Lawson LY, Migotsky N, Chermside-Scabbo CJ, Shuster JT, Joeng KS, Civitelli R, Silva MJ Loading-Induced Bone Formation is Mediated by Wnt1 Induction in Osteoblast-Lineage Cells , FASEB J: 2022

3., Zhong L, Yao L, Holdreith N, Yu W, Gui T, Miao Z, Elkaim Y, Li M, Gong Y, Pacifici M, Maity A, Busch TM, Joeng KS, Cengel K, Seale P, Tong W, Qin L. Transient expansion and myofibroblast conversion of adipogenic lineage precursors mediate bone marrow repair after radiation , Journal of Clinical Investigation: 2022

2., Turin CG, Joeng KS, Kallish S, Raper A, Asher S, Campeau PM, Khan AN, Al Mukaddam M. Heterozygous variant in WNT1 gene in two brothers with early onset osteoporosis. , Bone Report: 2021

Marom R, Burrage LC, Venditti R, Clément A, Blanco-Sánchez B, Jain M, Scott DA, Rosenfeld JA, Sutton VR, Shinawi M, Mirzaa G, DeVile C, Roberts R, Calder AD, Allgrove J, Grafe I, Lanza DG, Li X, Joeng KS, Eyre DR, Westerfield M, De Matteis MA, Lee B. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. , Am J Hum Genet: 2021

Park NR, Shetye S, Bougsh I, Keene DR, Tufa S, Hudson DM, Archer M, Qin L, Soslowsky LJ, Dyment NA, and Joeng KS. Reticulocalbin 3 is Involved in Postnatal Tendon Development by Regulating Collagen Fibrillogenesis and cellular maturation , Scientific reports: 2021

Shatha Alhamdi, Yi‐Chien Lee, Shimul Chowdhury, Peter H. Byers, Michael Gottschalk, Ryan J. Taft, Kyu Sang Joeng, Brendan H. Lee, Lynne M. Bird Heterozygous WNT1 variant causing a variable bone phenotype. , American Journal of Medical Genetics: 2018

Lim J, Munivez E, Jiang MM, Song IW, Gannon F, Keene DR, Schweitzer R, Lee BH, Joeng KS. mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development. , Sci Rep.: 2017

Joeng KS, Lee YC, Lim J, Chen Y, Jiang MM, Munivez E, Ambrose C, Lee BH Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis. , J Clin Invest, 127(7): 2017,2678-88

Hudson DM, Weis M, Rai J, Joeng KS, Dimori M, Lee BH, Morello R, Eyre DR P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA. , J Biol Chem, 292(9): 2017,3877-87

Rajagopal A, Homan EP, Joeng KS, Suzuki M, Bertin T, Cela R, Munivez E, Dawson B, Jiang MM, Gannon F, Crawford S, Lee BH Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice. , Mol Genet Metab, 117(3): 2016,378-82