Publications Archive

Evaluation of SORL1 in Lewy body dementia identifies no significant associations (letter)

Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population (letter)

GRN mutations are associated with Lewy body dementia.

Toffoli et al 2022 Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson's disease-associated GBA gene. Commun Biol

Multi-Platform Proteomic Analysis of Alzheimer’s Disease Cerebrospinal Fluid and Plasma Reveals Network Biomarkers Associated with Proteostasis and the Matrisome.

Deficiency in endocannabinoid synthase 1 DAGLB contributes to Parkinson's disease and dopaminergic neuron dysfunction.

The Parkinson’s disease protein alpha-synuclein is a direct modulator of RNA Processing-bodies and mRNA stability.

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.