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

The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.

European journal of human genetics : EJHG - 1 Dec 2013

Kanduri Chakravarthi, Ukkola-Vuoti Liisa, Oikkonen Jaana, Buck Gemma, Blancher Christine, Raijas Pirre, Karma Kai, Lähdesmäki Harri, Järvelä Irma

Abstract excerpt

Here we characterized the genome-wide architecture of copy number variations (CNVs) in 286 healthy, unrelated Finnish individuals belonging to the MUSGEN study, where molecular background underlying musical aptitude and related traits are studied. By using Illumina HumanOmniExpress-12v.1.0 beadchip, we identified 5493 CNVs that were spread across 467 different cytogenetic regions, spanning a total size of...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged, 80 and over

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Founder Effect

Share to Genetics, Population

Share to Genome, Human

Share to Genome-Wide Association Study

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 23591402
DOI: 10.1038/ejhg.2013.60
PMCID: PMC3831076

Genes

GALM

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

The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.PMID 23591402Read ↗

Global variation in copy number in the human genome.Semantic proximity Read ↗

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.Semantic proximity Read ↗

Copy number variations in the human genome and strategies for analysis.Semantic proximity Read ↗

A comprehensive analysis of common copy-number variations in the human genome.Semantic proximity Read ↗

CNVs and genetic medicine (excitement and consequences of a rediscovery).Semantic proximity Read ↗

Population analysis of large copy number variants and hotspots of human genetic disease.Semantic proximity Read ↗

Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.Semantic proximity Read ↗

A copy number variation map of the human genome.Semantic proximity Read ↗

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Semantic proximity Read ↗

Clinical significance of germline copy number variation in susceptibility of human diseases.Semantic proximity Read ↗

Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.Semantic proximity Read ↗

The landscape of copy number variations in Finnish families with autism spectrum disorders.Semantic proximity Read ↗

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