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

Identification of a novel Parkinson's disease locus via stratified genome-wide association study.

BMC genomics - 10 Feb 2014

Hill-Burns Erin M, Wissemann William T, Hamza Taye H, Factor Stewart A, Zabetian Cyrus P, Payami Haydeh

Abstract excerpt

BACKGROUND: Parkinson's disease (PD) is complex and heterogeneous. The numerous susceptibility loci that have been identified reaffirm the complexity of PD but do not fully explain it; e.g., it is not known if any given PD susceptibility gene is associated with all PD or a disease subtype. We also suspect that important disease genes may have escaped detection because of this heterogeneity. We used...

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 Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Loci

Share to Genome, Human

Share to Genome-Wide Association Study

Share to HLA Antigens

Share to Odds Ratio

Share to Parkinson Disease

Source

Open in PubMed Open full text

Identifiers

PMID: 24511991
DOI: 10.1186/1471-2164-15-118
PMCID: PMC3925254

Genes

MAPT
OLFM3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Identification of a novel Parkinson's disease locus via stratified genome-wide association study.PMID 24511991Read ↗

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.Semantic proximity Read ↗

Genome-wide association study reveals genetic risk underlying Parkinson's disease.Semantic proximity Read ↗

Association Studies of Sporadic Parkinson’s Disease in the Genomic EraSemantic proximity Read ↗

Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable riskSemantic proximity Read ↗

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.Semantic proximity Read ↗

What have we learned from genome-wide association studies (GWAS) in Parkinson's disease?Semantic proximity Read ↗

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.Semantic proximity Read ↗

Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease.Semantic proximity Read ↗

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.Semantic proximity Read ↗

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese populationSemantic proximity Read ↗

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.Semantic proximity Read ↗

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Semantic proximity Read ↗

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