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Nature Communications|January 13, 2021
A logical network-based drug-screening platform for Alzheimer's disease representing pathological features of human brain organoidsJong-Chan Park, So-Yeong Jang, Dongjoon Lee, et al.
Brain : a Journal of Neurology|September 25, 2025
Normalization of network activity in an epilepsy model with a constitutively active GABBR2 variantMichal Stawarski, Daniel Ulrich, Sebastian Reinartz, et al.
Nature Genetics|September 15, 2014
Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammationNeil Romberg, Khatoun Al Moussawi, Carol Nelson-Williams, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Fam83h null mice support a neomorphic mechanism for human ADHCAIShih-Kai Wang, Yuanyuan Hu, Jie Yang, et al.
Scientific Reports|November 25, 2015
Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasiaBeryl Royer-Bertrand, Silvia Castillo-Taucher, Rodrigo Moreno-Salinas, et al.
The New England Journal of Medicine|May 16, 2014
A form of the metabolic syndrome associated with mutations in DYRK1BAli R Keramati, Mohsen Fathzadeh, Gwang-Woong Go, et al.
Science Advances|March 14, 2025
Inhibiting EZH2 complements steroid effects in Duchenne muscular dystrophyEun Young Jeon, Yejin Kwak, Hyeji Kang, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 22, 2016
Epigenetic regulation of Kcna3-encoding Kv1.3 potassium channel by cereblon contributes to regulation of CD4+ T-cell activationJung-Ah Kang, Sang-Heon Park, Sang Phil Jeong, et al.
Cancers|July 2, 2021
Overexpression of Replication-Dependent Histone Signifies a Subset of Dedifferentiated Liposarcoma with Increased AggressivenessYongjin Yoo, Sang-Yoon Park, Eun Byeol Jo, et al.
Journal of Hepatology|April 23, 2021
Disease-specific eQTL screening reveals an anti-fibrotic effect of AGXT2 in non-alcoholic fatty liver diseaseTaekyeong Yoo, Sae Kyung Joo, Hyo Jung Kim, et al.
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