Julian C Knight
occupation: researcher
Articles 108
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Transcriptomic Analysis of Inflammatory Cardiomyopathy Identifies Molecular Signatures of Disease and Informs <i>in silico</i> Prediction of a Network-Based Rationale for Therapy
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Using de novo assembly to identify structural variation of eight complex immune system gene regions
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Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus
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The Polygenic and Monogenic Basis of Blood Traits and Diseases
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Early-onset autoimmunity associated with SOCS1 haploinsufficiency
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Host genetics and infectious disease: new tools, insights and translational opportunities
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Genetic mechanisms of critical illness in Covid-19
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Antibody testing for COVID-19: A report from the National COVID Scientific Advisory Panel
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Peripheral CD8+ T cell characteristics associated with durable responses to immune checkpoint blockade in patients with metastatic melanoma
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Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis
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Context-specific regulation of surface and soluble IL7R expression by an autoimmune risk allele
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The association between endometriosis and autoimmune diseases: a systematic review and meta-analysis
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Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series
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Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leucocyte antigen locus
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A genetics-led approach defines the drug target landscape of 30 immune-related traits
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Transcriptomic Signatures in Sepsis and a Differential Response to Steroids: From the VANISH Randomized Trial
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AltHapAlignR: improved accuracy of RNA-seq analyses through the use of alternative haplotypes
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Translating GWAS in rheumatic disease: approaches to establishing mechanism and function for genetic associations with ankylosing spondylitis
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Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis
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A community approach to mortality prediction in sepsis via gene expression analysis.
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Evidence for a second ankylosing spondylitis-associated RUNX3 regulatory polymorphism.
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Genomic Response to Vitamin D Supplementation in the Setting of a Randomized, Placebo-Controlled Trial.
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Distinct HLA associations of LGI1 and CASPR2-antibody diseases.
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Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study
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Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis.
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High resolution HLA haplotyping by imputation for a British population bioresource
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Enhanced understanding of the host-pathogen interaction in sepsis: new opportunities for omic approaches.
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Shared and Distinct Aspects of the Sepsis Transcriptomic Response to Fecal Peritonitis and Pneumonia.
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Unique transcriptome signatures and GM-CSF expression in lymphocytes from patients with spondyloarthritis.
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Microvesicle Subsets in Sepsis Due to Community Acquired Pneumonia Compared to Faecal Peritonitis.
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"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
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XGR software for enhanced interpretation of genomic summary data, illustrated by application to immunological traits.
Human - wd:Q40247846