Sayaka Ogikubo

Correlation between Clinical Phenotypes and X-inactivation Patterns in Six Female Carriers with Heterozygote Vasopressin Type 2 Receptor Gene Mutations

Mari Satoh, Sayaka Ogikubo, Atsuko Yoshizawa-Ogasawara · Endocrine Journal · 2008 · 44 citations · Full text

X-inactivation Patterns, Clinical Symptoms, Human Growth +17

Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene

Atsuko Yoshizawa-Ogasawara, Sayaka Ogikubo, Mari Satoh et al. · Journal of Pediatric Endocrinology and Metabolism · 2012 · 27 citations

Novel Mutation, Developmental Biology, Biochemistry +15

Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene

Mari Satoh, Keiko Aso, Sayaka Ogikubo et al. · Journal of Pediatric Endocrinology and Metabolism · 2014 · 27 citations

Duox2 Gene, Genetics, Parathyroid Disease +18

Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2

Atsuko Yoshizawa-Ogasawara, Kiyomi Abe, Sayaka Ogikubo et al. · Journal of Pediatric Endocrinology and Metabolism · 2015 · 15 citations

Nadph-oxidase Domain, Biochemistry, Thyroid Function +15

Genetic Analysis in Children with Transient Thyroid Dysfunction or Subclinical Hypothyroidism Detected on Neonatal Screening

Mari Satoh, Keiko Aso, Sayaka Ogikubo et al. · Clinical Pediatric Endocrinology · 2009 · 12 citations · Full text

Genetics, Genetic Epidemiology, Thyroid Peroxidase +16