Patrinos GP - Search Results

1

The cypriot and Iranian National Mutation Frequency Databases.

Kleanthous M, Patsalis PC, Drousiotou A, Motazacker M, Christodoulou K, Cariolou M, Baysal E, Khrizi K, Moghimi B, Pourfarzad F, van Baal S, Deltas C, Najmabadi H, Patrinos GP. Kleanthous M, et al. Among authors: patrinos gp. Hum Mutat. 2006 Jun;27(6):598-9. doi: 10.1002/humu.9422. Hum Mutat. 2006. PMID: 16705699

2

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.

Hardison RC, Chui DH, Giardine B, Riemer C, Patrinos GP, Anagnou N, Miller W, Wajcman H. Hardison RC, et al. Among authors: patrinos gp. Hum Mutat. 2002 Mar;19(3):225-33. doi: 10.1002/humu.10044. Hum Mutat. 2002. PMID: 11857738

3

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

Patrinos GP, van Baal S, Petersen MB, Papadakis MN. Patrinos GP, et al. Hum Mutat. 2005 Apr;25(4):327-33. doi: 10.1002/humu.20157. Hum Mutat. 2005. PMID: 15776445

4

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.

Patrinos GP, Kollia P, Papadakis MN. Patrinos GP, et al. Hum Mutat. 2005 Nov;26(5):399-412. doi: 10.1002/humu.20225. Hum Mutat. 2005. PMID: 16138310 Review.

5

National and ethnic mutation databases: recording populations' genography.

Patrinos GP. Patrinos GP. Hum Mutat. 2006 Sep;27(9):879-87. doi: 10.1002/humu.20376. Hum Mutat. 2006. PMID: 16868936

6

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.

van Baal S, Kaimakis P, Phommarinh M, Koumbi D, Cuppens H, Riccardino F, Macek M Jr, Scriver CR, Patrinos GP. van Baal S, et al. Among authors: patrinos gp. Nucleic Acids Res. 2007 Jan;35(Database issue):D690-5. doi: 10.1093/nar/gkl934. Epub 2006 Nov 28. Nucleic Acids Res. 2007. PMID: 17135191 Free PMC article.

7

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Giardine B, van Baal S, Kaimakis P, Riemer C, Miller W, Samara M, Kollia P, Anagnou NP, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: patrinos gp. Hum Mutat. 2007 Feb;28(2):206. doi: 10.1002/humu.9479. Hum Mutat. 2007. PMID: 17221864

8

Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database.

Zlotogora J, van Baal S, Patrinos GP. Zlotogora J, et al. Among authors: patrinos gp. Hum Mutat. 2007 Oct;28(10):944-9. doi: 10.1002/humu.20551. Hum Mutat. 2007. PMID: 17492749

9

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

10

An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.

Lederer CW, Basak AN, Aydinok Y, Christou S, El-Beshlawy A, Eleftheriou A, Fattoum S, Felice AE, Fibach E, Galanello R, Gambari R, Gavrila L, Giordano PC, Grosveld F, Hassapopoulou H, Hladka E, Kanavakis E, Locatelli F, Old J, Patrinos GP, Romeo G, Taher A, Traeger-Synodinos J, Vassiliou P, Villegas A, Voskaridou E, Wajcman H, Zafeiropoulos A, Kleanthous M. Lederer CW, et al. Among authors: patrinos gp. Hemoglobin. 2009;33(3):163-76. doi: 10.1080/03630260903089177. Hemoglobin. 2009. PMID: 19657830

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