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Publications

Stratified analyses refine association between TLR7 rare variants and severe COVID-19

Boos J. et al, (2024), Human Genetics and Genomics Advances, 5

POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic-atonic seizures and ataxia.

Symonds JD. et al, (2024), Epilepsia

Longitudinal landscape of immune reconstitution after acute SARS-CoV-2 infection at single-cell resolution.

Ren L. et al, (2024), Science bulletin

A disease-associated gene desert directs macrophage inflammation through ETS2.

Stankey CT. et al, (2024), Nature

High-throughput mass spectrometry maps the sepsis plasma proteome and differences in patient response.

Mi Y. et al, (2024), Sci Transl Med, 16

eQTLs identify regulatory networks and drivers of variation in the individual response to sepsis.

Burnham KL. et al, (2024), Cell genomics

Characterization of the genetic determinants of context-specific DNA methylation in primary monocytes.

Gilchrist JJ. et al, (2024), Cell genomics

Optimized protocol for CRISPR knockout of human iPSC-derived macrophages

Navarro-Guerrero E. et al, (2024), STAR Protocols, 5, 102903 - 102903

Patient stratification using plasma cytokines and their regulators in sepsis: relationship to outcomes, treatment effect and leucocyte transcriptomic subphenotypes.

Antcliffe DB. et al, (2024), Thorax

A common NFKB1 variant detected through antibody analysis in UK Biobank predicts risk of infection and allergy.

Chong AY. et al, (2024), American journal of human genetics, 111, 295 - 308

Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study.

Hägele P. et al, (2024), The Lancet. Haematology, 11, e114 - e126

Reframing sepsis immunobiology for translation: towards informative subtyping and targeted immunomodulatory therapies.

Shankar-Hari M. et al, (2024), The Lancet. Respiratory medicine

Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expression

Nassiri I. et al, (2024), Bioinformatics Advances, 4

BurkHostGEN: a study protocol for evaluating variations in the Burkholderia pseudomallei and host genomes associated with melioidosis infection

Angchagun K. et al, (2023), Wellcome Open Research, 8, 347 - 347

Single cell spatial analysis reveals inflammatory foci of immature neutrophil and CD8 T cells in COVID-19 lungs.

Weeratunga P. et al, (2023), Nature communications, 14

Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance.

Amarasinghe HE. et al, (2023), BMC genomics, 24

Uncovering heterogeneity in sepsis: a comparative analysis of subphenotypes.

van Amstel RBE. et al, (2023), Intensive care medicine

A second update on mapping the human genetic architecture of COVID-19.

COVID-19 Host Genetics Initiative None., (2023), Nature, 621, E7 - E26

A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.

Akbari P. et al, (2023), Nature communications, 14

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Pairo-Castineira E. et al, (2023), Nature, 619, E61 - E61

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