Evgeniia Golovina

The paper identifies infection-dependent changes in lung-specific gene expression and chromatin remodelling associated with SARS-CoV-2 risk variants.

This study identifies causal genes and genetic loci linking autism to co-occurring traits using Mendelian Randomisation and eQTL integration.

This study identifies genetic variants and genes associated with COPD and co-occurring traits by integrating multi-omics data and gene regulatory networks.

This study identifies gene regulatory networks influenced by Parkinson's disease risk SNPs using eQTL and chromosomal conformation data across multiple tissues.

This study identifies shared genetic mechanisms across 18 autoimmune diseases by integrating chromatin contact, expression quantitative trait loci, and protein-protein interaction data.

The paper identifies ASD-associated SNPs in fetal and adult cortex tissues and links them to regulatory processes and pathways, highlighting differences in their impact across developmental stages.

This study identifies 33 genes and 62 pathways impacted by GWAS SNPs associated with psychiatric disorders and cognitive functioning, revealing shared regulatory mechanisms despite no common SNPs or eQTLs.

The paper identifies regulatory elements within the ACE2 locus that control host gene expression, suggesting they may contribute to a pro-viral environment for SARS-CoV-2.