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Nature Genetics|May 29, 2025
Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genesAdam Jackson, Nishi Thaker, Alexander Blakes, et al.
Clinical Genetics|February 24, 2026
Exploring the Impact of RNU4-2 Defects on Neurodevelopmental Disorders in a Korean PopulationJuhyeon Hong, Seungbok Lee, Soo Yeon Kim, et al.
Plos One|January 30, 2020
Determining the cut-off score for the Modified Barthel Index and the Modified Rankin Scale for assessment of functional independence and residual disability after strokeSeung Yeol Lee, Deog Young Kim, Min Kyun Sohn, et al.
Frontiers in Genetics|October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseasesSoojin Park, Se Song Jang, Seungbok Lee, et al.
Scientific Reports|January 31, 2020
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred populationYoungha Lee, Soojin Park, Jin Sook Lee, et al.
Communications Biology|May 11, 2021
Mitofusin-2 boosts innate immunity through the maintenance of aerobic glycolysis and activation of xenophagy in micePrashanta Silwal, Jin Kyung Kim, Sang Min Jeon, et al.
Korean Journal of Radiology|January 7, 2024
Unenhanced Breast MRI With Diffusion-Weighted Imaging for Breast Cancer Detection: Effects of Training on Performance and Agreement of Subspecialty RadiologistsYeon Soo Kim, Su Hyun Lee, Soo-Yeon Kim, et al.
Journal of Breast Cancer|March 3, 2024
Omission of Breast Surgery in Predicted Pathologic Complete Response after Neoadjuvant Systemic Therapy: A Multicenter, Single-Arm, Non-inferiority TrialJi-Jung Jung, Jong-Ho Cheun, Soo-Yeon Kim, et al.
Breast Cancer Research and Treatment|May 18, 2020
Prediction of pathologic complete response using image-guided biopsy after neoadjuvant chemotherapy in breast cancer patients selected based on MRI findings: a prospective feasibility trialHan-Byoel Lee, Wonshik Han, Soo-Yeon Kim, et al.
Genome Medicine|August 7, 2025
Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disordersJihoon G Yoon, Hyunsoo Jang, Seungbok Lee, et al.
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