Publications Archive

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

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

Toffoli et al 2021 Movement Disorders. Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease

Dong et al 2021 Briefings in Functional Genomics. Review of multi-omics data resources and integrative analysis for human brain disorders