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From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies

Schizophrenia (SZ) is a severe mental disorder afflicting around 1% of the population. It is highly heritable but with complex genetics. Recent research has unraveled a plethora of risk loci for SZ. Accordingly, our conceptual understanding of SZ genetics has been rapidly evolving, from oligogenic m...

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Detalles Bibliográficos
Autores principales: Duan, Jubao, Sanders, Alan R., Gejman, Pablo V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760308/
https://www.ncbi.nlm.nih.gov/pubmed/31555746
http://dx.doi.org/10.20900/jpbs.20190014
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author Duan, Jubao
Sanders, Alan R.
Gejman, Pablo V.
author_facet Duan, Jubao
Sanders, Alan R.
Gejman, Pablo V.
author_sort Duan, Jubao
collection PubMed
description Schizophrenia (SZ) is a severe mental disorder afflicting around 1% of the population. It is highly heritable but with complex genetics. Recent research has unraveled a plethora of risk loci for SZ. Accordingly, our conceptual understanding of SZ genetics has been rapidly evolving, from oligogenic models towards polygenic or even omnigenic models. A pressing challenge to the field, however, is the translation of the many genetic findings of SZ into disease biology insights leading to more effective treatments. Bridging this gap requires the integration of genetic findings and functional genomics using appropriate cellular models. Harnessing new technologies, such as the development of human induced pluripotent stem cells (hiPSC) and the CRISPR/Cas-based genome/epigenome editing approach are expected to change our understanding of SZ disease biology to a fundamentally higher level. Here, we discuss some new developments.
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spelling pubmed-67603082019-09-25 From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies Duan, Jubao Sanders, Alan R. Gejman, Pablo V. J Psychiatr Brain Sci Article Schizophrenia (SZ) is a severe mental disorder afflicting around 1% of the population. It is highly heritable but with complex genetics. Recent research has unraveled a plethora of risk loci for SZ. Accordingly, our conceptual understanding of SZ genetics has been rapidly evolving, from oligogenic models towards polygenic or even omnigenic models. A pressing challenge to the field, however, is the translation of the many genetic findings of SZ into disease biology insights leading to more effective treatments. Bridging this gap requires the integration of genetic findings and functional genomics using appropriate cellular models. Harnessing new technologies, such as the development of human induced pluripotent stem cells (hiPSC) and the CRISPR/Cas-based genome/epigenome editing approach are expected to change our understanding of SZ disease biology to a fundamentally higher level. Here, we discuss some new developments. 2019-09-19 2019 /pmc/articles/PMC6760308/ /pubmed/31555746 http://dx.doi.org/10.20900/jpbs.20190014 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms and conditions of Creative Commons Attribution 4.0 International License.
spellingShingle Article
Duan, Jubao
Sanders, Alan R.
Gejman, Pablo V.
From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title_full From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title_fullStr From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title_full_unstemmed From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title_short From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies
title_sort from schizophrenia genetics to disease biology: harnessing new concepts and technologies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760308/
https://www.ncbi.nlm.nih.gov/pubmed/31555746
http://dx.doi.org/10.20900/jpbs.20190014
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