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Data on a genome-wide association study of type 2 diabetes in a Maya population.玛雅人群2型糖尿病全基因组关联研究的数据。
Data Brief. 2019 Nov 22;28:104866. doi: 10.1016/j.dib.2019.104866. eCollection 2020 Feb.
2
Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population.在玛雅人群中进行的全基因组关联研究鉴定出 2 型糖尿病的新风险位点。
Gene. 2018 Nov 30;677:324-331. doi: 10.1016/j.gene.2018.08.041. Epub 2018 Aug 18.
3
Whole-exome sequencing in maya indigenous families: variant in PPP1R3A is associated with type 2 diabetes.玛雅原住民家族的全外显子组测序:PPP1R3A 中的变异与 2 型糖尿病相关。
Mol Genet Genomics. 2018 Oct;293(5):1205-1216. doi: 10.1007/s00438-018-1453-2. Epub 2018 Jun 11.
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Front Endocrinol (Lausanne). 2023 Dec 19;14:1293124. doi: 10.3389/fendo.2023.1293124. eCollection 2023.
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Maya gene variants related to the risk of type 2 diabetes in a family-based association study.基于家系的关联研究发现与 2 型糖尿病风险相关的玛雅基因变异。
Gene. 2020 Mar 10;730:144259. doi: 10.1016/j.gene.2019.144259. Epub 2019 Nov 21.
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Cancer Epidemiol Biomarkers Prev. 2011 Aug;20(8):1599-610. doi: 10.1158/1055-9965.EPI-11-0312. Epub 2011 Jun 29.

本文引用的文献

1
Association of common polymorphisms in the and genes with type 2 diabetes-related traits in Mexicans.墨西哥人群中[具体基因名称缺失]基因常见多态性与2型糖尿病相关性状的关联。
Arch Med Sci. 2018 Oct;14(6):1361-1373. doi: 10.5114/aoms.2018.74757. Epub 2018 Mar 28.
2
Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population.在玛雅人群中进行的全基因组关联研究鉴定出 2 型糖尿病的新风险位点。
Gene. 2018 Nov 30;677:324-331. doi: 10.1016/j.gene.2018.08.041. Epub 2018 Aug 18.
3
The ADRA2A rs553668 variant is associated with type 2 diabetes and five variants were associated at nominal significance levels in a population-based case-control study from Mexico City.ADRA2A rs553668 变异与 2 型糖尿病相关,在一项来自墨西哥城的基于人群的病例对照研究中,有五个变异与该疾病在名义显著水平相关。
Gene. 2018 Aug 30;669:28-34. doi: 10.1016/j.gene.2018.05.078. Epub 2018 May 22.
4
Diabetes susceptibility in Mayas: Evidence for the involvement of polymorphisms in HHEX, HNF4α, KCNJ11, PPARγ, CDKN2A/2B, SLC30A8, CDC123/CAMK1D, TCF7L2, ABCA1 and SLC16A11 genes.玛雅人的糖尿病易感性:HHEX、HNF4α、KCNJ11、PPARγ、CDKN2A/2B、SLC30A8、CDC123/CAMK1D、TCF7L2、ABCA1和SLC16A11基因多态性参与的证据
Gene. 2015 Jul 1;565(1):68-75. doi: 10.1016/j.gene.2015.03.065. Epub 2015 Mar 31.
5
Replication of obesity and diabetes-related SNP associations in individuals from Yucatán, México.肥胖和糖尿病相关单核苷酸多态性关联在墨西哥尤卡坦半岛个体中的复制。
Front Genet. 2014 Nov 18;5:380. doi: 10.3389/fgene.2014.00380. eCollection 2014.
6
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.常见遗传变异对墨西哥梅斯蒂索人群 2 型糖尿病发病风险的影响。
Diabetes. 2012 Dec;61(12):3314-21. doi: 10.2337/db11-0550. Epub 2012 Aug 24.
7
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm.基于 imputation 和一种新的混合 SNP 选择算法,为东亚、非裔美国人和拉丁裔个体设计并覆盖高通量基因分型阵列,以实现优化。
Genomics. 2011 Dec;98(6):422-30. doi: 10.1016/j.ygeno.2011.08.007. Epub 2011 Aug 28.
8
A replication study of the IRS1, CAPN10, TCF7L2, and PPARG gene polymorphisms associated with type 2 diabetes in two different populations of Mexico.对墨西哥两个不同人群中与2型糖尿病相关的IRS1、CAPN10、TCF7L2和PPARG基因多态性的重复研究。
Ann Hum Genet. 2011 Sep;75(5):612-20. doi: 10.1111/j.1469-1809.2011.00668.x.
9
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array.下一代全基因组关联工具:高通量欧洲优化 SNP 芯片的设计和覆盖度。
Genomics. 2011 Aug;98(2):79-89. doi: 10.1016/j.ygeno.2011.04.005. Epub 2011 Apr 30.
10
Robust genomic control for association studies.用于关联研究的稳健基因组控制。
Am J Hum Genet. 2006 Feb;78(2):350-6. doi: 10.1086/500054. Epub 2005 Dec 22.

玛雅人群2型糖尿病全基因组关联研究的数据。

Data on a genome-wide association study of type 2 diabetes in a Maya population.

作者信息

Totomoch-Serra Armando, Domínguez-Cruz Miriam Givisay, Muñoz María de Lourdes, García-Escalante María Guadalupe, Burgueño Juan, Díaz-Badillo Álvaro, Valadez-González Nina, Escalante Doris Pinto

机构信息

Department of Genetics and Molecular Biology, Centro de Investigación y de Estudios Avanzados Del Instituto Politécnico Nacional, Mexico City, Mexico.

PhD Program in Medical Sciences, Universidad de La Frontera, Chile.

出版信息

Data Brief. 2019 Nov 22;28:104866. doi: 10.1016/j.dib.2019.104866. eCollection 2020 Feb.

DOI:10.1016/j.dib.2019.104866
PMID:31872004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6909262/
Abstract

Maya communities have been shown to exhibit type 2 diabetes (T2D) with high prevalence compared with Mexican mestizo populations. Furthermore, some variants associated with the risk for T2D have been described. In this study, we describe the results of a pilot genome wide association study (GWAS) using 817,823 single nucleotide polymorphisms (SNPs) to identify candidate variants for replication in future studies. Herein, we present the GWAS study data, which were divided into three parts: first, 1289 ancestry informative markers (AIMs) were selected for Latino populations containing European, African, and Native American SNPs obtained from the literature; second, a GWAS hypothesis free to select candidate genes associated with T2D was performed, which identified 24 candidate genes; and third, 39 SNPs previously associated with T2D or related traits were replicated. This article is associated with the original article published in "Gene" under the title Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population".

摘要

与墨西哥混血人群相比,玛雅人群的2型糖尿病(T2D)患病率较高。此外,已经描述了一些与T2D风险相关的变异。在本研究中,我们描述了一项先导全基因组关联研究(GWAS)的结果,该研究使用817,823个单核苷酸多态性(SNP)来识别未来研究中用于复制的候选变异。在此,我们展示了GWAS研究数据,这些数据分为三个部分:第一,从文献中获取的包含欧洲、非洲和美洲原住民SNP的1289个祖先信息标记(AIM)被选用于拉丁裔人群;第二,进行了一项无GWAS假设的研究,以选择与T2D相关的候选基因,该研究确定了24个候选基因;第三,对先前与T2D或相关性状相关的39个SNP进行了复制。本文与发表在《基因》杂志上的题为“在玛雅人群中进行的先导全基因组关联研究,识别2型糖尿病的新风险位点”的原始文章相关。