Kazumichi Onigata

Deletions of the Homeobox Gene<i>SHOX</i>(Short Stature Homeobox) Are an Important Cause of Growth Failure in Children with Short Stature

Gudrun Rappold, Maki Fukami, Beate Niesler et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 208 citations

Short Stature, Human Growth, Complete Gene Deletions +17

Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital Hypothyroidism

I. Zamproni, Helmut Grasberger, Francesca Cortinovis et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 177 citations · Full text

Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects

Hidekazu Nishigori, Hideaki Tomura, Naoko Tonooka et al. · Proceedings of the National Academy of Sciences · 2001 · 167 citations · Full text

Clinical and genetic aspects of hypophosphatasia in Japanese patients

Takeshi Taketani, Kazumichi Onigata, Hironori Kobayashi et al. · Archives of Disease in Childhood · 2013 · 89 citations

Detection of Skewed X-Inactivation in Two Female Carriers of Vasopressin Type 2 Receptor Gene Mutation

Yoko Nomura, Kazumichi Onigata, Tomohisa Nagashima et al. · The Journal of Clinical Endocrinology & Metabolism · 1997 · 74 citations

Vasopressin Type 2, Genetics, Genetic Epidemiology +25