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

ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics.

Human mutation - 1 Sept 2012

Abel Olubunmi, Powell John F, Andersen Peter M, Al-Chalabi Ammar

Abstract excerpt

Amyotrophic lateral sclerosis (ALS) is the commonest adult onset motor neuron disease, with a peak age of onset in the seventh decade. With advances in genetic technology, there is an enormous increase in the volume of genetic data produced, and a corresponding need for storage, analysis, and interpretation, particularly as our understanding of the relationships between genotype and phenotype mature. Here, we...

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis
Share to Databases, Genetic
Share to Geography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Storage and Retrieval

Share to Internet

Share to Superoxide Dismutase

Share to Superoxide Dismutase-1

Share to User-Computer Interface

Source

Identifiers

PMID: 22753137
DOI: 10.1002/humu.22157

Genes

SOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics.PMID 22753137Read ↗

ALSOD: the Amyotrophic Lateral Sclerosis Online Database.Semantic proximity Read ↗

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases.Semantic proximity Read ↗

SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in<i>SOD1</i>amyotrophic lateral sclerosisSemantic proximity Read ↗

SOD-1 Variants in Amyotrophic Lateral Sclerosis: Systematic Re-Evaluation According to ACMG-AMP GuidelinesSemantic proximity Read ↗

Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery.Semantic proximity Read ↗

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA NGS data of ALS patientsSemantic proximity Read ↗

ALSODatabase: database of SOD1 (and other) gene mutations in ALS on the Internet. European FALS Group and ALSOD Consortium.Semantic proximity Read ↗

A mutation database for amyotrophic lateral sclerosis.Semantic proximity Read ↗

Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis GenesSemantic proximity Read ↗

Evaluating the utility of REVEL and CADD for interpreting variants in amyotrophic lateral sclerosis genesSemantic proximity Read ↗

Structural and functional analysis of human SOD1 in amyotrophic lateral sclerosis.Semantic proximity Read ↗

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the publicSemantic proximity Read ↗

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