H.‐W. Yoo

Characteristics of CADASIL in Korea

Y. Kim, Eun Jung Choi, Choong Gon Choi et al. · Neurology · 2006 · 98 citations

Life Sciences, Genetics, Neurology +17

Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene.

Cecilia A. Warner, H.‐W. Yoo, A G Roberts et al. · Journal of Clinical Investigation · 1992 · 68 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndrome

Adam Stevens, Peter Clayton, Luciano Tatò et al. · The Pharmacogenomics Journal · 2013 · 36 citations · Full text

Medicine, Endocrinology, Genetics +17

Molecular and Clinical Characterization of Korean Patients with Congenital Lipoid Adrenal Hyperplasia

H.‐W. Yoo, G H Kim · Journal of Pediatric Endocrinology and Metabolism · 1998 · 35 citations

Life Sciences, Endocrinology, Genetics +17

A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome

Peter Clayton, Pierre Chatelain, Luciano Tatò et al. · European Journal of Endocrinology · 2013 · 34 citations · Full text

Medicine, Genetics, Pediatrics +17