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Cited by 1,358

The DOI matches its Crossref record; 185 of the 185 references it cites were found in a registry or an index.

Genetics of Parkinson's Disease

Open access
Klein, C., Westenberger, A.·2012·Cold Spring Harbor Perspectives in Medicine

Abstract

Fifteen years of genetic research in Parkinson's disease (PD) have led to the identification of several monogenic forms of the disorder and of numerous genetic risk factors increasing the risk to develop PD. Monogenic forms, caused by a single mutation in a dominantly or recessively inherited gene, are well-established, albeit relatively rare types of PD. They collectively account for about 30% of the familial and 3%-5% of the sporadic cases. In this article, we will summarize the current knowledge and understanding of the molecular genetics of PD. In brief, we will review familial forms of PD, basic genetic principles of inheritance (and their exceptions in PD), followed by current methods for the identification of PD genes and risk factors, and implications for genetic testing.

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Metadata

Authors
Klein, C., & Westenberger, A.
Venue
Cold Spring Harbor Perspectives in Medicine
Published
2012-01-01
Volume
2
Issue
1
Pages
a008888-a008888
ISSN
2157-1422 (ISSN-L)
OpenAlex
W2143906078
Cited by
1,358
References
185
Type
posted content
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Genetics of Parkinson's Disease. https://app.cochat.ai/papers/10.1101/cshperspect.a008888
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Klein, C., & Westenberger, A. (2012). Genetics of Parkinson's Disease. Cold Spring Harbor Perspectives in Medicine. https://doi.org/10.1101/cshperspect.a008888

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.