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Journal of the American Society of Nephrology : JASN|April 13, 2016
The Role of TNF Superfamily Member 13 in the Progression of IgA NephropathySeung Seok Han, Seung Hee Yang, Murim Choi, et al.Science (New York, N.Y.)|February 12, 2011
K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertensionMurim Choi, Ute I Scholl, Peng Yue, et al.Human Molecular Genetics|January 11, 2015
Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencingJohn W Kunstman, C Christofer Juhlin, Gerald Goh, et al.Signal Transduction and Targeted Therapy|May 6, 2026
ADAMTS4 elicits myeloid-derived immune cell recruitment and liver fibrogenesis in metabolic dysfunction-associated steatotic liver diseaseJeongwoo Park, Taeeung Kim, Wan Seob Shim, et al.Nature Communications|August 2, 2024
Prion-like domain mediated phase separation of ARID1A promotes oncogenic potential of Ewing's sarcomaYong Ryoul Kim, Jaegeon Joo, Hee Jung Lee, et al.Nature Genetics|April 22, 2014
Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumorsGerald Goh, Ute I Scholl, James M Healy, et al.Experimental & Molecular Medicine|July 31, 2024
Comprehensive molecular characterization of TFE3-rearranged renal cell carcinomaCho-Rong Lee, Jungyo Suh, Dongjun Jang, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegenerationKaya Bilguvar, Navneet K Tyagi, Cigdem Ozkara, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2025
Biallelic BRF2 mutations disrupt redox homeostasis as etiological factors in syndromic immunodeficiency and developmental disordersSeobin Yoon, Seungbok Lee, Haeyoon Kwon, et al.Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.Pageof 18