Yeon-Joo Kim

Diagnostic mutational analysis of MECP2 in Korean patients with Rett syndrome

Hoon-Chul Kang, H. Kim, C. Kim, 2006, Experimental & Molecular Medicine.

Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome

J. Y. Lee, M. Levine, S. McCormack, 2017, The Journal of clinical endocrinology and metabolism.

Loss of Kallmann syndrome-associated gene WDR11 disrupts primordial germ cell development by affecting canonical and non-canonical Hedgehog signalling

Hyung-Goo Kim, D. Bennett, L. Layman, 2020, bioRxiv.

Digenic Inheritance of PROKR 2 and WDR 11 Mutations in Pituitary Stalk Interruption Syndrome and Hormone Deficiencies

J. Y. Lee, --Manuscript Draft, M. Levine, 2017 .

WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

Cheol‐Hee Kim, Hyung-Goo Kim, T. Raivio, 2017, EMBO reports.

WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

Cheol‐Hee Kim, Hyung-Goo Kim, T. Raivio, 2017, bioRxiv.

Overexpression and unique rearrangement of VH2 transcripts in immunoglobulin variable heavy chain genes in ankylosing spondylitis patients

Nayoung Kim, H. Choi, Yeon-Joo Kim, 2010, Experimental & Molecular Medicine.

Development of early diagnostic systems for ankylosing spondylitis

Yeon-Joo Kim, 2012 .