Fostira F - Search Results

1

Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation.

Apostolou P, Pertesi M, Aleporou-Marinou V, Dimitrakakis C, Papadimitriou C, Razis E, Christodoulou C, Fountzilas G, Yannoukakos D, Konstantopoulou I, Fostira F. Apostolou P, et al. Among authors: fostira f. Clin Genet. 2017 Mar;91(3):482-487. doi: 10.1111/cge.12824. Epub 2016 Aug 22. Clin Genet. 2017. PMID: 27357818

2

Hereditary cancer syndromes.

Fostira F, Thodi G, Konstantopoulou I, Sandaltzopoulos R, Yannoukakos D. Fostira F, et al. J BUON. 2007 Sep;12 Suppl 1:S13-22. J BUON. 2007. PMID: 17935271 Review.

3

Culture of primary epithelial adenoma cells from familial adenomatous polyposis patients.

Fostira F, Apessos A, Oikonomou E, Kouklis P, Baratsis S, Manifikos G, Andera L, Yannoukakos D, Pintzas A, Nasioulas G. Fostira F, et al. Anticancer Res. 2008 Mar-Apr;28(2A):843-6. Anticancer Res. 2008. PMID: 18507027 Free article.

4

Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases.

Armaou S, Pertesi M, Fostira F, Thodi G, Athanasopoulos PS, Kamakari S, Athanasiou A, Gogas H, Yannoukakos D, Fountzilas G, Konstantopoulou I. Armaou S, et al. Among authors: fostira f. Br J Cancer. 2009 Jul 7;101(1):32-7. doi: 10.1038/sj.bjc.6605115. Epub 2009 Jun 2. Br J Cancer. 2009. PMID: 19491894 Free PMC article.

5

Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now?

Konstantopoulou I, Pertesi M, Fostira F, Grivas A, Yannoukakos D. Konstantopoulou I, et al. Among authors: fostira f. J BUON. 2009 Sep;14 Suppl 1:S187-92. J BUON. 2009. PMID: 19785065 Review.

6

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.

Fostira F, Yannoukakos D. Fostira F, et al. Fam Cancer. 2010 Sep;9(3):395-400. doi: 10.1007/s10689-009-9317-x. Fam Cancer. 2010. PMID: 20033787

7

An in-frame exon-skipping MUTYH mutation is associated with early-onset colorectal cancer.

Fostira F, Papademitriou C, Efremidis A, Yannoukakos D. Fostira F, et al. Dis Colon Rectum. 2010 Aug;53(8):1197-201. doi: 10.1007/DCR.0b013e3181dcf0c1. Dis Colon Rectum. 2010. PMID: 20628285

8

Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients.

Fostira F, Thodi G, Sandaltzopoulos R, Fountzilas G, Yannoukakos D. Fostira F, et al. BMC Cancer. 2010 Jul 22;10:389. doi: 10.1186/1471-2407-10-389. BMC Cancer. 2010. PMID: 20649969 Free PMC article.

9

Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families.

Thodi G, Fostira F, Sandaltzopoulos R, Nasioulas G, Grivas A, Boukovinas I, Mylonaki M, Panopoulos C, Magic MB, Fountzilas G, Yannoukakos D. Thodi G, et al. Among authors: fostira f. BMC Cancer. 2010 Oct 11;10:544. doi: 10.1186/1471-2407-10-544. BMC Cancer. 2010. PMID: 20937110 Free PMC article.

10

ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes.

Spurdle AB, Healey S, Devereau A, Hogervorst FB, Monteiro AN, Nathanson KL, Radice P, Stoppa-Lyonnet D, Tavtigian S, Wappenschmidt B, Couch FJ, Goldgar DE; ENIGMA. Spurdle AB, et al. Hum Mutat. 2012 Jan;33(1):2-7. doi: 10.1002/humu.21628. Epub 2011 Nov 3. Hum Mutat. 2012. PMID: 21990146 Free PMC article.

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