
Within the group of Professor Nicole Soranzo, my research combines experimental and computational approaches to uncover the genetic mechanisms underlying autoimmune and cardiovascular diseases. I focus on using quantitative trait locus (QTL) analyses integrated with genome-wide association studies (GWAS) to identify how genetic variation influences molecular and cellular phenotypes relevant to disease.
I have developed high-throughput laboratory pipelines for generating population-scale multi-omic datasets, enabling the systematic investigation of gene regulation across diverse cohorts. Currently, I lead a high-throughput single-cell genomics laboratory, where we apply cutting-edge technologies to dissect gene expression and chromatin dynamics at single-cell resolution.
These approaches have been applied to assay transcriptomic and epigenomic landscapes across large-scale population cohorts, including the EU Blueprint, UK Biobank, and Genes & Health studies, providing new insights into how genetic variation shapes human health and disease.
My timeline
Senior Staff Scientist, Human Complex Traits laboratory, WTSI
Senior Scientific Officer, Regulatory systems biology laboratory, CRUK
Senior Research Assistant, Fission Yeast Functional Genomics Group, WTSI
Research Assistant, Cancer Genome Project, WTSI
Human Genome Project Sequencing team, WTSI
Bsc Biology, University of Paisley
My publications
Genetic perturbation of PU. 1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease
Rapid turnover of long noncoding RNAs and the evolution of gene expression