Hiromi Kamura

Setagaya, 1578535, Japan

Last Updated: 09/26/2026

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Found 17 publications

DNA methylation changes following rapid maxillary expansion in children.

DNA methylation changes following rapid maxillary expansion in children.

Journal: Scientific reports

Published: May 26, 2026

Helios expression in naive CD4+ T cells decreases from neonates to older adults.

Helios expression in naive CD4+ T cells decreases from neonates to older adults.

Journal: Clinical and experimental immunology

Published: August 20, 2025

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

Vaginal microbiota composition in pregnant women following cervical conization and radical trachelectomy.

Vaginal microbiota composition in pregnant women following cervical conization and radical trachelectomy.

Journal: Scientific reports

Published: April 10, 2025

Maternal Vitamin D Deficiency Is a Risk Factor for Infants' Epigenetic Gestational Age Acceleration at Birth in Japan: A Cohort Study.

Maternal Vitamin D Deficiency Is a Risk Factor for Infants' Epigenetic Gestational Age Acceleration at Birth in Japan: A Cohort Study.

Journal: Nutrients

Published: December 25, 2024

A prenatally diagnosed Klinefelter syndrome case of 46,XX/47,XXY mosaicism with partial deletion of Y chromosome.

A prenatally diagnosed Klinefelter syndrome case of 46,XX/47,XXY mosaicism with partial deletion of Y chromosome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 02, 2024

Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia.

Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia.

Journal: Human genome variation

Published: April 24, 2024

Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism.

Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism.

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 30, 2023

Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome.

Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome.

Journal: Genetics in medicine open

Published: July 18, 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

Genome-wide association study of preterm birth and gestational age in a Japanese population.

Genome-wide association study of preterm birth and gestational age in a Japanese population.

Journal: Human genome variation

Published: December 26, 2022

Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data.

Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data.

Journal: Scientific reports

Published: September 20, 2020

Showing 1-12 of 17

Last Updated: 09/26/2026