Contact information
Professor Knight's Research Group
https://orcid.org/0000-0002-0377-5536
Henry Wellcome Building of Genomic Medicine
Colleges
Websites
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Knight lab research group
Knight research group
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CAS GMSA
Central and South NHS Genomic Medicine Service
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Sepsis science
Background on sepsis research for public and professionals
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GMS DPhil programme
Genomic Medicine and Statistics DPhil programme at Oxford
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MSc Genomic Medicine
MSc in Genomic Medicine at Oxford
Julian Knight
Professor of Genomic Medicine
- Principal Investigator
- Deputy Director, Centre for Human Genetics
- Honorary Consultant Physician
- Tutor and Fellow, Merton College
- Director, Medical Sciences Division Graduate School
- Genomic Medicine Theme Lead, NIHR Oxford Biomedical Research Centre
- Research Director, Central and South NHS Genomic Medicine Service Alliance
My work aims to promote excellence in translational genomic science and delivery into the clinic for patient benefit. I do this through an active research programme and leadership in local and national initiatives establishing use of genomic medicine through education and clinical implementation.
Our research uses a genetics and -omics led approach to understand why some individuals develop an inappropriate or dysregulated immune response, how this may contribute to disease, and opportunities to advance personalised medicine approaches. This includes application to the severe infection and critical illness together with autoimmune disease.
For example, in acute sepsis we found patients can be stratified from white blood cell RNA signatures, independent of aetiology and predictive of their immune response state, outcome, and differential response to therapy with a specific poor outcome endotype driven by neutrophil and bone marrow dysfunction.
During the recent pandemic we investigated immunological drivers of severe COVID-19 including through the COVID-19 Multi-omic Blood ATlas (COMBAT) Consortium. With the Oxford Vaccine Group we found specific HLA alleles are associated with vaccine immunogenicity and breakthrough infection.
Complementing this, we conduct research into genetic and epigenetic modulators of the induced innate immune response. This includes the nature and functional significance of disease associated genetic variants in relevant contexts such as following innate immune activation or in acute ankylosing spondylitis.
We are also innovating ways to integrate multi-omic datasets and establish causal relationships, and approaches to enhance the utility of human genetics for understanding disease pathogenesis and novel therapeutic targets.
I am clinically active, working in acute internal medicine; support implementation of research into practise through the Central and South NHS Genomic Medicine Service; capacity building genomic medicine in through education and training; use of genomics for diagnostics and drug target identification and validation; and public engagement.
Recent publications
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Stratified analyses refine association between TLR7 rare variants and severe COVID-19
Journal article
Boos J. et al, (2024), Human Genetics and Genomics Advances, 5
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Single-cell immune survey identifies a novel pathogenic role for T cells in anti-NMDA receptor encephalitis
Preprint
Kwok AJ. et al, (2024)
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POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia.
Journal article
Symonds JD. et al, (2024), Epilepsia
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Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Preprint
Fairfax B. et al, (2024)
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eQTLs identify regulatory networks and drivers of variation in the individual response to sepsis.
Journal article
Burnham KL. et al, (2024), Cell genomics, 4