مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Title

ETHICAL ISSUES OF GENETIC INFORMATION BANKS

Pages

  53-82

Abstract

BIOBANKs are an essential and important tool of genetic epidemiology and screening. BIOBANKs cacould investigates the roles, effects and influences of genetic factors and their interaction with environmental factors such as nutrition, stress, etc (in a broad meaning) for the occurrence of behaviors, health conditions, diseases, and quality of life in human populations. BIOBANKs aims are to understand the influence and impact of genetics parameters on the development of behaviors, health conditions, diseases, and quality of life, their course and the clinical implications, with the final goal to improve prevention, diagnostics and therapy. The unexpected progress of genetics fields in the last two decades - with respect to the understanding of the meaning of genes for human health, as well as the availability of cost-effective high throughput methods in the lab and techniques, has opened massive opportunities to study genetic factors and their influence in human health condition. In addition, for establishment of a effective BIOBANK access to large cases and samples of patients or from the population is needed. This can be realized via collaboration of several BIOBANKs. Large BIOBANKs with 500, 000 or more participants are being established or planned in the UK, Japan, Iceland, Taiwan, Canada, Australia, Italia, Sweden and the US.However, in Germany only two smaller activities are ongoing, KORA-gen in the south and POPGEN in the north. Possibilities to reach larger numbers for Germany, based on existing cohorts or disease networks, are discussed between scientist and government. For the implementation and use of BIOBANKs, stringent ethical, social and legal boundary circumstances have to be taken into account. The opinion of the German National Ethics Council on BIOBANKs for Research as well as the new advices of the Telematic Platform (TMF), which has been developed in close collaboration with the Data Protection Officers, improve transparency and legal security.

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    APA: Copy

    KAZEMI, ABDOLHASSAN, FEIZOLLAHI, NEJAT, ABBASI, MAHMOUD, & KIANI, MEHRZAD. (2010). ETHICAL ISSUES OF GENETIC INFORMATION BANKS. MEDICAL ETHICS, 4(11), 53-82. SID. https://sid.ir/paper/195696/en

    Vancouver: Copy

    KAZEMI ABDOLHASSAN, FEIZOLLAHI NEJAT, ABBASI MAHMOUD, KIANI MEHRZAD. ETHICAL ISSUES OF GENETIC INFORMATION BANKS. MEDICAL ETHICS[Internet]. 2010;4(11):53-82. Available from: https://sid.ir/paper/195696/en

    IEEE: Copy

    ABDOLHASSAN KAZEMI, NEJAT FEIZOLLAHI, MAHMOUD ABBASI, and MEHRZAD KIANI, “ETHICAL ISSUES OF GENETIC INFORMATION BANKS,” MEDICAL ETHICS, vol. 4, no. 11, pp. 53–82, 2010, [Online]. Available: https://sid.ir/paper/195696/en

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