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The complex genetics of multiple sclerosis: pitfalls and prospects
The genetics of complex disease is entering a new and exciting era. The exponentially growing knowledge and technological capabilities emerging from the human genome project have finally reached the point where relevant genes can be readily and affordably identified. As a result, the last 12 months...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639203/ https://www.ncbi.nlm.nih.gov/pubmed/18490360 http://dx.doi.org/10.1093/brain/awn081 |
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author | Sawcer, Stephen |
author_facet | Sawcer, Stephen |
author_sort | Sawcer, Stephen |
collection | PubMed |
description | The genetics of complex disease is entering a new and exciting era. The exponentially growing knowledge and technological capabilities emerging from the human genome project have finally reached the point where relevant genes can be readily and affordably identified. As a result, the last 12 months has seen a virtual explosion in new knowledge with reports of unequivocal association to relevant genes appearing almost weekly. The impact of these new discoveries in Neuroscience is incalculable at this stage but potentially revolutionary. In this review, an attempt is made to illuminate some of the mysteries surrounding complex genetics. Although focused almost exclusively on multiple sclerosis all the points made are essentially generic and apply equally well, with relatively minor addendums, to any other complex trait, neurological or otherwise. |
format | Text |
id | pubmed-2639203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26392032009-02-25 The complex genetics of multiple sclerosis: pitfalls and prospects Sawcer, Stephen Brain Review Article The genetics of complex disease is entering a new and exciting era. The exponentially growing knowledge and technological capabilities emerging from the human genome project have finally reached the point where relevant genes can be readily and affordably identified. As a result, the last 12 months has seen a virtual explosion in new knowledge with reports of unequivocal association to relevant genes appearing almost weekly. The impact of these new discoveries in Neuroscience is incalculable at this stage but potentially revolutionary. In this review, an attempt is made to illuminate some of the mysteries surrounding complex genetics. Although focused almost exclusively on multiple sclerosis all the points made are essentially generic and apply equally well, with relatively minor addendums, to any other complex trait, neurological or otherwise. Oxford University Press 2008-12 2008-05-18 /pmc/articles/PMC2639203/ /pubmed/18490360 http://dx.doi.org/10.1093/brain/awn081 Text en © 2008 The Author(s) 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/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Sawcer, Stephen The complex genetics of multiple sclerosis: pitfalls and prospects |
title | The complex genetics of multiple sclerosis: pitfalls and prospects |
title_full | The complex genetics of multiple sclerosis: pitfalls and prospects |
title_fullStr | The complex genetics of multiple sclerosis: pitfalls and prospects |
title_full_unstemmed | The complex genetics of multiple sclerosis: pitfalls and prospects |
title_short | The complex genetics of multiple sclerosis: pitfalls and prospects |
title_sort | complex genetics of multiple sclerosis: pitfalls and prospects |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639203/ https://www.ncbi.nlm.nih.gov/pubmed/18490360 http://dx.doi.org/10.1093/brain/awn081 |
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