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

Missing heritability in Parkinson's disease: the emerging role of non-coding genetic variation.

Journal of neural transmission (Vienna, Austria : 1996) - 1 May 2020

Ohnmacht Jochen, May Patrick, Sinkkonen Lasse, Krüger Rejko

Abstract excerpt

Parkinson's disease (PD) is a neurodegenerative disorder caused by a complex interplay of genetic and environmental factors. For the stratification of PD patients and the development of advanced clinical trials, including causative treatments, a better understanding of the underlying genetic architecture of PD is required. Despite substantial efforts, genome-wide association studies have not been able to explain...

Read the complete abstract on PubMed

Topics

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

Share to Cancer-related gene regulation
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomics and Chromatin Dynamics

Share to Parkinson Disease

Share to Parkinson's Disease Mechanisms and Treatments

Source

Open in PubMed Open full text

Identifiers

PMID: 32248367
DOI: 10.1007/s00702-020-02184-0
PMCID: PMC7242266

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

Missing heritability in Parkinson's disease: the emerging role of non-coding genetic variation.PMID 32248367Read ↗

Genetic risk factors in Parkinson's disease.Semantic proximity Read ↗

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

Genetic Determinants of Parkinson's Disease: Can They Help to Stratify the Patients Based on the Underlying Molecular Defect?Semantic proximity Read ↗

Genetic Risk Profiling in Parkinson's Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological Pathways.Semantic proximity Read ↗

Progress in unraveling the genetic etiology of Parkinson disease in a genomic era.Semantic proximity Read ↗

Molecular pathogenesis of Parkinson's disease: update.Semantic proximity Read ↗

Identifying PD-causing genes and genetic susceptibility factors: current approaches and future prospects.Semantic proximity Read ↗

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine.Semantic proximity Read ↗

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

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

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

The Genetics of Parkinson's Disease and Implications for Clinical Practice.Semantic proximity Read ↗

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