Nicolaou M - Search Results

1

Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology.

Jun G, Nicolaou M, Morrison MA, Buros J, Morgan DJ, Radeke MJ, Yonekawa Y, Tsironi EE, Kotoula MG, Zacharaki F, Mollema N, Yuan Y, Miller JW, Haider NB, Hageman GS, Kim IK, Schaumberg DA, Farrer LA, DeAngelis MM. Jun G, et al. Among authors: nicolaou m. PLoS One. 2011;6(10):e25775. doi: 10.1371/journal.pone.0025775. Epub 2011 Oct 6. PLoS One. 2011. PMID: 21998696 Free PMC article.

2

Genetic predisposition to stroke in relatives of hypertensives.

Nicolaou M, DeStefano AL, Gavras I, Cupples LA, Manolis AJ, Baldwin CT, Gavras H, Farrer LA. Nicolaou M, et al. Stroke. 2000 Feb;31(2):487-92. doi: 10.1161/01.str.31.2.487. Stroke. 2000. PMID: 10657427

3

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

4

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

5

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.

6

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

7

Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease.

Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, Farrer LA, St Georg-Hyslop P, Rogaeva EA. Nicolaou M, et al. Neurogenetics. 2001 Oct;3(4):203-6. doi: 10.1007/s100480100123. Neurogenetics. 2001. PMID: 11714100

8

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

9

Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD.

Riazanskaia N, Lukiw WJ, Grigorenko A, Korovaitseva G, Dvoryanchikov G, Moliaka Y, Nicolaou M, Farrer L, Bazan NG, Rogaev E. Riazanskaia N, et al. Among authors: nicolaou m. Mol Psychiatry. 2002;7(8):891-8. doi: 10.1038/sj.mp.4001101. Mol Psychiatry. 2002. PMID: 12232783

10

Neurokinin-1 receptor and substance P messenger RNA levels increase during intraabdominal adhesion formation.

Reed KL, Fruin AB, Bishop-Bartolomei KK, Gower AC, Nicolaou M, Stucchi AF, Leeman SE, Becker JM. Reed KL, et al. Among authors: nicolaou m. J Surg Res. 2002 Nov;108(1):165-72. doi: 10.1006/jsre.2002.6533. J Surg Res. 2002. PMID: 12443729

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