Anni K. Moore

The paper identifies decreased SNCA expression in Parkinson's Disease blood samples after correcting for immune cell effects, suggesting it as a potential transcriptomic biomarker.

This study uses multi-omics data to connect MRI-derived cardiac measures with gene and protein changes in heart failure, identifying shared pathways and novel insights into disease mechanisms.

This study uses PheWAS to find cross-phenotype associations between Alzheimer's Disease and other conditions, identifying immune and cardiac disease links.

This study investigates the genetic and genomic links between NBIA and PD, finding no strong association and suggesting they may be distinct conditions.

The paper describes a virtual hackathon event that brought together early career scientists to develop tools for Parkinson's disease research using open science principles.

This study identifies 3,154 high-confidence structural variants in Parkinson's disease using short-read sequencing and validates some with long-read data, highlighting limitations of short-read methods.

This study examines the genetic association between ANG variants and Parkinson's disease using large-scale genotype and whole genome sequencing data, finding no significant association.

This study investigates the genetic and transcriptomic link between KTN1 and Parkinson's disease using GWAS, eQTL, and transcriptomics data, finding no genetic associations but potential expression differences.

This paper identifies five new genetic risk loci for Lewy body dementia through whole-genome sequencing and shows shared risk profiles with Alzheimer’s and Parkinson’s disease.