Hidenobu Soejima

Saga, 8498501, Japan

Last Updated: 09/26/2026

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Found 54 publications

Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.

Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.

Journal: Human genomics

Published: March 21, 2026

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site.

Methylation profile characteristics in the H19/IGF2:IG-DMR revealed by long-read sequencing analysis in patients with Beckwith-Wiedemann syndrome having defects in the OCT4/SOX2 binding site.

Journal: Clinical epigenetics

Published: July 14, 2025

Variants of NLRP genes encoding subcortical maternal complex components are linked to biparental placental mesenchymal dysplasia.

Variants of NLRP genes encoding subcortical maternal complex components are linked to biparental placental mesenchymal dysplasia.

Journal: Human genomics

Published: March 23, 2025

Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.

Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.

Journal: Communications biology

Published: August 07, 2024

Epigenetic Changes Cause Aberrantly High Expression of SOX11, Leading to Systemic Sclerosis.

Epigenetic Changes Cause Aberrantly High Expression of SOX11, Leading to Systemic Sclerosis.

Journal: The Journal of investigative dermatology

Published: June 19, 2024

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Journal: Clinical epigenetics

Published: May 13, 2024

Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.

Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.

Journal: Journal of medical genetics

Published: September 07, 2023

Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cells.

Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cells.

Journal: Glycoconjugate journal

Published: November 30, 2022

Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome.

Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome.

Journal: Cancers

Published: October 18, 2022

DNA Methylation Analysis Using Bisulfite Pyrosequencing.

DNA Methylation Analysis Using Bisulfite Pyrosequencing.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: September 29, 2022

Formation and evolution of carbonaceous asteroid Ryugu: Direct evidence from returned samples.

Formation and evolution of carbonaceous asteroid Ryugu: Direct evidence from returned samples.

Journal: Science (New York, N.Y.)

Published: September 22, 2022

Donor cord blood aging accelerates in recipients after transplantation.

Donor cord blood aging accelerates in recipients after transplantation.

Journal: Scientific reports

Published: September 13, 2022

Showing 1-12 of 54

Last Updated: 09/26/2026