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Page 1
Molecular predictive markers in tumors of the gastrointestinal tract.
Papadopoulou E, Metaxa-Mariatou V, Tsaousis G, Tsoulos N, Tsirigoti A, Efstathiadou C, Apessos A, Agiannitopoulos K, Pepe G, Bourkoula E, Nasioulas G. Papadopoulou E, et al. Among authors: tsaousis g. World J Gastrointest Oncol. 2016 Nov 15;8(11):772-785. doi: 10.4251/wjgo.v8.i11.772. World J Gastrointest Oncol. 2016. PMID: 27895815 Free PMC article. Review.
Tumor molecular profiling of NSCLC patients using next generation sequencing.
Tsoulos N, Papadopoulou E, Metaxa-Mariatou V, Tsaousis G, Efstathiadou C, Tounta G, Scapeti A, Bourkoula E, Zarogoulidis P, Pentheroudakis G, Kakolyris S, Boukovinas I, Papakotoulas P, Athanasiadis E, Floros T, Koumarianou A, Barbounis V, Dinischiotu A, Nasioulas G. Tsoulos N, et al. Among authors: tsaousis g. Oncol Rep. 2017 Dec;38(6):3419-3429. doi: 10.3892/or.2017.6051. Epub 2017 Oct 23. Oncol Rep. 2017. PMID: 29130105 Free PMC article.
Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center.
Apessos A, Agiannitopoulos K, Pepe G, Tsaousis GN, Papadopoulou E, Metaxa-Mariatou V, Tsirigoti A, Efstathiadou C, Markopoulos C, Xepapadakis G, Venizelos V, Tsiftsoglou A, Natsiopoulos I, Nasioulas G. Apessos A, et al. Among authors: tsaousis gn. Cancer Genet. 2018 Jan;220:1-12. doi: 10.1016/j.cancergen.2017.10.002. Epub 2017 Oct 19. Cancer Genet. 2018. PMID: 29310832
Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations.
Tsaousis GN, Papadopoulou E, Apessos A, Agiannitopoulos K, Pepe G, Kampouri S, Diamantopoulos N, Floros T, Iosifidou R, Katopodi O, Koumarianou A, Markopoulos C, Papazisis K, Venizelos V, Xanthakis I, Xepapadakis G, Banu E, Eniu DT, Negru S, Stanculeanu DL, Ungureanu A, Ozmen V, Tansan S, Tekinel M, Yalcin S, Nasioulas G. Tsaousis GN, et al. BMC Cancer. 2019 Jun 3;19(1):535. doi: 10.1186/s12885-019-5756-4. BMC Cancer. 2019. PMID: 31159747 Free PMC article.
Clinical feasibility of NGS liquid biopsy analysis in NSCLC patients.
Papadopoulou E, Tsoulos N, Tsantikidi K, Metaxa-Mariatou V, Stamou PE, Kladi-Skandali A, Kapeni E, Tsaousis G, Pentheroudakis G, Petrakis D, Lampropoulou DI, Aravantinos G, Varthalitis I, Kesisis G, Boukovinas I, Papakotoulas P, Katirtzoglou N, Athanasiadis E, Stavridi F, Christodoulou C, Koumarianou A, Eralp Y, Nasioulas G. Papadopoulou E, et al. Among authors: tsaousis g. PLoS One. 2019 Dec 20;14(12):e0226853. doi: 10.1371/journal.pone.0226853. eCollection 2019. PLoS One. 2019. PMID: 31860648 Free PMC article.
miRNA polymorphisms and risk of premature coronary artery disease.
Agiannitopoulos K, Samara P, Papadopoulou M, Efthymiadou A, Papadopoulou E, Tsaousis GN, Mertzanos G, Babalis D, Lamnissou K. Agiannitopoulos K, et al. Among authors: tsaousis gn. Hellenic J Cardiol. 2021 Jul-Aug;62(4):278-284. doi: 10.1016/j.hjc.2020.01.005. Epub 2020 Feb 21. Hellenic J Cardiol. 2021. PMID: 32092393 Free article.
Report of a germline double heterozygote in MSH2 and PALB2.
Agiannitopoulos K, Papadopoulou E, Tsaousis GN, Pepe G, Kampouri S, Patsea E, Lypas G, Nasioulas G. Agiannitopoulos K, et al. Among authors: tsaousis gn. Mol Genet Genomic Med. 2020 Oct;8(10):e1242. doi: 10.1002/mgg3.1242. Epub 2020 Aug 27. Mol Genet Genomic Med. 2020. PMID: 32853479 Free PMC article.
Comprehensive tumor molecular profile analysis in clinical practice.
Özdoğan M, Papadopoulou E, Tsoulos N, Tsantikidi A, Mariatou VM, Tsaousis G, Kapeni E, Bourkoula E, Fotiou D, Kapetsis G, Boukovinas I, Touroutoglou N, Fassas A, Adamidis A, Kosmidis P, Trafalis D, Galani E, Lypas G, Orhan B, Tansan S, Özatlı T, Kırca O, Çakır O, Nasioulas G. Özdoğan M, et al. Among authors: tsaousis g. BMC Med Genomics. 2021 Apr 14;14(1):105. doi: 10.1186/s12920-021-00952-9. BMC Med Genomics. 2021. PMID: 33853586 Free PMC article.
55 results