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Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges

The past decade has been proclaimed as a hugely successful era of gene discovery through the high yields of many genome-wide association studies (GWAS). However, much of the perceived benefit of such discoveries lies in the promise that the identification of genes that influence disease would direct...

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Detalles Bibliográficos
Autores principales: Paternoster, Lavinia, Tilling, Kate, Davey Smith, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628782/
https://www.ncbi.nlm.nih.gov/pubmed/28981501
http://dx.doi.org/10.1371/journal.pgen.1006944
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author Paternoster, Lavinia
Tilling, Kate
Davey Smith, George
author_facet Paternoster, Lavinia
Tilling, Kate
Davey Smith, George
author_sort Paternoster, Lavinia
collection PubMed
description The past decade has been proclaimed as a hugely successful era of gene discovery through the high yields of many genome-wide association studies (GWAS). However, much of the perceived benefit of such discoveries lies in the promise that the identification of genes that influence disease would directly translate into the identification of potential therapeutic targets, but this has yet to be realized at a level reflecting expectation. One reason for this, we suggest, is that GWAS, to date, have generally not focused on phenotypes that directly relate to the progression of disease and thus speak to disease treatment.
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spelling pubmed-56287822017-10-20 Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges Paternoster, Lavinia Tilling, Kate Davey Smith, George PLoS Genet Review The past decade has been proclaimed as a hugely successful era of gene discovery through the high yields of many genome-wide association studies (GWAS). However, much of the perceived benefit of such discoveries lies in the promise that the identification of genes that influence disease would directly translate into the identification of potential therapeutic targets, but this has yet to be realized at a level reflecting expectation. One reason for this, we suggest, is that GWAS, to date, have generally not focused on phenotypes that directly relate to the progression of disease and thus speak to disease treatment. Public Library of Science 2017-10-05 /pmc/articles/PMC5628782/ /pubmed/28981501 http://dx.doi.org/10.1371/journal.pgen.1006944 Text en © 2017 Paternoster et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Paternoster, Lavinia
Tilling, Kate
Davey Smith, George
Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title_full Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title_fullStr Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title_full_unstemmed Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title_short Genetic epidemiology and Mendelian randomization for informing disease therapeutics: Conceptual and methodological challenges
title_sort genetic epidemiology and mendelian randomization for informing disease therapeutics: conceptual and methodological challenges
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628782/
https://www.ncbi.nlm.nih.gov/pubmed/28981501
http://dx.doi.org/10.1371/journal.pgen.1006944
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