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Results: 1 to 20 of 148

Similar articles for PubMed (Select 11156623)

1.

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

Fallin D, Cohen A, Essioux L, Chumakov I, Blumenfeld M, Cohen D, Schork NJ.

Genome Res. 2001 Jan;11(1):143-51.

2.

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.

Fullerton SM, Clark AG, Weiss KM, Nickerson DA, Taylor SL, Stengârd JH, Salomaa V, Vartiainen E, Perola M, Boerwinkle E, Sing CF.

Am J Hum Genet. 2000 Oct;67(4):881-900. Epub 2000 Sep 13.

4.

Association studies testing for risk for late-onset Alzheimer's disease with common variants in the beta-amyloid precursor protein (APP).

Nowotny P, Simcock X, Bertelsen S, Hinrichs AL, Kauwe JS, Mayo K, Smemo S, Morris JC, Goate A.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):469-74.

PMID:
17427190
5.

Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci.

North BV, Curtis D, Martin ER, Lai EH, Roses AD, Sham PC.

Ann Hum Genet. 2004 May;68(Pt 3):240-8.

PMID:
15180704
6.

Dynamin-binding protein gene on chromosome 10q is associated with late-onset Alzheimer's disease.

Kuwano R, Miyashita A, Arai H, Asada T, Imagawa M, Shoji M, Higuchi S, Urakami K, Kakita A, Takahashi H, Tsukie T, Toyabe S, Akazawa K, Kanazawa I, Ihara Y; Japanese Genetic Study Consortium for Alzeheimer's Disease.

Hum Mol Genet. 2006 Jul 1;15(13):2170-82. Epub 2006 Jun 1.

7.

Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.

Verpillat P, Bouley S, Campion D, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Antérion C, Agid Y, Brice A, Clerget-Darpoux F.

Eur J Hum Genet. 2001 Jun;9(6):464-8.

8.

Apolipoprotein E promoter polymorphisms (-491A/T and -427T/C) and Alzheimer's disease: no evidence of association in the Irish population.

Lynch CA, Brazil J, Cullen B, Coakley D, Gill M, Lawlor BA, Hawi Z.

Ir J Med Sci. 2008 Mar;177(1):29-33. Epub 2007 Dec 5.

PMID:
18057979
10.

Genetic association study between senile dementia of Alzheimer's type and APOE/C1/C2 gene cluster.

Kamino K, Yoshiiwa A, Nishiwaki Y, Nagano K, Yamamoto H, Kobayashi T, Nonomura Y, Yoneda H, Sakai T, Imagawa M, Miki T, Ogihara T.

Gerontology. 1996;42 Suppl 1:12-9.

PMID:
8804993
11.

Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures.

Kamboh MI, Minster RL, Feingold E, DeKosky ST.

Mol Psychiatry. 2006 Mar;11(3):273-9.

PMID:
16302009
12.

Apolipoprotein E -491 promoter polymorphism is an independent risk factor for Alzheimer's disease in the Chinese population.

Yang JD, Feng GY, Zhang J, Cheung J, St Clair D, He L, Ichimura K.

Neurosci Lett. 2003 Oct 16;350(1):25-8. Erratum in: Neurosci Lett. 2003 May;30(2):215.

PMID:
12962909
13.

Joint analysis of candidate genes related to Alzheimer's disease in a Spanish population.

Clarimón J, Bertranpetit J, Calafell F, Boada M, Tàrraga L, Comas D.

Psychiatr Genet. 2003 Jun;13(2):85-90.

PMID:
12782964
14.

APOE and APOC1 promoter polymorphisms and the risk of Alzheimer disease in African American and Caribbean Hispanic individuals.

Tycko B, Lee JH, Ciappa A, Saxena A, Li CM, Feng L, Arriaga A, Stern Y, Lantigua R, Shachter N, Mayeux R.

Arch Neurol. 2004 Sep;61(9):1434-9. Erratum in: Arch Neurol. 2005 Feb;62(2):332.

PMID:
15364690
15.

Sequential haplotype scan methods for association analysis.

Yu Z, Schaid DJ.

Genet Epidemiol. 2007 Sep;31(6):553-64.

PMID:
17487883
16.

Quantifying the amount of missing information in genetic association studies.

Nicolae DL.

Genet Epidemiol. 2006 Dec;30(8):703-17.

PMID:
16986163
17.

Molecular evolution and genetics of the Saitohin gene and tau haplotype in Alzheimer's disease and argyrophilic grain disease.

Conrad C, Vianna C, Schultz C, Thal DR, Ghebremedhin E, Lenz J, Braak H, Davies P.

J Neurochem. 2004 Apr;89(1):179-88.

PMID:
15030402
18.

Association of ApoE genetic variants with obstructive sleep apnea in children.

Kalra M, Pal P, Kaushal R, Amin RS, Dolan LM, Fitz K, Kumar S, Sheng X, Guha S, Mallik J, Deka R, Chakraborty R.

Sleep Med. 2008 Mar;9(3):260-5. Epub 2007 Jul 19.

PMID:
17658295
19.

Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.

Hum Mutat. 2006 Aug;27(8):778-85.

PMID:
16835882
20.
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