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

Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity.

Hormone research in paediatrics - 1 Jan 2021

Madeo Simona Filomena, Stanghellini Ilaria, Predieri Barbara, Ciancia Silvia, Leo Francesco, Bruzzi Patrizia, Calabrese Olga, Iughetti Lorenzo

Abstract excerpt

BACKGROUND/AIMS: Obesity is a multifactorial disease caused by the interaction of genetic, environmental, and behavioral factors. Currently, only a small number of obese children undergo genetic analysis, usually when obesity is associated with dysmorphic features. The aim of this study was to identify genomic rearrangement causing obesity. METHODS: We analyzed the DNA of children and adolescents by...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to DNA Copy Number Variations

Share to Genetic Testing

Share to Intellectual Disability

Share to Mutation

Share to Pediatric Obesity

Source

Identifiers

PMID: 34482307
DOI: 10.1159/000519299

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity.PMID 34482307Read ↗

New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.Semantic proximity Read ↗

Identification of genomic copy number variations associated with obesity-related phenotypesSemantic proximity Read ↗

Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in Koreans.Semantic proximity Read ↗

Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies.Semantic proximity Read ↗

A genome-wide study reveals copy number variants exclusive to childhood obesity cases.Semantic proximity Read ↗

Large copy-number variations are enriched in cases with moderate to extreme obesity.Semantic proximity Read ↗

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.Semantic proximity Read ↗

Large, rare chromosomal deletions associated with severe early-onset obesity.Semantic proximity Read ↗

Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study.Semantic proximity Read ↗

Interactions between obesity-related copy number variants and dietary behaviors in childhood obesity.Semantic proximity Read ↗

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan.Semantic proximity Read ↗

Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.Semantic proximity Read ↗

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