Nicolaou M - Search Results

1

Aniridia due to a novel microdeletion affecting PAX6 regulatory enhancers: case report and review of the literature.

Syrimis A, Nicolaou N, Alexandrou A, Papaevripidou I, Nicolaou M, Loukianou E, Christophidou-Anastasiadou V, Malas S, Sismani C, Tanteles GA. Syrimis A, et al. Among authors: nicolaou m, nicolaou n. J Genet. 2018 Jun;97(2):555-562. J Genet. 2018. PMID: 29932076 Free article. Review.

2

Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas.

Tanteles GA, Nicolaou M, Neocleous V, Shammas C, Loizidou MA, Alexandrou A, Ellina E, Patsia N, Sismani C, Phylactou LA, Christophidou-Anastasiadou V. Tanteles GA, et al. Among authors: nicolaou m. J Genet. 2015 Dec;94(4):749-54. doi: 10.1007/s12041-015-0564-3. J Genet. 2015. PMID: 26690531 Free article. No abstract available.

3

Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation.

Syrimis A, Nicolaou N, Alexandrou A, Papaevripidou I, Nicolaou M, Loukianou E, Sismani C, Malas S, Christophidou-Anastasiadou V, Tanteles GA. Syrimis A, et al. Among authors: nicolaou m, nicolaou n. Mol Med Rep. 2018 Aug;18(2):1623-1627. doi: 10.3892/mmr.2018.9126. Epub 2018 Jun 5. Mol Med Rep. 2018. PMID: 29901133 Free PMC article.

4

Novel TBX3 mutation in a family of Cypriot ancestry with ulnar-mammary syndrome.

Tanteles GA, Nicolaou N, Syrimis A, Metaxa R, Nicolaou M, Christophidou-Anastasiadou V, Skordis N. Tanteles GA, et al. Among authors: nicolaou m, nicolaou n. Clin Dysmorphol. 2017 Apr;26(2):61-65. doi: 10.1097/MCD.0000000000000170. Clin Dysmorphol. 2017. PMID: 28145909

5

A rare cause of pruritic ichthyosis: Sjögren-Larsson syndrome in the first reported patients of Cypriot descent.

Tanteles GA, Nicolaou M, Patsia N, Delikurt-Tuncalp T, Spanou-Aristidou E, Leonidou E, Kyriakides T, Christophidou-Anastasiadou V. Tanteles GA, et al. Among authors: nicolaou m. Eur J Dermatol. 2015 Sep-Oct;25(5):495-6. doi: 10.1684/ejd.2015.2615. Eur J Dermatol. 2015. PMID: 26394537 No abstract available.

6

Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.

DeStefano AL, Baldwin CT, Burzstyn M, Gavras I, Handy DE, Joost O, Martel T, Nicolaou M, Schwartz F, Streeten DH, Farrer LA, Gavras H. DeStefano AL, et al. Among authors: nicolaou m. Am J Hum Genet. 1998 Nov;63(5):1425-30. doi: 10.1086/302096. Am J Hum Genet. 1998. PMID: 9792870 Free PMC article.

7

Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.

Baima J, Nicolaou M, Schwartz F, DeStefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, Gavras H. Baima J, et al. Among authors: nicolaou m. Hypertension. 1999 Jul;34(1):4-7. doi: 10.1161/01.hyp.34.1.4. Hypertension. 1999. PMID: 10406815

8

Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension.

Baldwin CT, Schwartz F, Baima J, Burzstyn M, DeStefano AL, Gavras I, Handy DE, Joost O, Martel T, Manolis A, Nicolaou M, Bresnahan M, Farrer L, Gavras H. Baldwin CT, et al. Among authors: nicolaou m. Am J Hypertens. 1999 Sep;12(9 Pt 1):853-7. doi: 10.1016/s0895-7061(99)00070-9. Am J Hypertens. 1999. PMID: 10509541

9

Power of concordant versus discordant sib pairs at different penetrance levels.

Nicolaou M, Premkumar S, DeStefano AL, Farrer LA, Cupples LA. Nicolaou M, et al. Genet Epidemiol. 1999;17 Suppl 1:S679-84. doi: 10.1002/gepi.13701707111. Genet Epidemiol. 1999. PMID: 10597513

10

Stratification techniques to explore genotype environment interactions.

Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, Couropmitree NN. Wilk JB, et al. Among authors: nicolaou m. Genet Epidemiol. 1999;17 Suppl 1:S761-6. doi: 10.1002/gepi.13701707125. Genet Epidemiol. 1999. PMID: 10597527

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