scholarly journals The Interface Between the Practice of Medical Genetics and Human Genetic Research: What Every Genetic Counselor Needs to Know

2004 ◽  
Vol 13 (5) ◽  
pp. 351-368 ◽  
Author(s):  
Dorene S. Markel ◽  
Beverly M. Yashar
2011 ◽  
pp. 1-14
Author(s):  
Somparn Promta

What the author is trying to do in this chapter is to explore how Buddhism, especially Theravada Buddhism as adopted in Thailand, responds to the advancements of human genetic research in the modern world. Buddhism has a certain number of doctrinal beliefs normally differing from those in the theistic tradition, making Buddhism respond to genetic research in a certain way. The way Buddhism responds to genetic research could be characterized as a kind of humanistic view. This kind of view is mainly based on human wisdom and rational investigation of the problem. Belief as normally understood in terms of religion plays a lesser role in Buddhist ethics. The following will show the positions of Buddhism on the problems raised by genetic research. As the concept of personhood plays the key role in the debates over human genetic research, the author will start with this point. As human genetic research raises so many issues that it is impossible to explore all of them, the chapter will then focus on some of these issues, namely human cloning and the use of embryonic stem cells in medical practice.


2018 ◽  
pp. 1-24 ◽  
Author(s):  
Angela R. Bradbury ◽  
Linda Patrick-Miller ◽  
Brian L. Egleston ◽  
Kara N. Maxwell ◽  
Laura DiGiovanni ◽  
...  

Purpose Understanding the outcomes of returning individual genetic research results to participants is critical because some genetic variants are found to be associated with health outcomes and have become available for clinical testing. Materials and Methods BRCA1/2-negative women with early-onset breast cancer, multiple primary cancers, or a family history of breast cancer who participated in a gene discovery cancer registry were offered the opportunity to learn their individual genetic research results of 24 breast cancer susceptibility genes with a genetic counselor after predisclosure genetic counseling. Outcomes included uptake of research results, knowledge, informed choice, psychosocial adjustment, uncertainty, satisfaction, and uptake of clinical confirmation testing. Results Four hundred two potential participants were contacted. One hundred ninety-four participants (48%) did not respond despite multiple attempts, and 85 participants (21%) actively or passively declined. One hundred seven participants (27%) elected for predisclosure counseling and were more likely to be younger, married, and white. Ninety percent of participants who had predisclosure counseling elected to receive their genetic research results, and 89% made an informed choice. Knowledge increased significantly after predisclosure counseling, and anxiety, intrusive cancer-specific distress, uncertainty, and depression declined significantly after receipt of results. General anxiety and intrusive cancer-specific distress declined significantly for both participants with a positive result and those with a negative result. Sixty-four percent of participants had clinical confirmation testing when recommended, including all participants with a mutation in a high-penetrance gene. Conclusion Uptake of genetic research results may be lower than anticipated by hypothetical reports and small select studies. Participants who elected to receive research results with genetic providers did not experience increases in distress or uncertainty, but not all patients return for confirmation testing.


2014 ◽  
Vol 15 (1) ◽  
Author(s):  
Yasuko Takezawa ◽  
Kazuto Kato ◽  
Hiroki Oota ◽  
Timothy Caulfield ◽  
Akihiro Fujimoto ◽  
...  

2005 ◽  
Vol 6 (1) ◽  
pp. 75-79 ◽  
Author(s):  
Bartha Maria Knoppers ◽  
Ruth Chadwick

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Yasue Uchida ◽  
Saiko Sugiura ◽  
Michihiko Sone ◽  
Hiromi Ueda ◽  
Tsutomu Nakashima

Age-related hearing impairment (ARHI) is a complex, multifactorial disorder that is attributable to confounding intrinsic and extrinsic factors. The degree of impairment shows substantial variation between individuals, as is also observed in the senescence of other functions. This individual variation would seem to refute the stereotypical view that hearing deterioration with age is inevitable and may indicate that there is ample scope for preventive intervention. Genetic predisposition could account for a sizable proportion of interindividual variation. Over the past decade or so, tremendous progress has been made through research into the genetics of various forms of hearing impairment, including ARHI and our knowledge of the complex mechanisms of auditory function has increased substantially. Here, we give an overview of recent investigations aimed at identifying the genetic risk factors involved in ARHI and of what we currently know about its pathophysiology. This review is divided into the following sections: (i) genes causing monogenic hearing impairment with phenotypic similarities to ARHI; (ii) genes involved in oxidative stress, biologic stress responses, and mitochondrial dysfunction; and (iii) candidate genes for senescence, other geriatric diseases, and neurodegeneration. Progress and prospects in genetic research are discussed.


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