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Epi4K: Gene discovery in 4,000 genomes
A major challenge in epilepsy research is to unravel the complex genetic mechanisms underlying both common and rare forms of epilepsy, as well as the genetic determinants of response to treatment. To accelerate progress in this area, the National Institute of Neurological Disorders and Stroke (NINDS...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418423/ https://www.ncbi.nlm.nih.gov/pubmed/22642626 http://dx.doi.org/10.1111/j.1528-1167.2012.03511.x |
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collection | PubMed |
description | A major challenge in epilepsy research is to unravel the complex genetic mechanisms underlying both common and rare forms of epilepsy, as well as the genetic determinants of response to treatment. To accelerate progress in this area, the National Institute of Neurological Disorders and Stroke (NINDS) recently offered funding for the creation of a “Center without Walls” to focus on the genetics of human epilepsy. This article describes Epi4K, the collaborative study supported through this grant mechanism and having the aim of analyzing the genomes of a minimum 4,000 subjects with highly selected and well-characterized epilepsy. |
format | Online Article Text |
id | pubmed-3418423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34184232012-09-17 Epi4K: Gene discovery in 4,000 genomes Epilepsia Special Report A major challenge in epilepsy research is to unravel the complex genetic mechanisms underlying both common and rare forms of epilepsy, as well as the genetic determinants of response to treatment. To accelerate progress in this area, the National Institute of Neurological Disorders and Stroke (NINDS) recently offered funding for the creation of a “Center without Walls” to focus on the genetics of human epilepsy. This article describes Epi4K, the collaborative study supported through this grant mechanism and having the aim of analyzing the genomes of a minimum 4,000 subjects with highly selected and well-characterized epilepsy. Blackwell Publishing Ltd 2012-08 2012-05-29 /pmc/articles/PMC3418423/ /pubmed/22642626 http://dx.doi.org/10.1111/j.1528-1167.2012.03511.x Text en Wiley Periodicals, Inc. © 2012 International League Against Epilepsy http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Special Report Epi4K: Gene discovery in 4,000 genomes |
title | Epi4K: Gene discovery in 4,000 genomes |
title_full | Epi4K: Gene discovery in 4,000 genomes |
title_fullStr | Epi4K: Gene discovery in 4,000 genomes |
title_full_unstemmed | Epi4K: Gene discovery in 4,000 genomes |
title_short | Epi4K: Gene discovery in 4,000 genomes |
title_sort | epi4k: gene discovery in 4,000 genomes |
topic | Special Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418423/ https://www.ncbi.nlm.nih.gov/pubmed/22642626 http://dx.doi.org/10.1111/j.1528-1167.2012.03511.x |
work_keys_str_mv | AT epi4kgenediscoveryin4000genomes |