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Greek BRCA1 and BRCA2 mutation spectrum: two BRCA1 mutations account for half the carriers found among high-risk breast/ovarian cancer patients.
Konstantopoulou I, Rampias T, Ladopoulou A, Koutsodontis G, Armaou S, Anagnostopoulos T, Nikolopoulos G, Kamakari S, Nounesis G, Stylianakis A, Karanikiotis C, Razis E, Gogas H, Keramopoulos A, Gaki V, Markopoulos C, Skarlos D, Pandis N, Bei T, Arzimanoglou I, Fountzilas G, Yannoukakos D. Konstantopoulou I, et al. Among authors: nikolopoulos g. Breast Cancer Res Treat. 2008 Feb;107(3):431-41. doi: 10.1007/s10549-007-9571-2. Epub 2007 Apr 24. Breast Cancer Res Treat. 2008. PMID: 17453335
Thermal unfolding of human BRCA1 BRCT-domain variants.
Nikolopoulos G, Pyrpassopoulos S, Thanassoulas A, Klimentzou P, Zikos C, Vlassi M, Vorgias CE, Yannoukakos D, Nounesis G. Nikolopoulos G, et al. Biochim Biophys Acta. 2007 Jun;1774(6):772-80. doi: 10.1016/j.bbapap.2007.03.018. Epub 2007 Apr 6. Biochim Biophys Acta. 2007. PMID: 17493881
Apoptosis and hepatitis C virus infection in renal transplant recipients.
Delladetsima I, Psichogiou M, Alexandrou P, Nikolopoulos G, Revenas K, Hatzakis A, Boletis J. Delladetsima I, et al. Among authors: nikolopoulos g. Am J Clin Pathol. 2008 May;129(5):744-8. doi: 10.1309/U90671UBGT1GLKLL. Am J Clin Pathol. 2008. PMID: 18426734
Molecular epidemiology of HIV among people who inject drugs after the HIV-outbreak in Athens, Greece: Evidence for a 'slow burn' outbreak.
Kostaki EG, Roussos S, Kefala AM, Limnaios S, Psichogiou M, Papachristou E, Nikolopoulos G, Flountzi E, Friedman SR, Lagiou P, Hatzakis A, Sypsa V, Magiorkinis G, Beloukas A, Paraskevis D. Kostaki EG, et al. Among authors: nikolopoulos g. Infect Genet Evol. 2024 Jul;121:105597. doi: 10.1016/j.meegid.2024.105597. Epub 2024 Apr 23. Infect Genet Evol. 2024. PMID: 38663466 Free article.
Rotational Thromboelastometry as a Diagnostic Tool for Persistent Infection in Two-Stage Exchange Arthroplasty.
Tsantes AG, Papadopoulos DV, Goumenos S, Trikoupis IG, Tsante KA, Koutserimpas C, Koulouvaris P, Petrakis V, Vaiopoulos AG, Piovani D, Nikolopoulos GK, Mavrogenis AF, Papagelopoulos PJ, Bonovas S, Tsantes AE. Tsantes AG, et al. Among authors: nikolopoulos gk. J Clin Med. 2024 Mar 27;13(7):1942. doi: 10.3390/jcm13071942. J Clin Med. 2024. PMID: 38610707 Free PMC article.
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium. Smith CEL, et al. Among authors: nikolopoulos g. J Med Genet. 2024 Apr 8:jmg-2023-109728. doi: 10.1136/jmg-2023-109728. Online ahead of print. J Med Genet. 2024. PMID: 38458752 Free article.
226 results