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Current status on Alzheimer disease molecular genetics: from past, to present, to future
Linkage studies, candidate gene and whole-genome association studies have resulted in a tremendous amount of putative risk genes for Alzheimer's disease (AD). Yet, besides the three causal genes—amyloid precursor protein and presenilin 1 and 2 genes—and one risk gene apolipoprotein E (APOE), no...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875058/ https://www.ncbi.nlm.nih.gov/pubmed/20388643 http://dx.doi.org/10.1093/hmg/ddq142 |
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author | Bettens, Karolien Sleegers, Kristel Van Broeckhoven, Christine |
author_facet | Bettens, Karolien Sleegers, Kristel Van Broeckhoven, Christine |
author_sort | Bettens, Karolien |
collection | PubMed |
description | Linkage studies, candidate gene and whole-genome association studies have resulted in a tremendous amount of putative risk genes for Alzheimer's disease (AD). Yet, besides the three causal genes—amyloid precursor protein and presenilin 1 and 2 genes—and one risk gene apolipoprotein E (APOE), no single functional risk variant was identified. Discussing the possible involvement of rare alleles and other types of genetic variants, this review summarizes the current knowledge on the genetic spectrum of AD and integrates different approaches and recent discoveries by genome-wide association studies. |
format | Text |
id | pubmed-2875058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28750582010-05-25 Current status on Alzheimer disease molecular genetics: from past, to present, to future Bettens, Karolien Sleegers, Kristel Van Broeckhoven, Christine Hum Mol Genet Reviews Linkage studies, candidate gene and whole-genome association studies have resulted in a tremendous amount of putative risk genes for Alzheimer's disease (AD). Yet, besides the three causal genes—amyloid precursor protein and presenilin 1 and 2 genes—and one risk gene apolipoprotein E (APOE), no single functional risk variant was identified. Discussing the possible involvement of rare alleles and other types of genetic variants, this review summarizes the current knowledge on the genetic spectrum of AD and integrates different approaches and recent discoveries by genome-wide association studies. Oxford University Press 2010-04-15 2010-04-13 /pmc/articles/PMC2875058/ /pubmed/20388643 http://dx.doi.org/10.1093/hmg/ddq142 Text en © The Author 2010. Published by Oxford University Press http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Bettens, Karolien Sleegers, Kristel Van Broeckhoven, Christine Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title | Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title_full | Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title_fullStr | Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title_full_unstemmed | Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title_short | Current status on Alzheimer disease molecular genetics: from past, to present, to future |
title_sort | current status on alzheimer disease molecular genetics: from past, to present, to future |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875058/ https://www.ncbi.nlm.nih.gov/pubmed/20388643 http://dx.doi.org/10.1093/hmg/ddq142 |
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