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

Nanopore sequencing as a novel method of characterising anorexia nervosa risk loci.

BMC genomics - 31 Dec 2024

Berthold Natasha, Gaudieri Silvana, Hood Sean, Tschochner Monika, Miller Allison L, Jordan Jennifer, Thornton Laura M, Bulik Cynthia M, Akkari Patrick Anthony, Kennedy Martin A

Abstract excerpt

BACKGROUND: Anorexia nervosa (AN) is a polygenic, severe metabopsychiatric disorder with poorly understood aetiology. Eight significant loci have been identified by genome-wide association studies (GWAS) and single nucleotide polymorphism (SNP)-based heritability was estimated to be ~ 11-17, yet causal variants remain elusive. It is therefore important to define the full spectrum of genetic variants in the wider...

Read the complete abstract on PubMed

Topics

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

Share to Anorexia Nervosa
Share to Computational Biology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Loci

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Nanopore Sequencing

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 39741260
DOI: 10.1186/s12864-024-11172-7
PMCID: PMC11687000

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nanopore sequencing as a novel method of characterising anorexia nervosa risk loci.PMID 39741260Read ↗

Nanopore Sequencing as a Novel Method of Characterising Anorexia Nervosa Risk LociSemantic proximity Read ↗

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.Semantic proximity Read ↗

Bridging the gap: Short structural variants in the genetics of anorexia nervosa.Semantic proximity Read ↗

A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa.Semantic proximity Read ↗

A genome-wide association study of anorexia nervosa.Semantic proximity Read ↗

Utilising genomic association data for causal inference in anorexia nervosa.Semantic proximity Read ↗

Long-read nanopore sequencing reveals novel common genetic structural variants in Prader-Willi syndrome and associated psychosisSemantic proximity Read ↗

Multiomic prioritisation of risk genes for anorexia nervosa.Semantic proximity Read ↗

Integrative GWAS identifies novel loci and genetic links between psychiatric and metabolic factors in anorexia nervosa.Semantic proximity Read ↗

Multiomic prioritisation of risk genes for anorexia nervosaSemantic proximity Read ↗

Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.Semantic proximity Read ↗

Genetic association of FMRP targets with psychiatric disordersSemantic proximity Read ↗

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