Linn Nilsen Rødevand

This study investigates genetic overlaps between psychiatric disorders, cardiometabolic diseases, and brain structure to understand shared and distinct genetic pathways contributing to comorbidity.

The paper identifies sex differences in genetic and biological factors contributing to ischaemic heart disease-depression comorbidity, finding higher genetic correlation in females and distinct risk factors by sex.

This study analyzes GWAS data from nearly 1 million cases to show widespread genetic overlap between neurological and psychiatric disorders, with shared biological processes and divergent effect sizes.

This study identifies distinct genetic overlaps between Alzheimer's and Parkinson's disease and metabolic markers, revealing disease-specific pathways involving lipid metabolism and synaptic processes.

This study identifies 14 novel opioid use disorder loci and 7 shared loci with schizophrenia, bipolar disorder, and major depression using genome-wide association summary statistics.