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

Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypes.

Journal of chemical neuroanatomy - 1 Oct 2011

Crosiers David, Theuns Jessie, Cras Patrick, Van Broeckhoven Christine

Abstract excerpt

In the past 15 years, insights in clinical and genetic characteristics of Parkinson disease (PD) have increased substantially. Sequence or copy number variants in at least six genes (SNCA, LRRK2, PARK2, PINK1, DJ-1 and ATP13A2) have been identified to cause monogenic forms of PD. Routine clinical testing for mutations in these genes is feasible and available, but overlapping phenotypes in monogenic and sporadic...

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder Research
Share to PINK1 gene

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to SNCA gene

Share to Genetic Association Studies

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Parkinson Disease

Share to Parkinson's Disease Mechanisms and Treatments

Source

Identifiers

PMID: 21810464
DOI: 10.1016/j.jchemneu.2011.07.003

Genes

PINK1
SNCA

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Parkinson disease: insights in clinical, genetic and pathological features of monogenic disease subtypes.PMID 21810464Read ↗

Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations.Semantic proximity Read ↗

Implications of genetics on the diagnosis and care of patients with Parkinson disease.Semantic proximity Read ↗

An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.Semantic proximity Read ↗

Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing.Semantic proximity Read ↗

The genetics and neuropathology of Parkinson's disease.Semantic proximity Read ↗

Parkinson's disease: from monogenic forms to genetic susceptibility factors.Semantic proximity Read ↗

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.Semantic proximity Read ↗

Genetic Forms of Parkinson's Disease.Semantic proximity Read ↗

Genetics of Parkinson disease.Semantic proximity Read ↗

The genetics of Parkinson disease.Semantic proximity Read ↗

Genetics of Parkinson's disease.Semantic proximity Read ↗

Parkinson's disease: a genetic perspective.Semantic proximity Read ↗

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