Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Frequency and characterization of DNA methylation defects in children born SGA.

European journal of human genetics : EJHG - 1 Aug 2013

Bens Susanne, Haake Andrea, Richter Julia, Leohold Judith, Kolarova Julia, Vater Inga, Riepe Felix G, Buiting Karin, Eggermann Thomas, Gillessen-Kaesbach Gabriele, Platzer Konrad, Prawitt Dirk, Caliebe Almuth, Siebert Reiner

Abstract excerpt

Various genes located at imprinted loci and regulated by epigenetic mechanisms are involved in the control of growth and differentiation. The broad phenotypic variability of imprinting disorders suggests that individuals with inborn errors of imprinting might remain undetected among patients born small for gestational age (SGA). We evaluated quantitative DNA methylation analysis at differentially methylated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abnormalities, Multiple
Share to DNA Methylation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Genetic Loci

Share to Genomic Imprinting

Share to Infant, Newborn

Share to Infant, Small for Gestational Age

Share to Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 23232699
DOI: 10.1038/ejhg.2012.262
PMCID: PMC3722674

Genes

GRB10
IGF2
NDN
PLAGL1
SNRPN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Frequency and characterization of DNA methylation defects in children born SGA.PMID 23232699Read ↗

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

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting DisordersSemantic proximity Read ↗

Epigenetic anomalies in childhood growth disorders.Semantic proximity Read ↗

Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants.Semantic proximity Read ↗

Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.Semantic proximity Read ↗

Genetic Analyses in Small-for-Gestational-Age Newborns.Semantic proximity Read ↗

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.Semantic proximity Read ↗

Epigenetic deregulation of imprinting in congenital diseases of aberrant growthSemantic proximity Read ↗

Methylation profiling in individuals with Russell–Silver syndromeSemantic proximity Read ↗

New clinical and molecular insights into Silver-Russell syndrome.Semantic proximity Read ↗

DNA methylation of<i>IGF2</i>,<i>GNASAS</i>,<i>INSIGF</i>and<i>LEP</i>and being born small for gestational ageSemantic proximity Read ↗

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndromeSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.