C. Stavropoulou

GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates

S. Zachaki, A. Daraki, E. Polycarpou, 2017, American Journal of Perinatology.

Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A313G germline polymorphism and chromosomal abnormalities

S. Zachaki, A. Daraki, C. Stavropoulou, 2014, Leukemia & lymphoma.

Association of A313G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome

E. Kanavakis, G. Pantelias, T. Koromila, 2013, Leukemia & lymphoma.

Characterising Long Covid: a living systematic review update with controlled studies

P. Olliaro, I. Shemilt, C. Hastie, 2022, medRxiv.

High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.

E. Kanavakis, D. Koumbi, P. Kollia, 2013, Leukemia research.

polymorphism in MDS/AML with trisomy 8

E. Kanavakis, D. Koumbi, P. Kollia, 2013 .

Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis

D. Koumbi, P. Kollia, S. Zachaki, 2015, The International journal of neuroscience.

The C609T inborn polymorphism in NAD(P)H:quinone oxidoreductase 1 is associated with susceptibility to multiple sclerosis and affects the risk of development of the primary progressive form of the disease.

G. Terzoudi, G. Pantelias, S. Zachaki, 2011, Free radical biology & medicine.