☰

Michael S. Nicolaou, Ph.D. - Publications

Affiliations: 
2002 Boston University, Boston, MA, United States 
Area:
Biostatistics Biology, Genetics, Public Health
Tree Info Similar researchers PubMed Report error

10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2011 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, et al. Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology. Plos One. 6: e25775. PMID 21998696 DOI: 10.1371/Journal.Pone.0025775  0.327
2008 Lukiw WJ, Riazanskaya N, Grigorenko A, Korovaitseva G, Dvoryanchikov G, Molyaka Y, Nicolaou M, Farrer L, Bazan NG, Rogaev EI. DNA polymorphism in the human presenilin-2 promoter: altered gene activity and potential contribution to the risk for AD Journal of Neurochemistry. 81: 76-76. DOI: 10.1046/J.1471-4159.81.S1.44_2.X  0.346
2002 Riazanskaia N, Lukiw WJ, Grigorenko A, Korovaitseva G, Dvoryanchikov G, Moliaka Y, Nicolaou M, Farrer L, Bazan NG, Rogaev E. Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD. Molecular Psychiatry. 7: 891-8. PMID 12232783 DOI: 10.1038/Sj.Mp.4001101  0.349
2001 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, et al. Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Neurogenetics. 3: 203-6. PMID 11714100 DOI: 10.1007/S100480100123  0.309
2000 Rogaeva EA, Song YQ, Paterson A, Richard E, Nicolaou M, Sato C, Liang Y, Farrer LA. A genetic linkage study on late-onset familial Alzheimer's disease does not provide strong evidence for linkage to chromosome 1Q22, 9Q21.1, 10Q23, and chromosome 11Q23.3 Neurobiology of Aging. 21: 103. DOI: 10.1016/S0197-4580(00)82264-2  0.342
1999 Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, Couropmitree NN. Stratification techniques to explore genotype environment interactions. Genetic Epidemiology. 17: S761-6. PMID 10597527 DOI: 10.1002/Gepi.13701707125  0.383
1999 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. Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension. American Journal of Hypertension. 12: 853-7. PMID 10509541 DOI: 10.1016/S0895-7061(99)00070-9  0.301
1999 Baima J, Nicolaou M, Schwartz F, DeStefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, Gavras H. Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17 Hypertension. 34: 4-7. PMID 10406815 DOI: 10.1161/01.Hyp.34.1.4  0.389
1998 DeStefano AL, Baldwin CT, Burzstyn M, Gavras I, Handy DE, Joost O, Martel T, Nicolaou M, Schwartz F, Streeten DH, Farrer LA, Gavras H. Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q. American Journal of Human Genetics. 63: 1425-30. PMID 9792870 DOI: 10.1086/302096  0.334
1998 DeStefano AL, Gavras H, Burzstyn M, Gavras J, Handy DE, Joost O, Nicolaou M, Streeten D, Schwartz F, Farrer LA, Baldwin CT. Localization of a gene for blood pressure regulation to human chromosome 18q American Journal of Hypertension. 11. DOI: 10.1016/S0895-7061(97)90719-6  0.345
Show low-probability matches.