We are a computational genomics group studying the genetic basis of complex traits in human populations, including intermediate and end-point phenotypes. Our primary research focus is on understanding the causes and consequences of epigenetic variation in humans. Most projects in the lab are multidisciplinary and combine the analysis of large-scale genomic datasets (e.g. DNA methylation, DNA sequence, 16S microbiome) with statistical genetic and epigenetic tools.


I am a Senior Lecturer in the Department for Twin Research and Genetic Epidemiology at King's College London. My group uses computational methods to study research questions in genomics, with a focus on human epigenetic variation. Research areas include genetic and environmental basis of epigenetic variation, epigenome-wide association scans, gene-gene & gene-environment interactions, the human microbiome, and ageing. See Research for details.

Recent publications include:

DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation - Castillo-Fernandez et al. compare the epigenomes of IVF and naturally conceived newborn twins, identifying small changes.

Highlighted in The Conversation

Heritable components of the human fecal microbiome are associated with visceral fat - Beaumont et al. find that heritable elements of the human microbiome are associated with visceral fat, a key cardio-metabolic disease risk factor.