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

Gene-based copy number variation study reveals a microdeletion at 12q24 that influences height in the Korean population.

Genomics - 1 Feb 2013

Kim Yun Kyoung, Moon Sanghoon, Hwang Mi Yeong, Kim Dong-Joon, Oh Ji Hee, Kim Young Jin, Han Bok-Ghee, Lee Jong-Young, Kim Bong-Jo

Abstract excerpt

Height is a classic polygenic trait with high heritability (h(2)=0.8). Recent genome-wide association studies have revealed many independent loci associated with human height. In addition, although many studies have reported an association between copy number variation (CNV) and complex diseases, few have explored the relationship between CNV and height. Recent studies reported that single nucleotide...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Body Height

Share to Chromosome Deletion

Share to Chromosomes, Human, Pair 12

Share to Gene Dosage

Share to Genetics, Population

Share to Receptors, G-Protein-Coupled

Source

Identifiers

PMID: 23147675
DOI: 10.1016/j.ygeno.2012.11.002

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

Gene-based copy number variation study reveals a microdeletion at 12q24 that influences height in the Korean population.PMID 23147675Read ↗

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.Semantic proximity Read ↗

Rare copy number variants are a common cause of short stature.Semantic proximity Read ↗

Genome-wide association study identified CNP12587 region underlying height variation in Chinese females.Semantic proximity Read ↗

Rare protein-coding variation and the genetic architecture of height in >1.4 million individualsSemantic proximity Read ↗

A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK Biobank.Semantic proximity Read ↗

A phenome-wide association study of CNVs genotyped from genome sequencing read depth in the UK BiobankSemantic proximity Read ↗

Copy number variant association analysis in 94,730 Chinese adults reveals loci influencing anthropometric and cardiometabolic traitsSemantic proximity Read ↗

The individual and global impact of copy number variants on complex human traitsSemantic proximity Read ↗

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

Hundreds of variants clustered in genomic loci and biological pathways affect human height.Semantic proximity Read ↗

Influence of polygenic risk on height and BMI in adults with a 22q11.2 microdeletionSemantic proximity Read ↗

Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study.Semantic proximity Read ↗

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