Genetic epidemiology and human genomics

We investigate how genetic variation shapes health and disease across the lifespan, with a particular focus on understanding sex differences. Our research bridges genetic epidemiology and molecular genomics to uncover the biological mechanisms underlying disparities between sexes in disease risk, progression, and outcomes.

Our two core research areas are:

• Sex Chromosome Genomics: Exploring the unique biology of the X and Y chromosomes and their role in health and disease.
• Women’s Health and Reproduction: Studying how reproductive history and pregnancy-related biology influence disease risk in both mother and child.

We work closely with other research groups, particularly in cardiometabolic diseases, to bring genetic insights into broader health topics. By integrating large-scale population data with cutting-edge genomic tools, we aim to inform precision medicine and promote equitable healthcare.