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MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21.
Tsaliki E, Papageorgiou EA, Spyrou C, Koumbaris G, Kypri E, Kyriakou S, Sotiriou C, Touvana E, Keravnou A, Karagrigoriou A, Lamnissou K, Velissariou V, Patsalis PC. Tsaliki E, et al. Among authors: velissariou v. Prenat Diagn. 2012 Oct;32(10):996-1001. doi: 10.1002/pd.3947. Epub 2012 Jul 26. Prenat Diagn. 2012. PMID: 22833530
Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.
Koumbaris G, Kypri E, Tsangaras K, Achilleos A, Mina P, Neofytou M, Velissariou V, Christopoulou G, Kallikas I, González-Liñán A, Benusiene E, Latos-Bielenska A, Marek P, Santana A, Nagy N, Széll M, Laudanski P, Papageorgiou EA, Ioannides M, Patsalis PC. Koumbaris G, et al. Among authors: velissariou v. Clin Chem. 2016 Jun;62(6):848-55. doi: 10.1373/clinchem.2015.252502. Epub 2016 Apr 26. Clin Chem. 2016. PMID: 27117469
Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.
Evangelidou P, Alexandrou A, Moutafi M, Ioannides M, Antoniou P, Koumbaris G, Kallikas I, Velissariou V, Sismani C, Patsalis PC. Evangelidou P, et al. Among authors: velissariou v. Biomed Res Int. 2013;2013:346762. doi: 10.1155/2013/346762. Epub 2013 Mar 4. Biomed Res Int. 2013. PMID: 23555083 Free PMC article. Review.
Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test.
Kypri E, Ioannides M, Touvana E, Neophytou I, Mina P, Velissariou V, Vittas S, Santana A, Alexidis F, Tsangaras K, Achilleos A, Patsalis P, Koumbaris G. Kypri E, et al. Among authors: velissariou v. Mol Cytogenet. 2019 Jul 15;12:34. doi: 10.1186/s13039-019-0446-0. eCollection 2019. Mol Cytogenet. 2019. PMID: 31338126 Free PMC article.
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations.
Evangelidou P, Sismani C, Ioannides M, Christodoulou C, Koumbaris G, Kallikas I, Georgiou I, Velissariou V, Patsalis PC. Evangelidou P, et al. Among authors: velissariou v. Mol Cytogenet. 2010 Nov 26;3:24. doi: 10.1186/1755-8166-3-24. Mol Cytogenet. 2010. PMID: 21110858 Free PMC article.
Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases.
Koumbaris G, Achilleos A, Nicolaou M, Loizides C, Tsangaras K, Kypri E, Mina P, Sismani C, Velissariou V, Christopoulou G, Constantoulakis P, Manolakos E, Papoulidis I, Stambouli D, Ioannides M, Patsalis P. Koumbaris G, et al. Among authors: velissariou v. Mol Cytogenet. 2019 Nov 21;12:48. doi: 10.1186/s13039-019-0459-8. eCollection 2019. Mol Cytogenet. 2019. PMID: 31832098 Free PMC article.
43 results