Selection of Recent Peer-Review Journal Publications

• Terzoudi G.I., Manola K.N., Pantelias G.E., Iliakis G., Checkpoint abrogation in G2 compromises repair of chromosomal breaks in ataxia telangiectasia cells. Cancer Research, 65(24):11292-6, 2005.
• Terzoudi G.I. and Pantelias G.E., Cytogenetic methods for biodosimetry and risk individualization after exposure to ionising radiation. Radiation Protection Dosimetry, 122(1-4):513-20, 2006.
• Stavropoulou C., Sambani C., Rigana H., Georgakakos V.N., Voutsinas G., Manola K.N., Pantelias G.E., Makropoulos V. Low frequency of the glutathione-S-transferase T1-null genotype in patients with primary myelodysplastic syndrome and 5q deletion. Leukemia,22(8):1643-6, 2008.
• Manola K.N., Georgakakos V.N., Stavropoulou C., Spyridonidis A., Angelopoulou M.K., Vlachadami I., Katsigiannis A., Roussou P., Pantelias G.E., Sambani C. Jumping translocations in hematological malignancies: A cytogenetic study of five cases. Cancer Genetics and Cytogenetics, 187(2):85-94, 2008.
• Terzoudi G.I., Singh S.K., Pantelias G.E., Iliakis G., Premature Chromosome Condensation Reveals DNA-PK Independent Pathways of Chromosome Break Repair. International Journal of Oncology, 33:871-879, 2008.
• Crescenzi B., La Starza R., Sambani C., Parcharidou A., Pierini V., Nofrini V., Brandimarte L., Matteucci C., Aversa F., Martelli M.F., Mecucci C. Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome. Br J Haematol, 144(1):116-9, 2009.
• Manola K.N. Cytogenetics of pediatric acute myeloid leukemia. Eur J Haematol, 83(5):391-405, 2009.
• Pantelias G.E., Terzoudi G.I., Functional cell-cycle chromatin conformation changes in the presence of DNA damage result into chromatid breaks: A new insight in the formation of radiation-induced chromosomal aberrations based on the direct observation of interphase chromatin. Mutat Res, 701(1):27-37, 2010.
• Terzoudi G.I., Donta-Bakoyianni C., Iliakis G., Pantelias G.E., Investigation of bystander effects in hybrid cells by means of cell fusion and premature chromosome condensation induction. Radiat Res. 173(6):789-801, 2010.
• Ximeri M., Galanopoulos A., Klaus M., Parcharidou A., Giannikou K., Psyllaki M., Symeonidis A., Pappa V., Kartasis Z., Liapi D., Hatzimichael E., Kokoris S., Korkolopoulou P., Sambani C., Pontikoglou C., Papadaki H.A., Hellenic MDS Study Group. Effect of lenalidomide therapy on hematopoiesis of patients with myelodysplastic syndrome associated with chromosome 5q deletion. Haematologica, 95(3):406-14, 2010.
• La Starza R., Matteucci C., Gorello P., Brandimarte L., Pierini V., Crescenzi B., Nofrini V., Rosati R., Gottardi E., Saglio G., Santucci A., Berchicci L., Arcioni F., Falini B., Martelli M.F., Sambani C., Aventin A., Mecucci C. NPM1 deletion is associated with gross chromosomal rearrangements in leukemia. PLoS One, 5(9):12855, 2010.
• Karakosta M., Tsakiridou A., Korantzis I., Manola K.N. Deletion of 5q as a rare abnormality in chronic lymphocytic leukemia. Cancer Genetics and Cytogenetics, 15:175-9, 2010.
• Stavropoulou C., Zachaki S., Alexoudi A., Chatzi I., Georgakakos V.N., Terzoudi G.I., Pantelias G.E., Karageorgiou C.E., Sambani C. 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. Free Radic Biol Med, 51(3):713-8, 2011.
• Terzoudi G.I., Hatzi V.I., Donta-Bakoyianni C., Pantelias G.E. Chromatin dynamics during cell cycle mediate conversion of DNA damage into chromatid breaks and affect formation of chromosomal aberrations: Biological and clinical significance. Mutation Research, 3;711(1-2):174-86, 2011.
• Pantelias G.E,, Terzoudi G.I., A standardized G2-assay for the prediction of individual radiosensitivity. Radiother Oncol, 101(1):28-34, 2011.
• Kulka U., Ainsbury L., Atkinson M., Barquinero J.F., Barrios L., Beinke C., Bognar G., Cucu A., Darroudi F., Fattibene P., Gil O., Gregoire E., Hadjidekova V., Haghdoost S., Herranz R., Jaworska A., Lindholm C., Mkacher R., Mortl S., Montoro A., Moquet J., Moreno M., Ogbazghi A., Oestreicher U., Palitti F., Pantelias G., Popescu I., Prieto M.J., Romm H., Rothkamm K., Sabatier L., Sommer S., Terzoudi G., Testa A., Thierens H., Trompier F., Turai I., Vandersickel V., Vaz P., Voisin P., Vral A., Ugletveit F., Woda C., Wojcik A., Realising the European Network of Biodosimetry (RENEB). Radiat Prot Dosimetry, Oct;151(4):621-5, 2012.
• Aziz K, Nowsheen S, Pantelias G, Iliakis G, Gorgoulis VG, Georgakilas AG. (2012). Targeting DNA damage and repair: Embracing the pharmacological era for successful cancer therapy. Pharmacology and Therapeutics: 2012 Mar;133(3):334-50.
• Garcia O., Di Giorgio M., Vallerga M.B., Radl A., Taja M.R., Seoane A., De Luca J., Stuck Oliveira M., Valdivia P., Lamadrid A.I., Gonzalez J.E., Romero I., Mandina T., Pantelias G., Terzoudi G., Guerrero-Carbajal C., Arceo Maldonado C., Espinoza M., Oliveros N., Martinez-Lopez W., Di Tomaso M.V., Mendez-Acuna L., Puig R., Roy L., Barquinero J.F., Interlaboratory comparison of dicentric chromosome assay using electronically transmitted images. Radiat Prot Dosimetry, Apr;154(1):18-25, 2013.
• Lamadrid Boada A.I., Romero Aguilera I., Terzoudi G.I., Gonzalez Mesa J.E., Pantelias G., Garcia O. Rapid assessment of high-dose radiation exposures through scoring of cell-fusion-induced premature chromosome condensation and ring chromosomes. Mutat Res, Sep 18;757(1):45-51, 2013.
• Zachaki S., Stavropoulou C., Koromila T., Manola K.N., Kalomoiraki M., Daraki A., Koumbi D., Athanasiadou A., Kanavakis E., Kollia P., Sambani C. High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8. Leuk Res, 37(7):742-6, 2013.
• Zachaki S, Stavropoulou C, Kalomoiraki M, Koromila T, Daraki A, Manola KN, Mavrou A, Kanavakis E, Pantelias GE, Sambani C. Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome. Leuk Lymphoma, 54(8):1756-61, 2013.
• Manola K.N. Cytogenetic abnormalities in acute leukaemia of ambiguous lineage: an overview. Br J Haematol, 163(1):24-39, 2013. Review.
• Daraki A., Zachaki S., Koromila T., Diamantopoulou P., Sambani C., Pantelias G.E., Aleporou V., Kollia P., Manola K.N. The G516T CYP2B6 germline polymorphism affects the risk of Acute Myeloid Leukemia and is associated with specific chromosomal abnormalities. Plos One, 2014 [In Press].
• Manola K.N., Panitsas F., Polychronopoulou S., Daraki A., Karakosta M., Stavropoulou C., Avgerinou G., Hatzipantelis E., Pantelias G., Sambani C., Pagoni M. Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome. Cancer Genet, 206(3):63-72, 2013.