Tomoko Fuke

Setagaya, 1578535, Japan

Last Updated: 09/26/2026

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Found 14 publications

Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.

Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.

Journal: Clinical epigenetics

Published: May 28, 2025

Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes.

Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes.

Journal: Clinical epigenetics

Published: December 14, 2022

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders.

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 28, 2022

Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system.

Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system.

Journal: Journal of human genetics

Published: February 17, 2022

Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome.

Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome.

Journal: Clinical epigenetics

Published: June 30, 2020

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum.

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 23, 2020

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.

Journal: Clinical epigenetics

Published: March 08, 2020

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.

Journal: Journal of medical genetics

Published: April 30, 2018

Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.

Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.

Journal: Clinical epigenetics

Published: February 12, 2017

Polyhydramnios associated with Prader-Willi syndrome.

Polyhydramnios associated with Prader-Willi syndrome.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Published: August 21, 2015

Polyhydramnios associated with Prader-Willi syndrome.

Polyhydramnios associated with Prader-Willi syndrome.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Published: August 14, 2015

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.

Journal: European journal of human genetics : EJHG

Published: May 06, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026