Aphrodite Loutradi‐Anagnostou

The molecular heterogeneity of β-thalassemia in Greece

Marina Boussiou, Photini Karababa, Klio Sinopoulou et al. · Blood Cells Molecules and Diseases · 2007 · 39 citations

Medicine, Genetics, Molecular Genetics +7

The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [Aγ–158C→T] results from two independent gene conversion events

George P. Patrinos, Panagoula Κollia, Aphrodite Loutradi‐Anagnostou et al. · Human Genetics · 1998 · 38 citations

Life Sciences, Genetics, Molecular Genetics +7

‘Silent’β‐thalassaemia caused by a ‘silent’β‐chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia

Phaedon Fessas, Dimitris Loukopoulos, Aphrodite Loutradi‐Anagnostou et al. · British Journal of Haematology · 1982 · 35 citations

Life Sciences, Genetics, Hematology +10

Gγ-196 C→T, Aγ-201 C→T: Two novel mutations in the promoter region of the γ-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece

Magdalini Tasiopoulou, Marina Boussiou, Klio Sinopoulou et al. · Blood Cells Molecules and Diseases · 2007 · 24 citations

Medicine, Genetics, Molecular Genetics +12

A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes

Manoussos N. Papadakis, George P. Patrinos, Panayotis Tsaftaridis et al. · Journal of Molecular Medicine · 2001 · 24 citations

Life Sciences, Genetics, Molecular Genetics +13