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本文引用的文献

1
An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study.一项关于身体成分和肥胖表型的基因连锁的探索性研究:魁北克家庭研究。
Obes Res. 1994 May;2(3):213-9. doi: 10.1002/j.1550-8528.1994.tb00050.x.
2
Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.肥胖在家族性非胰岛素依赖型糖尿病中的隐性遗传,以及与九个候选基因无连锁关系。
Am J Hum Genet. 1997 Sep;61(3):668-77. doi: 10.1086/515509.
3
Markers for the gene ob and serum leptin levels in human morbid obesity.人类病态肥胖中ob基因的标志物及血清瘦素水平
Hum Genet. 1997 May;99(5):559-64. doi: 10.1007/s004390050406.
4
Publication bias in obesity treatment trials?肥胖治疗试验中的发表偏倚?
Int J Obes Relat Metab Disord. 1996 Oct;20(10):931-7.
5
Random effects model for meta-analysis of multiple quantitative sibpair linkage studies.用于多个定量同胞对连锁研究荟萃分析的随机效应模型。
Genet Epidemiol. 1996;13(4):377-83. doi: 10.1002/(SICI)1098-2272(1996)13:4<377::AID-GEPI6>3.0.CO;2-1.
6
OB gene not linked to human obesity in Mexican American affected sib pairs from Starr County, Texas.在来自得克萨斯州斯塔尔县的墨西哥裔美国患病同胞对中,OB基因与人类肥胖症无关。
Hum Genet. 1996 Nov;98(5):590-5. doi: 10.1007/s004390050265.
7
Absence of linkage of obesity and energy metabolism to markers flanking homologues of rodent obesity genes in Pima Indians.皮马印第安人中肥胖与能量代谢和啮齿动物肥胖基因同源物侧翼标记物之间不存在连锁关系。
Diabetes. 1996 Sep;45(9):1229-32. doi: 10.2337/diab.45.9.1229.
8
Quantitative variation in obesity-related traits and insulin precursors linked to the OB gene region on human chromosome 7.与人类7号染色体上OB基因区域相关的肥胖相关性状和胰岛素前体的定量变异。
Am J Hum Genet. 1996 Sep;59(3):694-703.
9
Extreme obesity may be linked to markers flanking the human OB gene.极度肥胖可能与人类OB基因两侧的标记物有关。
Diabetes. 1996 May;45(5):691-4. doi: 10.2337/diab.45.5.691.
10
Indication for linkage of the human OB gene region with extreme obesity.人类肥胖基因区域与极度肥胖的连锁指征。
Diabetes. 1996 May;45(5):687-90. doi: 10.2337/diab.45.5.687.

最坏情况下连锁数据的荟萃分析:以人类OB区域为例的演示

Meta-analysis of linkage data under worst-case conditions: a demonstration using the human OB region.

作者信息

Allison D B, Heo M

机构信息

Obesity Research Center, St. Luke's/Roosevelt Hospital Center, Columbia University College of Physicians & Surgeons, New York, New York 10025, USA.

出版信息

Genetics. 1998 Feb;148(2):859-65. doi: 10.1093/genetics/148.2.859.

DOI:10.1093/genetics/148.2.859
PMID:9504931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1459818/
Abstract

To date, few methods have been developed explicitly for meta-analysis of linkage analyses. Moreover, the methods that have been developed or suggested generally depend on certain ideal situations and have not been widely applied. In this article, we apply standard statistical theory and meta-analytic techniques in novel ways to five published papers discussing the evidence of linkage of body mass index (BMI) to the region of the human genome containing the OB gene. These methods are "inference based," meaning that they allow one to make statements about the statistical significance of the entire body of evidence. As currently developed, they do not allow specific statements to be made about the amount of variance explained by any putative locus or allow precise confidence intervals to be placed around the putative location of a linked locus. By applying these techniques to the literature on linkage in the human OB gene region, we are able to show that the evidence for linkage somewhere in the region is extremely strong (P = 1.5 x 10[-5]).

摘要

迄今为止,专门针对连锁分析的荟萃分析所开发的方法很少。此外,已开发或建议的方法通常依赖于某些理想情况,尚未得到广泛应用。在本文中,我们以新颖的方式将标准统计理论和荟萃分析技术应用于五篇已发表的论文,这些论文讨论了体重指数(BMI)与包含OB基因的人类基因组区域之间连锁的证据。这些方法是“基于推断的”,这意味着它们允许人们对整个证据体的统计显著性做出陈述。按照目前的发展情况,它们不允许对任何假定基因座所解释的方差量做出具体陈述,也不允许在连锁基因座的假定位置周围放置精确的置信区间。通过将这些技术应用于人类OB基因区域连锁的文献,我们能够表明该区域某处存在连锁的证据极其有力(P = 1.5×10[-5])。