- Direct-to-consumer genetic testing
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Kim JW
- KMID: 2462048
- Genomics Inform.
- 2019 Sep;17(3):e34.
- doi: 10.5808/GI.2019.17.3.e34
Direct-to-consumer (DTC) genetic testing is a controversial issue although Korean Government is considering to expand DTC genetic testing. Preventing the exaggeration and abusing of DTC genetic testing is an important... -
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- Regulated sandbox and disease-related genetic tests as a direct-to-consumer test
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Kim JW
- KMID: 2445786
- J Korean Med Assoc.
- 2019 May;62(5):240-242.
- doi: 10.5124/jkma.2019.62.5.240
Recently, the Korean government introduced a regulatory sandbox that includes direct-to-consumer (DTC) genetic tests. Several genetic testing companies received approval for predictive DTC genetic tests for conditions ranging from cancer... -
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- Current Status and Issues of Genetic Testing in Korea
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Hong YJ, Min WK
- KMID: 1958258
- J Korean Med Assoc.
- 2006 Jul;49(7):597-602.
- doi: 10.5124/jkma.2006.49.7.597
Since the effectuation of a new bioethical law, the number of registered genetic testing laboratories in Korea has reached about one hundred and seventy, as of June 2006. For the purpose of supervision... -
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- Genetic Testing and Genetic Counseling
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Kim HJ
- KMID: 1958259
- J Korean Med Assoc.
- 2006 Jul;49(7):603-611.
- doi: 10.5124/jkma.2006.49.7.603
he successful completion of Human Genome Project (HGP) and further advances in genomic research and technology ushered a new era of genetic medicine in the 21st century. The discovery of a gene-disease... -
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- Direct-to-consumer genetic testing: advantages and pitfalls
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Oh B
- KMID: 2462047
- Genomics Inform.
- 2019 Sep;17(3):e33.
- doi: 10.5808/GI.2019.17.3.e33
No abstract available. -
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- From Genetic Testing to Treatment and Prevention of BRCA-Related Breast Cancer
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Ki CS
- KMID: 2460906
- Ann Lab Med.
- 2020 Mar;40(2):99-100.
- doi: 10.3343/alm.2020.40.2.99
No abstract available. -
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- Clinical Application of Genetic Testing
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Yoo HW
- KMID: 1958257
- J Korean Med Assoc.
- 2006 Jul;49(7):589-596.
- doi: 10.5124/jkma.2006.49.7.589
The completion of the human genome project enables us to understand the molecular pathophysiology of human genetic diseases more deeply. In addition, information from genomics has been utilized for the diagnosis of... -
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- Evidence-based Entry of Genetic Testing
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Lee YK
- KMID: 1958255
- J Korean Med Assoc.
- 2006 Jul;49(7):577-582.
- doi: 10.5124/jkma.2006.49.7.577
Before the completion of the Human Genome Project (HGP), the genetics tended to be reserved only to the experts in research fields. Now genetic information has become a matter of grave concern... -
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- Prenatal Genetic Test
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Han YJ, Ryu HM
- KMID: 2184485
- J Genet Med.
- 2011 Dec;8(2):100-104.
Genetic testing has been generalized for the diagnosis of diseases and is an important method of research with advances in the life sciences. In particular, we should give better attention... -
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- Genetic testing in clinical pediatric practice
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Yoo HW
- KMID: 2281306
- Korean J Pediatr.
- 2010 Mar;53(3):273-285.
- doi: 10.3345/kjp.2010.53.3.273
Completion of the human genome project has allowed a deeper understanding of molecular pathophysiology and has provided invaluable genomic information for the diagnosis of genetic disorders. Advent of new technologies... -
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- Strategies for Protecting the Privacy in Genetic Testing
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Cha YJ
- KMID: 1958254
- J Korean Med Assoc.
- 2006 Jul;49(7):571-576.
- doi: 10.5124/jkma.2006.49.7.571
As genetic information is not changeable lifelong and might be used as disease predictors in a family, it requires special protection. Private genetic information is kind of individually identifiable health information, also known... -
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- Multiple Group Testing Procedures for Analysis of High-Dimensional Genomic Data
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Ko H, Kim K, Sun H
- KMID: 2366435
- Genomics Inform.
- 2016 Dec;14(4):187-195.
- doi: 10.5808/GI.2016.14.4.187
In genetic association studies with high-dimensional genomic data, multiple group testing procedures are often required in order to identify disease/trait-related genes or genetic regions, where multiple genetic sites or variants... -
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- Molecular Genetic Diagnosis of Genetic Endocrine Diseases
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Choi JH, Kim GH, Yoo HW
- KMID: 2135608
- J Genet Med.
- 2010 Jun;7(1):16-23.
Many endocrine disorders have a genetic component. The genetic component is the major etiologic factor in monogenic disorders, while multiple genes in conjunction with environmental and lifestyle factors contribute to... -
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- Establishment and Management of Medical Genetic Clinic Based on Genetic Testing Network
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Lee YW, Ki CS, Shin HB, Choi TY, Kim JW, Kim SH, Lee YK
- KMID: 2238905
- Korean J Lab Med.
- 2006 Apr;26(2):137-141.
- doi: 10.3343/kjlm.2006.26.2.137
BACKGROUND: With the progress of the Human Genome Project, genetic testing has become widely available and useful for the confirmation and treatment planning of various conditions. Additionally, the need for... -
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- Hereditary Dilated Cardiomyopathy: Recent Advances in Genetic Diagnostics
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Park HY
- KMID: 2385380
- Korean Circ J.
- 2017 May;47(3):291-298.
- doi: 10.4070/kcj.2016.0017
Dilated cardiomyopathy (DCM) is the most common cause of heart failure in young adults and up to 50% of idiopathic DCM is thought to be caused by genetic mutations in... -
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- Integrated diagnostic approach of pediatric neuromuscular disorders
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Lee HN, Lee YM
- KMID: 2435943
- J Genet Med.
- 2018 Dec;15(2):55-63.
- doi: 10.5734/JGM.2018.15.2.55
Clinical and genetic heterogeneity in association with overlapping spectrum is characteristic in pediatric neuromuscular disorders, which makes confirmative diagnosis difficult and time consuming. Considering evolution of molecular genetic diagnosis and... -
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- Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel
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Lee EH
- KMID: 2409829
- Korean J Pediatr.
- 2018 Apr;61(4):101-107.
- doi: 10.3345/kjp.2018.61.4.101
Recent advances in genetics have determined that a number of epilepsy syndromes that occur in the first year of life are associated with genetic etiologies. These syndromes range from benign... -
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- Search for Novel Mutational Targets in Human Endocrine Diseases
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Park SY, Seo MH, Lee S
- KMID: 2441675
- Endocrinol Metab.
- 2019 Mar;34(1):23-28.
- doi: 10.3803/EnM.2019.34.1.23
The identification of disease-causing genetic variations is an important goal in the field of genetics. Advancements in genetic technology have changed scientific knowledge and made it possible to determine the... -
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- Clinical Aspects of Genetic Testing for Dementia
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Lee SH, Park KW
- KMID: 2338710
- J Korean Geriatr Soc.
- 2008 Mar;12(1):5-10.
Dementia is the progressive or chronic dysfunction of cortical or subcortical functions that results in complex cognitive decline and Alzheimer's disease is the most common etiology of dementia. Currently, causal... -
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- Controversial issues in the legal restriction for prenatal genetic testing in Korea
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Choi J, Jeong SY, Kim HJ
- KMID: 2288521
- J Genet Med.
- 2007 Dec;4(2):186-189.
More than 6,000 rare disorders including genetic diseases have been reported. Of them, 1,500 diseases (1,211 for clinical diagnosis and 289 for research only) are technically possible for genetic testing.... -
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