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Brain & Development
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February 12, 2018
Familial cases of progressive myoclonic epilepsy caused by maternal somatic mosaicism of a recurrent KCNC1 p.Arg320His mutation
Hyuna Kim, Sangmoon Lee, Murim Choi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 3, 2017
eIF2B-related multisystem disorder in two sisters with atypical presentations
Jin Sook Lee, Sangmoon Lee, Murim Choi, et al.
Cancer Investigation
|
May 22, 2024
Analytical and Clinical Validation of a Target-Enhanced Whole Genome Sequencing-Based Comprehensive Genomic Profiling Test
Stephanie Ferguson, Shruthi Sriram, Jonathan Kyle Wallace, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
March 28, 2025
CGE25-108: Uncovering APOBEC Mutational Signatures in Cancer: The Power of Whole Genome Sequencing for Comprehensive Genomic Profiling
Erin Connolly-Strong, Ryul Kim, Brain Beak-Lok Oh, et al.
Nature Medicine
|
July 10, 2021
A human three-dimensional neural-perivascular 'assembloid' promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology
Lu Wang, David Sievert, Alex E Clark, et al.
IEEE Transactions on Biomedical Circuits and Systems
|
December 10, 2025
A Behind-The-Ear Patch-Type Mental Healthcare Integrated Interface with Adaptive Multimodal Offset Compensation and Parasitic Cancellation
Hyunjoong Kim, Sanghyeon Cho, Myeong Woo Kim, et al.
International Journal of Molecular Sciences
|
November 27, 2025
Cryopreserved Tissue Biospecimens Offer Superior Quality for Whole-Genome Sequencing of Various Cancers Compared to Paired Formalin-Fixed Paraffin-Embedded Tissues
Ken Dixon, Jeong-Hoon Lee, Ryan Miller, et al.
Case Reports in Oncology
|
February 26, 2024
Clinical Utility of Whole-Genome Analysis as One-for-All Test for Breast Cancer: A Case Series
Kabsoo Shin, Ryul Kim, Hansol Park, et al.
Scientific Reports
|
June 29, 2017
Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population
Sangmoon Lee, Jihae Seo, Jinman Park, et al.
American Journal of Medical Genetics. Part A
|
July 14, 2016
Atypical presentation of infantile-onset farber disease with novel ASAH1 mutations
Soo Yeon Kim, Sun Ah Choi, Sangmoon Lee, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
Brain & Development
|
February 12, 2018
Familial cases of progressive myoclonic epilepsy caused by maternal somatic mosaicism of a recurrent KCNC1 p.Arg320His mutation
Hyuna Kim, Sangmoon Lee, Murim Choi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 3, 2017
eIF2B-related multisystem disorder in two sisters with atypical presentations
Jin Sook Lee, Sangmoon Lee, Murim Choi, et al.
Cancer Investigation
|
May 22, 2024
Analytical and Clinical Validation of a Target-Enhanced Whole Genome Sequencing-Based Comprehensive Genomic Profiling Test
Stephanie Ferguson, Shruthi Sriram, Jonathan Kyle Wallace, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
March 28, 2025
CGE25-108: Uncovering APOBEC Mutational Signatures in Cancer: The Power of Whole Genome Sequencing for Comprehensive Genomic Profiling
Erin Connolly-Strong, Ryul Kim, Brain Beak-Lok Oh, et al.
Nature Medicine
|
July 10, 2021
A human three-dimensional neural-perivascular 'assembloid' promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology
Lu Wang, David Sievert, Alex E Clark, et al.
IEEE Transactions on Biomedical Circuits and Systems
|
December 10, 2025
A Behind-The-Ear Patch-Type Mental Healthcare Integrated Interface with Adaptive Multimodal Offset Compensation and Parasitic Cancellation
Hyunjoong Kim, Sanghyeon Cho, Myeong Woo Kim, et al.
International Journal of Molecular Sciences
|
November 27, 2025
Cryopreserved Tissue Biospecimens Offer Superior Quality for Whole-Genome Sequencing of Various Cancers Compared to Paired Formalin-Fixed Paraffin-Embedded Tissues
Ken Dixon, Jeong-Hoon Lee, Ryan Miller, et al.
Case Reports in Oncology
|
February 26, 2024
Clinical Utility of Whole-Genome Analysis as One-for-All Test for Breast Cancer: A Case Series
Kabsoo Shin, Ryul Kim, Hansol Park, et al.
Scientific Reports
|
June 29, 2017
Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population
Sangmoon Lee, Jihae Seo, Jinman Park, et al.
American Journal of Medical Genetics. Part A
|
July 14, 2016
Atypical presentation of infantile-onset farber disease with novel ASAH1 mutations
Soo Yeon Kim, Sun Ah Choi, Sangmoon Lee, et al.
Page
of 6