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

A DNA resequencing array for genes involved in Parkinson's disease.

Parkinsonism & related disorders - 1 May 2012

Wilkins E J, Rubio J P, Kotschet K E, Cowie T F, Boon W C, O'Hely M, Burfoot R, Wang W, Sue C M, Speed T P, Stankovitch J, Horne M K

Abstract excerpt

Parkinson's disease (PD) is aetiologically complex with both familial and sporadic forms. Familial PD results from rare, highly penetrant pathogenic mutations whereas multiple variants of low penetrance may contribute to the risk of sporadic PD. Common variants implicated in PD risk appear to explain only a minor proportion of the familial clustering observed in sporadic PD. It is therefore plausible that...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Synuclein
Share to Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Oligonucleotide Array Sequence Analysis

Share to Parkinson Disease

Share to Protein Kinases

Share to Protein Serine-Threonine Kinases

Share to Reproducibility of Results

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 22243833
DOI: 10.1016/j.parkreldis.2011.12.012

Genes

SNCA

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

A DNA resequencing array for genes involved in Parkinson's disease.PMID 22243833Read ↗

Parkinson’s Families Project: a UK-wide study of early onset and familial Parkinson’s diseaseSemantic proximity Read ↗

Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls.Semantic proximity Read ↗

Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.Semantic proximity Read ↗

A population scale analysis of rare SNCA variation in the UK Biobank.Semantic proximity Read ↗

Genetics of neurodegenerative diseases: insights from high-throughput resequencingSemantic proximity Read ↗

Integrated Sequencing & Array Comparative Genomic Hybridization in Familial Parkinson’s DiseaseSemantic proximity Read ↗

Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci.Semantic proximity Read ↗

High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.Semantic proximity Read ↗

Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.Semantic proximity Read ↗

Whole-Exome Sequencing in Familial Parkinson Disease.Semantic proximity Read ↗

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.Semantic proximity Read ↗

Comparative genome hybridization array analysis for sporadic Parkinson's disease.Semantic proximity Read ↗

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