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

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.

Neurobiology of aging - 1 Aug 2012

van Blitterswijk Marka, Blokhuis Anna, van Es Michael A, van Vught Paul W J, Rowicka Paulina A, Schelhaas Helenius J, van der Kooi Anneke J, de Visser Marianne, Veldink Jan H, van den Berg Leonard H

Abstract excerpt

Polymorphisms in the paraoxonase family (PON) have been reported in patients with amyotrophic lateral sclerosis (ALS), but a recent meta-analysis did not show a clear association. Recently, PON mutations have also been identified in ALS patients. In this study, we assessed the frequency of PON va...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Amyotrophic Lateral Sclerosis
Share to Aryldialkylphosphatase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Netherlands

Share to Prevalence

Share to Risk Factors

Share to Young Adult

Source

Identifiers

PMID: 22330174
DOI: 10.1016/j.neurobiolaging.2012.01.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22330174-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.PMID 22330174Read ↗

Paraoxonase gene mutations in amyotrophic lateral sclerosis.Semantic proximity Read ↗

Association analysis of PON polymorphisms in sporadic ALS in a Chinese population.Semantic proximity Read ↗

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.Semantic proximity Read ↗

Lack of association of PON polymorphisms with sporadic ALS in an Italian population.Semantic proximity Read ↗

A common haplotype within the PON1 promoter region is associated with sporadic ALS.Semantic proximity Read ↗

Incidence of amyotrophic lateral sclerosis-associated genetic variants: a clinic-based study.Semantic proximity Read ↗

Common mutations of interest in the diagnosis of amyotrophic lateral sclerosis: how common are common mutations in ALS genes?Semantic proximity Read ↗

Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: a comprehensive meta-analysis.Semantic proximity Read ↗

Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome.Semantic proximity Read ↗

Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

No evidence of association between polymorphisms in four genes and sporadic amyotrophic lateral sclerosis in Han Chinese.Semantic proximity Read ↗

Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden.Semantic proximity Read ↗

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