Genetics of Parkinson's disease

By Tim Postmus. 2018

692 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/769a1b155aed5397270381d07de88850c1412ab0

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

1. Diane Moujalled
2. J. R. Liddell
3. O. Tysnes
4. A. Strasser
5. A. Storstein
6. Bor Luen Tang
7. Jerry M. Adams

Citations in the corpus

• Sirt1 and the Mitochondria (2016, background): “The mitophagy regulators PINK1 and Parkin are both encoded by PD susceptibility genes that are mutated in patients with juvenile or early-onset Parkinsonism (Mullin and Schapira, 2015).”
• Epidemiology of Parkinson’s disease (2017, background): “It is generally considered that known genetic causes may be relevant in more than 5% of the total PD population and that monogenetic causes are rare, but some propose that monogenetic causes may be involved in as many as 5–10% of the PD population (Lill 2016).”
• Molecular mechanisms of cell death in neurological diseases (2021, background): “Inherited forms of PD are associated with mutations in genes associated with mitochondrial function, such as PRKN, LRRK2, PINK1 and PARK7 [49].”