Hiroko Kawata-Ogata

Setagaya, 1578535, Japan

Last Updated: 09/26/2026

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Found 25 publications

A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genes.

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

Isolation of Nucleated Red Blood Cells With Intact Genomic DNA From Cord Blood by Applying G&T-Seq.

Isolation of Nucleated Red Blood Cells With Intact Genomic DNA From Cord Blood by Applying G&T-Seq.

Journal: Reproductive medicine and biology

Published: March 12, 2025

Approaches to Evaluate Whole Exome Sequencing Data That Incorporate Genetic Intolerance Scores for Congenital Anomalies, Including Intronic Regions Adjacent to Exons.

Approaches to Evaluate Whole Exome Sequencing Data That Incorporate Genetic Intolerance Scores for Congenital Anomalies, Including Intronic Regions Adjacent to Exons.

Journal: Molecular genetics & genomic medicine

Published: May 28, 2024

Rare sequence variants associated with the risk of non-syndromic biliary atresia.

Rare sequence variants associated with the risk of non-syndromic biliary atresia.

Journal: Hepatology research : the official journal of the Japan Society of Hepatology

Published: June 14, 2023

Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.

Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.

Journal: Human reproduction (Oxford, England)

Published: June 13, 2023

Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis.

Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis.

Journal: European journal of medical genetics

Published: February 13, 2023

Variations in gender identity and sexual orientation of university students.

Variations in gender identity and sexual orientation of university students.

Journal: Sexual medicine

Published: December 07, 2022

Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome.

Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome.

Journal: Reproductive medicine and biology

Published: November 21, 2022

Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers.

Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers.

Journal: Cancer medicine

Published: May 12, 2022

NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia.

NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia.

Journal: Blood advances

Published: June 11, 2021

Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles.

Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles.

Journal: BMC research notes

Published: May 06, 2021

Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing.

Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing.

Journal: Reproductive medicine and biology

Published: April 15, 2021

Showing 1-12 of 25

Last Updated: 09/26/2026