Hitomi Yatsuki
Saga, 8498501, Japan
Last Updated: 09/26/2026
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Found 16 publications
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.
Journal: Communications biology
Published: August 07, 2024
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
Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.
Journal: Clinical epigenetics
Published: December 22, 2021
Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.
Journal: American journal of medical genetics. Part A
Published: November 28, 2020
Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome.
Journal: Journal of medical genetics
Published: February 17, 2020
The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome.
Journal: Journal of human genetics
Published: April 19, 2019
Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.
Journal: Clinical epigenetics
Published: September 12, 2018
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.
Journal: Epigenetics & chromatin
Published: March 09, 2018
Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.
Journal: Human molecular genetics
Published: December 28, 2015
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.
Journal: Gene
Published: September 01, 2015
Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.
Journal: Clinical genetics
Published: July 08, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 10, 2013
Last Updated: 09/26/2026