Patrinos GP - Search Results

1

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

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

Association study of human VN1R1 pheromone receptor gene alleles and gender.

Mitropoulos C, Papachatzopoulou A, Menounos PG, Kolonelou C, Pappa M, Bertolis G, Gerou S, Patrinos GP. Mitropoulos C, et al. Among authors: patrinos gp. Genet Test. 2007 Summer;11(2):128-32. doi: 10.1089/gte.2006.0516. Genet Test. 2007. PMID: 17627382

4

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.

5

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software.

Zaimidou S, van Baal S, Smith TD, Mitropoulos K, Ljujic M, Radojkovic D, Cotton RG, Patrinos GP. Zaimidou S, et al. Among authors: patrinos gp. Hum Mutat. 2009 Mar;30(3):308-13. doi: 10.1002/humu.20857. Hum Mutat. 2009. PMID: 19021233

6

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

7

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.

8

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.

9

First report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic population.

Georgitsi M, Papachatzopoulou A, Linardaki E, Maroulis V, Papadakis MN, Patrinos GP. Georgitsi M, et al. Among authors: patrinos gp. Hemoglobin. 2011;35(1):91-5. doi: 10.3109/03630269.2011.549071. Hemoglobin. 2011. PMID: 21250887

10

Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobin.

Papachatzopoulou A, Patrinos GP. Papachatzopoulou A, et al. Among authors: patrinos gp. Hemoglobin. 2011;35(2):135-41. doi: 10.3109/03630269.2011.553019. Hemoglobin. 2011. PMID: 21417570

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