors: patrinos gp. Nat Genet. 2010 Sep;42(9):801-5. doi: 10.1038/ng.630. Epub 2010 Aug 1. Nat Genet. 2010. PMID: 20676099 Free PMC article.

10

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Patrinos GP, Al Aama J, Al Aqeel A, Al-Mulla F, Borg J, Devereux A, Felice AE, Macrae F, Marafie MJ, Petersen MB, Qi M, Ramesar RS, Zlotogora J, Cotton RG. Patrinos GP, et al. Hum Mutat. 2011 Jan;32(1):2-9. doi: 10.1002/humu.21397. Hum Mutat. 2011. PMID: 21089065 Free PMC article.

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