Yasuko Ogiwara
Setagaya, 1578535, Japan
Last Updated: 09/26/2026
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Found 9 publications
A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genes.
Journal: Genome medicine
Published: May 02, 2025
De novo retrotransposon insertion into the FGFR1 gene in a boy with congenital hypogonadotropic hypogonadism: a case report.
Journal: Frontiers in endocrinology
Published: January 23, 2025
Cutoff value of serum 25-hydroxyvitamin D leading to vitamin D deficiency for children in Japan.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: September 30, 2024
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 1.
Journal: Cytogenetic and genome research
Published: February 29, 2024
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation.
Journal: Cytogenetic and genome research
Published: October 19, 2022
Genetic Analysis of Japanese Children Clinically Diagnosed with Familial Hypercholesterolemia.
Journal: Journal of atherosclerosis and thrombosis
Published: May 20, 2021
Structural and numerical Y chromosomal variations in elderly men identified through multiplex ligation-dependent probe amplification.
Journal: Journal of human genetics
Published: March 09, 2021
Rapid Hypercalciuria Induction With Bone Formation Marker Reduction During Immobilization in Children.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: February 08, 2021
Treatment of adrenal crisis in patients with primary hypoadrenalism can lead to hypertension.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: December 01, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026