Anastasiadou V - Search Results

1

Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus.

Loizidou M, Marcou Y, Anastasiadou V, Newbold R, Hadjisavvas A, Kyriacou K. Loizidou M, et al. Among authors: anastasiadou v. Clin Genet. 2007 Feb;71(2):165-70. doi: 10.1111/j.1399-0004.2007.00747.x. Clin Genet. 2007. PMID: 17250666

2

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

Patsalis PC, Sismani C, Hettinger JA, Boumba I, Georgiou I, Stylianidou G, Anastasiadou V, Koukoulli R, Pagoulatos G, Syrrou M. Patsalis PC, et al. Among authors: anastasiadou v. Am J Med Genet. 1999 May 28;84(3):184-90. Am J Med Genet. 1999. PMID: 10331587

3

Geographical clustering of low density lipoprotein receptor gene mutations (C292X; Q363X; D365E & C660X) in Cyprus.

Xenophontos SL, Pierides A, Demetriou K, Avraamides P, Manoli P, Ayrton N, Skordis N, Anastasiadou V, Miltiadous G, Cariolou MA. Xenophontos SL, et al. Among authors: anastasiadou v. Hum Mutat. 2000 Apr;15(4):380. doi: 10.1002/(SICI)1098-1004(200004)15:4<380::AID-HUMU11>3.0.CO;2-T. Hum Mutat. 2000. PMID: 10737984

4

Sandhoff disease in Cyprus: population screening by biochemical and DNA analysis indicates a high frequency of carriers in the Maronite community.

Drousiotou A, Stylianidou G, Anastasiadou V, Christopoulos G, Mavrikiou E, Georgiou T, Kalakoutis G, Oladimeji A, Hara Y, Suzuki K, Furihata K, Ueno I, Ioannou PA, Fensom AH. Drousiotou A, et al. Among authors: anastasiadou v. Hum Genet. 2000 Jul;107(1):12-7. doi: 10.1007/s004390000324. Hum Genet. 2000. PMID: 10982028

5

Novel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis.

Hadjisavvas A, Papasavva T, Loizidou M, Malas S, Potamitis G, Christodoulou C, Pavlides G, Papamichael D, Klonis C, Nasioulas G, Anastasiadou V, Kyriacou K. Hadjisavvas A, et al. Among authors: anastasiadou v. Clin Genet. 2006 May;69(5):404-9. doi: 10.1111/j.1399-0004.2006.00617.x. Clin Genet. 2006. PMID: 16650078

6

High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

Neocleous V, Aspris A, Shahpenterian V, Nicolaou V, Panagi C, Ioannou I, Kyamides Y, Anastasiadou V, Phylactou LA. Neocleous V, et al. Among authors: anastasiadou v. Genet Test. 2006 Winter;10(4):285-9. doi: 10.1089/gte.2006.10.285. Genet Test. 2006. PMID: 17253936

7

The BRCA1 variant p.Ser36Tyr abrogates BRCA1 protein function and potentially confers a moderate risk of breast cancer.

Christou CM, Hadjisavvas A, Kyratzi M, Flouri C, Neophytou I, Anastasiadou V, Loizidou MA, Kyriacou K. Christou CM, et al. Among authors: anastasiadou v. PLoS One. 2014 Apr 2;9(4):e93400. doi: 10.1371/journal.pone.0093400. eCollection 2014. PLoS One. 2014. PMID: 24695549 Free PMC article.

8

Molecular analysis of Cypriot patients with Glutaric aciduria type I: identification of two novel mutations.

Georgiou T, Nicolaidou P, Hadjichristou A, Ioannou R, Dionysiou M, Siama E, Chappa G, Anastasiadou V, Drousiotou A. Georgiou T, et al. Among authors: anastasiadou v. Clin Biochem. 2014 Sep;47(13-14):1300-5. doi: 10.1016/j.clinbiochem.2014.06.017. Epub 2014 Jun 25. Clin Biochem. 2014. PMID: 24973495

9

The mutational spectrum of Lynch syndrome in cyprus.

Loizidou MA, Neophytou I, Papamichael D, Kountourakis P, Vassiliou V, Marcou Y, Kakouri E, Ioannidis G, Philippou C, Spanou E, Tanteles GA, Anastasiadou V, Hadjisavvas A, Kyriacou K. Loizidou MA, et al. Among authors: anastasiadou v. PLoS One. 2014 Aug 18;9(8):e105501. doi: 10.1371/journal.pone.0105501. eCollection 2014. PLoS One. 2014. PMID: 25133505 Free PMC article.

10

Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.

Neocleous V, Costi C, Shammas C, Spanou E, Anastasiadou V, Tanteles GA, Phylactou LA. Neocleous V, et al. Among authors: anastasiadou v. J Genet. 2014 Aug;93(2):471-6. doi: 10.1007/s12041-014-0365-0. J Genet. 2014. PMID: 25189242 Free article. No abstract available.

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