Correction: Association of Genetic Variants with Isolated Fasting Hyperglycaemia and Isolated Postprandial Hyperglycaemia in a Han Chinese Population
Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects we...
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| Published in | PloS one Vol. 8; no. 8 |
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| Main Authors | , , , , , , , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
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United States
Public Library of Science
2013
Public Library of Science (PLoS) |
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| Online Access | Get full text |
| ISSN | 1932-6203 1932-6203 |
| DOI | 10.1371/annotation/936a4359-1bf5-4c33-be7d-1468e75eaa8b |
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| Abstract | Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects were not significantly more than that in the control group (ptrend = 0.2752; Figure 2A); and the number of risk alleles did not increase the risk of IFH (1.053 [0.963-1.150] per allele, p = 0.2564; Figure 2C). |
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| AbstractList | [This corrects the article DOI: 10.1371/journal.pone.0071399.].[This corrects the article DOI: 10.1371/journal.pone.0071399.]. [This corrects the article DOI: 10.1371/journal.pone.0071399.]. Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects were not significantly more than that in the control group (ptrend = 0.2752; Figure 2A); and the number of risk alleles did not increase the risk of IFH (1.053 [0.963-1.150] per allele, p = 0.2564; Figure 2C). Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the above loci than controls (ptrend < 0.0001; Figure 2A). In SNPs associated with IPH, the numbers of risk alleles carried in IFH subjects were not significantly more than that in the control group (ptrend = 0.2752; Figure 2A); and the number of risk alleles did not increase the risk of IFH (1.053 [0.963-1.150] per allele, p = 0.2564; Figure 2C). |
| Author | Jia, Weiping Yang, Wenying Lu, Juming Tian, Haoming Zhu, Dalong Chen, Ying Shan, Guangliang Chen, Li Guo, Xiaohui Liu, Jie Ji, Qiuhe Li, Qiang Xiao, Jianzhong Chen, Gang Ge, Jiapu Zhou, Zhiguang Ji, Linong Zhao, Zhigang Weng, Jianping Shan, Zhongyan Hong, Jing Kong, Xiaomu |
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| Snippet | [This corrects the article DOI: 10.1371/journal.pone.0071399.]. Joint study of IPH associated SNPs, including TCF7L2, CDKAL1, KCNQ1, PRC1, TP53INP1 and GCKR, shows that individuals with IPH carry more risk alleles from the... [This corrects the article DOI: 10.1371/journal.pone.0071399.].[This corrects the article DOI: 10.1371/journal.pone.0071399.]. |
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| SubjectTerms | Genetic diversity Genetic variance Hyperglycemia |
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| Title | Correction: Association of Genetic Variants with Isolated Fasting Hyperglycaemia and Isolated Postprandial Hyperglycaemia in a Han Chinese Population |
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