Dr Carla Cohen
Postdoctoral fellow
Ankylosing spondylitis (AS) is a chronic inflammatory arthritis affecting 1-2% of people in the UK. It is a polygenic disease, with over 40 associated genetic loci identified by genome-wide association studies. My research focus is to determine which particular single nucleotide polymorphisms (SNPs) play a causative role in the pathogenesis of AS. We have performed comprehensive epigenomic profiling of lymphocyte populations in AS patients and healthy controls. We are now analysing these data to identify how differential chromatin regions are linked to loci that are genetically associated with AS. Understanding these regulatory mechanisms may lead to the development of novel therapies for this debilitating condition.
I completed my DPhil at Oxford and went on to a postdoctoral position with Prof Dixie Mager, where I studied regulatory elements involving transposable elements, in Vancouver, Canada. During that time I developed an interest in epigenetic regulation which led me to return to Oxford and join Prof Wordsworth’s research group. In 2019 I joined Julian Knight's research team.
I am funded on a grant from Wyeth Pharmaceuticals and recently obtained awards from the University of Oxford Returning Carers’ Fund and the COVID Rebuilding Research Momentum Fund.
Twitter: @DrCarlaCohen @KnightGenetics
Recent publications
-
Single nucleus and spatial transcriptomic profiling of healthy human hamstring tendon.
Journal article
Mimpen JY. et al, (2024), FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 38
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs target discovery in ankylosing spondylitis
Journal article
Brown AC. et al, (2023), Cell Genomics, 3, 100306 - 100306
-
Chromosome conformation capture approaches to investigate 3D genome architecture in Ankylosing Spondylitis
Journal article
Davidson C. et al, (2023), Frontiers in Genetics, 14
-
Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter
Journal article
Cohen CJ. et al, (2022), Frontiers in Genetics, 12
-
FUNCTIONAL GENOMICS INVESTIGATION OF THE ANKYLOSING SPONDYLITIS ASSOCIATED LOCUS RUNX3
Conference paper
Cohen C. et al, (2022), ANNALS OF THE RHEUMATIC DISEASES, 81, 231 - 231