Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations (Q34675182)

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English	Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations	scientific article

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17 March 2020

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations (English)

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17 March 2020

Beckwith-Wiedemann syndrome

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17 March 2020

Hidenobu Soejima

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17 March 2020

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Toshiyuki Maeda

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17 March 2020

Ken Higashimoto

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17 March 2020

Kosuke Jozaki

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17 March 2020

Hitomi Yatsuki

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17 March 2020

Kazuhiko Nakabayashi

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17 March 2020

Yoshio Makita

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17 March 2020

Hidefumi Tonoki

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17 March 2020

Nobuhiko Okamoto

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17 March 2020

Fumio Takada

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17 March 2020

Hirofumi Ohashi

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17 March 2020

Makoto Migita

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17 March 2020

Rika Kosaki

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17 March 2020

Keiko Matsubara

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17 March 2020

Muneaki Matsuo

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17 March 2020

Yuhei Hamasaki

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17 March 2020

Yasufumi Ohtsuka

17

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17 March 2020

Kenichi Nishioka

18

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17 March 2020

Keiichiro Joh

19

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17 March 2020

Tsunehiro Mukai

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17 March 2020

Kenichiro Hata

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17 March 2020

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8 May 2014

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17 March 2020

Genetics in Medicine

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17 March 2020

16

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12

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17 March 2020

903-912

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17 March 2020

https://scigraph.springernature.com/pub.10.1038/gim.2014.46

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Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.

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Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology

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7 July 2018

Single-cell DNA-methylation analysis reveals epigenetic chimerism in preimplantation embryos

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7 July 2018

Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders

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7 July 2018

A systematic comparison of quantitative high-resolution DNA methylation analysis and methylation-specific PCR.

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7 July 2018

Genomic imprinting and its relevance to congenital disease, infertility, molar pregnancy and induced pluripotent stem cell.

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7 July 2018

Genomic imprinting: recognition and marking of imprinted loci

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7 July 2018

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

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Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2.

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7 July 2018

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4262761

7 July 2018

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

1 reference

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7 July 2018

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

1 reference

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7 July 2018

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

1 reference

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7 July 2018

Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry

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7 July 2018

Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer

1 reference

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7 July 2018

Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing

1 reference

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7 July 2018

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

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7 July 2018

A GNAS1 imprinting defect in pseudohypoparathyroidism type IB

1 reference

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7 July 2018

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

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7 July 2018

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

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7 July 2018

Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders.

1 reference

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21 January 2018

Quantitative analysis of DNA methylation at all human imprinted regions reveals preservation of epigenetic stability in adult somatic tissue.

1 reference

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21 January 2018

Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.46

21 January 2018

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.46

21 January 2018

Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions.

1 reference

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21 January 2018

A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.

1 reference

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26 October 2018

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies

1 reference

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21 January 2018

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/24810686

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2014.46

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17 March 2020

1 reference

Europe PubMed Central

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17 March 2020

1 reference

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17 March 2020

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