Websites
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Ancestrally Inclusive Musculoskeletal Single-cell (AIMS) Network
Creating a global atlas of the musculoskeletal system
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Snelling Group
Soft Tissue Repair
- Human Cell Atlas project
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Chan Zuckerberg Initiative
An Ancestrally Inclusive Atlas of Healthy Musculoskeletal Tissues
Carla Cohen
Computational Biologist
- Analysis of single-cell RNA-seq data from musculoskeletal tissues
- Trainer in computational biology
Delivering an ethnically diverse cell atlas of human musculoskeletal tissue
I am a computational biologist working in David Sims' Computational Biology group at the WIMM and in Sarah Snelling’s Soft Tissue Repair group at the Botnar Research Centre.
I work on the Human Cell Atlas project, a global consortium which aims to map all cells in the healthy human body. I analyse single-nuclear RNA-seq data from musculoskeletal tissues including tendon, muscle, bone and capsule to create an ethnically diverse atlas of healthy cells in the adult joint. This work will produce an open-source comprehensive resource for researchers around the world and will provide a foundation for further studies on human disease.
I am also a trainer in computational methods including Linux, R programming and core/advanced methods in single-cell RNA-seq analysis using R and Python, in collaboration with the African Institute of Biomedical Science and Technology in Harare, Zimbabwe.
My work is funded from the Chan-Zuckerberg Initiative and fits within their ambitious goal to solve human disease by 2100.
I completed my DPhil in the Dunn School of Pathology with William James, and went on to a postdoctoral position with Dixie Mager in the Terry Fox Laboratory, Vancouver, Canada. From 2011-2022 I worked in the University of Oxford with Paul Wordsworth and Julian Knight on the genetics and epigenetics of ankylosing spondylitis, an inflammatory arthritis. I took a career break from 2013-2017 when I had young children, and received funding from the University’s Returning Carer’s Fund when I returned to work. I am a keen supporter of public engagement with science, and improving equality, diversity and inclusion in science.
Key publications
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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, 100306 - 100306
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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, (2021), Front Genet, 12
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A RUNX3 enhancer polymorphism associated with ankylosing spondylitis influences recruitment of Interferon Regulatory Factor 5 and factors of the Nucleosome Remodelling Deacetylase Complex in CD8+ T-cells
Journal article
Vecellio M. et al, (2019)
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An ankylosing spondylitis-associated genetic variant in the IL23R-IL12RB2 intergenic region modulates enhancer activity and is associated with increased Th1-cell differentiation.
Journal article
Roberts AR. et al, (2016), Ann Rheum Dis, 75, 2150 - 2156
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Human Th1 and Th17 cells exhibit epigenetic stability at signature cytokine and transcription factor loci.
Journal article
Cohen CJ. et al, (2011), J Immunol, 187, 5615 - 5626
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Placenta-specific expression of the interleukin-2 (IL-2) receptor β subunit from an endogenous retroviral promoter.
Journal article
Cohen CJ. et al, (2011), J Biol Chem, 286, 35543 - 35552
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The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression.
Journal article
Vecellio M. et al, (2016), Ann Rheum Dis, 75, 1534 - 1540
Recent publications
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Exploring cellular changes in ruptured human quadriceps tendons at single-cell resolution
Preprint
Mimpen JY. et al, (2024)
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Single nucleus and spatial transcriptomic profiling of healthy human hamstring tendon.
Journal article
Mimpen JY. et al, (2024), FASEB J, 38
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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, 100306 - 100306
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Chromosome conformation capture approaches to investigate 3D genome architecture in Ankylosing Spondylitis.
Journal article
Davidson C. et al, (2023), Front Genet, 14
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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
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Functional Genomic Analysis of a RUNX3 Polymorphism Associated With Ankylosing Spondylitis.
Journal article
Vecellio M. et al, (2021), Arthritis Rheumatol, 73, 980 - 990
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INVESTIGATING THE ANKYLOSING SPONDYLITIS-ASSOCIATED REGULATORY SNPS AT THE RUNX3 LOCUS WITH A FUNCTIONAL GENOMICS APPROACH
Conference paper
Vecellio M. et al, (2021), ANNALS OF THE RHEUMATIC DISEASES, 80, 411 - 411
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COMPREHENSIVE EPIGENOMIC PROFILING REVEALS DISEASE-SPECIFIC CHROMATIN STATES IN ANKYLOSING SPONDYLITIS
Conference paper
Cohen CJ. et al, (2021), CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 39, 1155 - 1155