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Hidenobu Soejima

Saga University
Saga Group

116

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Genomic Imprinting Disorders (Including Mesenchymal Placental Dysplasia)

2021
- Hidenobu Soejima
- Takashi Ohba
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An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.

2021 Annals of Human Genetics
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Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.

2021 American Journal of Medical Genetics Part A
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Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series.

2021 Journal of Obstetrics and Gynaecology Research
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Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome.

2020 Journal of Medical Genetics
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IFPA meeting 2018 workshop report I: Reproduction and placentation among ocean-living species; placental imaging; epigenetics and extracellular vesicles in pregnancy

2019 Placenta
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One‐week, but not 12‐hours, cast immobilization alters promotor DNA methylation patterns in the nNOS gene in mouse skeletal muscle

2019 The Journal of Physiology
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The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome

2019 Journal of Human Genetics
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DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2 ‐DMR0 as a DNA methylation‐dependent, P0 promoter‐specific enhancer

2019 The FASEB Journal
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Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.

2018 Epigenetics & Chromatin
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