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Journal of Microbiology and Biotechnology|July 5, 2008
Genome-wide identification of haploinsufficiency in fission yeastSeung Tae Baek, Sangjo Han, Miyoung Nam, et al.Journal of Medical Genetics|March 23, 2021
Rising of LOXHD1 as a signature causative gene of down-sloping hearing loss in people in their teens and 20sBong Jik Kim, Hyoung Won Jeon, Woosung Jeon, et al.Journal of Microbiology and Biotechnology|March 1, 2008
Genome-wide drug-induced haploinsufficient screening of fission yeast for identification of hydrazinocurcumin targetsSeung Tae Baek, Dong-Uk Kim, Sangjo Han, et al.American Journal of Human Genetics|May 31, 2016
BGN Mutations in X-Linked Spondyloepimetaphyseal DysplasiaSung Yoon Cho, Jun-Seok Bae, Nayoung K D Kim, et al.American Journal of Human Genetics|December 14, 2011
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic typeByung-Joo Min, Namshin Kim, Taesu Chung, et al.American Journal of Human Genetics|February 19, 2019
Hypomorphic Mutations in TONSL Cause SPONASTRIME DysplasiaHae Ryung Chang, Sung Yoon Cho, Jae Hoon Lee, et al.Nature Biotechnology|May 18, 2010
Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombeDong-Uk Kim, Jacqueline Hayles, Dongsup Kim, et al.Neuroscience Research|May 4, 2010
Two genetic variants of CD38 in subjects with autism spectrum disorder and controlsToshio Munesue, Shigeru Yokoyama, Kazuhiko Nakamura, et al.Pageof 11