Gene List:
ATP13A2, ATP1A3, ATP6AP2, ATP7B, C19orf12, CHCHD2, DCTN1, DNAJC6, EIF4G1, FBXO7, GBA, GCH1, HTRA2, LRRK2, MAPT, PARK2, PARK7, PINK1, PLA2G6, POLG, PRKN, PRKRA, RAB39B, SLC20A2, SLC6A3, SNCA, SPR, SYNJ1, TAF1, TH, UCHL1, VPS13A, VPS13C, VPS35, WDR45, XPR1

References:
Devanna,P, et al. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders. Mol Psychiatry 23, 1375–1384 (2018).

Farlow JL, et al. Whole-Exome Sequencing in Familial Parkinson Disease. JAMA Neurol. 2016;73(1):68–75.

Robak L, Excessive buyrden of lysosomal storage disorder gene variants in Parkinson’s disease. Brain. (140)12:3191–3203.

Zucca S, et al. Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management. BMC Bioinformatics 17, 339 (2016).