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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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Autores principales: Bettens, Karolien, Sleegers, Kristel, Van Broeckhoven, Christine
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
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.
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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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