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Πρωτεύουσες καρτέλες

Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.

2023
Avgeros, C., Patsatsi A., Dimitriadis D., Malousi A., Koletsa T., Papathemeli D., et al. (2023).  Dysregulation of Plasma miR-146a and miR-155 Expression Profile in Mycosis Fungoides Is Associated with rs2910164 and rs767649 Polymorphisms. International Journal of Molecular Sciences. 24(1), 271.
2021
Ntelios, D., Georgiou E., Alexouda S., Malousi A., Efthimiadis G., & Tzimagiorgis G. (2021).  A critical approach for successful use of circulating microRNAs as biomarkers in cardiovascular diseases: the case of hypertrophic cardiomyopathy.. Heart Fail Rev.
2019
Protonotariou, E., Meletis G., Chatzopoulou F., Malousi A., Chatzidimitriou D., & Skoura L. (2019).  Emergence of Klebsiella pneumoniae ST11 co-producing NDM-1 and OXA-48 carbapenemases in Greece.. J Glob Antimicrob Resist. 19, 81-82.
Malousi, A., Kouidou S., Tsagiopoulou M., Papakonstantinou N., Bouras E., Georgiou E., et al. (2019).  MeinteR: A framework to prioritize DNA methylation aberrations based on conformational and cis-regulatory element enrichment.. Sci Rep. 9(1), 19148.
2018
Malousi, A., Andreou A-Z., Georgiou E., Tzimagiorgis G., Kovatsi L., & Kouidou S. (2018).  Age-dependent methylation in epigenetic clock CpGs is associated with G-quadruplex, co-transcriptionally formed RNA structures and tentative splice sites.. Epigenetics. 13(8), 808-821.
2017
Karambataki, M., Malousi A., Tzimagiorgis G., Haitoglou C., Fragou A., Georgiou E., et al. (2017).  Association of two synonymous splicing-associated CpG single nucleotide polymorphisms in calpain 10 and solute carrier family 2 member 2 with type 2 diabetes.. Biomed Rep. 6(2), 146-158.
2014
Karambataki, M., Malousi A., & Kouidou S. (2014).  Risk-associated coding synonymous SNPs in type 2 diabetes and neurodegenerative diseases: genetic silence and the underrated association with splicing regulation and epigenetics.. Mutat Res. 770, 85-93.
2013
Athanasiadis, P., Malousi A., Kouidou S., & Maglaveras N. (2013).  GREMET: an integrative tool for the prediction of mutation effects on gene regulation.. Comput Methods Programs Biomed. 111(1), 214-9.
2012
Malousi, A., & Kouidou S. (2012).  DNA hypermethylation of alternatively spliced and repeat sequences in humans.. Mol Genet Genomics. 287(8), 631-42.
2010
Malousi, A., Chouvarda I., Koutkias V., Kouidou S., & Maglaveras N. (2010).  SpliceIT: a hybrid method for splice signal identification based on probabilistic and biological inference.. J Biomed Inform. 43(2), 208-17.
Koutkias, V. G., Chouvarda I., Triantafyllidis A., Malousi A., Giaglis G. D., & Maglaveras N. (2010).  A personalized framework for medication treatment management in chronic care.. IEEE Trans Inf Technol Biomed. 14(2), 464-72.
Karambataki, M., Malousi A., Maglaveras N., & Kouidou S. (2010).  Synonymous polymorphisms at splicing regulatory sites are associated with CpGs in neurodegenerative disease-related genes.. Neuromolecular Med. 12(3), 260-9.
2009
Kouidou, S., Malousi A., & Maglaveras N. (2009).  Li-Fraumeni and Li-Fraumeni-like syndrome mutations in p53 are associated with exonic methylation and splicing regulatory elements.. Mol Carcinog. 48(10), 895-902.
Kotoula, V., Charalambous E., Biesmans B., Malousi A., Vrettou E., Fountzilas G., et al. (2009).  Targeted KRAS mutation assessment on patient tumor histologic material in real time diagnostics.. PLoS One. 4(11), e7746.

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