Genetics of Parkinson's Disease: Discoveries and Therapeutics

A special issue of Brain Sciences (ISSN 2076-3425). This special issue belongs to the section "Neurodegenerative Diseases".

Deadline for manuscript submissions: 30 November 2024 | Viewed by 50

Special Issue Editor


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Guest Editor
Duke-NUS Medical School, Singapore 169857, Singapore
Interests: genetics of PD and related disorders; experimental and clinical therapeutics
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Genetic and environmental factors have been linked to Parkinson’s disease (PD), which is a neurological disorder with complex aetiologies. Several pathogenic genes are responsible for autosomal dominant (such as alpha synuclein and LRRK2) and recessive (such as Parkin and Pink1) PD. In addition, >90 gene loci have been associated with sporadic PD. Among these genes, GBA variants are associated with a high PD risk, and a common recurrent mutation, G2019S in LRRK2, accounts for up to 30–40% of cases in certain populations. In addition, LRRK2-coding polymorphic risk variants have been found in certain ethnic races. GWAS studies have also led to the development of the polygenic risk score.

Subsequently, the identification of genes has led to the creation of transgenic animal models and human ipsc-derived neuronal models. These models have provided pathophysiologic insights and have identified key molecular features associated with neurodegeneration, including mitochondrial dysfunction, oxidative stress, protein accumulation and neuroinflammation.

The study of genetic targets has translated into various clinical drug trials, including LRRK2 inhibitors and synuclein antibodies, among several others. The challenges and limitations faced by these trials have encouraged further efforts to better screen and stratify patients with a similar genetic background for future precision medicine approaches.

Given this background, this Special Issue is open to all studies related to clinical genetics, functional genomics and animal studies of genes and their related targets and pathways linked to PD.

Prof. Dr. Eng King Tan
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2200 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Parkinson’s disease
  • genes
  • animal models
  • clinical trials

Published Papers

This special issue is now open for submission.
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