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American Journal of Hematology|January 25, 2006
Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysisAdamantia Papachatzopoulou, Panagiotis G Menounos, Christina Kolonelou, et al.
Human Genomics|November 27, 2012
Association of genome variations in the renin-angiotensin system with physical performanceArgyro Sgourou, Vassilis Fotopoulos, Vassilis Kontos, et al.
British Journal of Haematology|March 11, 2004
Thalassaemia mutations within the 5'UTR of the human beta-globin gene disrupt transcriptionArgyro Sgourou, Samantha Routledge, Michael Antoniou, et al.
Human Genomics|December 12, 2019
The multi-faceted functioning portrait of LRF/ZBTB7ACaterina Constantinou, Magda Spella, Vasiliki Chondrou, et al.
European Journal of Haematology|March 8, 2006
Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermediaAdamantia Papachatzopoulou, Alexandra Kourakli, Panagiota Makropoulou, et al.
Hemoglobin|January 22, 2011
First report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic populationMarianthi Georgitsi, Adamantia Papachatzopoulou, Emmanouella Linardaki, et al.
Hemoglobin|July 21, 2010
Region-specific genetic heterogeneity of HBB mutation distribution in South-Western GreeceAdamantia Papachatzopoulou, Alexandra Kourakli, Eleana F Stavrou, et al.
Pharmacogenomics|August 27, 2014
Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patientsAikaterini Gravia, Vasiliki Chondrou, Argyro Sgourou, et al.
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