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Genetics of RA susceptibility, what comes next?

Genome-wide association studies (GWASs) have been used to great effect to identify genetic susceptibility loci for complex disease. A series of GWAS and meta-analyses have informed the discovery of over 100 loci for rheumatoid arthritis (RA). In common with findings in other autoimmune diseases the...

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Autores principales: Ding, James, Eyre, Stephen, Worthington, Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612696/
https://www.ncbi.nlm.nih.gov/pubmed/26509058
http://dx.doi.org/10.1136/rmdopen-2014-000028
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author Ding, James
Eyre, Stephen
Worthington, Jane
author_facet Ding, James
Eyre, Stephen
Worthington, Jane
author_sort Ding, James
collection PubMed
description Genome-wide association studies (GWASs) have been used to great effect to identify genetic susceptibility loci for complex disease. A series of GWAS and meta-analyses have informed the discovery of over 100 loci for rheumatoid arthritis (RA). In common with findings in other autoimmune diseases the lead signals for the majority of these loci do not map to known gene sequences. In order to realise the benefit of investment in GWAS studies it is vital we determine how disease associated alleles function to influence disease processes. This is leading to rapid development in our knowledge as to the function of non-coding regions of the genome. Here we consider possible functional mechanisms for intergenic RA-associated variants which lie within lncRNA sequences.
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spelling pubmed-46126962015-10-27 Genetics of RA susceptibility, what comes next? Ding, James Eyre, Stephen Worthington, Jane RMD Open Rheumatoid Arthritis Genome-wide association studies (GWASs) have been used to great effect to identify genetic susceptibility loci for complex disease. A series of GWAS and meta-analyses have informed the discovery of over 100 loci for rheumatoid arthritis (RA). In common with findings in other autoimmune diseases the lead signals for the majority of these loci do not map to known gene sequences. In order to realise the benefit of investment in GWAS studies it is vital we determine how disease associated alleles function to influence disease processes. This is leading to rapid development in our knowledge as to the function of non-coding regions of the genome. Here we consider possible functional mechanisms for intergenic RA-associated variants which lie within lncRNA sequences. BMJ Publishing Group 2015-04-15 /pmc/articles/PMC4612696/ /pubmed/26509058 http://dx.doi.org/10.1136/rmdopen-2014-000028 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Rheumatoid Arthritis
Ding, James
Eyre, Stephen
Worthington, Jane
Genetics of RA susceptibility, what comes next?
title Genetics of RA susceptibility, what comes next?
title_full Genetics of RA susceptibility, what comes next?
title_fullStr Genetics of RA susceptibility, what comes next?
title_full_unstemmed Genetics of RA susceptibility, what comes next?
title_short Genetics of RA susceptibility, what comes next?
title_sort genetics of ra susceptibility, what comes next?
topic Rheumatoid Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612696/
https://www.ncbi.nlm.nih.gov/pubmed/26509058
http://dx.doi.org/10.1136/rmdopen-2014-000028
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