Lee, Min Goo

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1

Klionsky, D. J., Abdel-Aziz, A. K., Abdelfatah, S., Abdellatif, M., Abdoli, A., Abel, S., Abeliovich, H., Abildgaard, M. H., Abudu, Y. P., Acevedo-Arozena, A., et al. (2021) · Autophagy

Autophagy in Disease and TherapyCalcium signaling and nucleotide metabolism

Cited by 2,897

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

Won, H., Lee, H.-R., Gee, H. Y., Mah, W., Kim, J.-I., Lee, J., Ha, S., Chung, C., Jung, E. S., Cho, Y. S., et al. (2012) · Nature

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 695

Targeting mutant KRAS with CRISPR-Cas9 controls tumor growth

Kim, W., Lee, S., Kim, H. S., Song, M., Cha, Y. H., Kim, Y.-H., Shin, J., Lee, E.-S., Joo, Y., Song, J. J., et al. (2018) · Genome Research

CRISPR and Genetic EngineeringVirus-based gene therapy research

Cited by 97

A predictive framework for stop-loss variants with C-terminal extensions

Yoon, J. G., Lee, S., Kim, Y., Gee, H. Y., Lee, M. G., & Lee, K.-A. (2025) · Nucleic Acids Research

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 3

A predictive framework for stop-loss variants with C-terminal extensions

Yoon, J. G., Lee, S., Kim, Y., Gee, H. Y., Lee, M. G., & Lee, K.-A. (2026) · Nucleic Acids Research

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 3

Syndromic craniosynostosis caused by a novel missense variant in MAP4K4 : Expanding the genotype–phenotype relationship in RASopathies

Yoon, J. G., Yu, J. W., Shim, K. W., Kim, Y. O., & Lee, M. G. (2024) · Clinical Genetics

Craniofacial Disorders and TreatmentsGenomics and Rare Diseases

Cited by 1