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  Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study.

Laumet, G., Chouraki, V., Grenier-Boley, B., Legry, V., Heath, S., Zelenika, D., et al. (2010). Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's Disease, 20(4), 1181-1188. doi:10.3233/JAD-2010-100126.

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Genre: Journal Article
Alternative Title : J Alzheimers Dis

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 Creators:
Laumet, G., Author
Chouraki, V., Author
Grenier-Boley, B., Author
Legry, V., Author
Heath, S., Author
Zelenika, D., Author
Fievet, N., Author
Hannequin, D., Author
Delepine, M., Author
Pasquier, F., Author
Hanon, O., Author
Brice, A., Author
Epelbaum, J., Author
Berr, C., Author
Dartigues, J. F., Author
Tzourio, C., Author
Campion, D., Author
Lathrop, M., Author
Bertram, L.1, Author           
Amouyel, P., Author
Lambert, J. C., Author more..
Affiliations:
1Neuropsychiatric Genetics (Lars Bertram), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479655              

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Free keywords: AlzGene database; Alzheimer's disease; association; GWAS; replication; risk factor; SNPs
 Abstract: We selected twenty genes from the "Top Results" list on the AlzGene database website and assessed their association with risk of developing Alzheimer's disease (AD) in a large, genome-wide association study (using 526 SNPs from 2,032 AD cases and 5,328 controls) performed in France. The APOE, CLU, PICALM, and CR1 loci were excluded, since they had already been extensively analyzed. Ten genes/loci (TFAM, SORL1, CHRNB2, SORCS1, DAPK1, MTHFR, GWA 14q32.13, BDNF, NEDD9, and CH25H) showed weak nominal association with AD risk, in line with previous studies. In the remaining ten genes/loci (TNK1, ACE, CST3, IL1B, hCG2039140, PRNP, GAB2, LOC651924, IL1A, and TF), no single nucleotide polymorphisms were associated in our dataset. Of the genes showing nominal association in our cohorts, TFAM and CHRNB2 appear particularly interesting and warrant further genetic and functional follow-up analyses.

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Language(s): eng - English
 Dates: 2010
 Publication Status: Issued
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Title: Journal of Alzheimer's Disease
  Alternative Title : J Alzheimers Dis
Source Genre: Journal
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Pages: - Volume / Issue: 20 (4) Sequence Number: - Start / End Page: 1181 - 1188 Identifier: ISSN: 1387-2877