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Opening the white box: Exploring the study of whiteness in contemporary genetics research

机译:打开白盒子:探索当代遗传学研究中的白度研究

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This article addresses the routine use of race and ethnicity in the context of applied population genetics, which includes research in genetic epidemiology into the causes of common, complex diseases and in pharmacogenetics - the study of the genetic basis of how people respond to pharmaceuticals. It investigates how categories of “whiteness” are operationalized in everyday scientific practice. It reviews the critique of the presumed homogeneity, invisibility and “common-sense” status of whiteness in the epidemiological and clinical literature, and draws on qualitative interviews conducted with twenty-eight UK-based researchers working in the areas of genetic epidemiology and pharmacogenetics. The study explores how researchers justify the inclusion of white/Caucasians in studies and the exclusion of other ethnic groups, operationalize white/Caucasian as a category by which volunteers or patients are selected in and out of studies, and show how genetic evidence can also challenge researchers' assumptions and problematize their everyday use of categories such as white/Caucasian.
机译:本文介绍了在应用的人口遗传学背景下种族和种族的常规使用,其中包括对常见,复杂疾病的成因进行遗传流行病学研究和药物遗传学研究-人们对药物反应方式的遗传基础研究。它研究了日常科学实践中如何操作“白度”类别。它回顾了对流行病学和临床文献中假定的同质性,隐形性和“常识”状态的白人的批评,并利用了对28名英国研究人员进行的定性访谈,这些研究人员从事基因流行病学和药物遗传学研究。该研究探索了研究人员如何证明将白人/高加索人包括在研究中以及排除其他种族群体是合理的,将白人/高加索人作为选择志愿者或患者进行研究或从研究中选出的一类,并展示遗传证据如何也可以挑战研究人员的假设并使他们日常使用诸如白人/高加索人等类别的问题。

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