George V. Z. Dedoussis
Department of Dietetics-Nutrition
Harokopio University
17671 Athens
Greece
Name/email consistency: high
- An age-dependent diet-modified effect of the PPARγ Pro12Ala polymorphism in children. Dedoussis, G.V., Manios, Y., Kourlaba, G., Kanoni, S., Lagou, V., Butler, J., Papoutsakis, C., Scott, R.A., Yannakoulia, M., Pitsiladis, Y.P., Hirschhorn, J.N., Lyon, H.N. Metab. Clin. Exp. (2011)
- Expression of inflammatory molecules and associations with BMI in children. Dedoussis, G.V., Kapiri, A., Samara, A., Dimitriadis, D., Lambert, D., Pfister, M., Siest, G., Visvikis-Siest, S. Eur. J. Clin. Invest. (2010)
- Dairy intake associates with the IGF rs680 polymorphism to height variation in periadolescent children. Dedoussis, G.V., Louizou, E., Papoutsakis, C., Skenderi, K.P., Yannakoulia, M. Eur. J. Clin. Nutr (2010)
- Adipokine expression in adipose tissue and in peripheral blood mononuclear cells in children Correlation with BMI and fatty acid content. Dedoussis, G.V., Kapiri, A., Kalogeropoulos, N., Samara, A., Dimitriadis, D., Lambert, D., Pfister, M., Siest, G., Visvikis-Siest, S. Clin. Chim. Acta (2009)
- Peroxisome proliferator-activated receptor-gamma (PPARgamma) Pro12Ala polymorphism and risk for pediatric obesity. Dedoussis, G.V., Vidra, N., Butler, J., Papoutsakis, C., Yannakoulia, M., Hirschhorn, J.N., Lyon, H.N. Clin. Chem. Lab. Med. (2009)
- Mediterranean diet and plasma concentration of inflammatory markers in old and very old subjects in the ZINCAGE population study. Dedoussis, G.V., Kanoni, S., Mariani, E., Cattini, L., Herbein, G., Fulop, T., Varin, A., Rink, L., Jajte, J., Monti, D., Marcellini, F., Malavolta, M., Mocchegiani, E. Clin. Chem. Lab. Med. (2008)
- Age-dependent dichotomous effect of superoxide dismutase Ala16Val polymorphism on oxidized LDL levels. Dedoussis, G.V., Kanoni, S., Panagiotakos, D.B., Louizou, E., Grigoriou, E., Chrysohoou, C., Pitsavos, C., Stefanadis, C. Exp. Mol. Med. (2008)
- Co-inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney disease. Dedoussis, G.V., Luo, Y., Starremans, P., Rossetti, S., Ramos, A.J., Cantiello, H.F., Katsareli, E., Ziroyannis, P., Lamnissou, K., Harris, P.C., Zhou, J. Eur. J. Clin. Invest. (2008)
- Apolipoprotein polymorphisms and familial hypercholesterolemia. Dedoussis, G.V. Pharmacogenomics (2007)
- The Pro12Ala polymorphism in PPARgamma2 gene affects lipid parameters in Greek primary school children: A case of gene-to-gender interaction. Dedoussis, G.V., Theodoraki, E.V., Manios, Y., Yiannakouris, N., Panagiotakos, D., Papoutsakis, C., Skenderi, K., Zampelas, A. Am. J. Med. Sci. (2007)
- Cholesteryl ester-transfer protein (CETP) polymorphism and the association of acute coronary syndromes by obesity status in Greek subjects: the CARDIO2000-GENE study. Dedoussis, G.V., Panagiotakos, D.B., Louizou, E., Mantoglou, I., Chrysohoou, C., Lamnisou, K., Pitsavos, C., Stefanadis, C. Hum. Hered. (2007)
- Human gene mutations. Gene symbol: SLC3A1. Disease: cystinuria. Dedoussis, G., Louzou, E., Michelekakis, H., Komianou, F., di Perna, M., Bisceglia, L. Hum. Genet. (2007)
- Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia. Dedoussis, G.V., Maumus, S., Skoumas, J., Choumerianou, D.M., Pitsavos, C., Stefanadis, C., Visvikis-Siest, S. J. Clin. Lab. Anal. (2006)
- Different genes and polymorphisms affecting high-density lipoprotein cholesterol levels in Greek familial hypercholesterolemia patients. Dedoussis, G.V., Maumus, S., Choumerianou, D.M., Skoumas, J., Pitsavos, C., Stefanadis, C., Visvikis-Siest, S. Genet. Test. (2006)
- Wilson disease: high prevalence in a mountainous area of Crete. Dedoussis, G.V., Genschel, J., Sialvera, T.E., Bochow, B., Manolaki, N., Manios, Y., Tsafantakis, E., Schmidt, H. Ann. Hum. Genet. (2005)
- Antiatherogenic effect of Pistacia lentiscus via GSH restoration and downregulation of CD36 mRNA expression. Dedoussis, G.V., Kaliora, A.C., Psarras, S., Chiou, A., Mylona, A., Papadopoulos, N.G., Andrikopoulos, N.K. Atherosclerosis (2004)
- FH clinical phenotype in Greek patients with LDL-R defective vs. negative mutations. Dedoussis, G.V., Skoumas, J., Pitsavos, C., Choumerianou, D.M., Genschel, J., Schmidt, H., Stefanadis, C. Eur. J. Clin. Invest. (2004)
- The IL-6 gene G-174C polymorphism related to health indices in Greek primary school children. Dedoussis, G.V., Manios, Y., Choumerianou, D.M., Yiannakouris, N., Panagiotakos, D.B., Skenderi, K., Zampelas, A. Obes. Res. (2004)
- FH-Pyrgos: a novel mutation in the promoter (-45delT) of the low-density lipoprotein receptor gene associated with familial hypercholesterolemia. Dedoussis, G.V., Pitsavos, C., Kelberman, D., Skoumas, J., Prassa, M.E., Choumerianou, D.M., Stefanadis, C., Humphries, S.E., Toutouzas, P. Clin. Genet. (2003)
- Inverse correlation of plasma leptin and soluble transferrin receptor levels in beta-thalassemia patients. Dedoussis, G.V., Kyrtsonis, M.C., Andrikopoulos, N.E., Voskaridou, E., Loutradis, A. Ann. Hematol. (2002)
- Glutathione depletion restores the susceptibility of cisplatin-resistant chronic myelogenous leukemia cell lines to Natural Killer cell-mediated cell death via necrosis rather than apoptosis. Dedoussis, G.V., Andrikopoulos, N.K. Eur. J. Cell Biol. (2001)
- HbF production in beta thalassaemia heterozygotes for the IVS-II-1 G-->A beta(0)-globin mutation. Implication of the haplotype and the (G)gamma-158 C-->T mutation on the HbF level. Dedoussis, G.V., Mandilara, G.D., Boussiu, M., Loutradis, A. Am. J. Hematol. (2000)
- Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVS-1 nt 110 (G-->A) beta+ thalassemia: a case study. Dedoussis, G.V., Sinopoulou, K., Gyparaki, M., Loutradis, A. Eur. J. Haematol. (2000)
- Endogenous interleukin 6 conveys resistance to cis-diamminedichloroplatinum-mediated apoptosis of the K562 human leukemic cell line. Dedoussis, G.V., Mouzaki, A., Theodoropoulou, M., Menounos, P., Kyrtsonis, M.C., Karameris, A., Maniatis, A. Exp. Cell Res. (1999)
- Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVSII-745 (C-->G) beta+ thalassemia: a case study. Dedoussis, G.V., Sinopoulou, K., Gyparaki, M., Loutradis, A. Am. J. Hematol. (1999)