Gee, Heon Yung

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

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

Sadowski, C. E., Lovric, S., Ashraf, S., Pabst, W. L., Gee, H. Y., Kohl, S., Engelmann, S., Vega-Warner, V., Fang, H., Halbritter, J., et al. (2015) · Journal of the American Society of Nephrology

Renal Diseases and GlomerulopathiesRenal and related cancers

Cited by 651

Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis

Nandadasa, S., Kraft, C. M., Wang, L. W., O’Donnell, A., Patel, R., Gee, H. Y., Grobe, K., Cox, T. C., Hildebrandt, F., & Apte, S. S. (2019) · Nature Communications

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 76

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