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Items: 20

1.

No association of SORL1 SNPs with Alzheimer's disease.

Minster RL, DeKosky ST, Kamboh MI.

Neurosci Lett. 2008 Aug 1;440(2):190-2. doi: 10.1016/j.neulet.2008.05.082. Epub 2008 May 27.

2.

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population.

Bettens K, Brouwers N, Engelborghs S, De Deyn PP, Van Broeckhoven C, Sleegers K.

Hum Mutat. 2008 May;29(5):769-70. doi: 10.1002/humu.20725.

PMID:
18407551
3.

A survey of genetic human cortical gene expression.

Myers AJ, Gibbs JR, Webster JA, Rohrer K, Zhao A, Marlowe L, Kaleem M, Leung D, Bryden L, Nath P, Zismann VL, Joshipura K, Huentelman MJ, Hu-Lince D, Coon KD, Craig DW, Pearson JV, Holmans P, Heward CB, Reiman EM, Stephan D, Hardy J.

Nat Genet. 2007 Dec;39(12):1494-9. Epub 2007 Nov 4.

PMID:
17982457
4.

Sorl1 as an Alzheimer's disease predisposition gene?

Webster JA, Myers AJ, Pearson JV, Craig DW, Hu-Lince D, Coon KD, Zismann VL, Beach T, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Huentelman MJ, Joshipura K, Walker D, Heward CB, Ravid R, Rogers J, Papassotiropoulos A, Hardy J, Reiman EM, Stephan DA.

Neurodegener Dis. 2008;5(2):60-4. Epub 2007 Nov 1.

5.

SORL1 variants and risk of late-onset Alzheimer's disease.

Li Y, Rowland C, Catanese J, Morris J, Lovestone S, O'Donovan MC, Goate A, Owen M, Williams J, Grupe A.

Neurobiol Dis. 2008 Feb;29(2):293-6. Epub 2007 Sep 16.

6.

A genome-wide association study of global gene expression.

Dixon AL, Liang L, Moffatt MF, Chen W, Heath S, Wong KC, Taylor J, Burnett E, Gut I, Farrall M, Lathrop GM, Abecasis GR, Cookson WO.

Nat Genet. 2007 Oct;39(10):1202-7. Epub 2007 Sep 16.

PMID:
17873877
7.

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.

Reiman EM, Webster JA, Myers AJ, Hardy J, Dunckley T, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Huentelman MJ, Craig DW, Coon KD, Liang WS, Herbert RH, Beach T, Rohrer KC, Zhao AS, Leung D, Bryden L, Marlowe L, Kaleem M, Mastroeni D, Grover A, Heward CB, Ravid R, Rogers J, Hutton ML, Melquist S, Petersen RC, Alexander GE, Caselli RJ, Kukull W, Papassotiropoulos A, Stephan DA.

Neuron. 2007 Jun 7;54(5):713-20.

8.

The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort.

Lee JH, Cheng R, Schupf N, Manly J, Lantigua R, Stern Y, Rogaeva E, Wakutani Y, Farrer L, St George-Hyslop P, Mayeux R.

Arch Neurol. 2007 Apr;64(4):501-6.

9.

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.

Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song YQ, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P.

Nat Genet. 2007 Feb;39(2):168-77. Epub 2007 Jan 14.

10.

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.

Bertram L, McQueen MB, Mullin K, Blacker D, Tanzi RE.

Nat Genet. 2007 Jan;39(1):17-23.

PMID:
17192785
11.

Haploview: analysis and visualization of LD and haplotype maps.

Barrett JC, Fry B, Maller J, Daly MJ.

Bioinformatics. 2005 Jan 15;21(2):263-5. Epub 2004 Aug 5.

PMID:
15297300
12.

APOE epsilon4 allele is associated with reduced cerebrospinal fluid levels of Abeta42.

Prince JA, Zetterberg H, Andreasen N, Marcusson J, Blennow K.

Neurology. 2004 Jun 8;62(11):2116-8.

PMID:
15184629
13.

Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism.

Katzov H, Chalmers K, Palmgren J, Andreasen N, Johansson B, Cairns NJ, Gatz M, Wilcock GK, Love S, Pedersen NL, Brookes AJ, Blennow K, Kehoe PG, Prince JA.

Hum Mutat. 2004 Apr;23(4):358-67.

PMID:
15024730
14.

Association between depressed mood in the elderly and a 5-HTR2A gene variant.

Jansson M, Gatz M, Berg S, Johansson B, Malmberg B, McClearn GE, Schalling M, Pedersen NL.

Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):79-84.

PMID:
12815744
15.

The Swedish Twin Registry in the third millennium.

Pedersen NL, Lichtenstein P, Svedberg P.

Twin Res. 2002 Oct;5(5):427-32. Review.

PMID:
12537870
16.

The Swedish Twin Registry: a unique resource for clinical, epidemiological and genetic studies.

Lichtenstein P, De Faire U, Floderus B, Svartengren M, Svedberg P, Pedersen NL.

J Intern Med. 2002 Sep;252(3):184-205. Review.

17.

Sensitivity, specificity, and stability of CSF-tau in AD in a community-based patient sample.

Andreasen N, Minthon L, Clarberg A, Davidsson P, Gottfries J, Vanmechelen E, Vanderstichele H, Winblad B, Blennow K.

Neurology. 1999 Oct 22;53(7):1488-94.

PMID:
10534256
18.

Towards an earlier diagnosis of Alzheimer's disease.

Vanmechelen E, Vanderstichele H.

J Biotechnol. 1998 Dec 11;66(2-3):229-31. No abstract available.

PMID:
9866871
19.

Tau protein in cerebrospinal fluid: a biochemical marker for axonal degeneration in Alzheimer disease?

Blennow K, Wallin A, Agren H, Spenger C, Siegfried J, Vanmechelen E.

Mol Chem Neuropathol. 1995 Dec;26(3):231-45.

PMID:
8748926
20.

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, Salvesen GS, Roses AD.

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1977-81.

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