Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasiaSu Jin Kim, Dong‐Kyu Jin, Andrea Superti‐Furga et al.|Human Genetics|2011Cited by 88
Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosisTadashi Kaname, Dong‐Kyu Jin, Chang‐Seok Ki et al.|Cellular Signalling|2014Cited by 53
BGN Mutations in X-Linked Spondyloepimetaphyseal DysplasiaSung Yoon Cho, Dong‐Kyu Jin, Jun-Seok Bae et al.|The American Journal of Human Genetics|2016Cited by 39
Osteogenesis imperfecta type V: Clinical and radiographic manifestations in mutation confirmed patientsOk‐Hwa Kim, Tae‐Joon Cho, Dong‐Kyu Jin et al.|American Journal of Medical Genetics Part A|2013Cited by 37
Identification and<i>In Vivo</i>Functional Characterization of Novel Compound Heterozygous<i>BMP1</i>Variants in Osteogenesis ImperfectaSung Yoon Cho, Dong‐Kyu Jin, P. V. Asharani et al.|Human Mutation|2014Cited by 32