Lang Liu

This study uses Mendelian Randomization to test if TNF pathway genes are genetically linked to Parkinson's disease or RBD, finding no evidence of such a link.

The paper investigates whether CPT1C loss-of-function variants cause hereditary spastic paraplegia (HSP) by analyzing genomic data from multiple cohorts and finds no causal association.

The paper analyzes resting-state fMRI data from bipolar disorder patients across four episodes and healthy controls to identify shared and individual-specific neural patterns using edge-centric functional connectomes.

The paper investigates genetic and causal links between post-traumatic stress disorder and rapid-eye-movement sleep behavior disorder using polygenic risk scores, genetic correlation, and Mendelian randomization analyses.

This study examines how genetic risk for bipolar disorder affects cortical thickness and network topology in adolescents using PRS and neuroimaging data from the ABCD cohort.

The paper uses machine learning to identify candidate genes, variants, and pathways potentially linked to Parkinson's disease from GWAS loci and genomic data.