Progress in genome-wide association studies of schizophrenia in Han Chinese populations

Abstract Since 2006, genome-wide association studies of schizophrenia have led to the identification of numerous novel risk loci for this disease. However, there remains a geographical imbalance in genome-wide association studies, which to date have primarily focused on Western populations. During t...

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Autores principales: Weihua Yue, Xin Yu, Dai Zhang
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Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/0f1d7b4cb3a64612bfa2bd3637d4e52d
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spelling oai:doaj.org-article:0f1d7b4cb3a64612bfa2bd3637d4e52d2021-12-02T12:30:09ZProgress in genome-wide association studies of schizophrenia in Han Chinese populations10.1038/s41537-017-0029-12334-265Xhttps://doaj.org/article/0f1d7b4cb3a64612bfa2bd3637d4e52d2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41537-017-0029-1https://doaj.org/toc/2334-265XAbstract Since 2006, genome-wide association studies of schizophrenia have led to the identification of numerous novel risk loci for this disease. However, there remains a geographical imbalance in genome-wide association studies, which to date have primarily focused on Western populations. During the last 6 years, genome-wide association studies in Han Chinese populations have identified both the sharing of susceptible loci across ethnicities and genes unique to Han Chinese populations. Here, we review recent progress in genome-wide association studies of schizophrenia in Han Chinese populations. Researchers have identified and replicated the sharing of susceptible genes, such as within the major histocompatibility complex, microRNA 137 (MIR137), zinc finger protein 804A (ZNF804A), vaccinia related kinase 2 (VRK2), and arsenite methyltransferase (AS3MT), across both European and East Asian populations. Several copy number variations identified in European populations have also been validated in the Han Chinese, including duplications at 16p11.2, 15q11.2-13.1, 7q11.23, and VIPR2 and deletions at 22q11.2, 1q21.1-q21.2, and NRXN1. However, these studies have identified some potential confounding factors, such as genetic heterogeneity and the effects of natural selection on tetraspanin 18 (TSPAN18) or zinc finger protein 323 (ZNF323), which may explain the population differences in genome-wide association studies. In the future, genome-wide association studies in Han Chinese populations should include meta-analyzes or mega-analyses with enlarged sample sizes across populations, deep sequencing, precision medicine treatment, and functional exploration of the risk genes for schizophrenia.Weihua YueXin YuDai ZhangNature PortfolioarticlePsychiatryRC435-571ENnpj Schizophrenia, Vol 3, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Psychiatry
RC435-571
spellingShingle Psychiatry
RC435-571
Weihua Yue
Xin Yu
Dai Zhang
Progress in genome-wide association studies of schizophrenia in Han Chinese populations
description Abstract Since 2006, genome-wide association studies of schizophrenia have led to the identification of numerous novel risk loci for this disease. However, there remains a geographical imbalance in genome-wide association studies, which to date have primarily focused on Western populations. During the last 6 years, genome-wide association studies in Han Chinese populations have identified both the sharing of susceptible loci across ethnicities and genes unique to Han Chinese populations. Here, we review recent progress in genome-wide association studies of schizophrenia in Han Chinese populations. Researchers have identified and replicated the sharing of susceptible genes, such as within the major histocompatibility complex, microRNA 137 (MIR137), zinc finger protein 804A (ZNF804A), vaccinia related kinase 2 (VRK2), and arsenite methyltransferase (AS3MT), across both European and East Asian populations. Several copy number variations identified in European populations have also been validated in the Han Chinese, including duplications at 16p11.2, 15q11.2-13.1, 7q11.23, and VIPR2 and deletions at 22q11.2, 1q21.1-q21.2, and NRXN1. However, these studies have identified some potential confounding factors, such as genetic heterogeneity and the effects of natural selection on tetraspanin 18 (TSPAN18) or zinc finger protein 323 (ZNF323), which may explain the population differences in genome-wide association studies. In the future, genome-wide association studies in Han Chinese populations should include meta-analyzes or mega-analyses with enlarged sample sizes across populations, deep sequencing, precision medicine treatment, and functional exploration of the risk genes for schizophrenia.
format article
author Weihua Yue
Xin Yu
Dai Zhang
author_facet Weihua Yue
Xin Yu
Dai Zhang
author_sort Weihua Yue
title Progress in genome-wide association studies of schizophrenia in Han Chinese populations
title_short Progress in genome-wide association studies of schizophrenia in Han Chinese populations
title_full Progress in genome-wide association studies of schizophrenia in Han Chinese populations
title_fullStr Progress in genome-wide association studies of schizophrenia in Han Chinese populations
title_full_unstemmed Progress in genome-wide association studies of schizophrenia in Han Chinese populations
title_sort progress in genome-wide association studies of schizophrenia in han chinese populations
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/0f1d7b4cb3a64612bfa2bd3637d4e52d
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