Keravnou A[Author] - Search Results

Year	Number of Results
2012	1
2014	1
2016	1
2017	1
2018	2
2020	2
2021	0

1

MicroRNAs in ascending thoracic aortic aneurysms.

Moushi A, Pillar N, Keravnou A, Soteriou M, Shomron N, Cariolou MA, Bashiardes E. Moushi A, et al. Among authors: keravnou a. Biosci Rep. 2020 Jul 31;40(7):BSR20200218. doi: 10.1042/BSR20200218. Biosci Rep. 2020. PMID: 32678444 Free PMC article.

2

Identification of novel splice mutation in SMAD3 in two Cypriot families with nonsyndromic thoracic aortic aneurysm. Two case reports.

Keravnou A, Bashiardes E, Barberis V, Michailidou K, Soteriou M, Tanteles GA, Cariolou MA. Keravnou A, et al. Mol Genet Genomic Med. 2020 Sep;8(9):e1378. doi: 10.1002/mgg3.1378. Epub 2020 Jun 29. Mol Genet Genomic Med. 2020. PMID: 32597575 Free PMC article.

3

Novel variants in the ACTA2 and MYH11 genes in a Cypriot family with thoracic aortic aneurysms: a case report.

Keravnou A, Bashiardes E, Michailidou K, Soteriou M, Moushi A, Cariolou M. Keravnou A, et al. BMC Med Genet. 2018 Dec 7;19(1):208. doi: 10.1186/s12881-018-0728-0. BMC Med Genet. 2018. PMID: 30526509 Free PMC article.

4

Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.

Neofytou MC, Tsangaras K, Kypri E, Loizides C, Ioannides M, Achilleos A, Mina P, Keravnou A, Sismani C, Koumbaris G, Patsalis PC. Neofytou MC, et al. Among authors: keravnou a. PLoS One. 2017 Feb 3;12(2):e0171319. doi: 10.1371/journal.pone.0171319. eCollection 2017. PLoS One. 2017. PMID: 28158220 Free PMC article.

5

MeDIP combined with in-solution targeted enrichment followed by NGS: Inter-individual methylation variability of fetal-specific biomarkers and their implementation in a proof of concept study for NIPT.

Keravnou A, Ioannides M, Loizides C, Tsangaras K, Achilleos A, Mina P, Kypri E, Hadjidaniel MD, Neofytou M, Kyriacou S, Sismani C, Koumbaris G, Patsalis PC. Keravnou A, et al. PLoS One. 2018 Jun 11;13(6):e0199010. doi: 10.1371/journal.pone.0199010. eCollection 2018. PLoS One. 2018. PMID: 29889893 Free PMC article.

6

Inter-individual methylation variability in differentially methylated regions between maternal whole blood and first trimester CVS.

Ioannides M, Papageorgiou EA, Keravnou A, Tsaliki E, Spyrou C, Hadjidaniel M, Sismani C, Koumbaris G, Patsalis PC. Ioannides M, et al. Among authors: keravnou a. Mol Cytogenet. 2014 Nov 1;7(1):73. doi: 10.1186/s13039-014-0073-8. eCollection 2014. Mol Cytogenet. 2014. PMID: 25426166 Free PMC article.

7

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: keravnou a. Prenat Diagn. 2012 Oct;32(10):996-1001. doi: 10.1002/pd.3947. Epub 2012 Jul 26. Prenat Diagn. 2012. PMID: 22833530

8

Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions.

Keravnou A, Ioannides M, Tsangaras K, Loizides C, Hadjidaniel MD, Papageorgiou EA, Kyriakou S, Antoniou P, Mina P, Achilleos A, Neofytou M, Kypri E, Sismani C, Koumbaris G, Patsalis PC. Keravnou A, et al. Genet Res (Camb). 2016 Nov 11;98:e15. doi: 10.1017/S0016672316000136. Genet Res (Camb). 2016. PMID: 27834155 Free PMC article.

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