Kanavakis E - Search Results

1

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases.

Tsipi M, Tzetis M, Kosma K, Moschos M, Braoudaki M, Poulou M, Kanavakis E, Kitsiou-Tzeli S. Tsipi M, et al. Among authors: kanavakis e. Meta Gene. 2016 Feb 16;8:37-43. doi: 10.1016/j.mgene.2016.02.002. eCollection 2016 Jun. Meta Gene. 2016. PMID: 27014590 Free PMC article.

2

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients.

Delaveri A, Rapti A, Poulou M, Fylaktou E, Tsipi M, Roussos C, Makrythanasis P, Kanavakis E, Tzetis M. Delaveri A, et al. Among authors: kanavakis e. Meta Gene. 2014 Aug 31;2:619-30. doi: 10.1016/j.mgene.2014.07.009. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606445 Free PMC article.

3

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.

Kitsiou-Tzeli S, Frysira H, Giannikou K, Syrmou A, Kosma K, Kakourou G, Leze E, Sofocleous C, Kanavakis E, Tzetis M. Kitsiou-Tzeli S, et al. Among authors: kanavakis e. Gene. 2012 Jan 15;492(1):319-24. doi: 10.1016/j.gene.2011.10.023. Epub 2011 Oct 20. Gene. 2012. PMID: 22037486

4

Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene.

Poulou M, Fylaktou I, Fotoulaki M, Kanavakis E, Tzetis M. Poulou M, et al. Among authors: kanavakis e. J Cyst Fibros. 2012 Jul;11(4):344-8. doi: 10.1016/j.jcf.2012.01.004. Epub 2012 Feb 11. J Cyst Fibros. 2012. PMID: 22326559 Free article.

5

Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.

Syrmou A, Tzetis M, Fryssira H, Kosma K, Oikonomakis V, Giannikou K, Makrythanasis P, Kitsiou-Tzeli S, Kanavakis E. Syrmou A, et al. Among authors: kanavakis e. Pediatr Res. 2013 Jun;73(6):772-6. doi: 10.1038/pr.2013.41. Epub 2013 Mar 12. Pediatr Res. 2013. PMID: 23481551

6

Are ALOX5AP gene SNPs a risk or protective factor for stroke?

Papapostolou A, Spengos K, Fylaktou I, Poulou M, Gountas I, Kitsiou-Tzeli S, Kanavakis E, Tzetis M. Papapostolou A, et al. Among authors: kanavakis e. Gene. 2014 Sep 10;548(1):56-60. doi: 10.1016/j.gene.2014.07.007. Epub 2014 Jul 8. Gene. 2014. PMID: 25010723

7

Association of TLR4 single-nucleotide polymorphisms and sarcoidosis in Greek patients.

Iliadi A, Makrythanasis P, Tzetis M, Tsipi M, Traeger-Synodinos J, Ioannou PC, Rapti A, Kanavakis E, Christopoulos TK. Iliadi A, et al. Among authors: kanavakis e. Genet Test Mol Biomarkers. 2009 Dec;13(6):849-53. doi: 10.1089/gtmb.2009.0117. Genet Test Mol Biomarkers. 2009. PMID: 19839752

8

Genetic polymorphisms in the UGT1A1 gene and breast cancer risk in Greek women.

Tsezou A, Tzetis M, Giannatou E, Gennatas C, Pampanos A, Kanavakis E, Kitsiou-Tzeli S. Tsezou A, et al. Among authors: kanavakis e. Genet Test. 2007 Fall;11(3):303-6. doi: 10.1089/gte.2007.0020. Genet Test. 2007. PMID: 17949292

9

Association of the CALM1 core promoter polymorphism with knee osteoarthritis in patients of Greek origin.

Poulou M, Kaliakatsos M, Tsezou A, Kanavakis E, Malizos KN, Tzetis M. Poulou M, et al. Among authors: kanavakis e. Genet Test. 2008 Jun;12(2):263-5. doi: 10.1089/gte.2007.0114. Genet Test. 2008. PMID: 18452398

10

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.

Tzetis M, Kitsiou-Tzeli S, Frysira H, Xaidara A, Kanavakis E. Tzetis M, et al. Among authors: kanavakis e. Expert Rev Mol Diagn. 2012 Jun;12(5):449-57. doi: 10.1586/erm.12.40. Expert Rev Mol Diagn. 2012. PMID: 22702362

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