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17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes.

Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease

Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia.

Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease.

Polygenic resilience modulates the penetrance of Parkinson's disease genetic risk factors

Senkevich et al 2019 Rare Variants In ARSA Are Associated With Parkinson’s Disease (P12-11.003)

Multi-modality machine learning predicting Parkinson’s disease

Analysis of Y Chromosome Haplogroups in Parkinson’s Disease.

Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk.

Dennis et al 2021 medrxiv. Machine Learning Prediction of Parkinson’s Disease Onset and Subtype Using Germline Variants