Emma E. Davenport

Hinxton, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 34 publications

Trans-eQTLs reveal the architecture of human gene regulatory networks.

Trans-eQTLs reveal the architecture of human gene regulatory networks.

Journal: medRxiv : the preprint server for health sciences
Published: April 29, 2026

The Lancet Commission on Sepsis: transforming sepsis care and outcomes.

The Lancet Commission on Sepsis: transforming sepsis care and outcomes.

Journal: Lancet (London, England)
Published: February 20, 2026

Single-Cell Level Characterization of B Cell Depletion and Repopulation Following Rituximab in Systemic Lupus Erythematosus.

Single-Cell Level Characterization of B Cell Depletion and Repopulation Following Rituximab in Systemic Lupus Erythematosus.

Journal: Arthritis & rheumatology (Hoboken, N.J.)
Published: May 23, 2025

Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis.

Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis.

Journal: Nature communications
Published: May 18, 2025

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Journal: Cell reports
Published: March 21, 2025

A consensus blood transcriptomic framework for sepsis.

A consensus blood transcriptomic framework for sepsis.

Journal: Nature medicine
Published: November 20, 2024

Pulmonary inflammation in severe pneumonia is characterised by compartmentalised and mechanistically distinct sub-phenotypes.

Pulmonary inflammation in severe pneumonia is characterised by compartmentalised and mechanistically distinct sub-phenotypes.

Journal: Nature communications
Published: September 20, 2024

The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding.

The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding.

Journal: Blood advances
Published: July 10, 2024

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Journal: American journal of human genetics
Published: January 12, 2024

The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes.

The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes.

Journal: Nature genetics
Published: December 05, 2023

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

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

Journal: Cell genomics
Published: November 07, 2023

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

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

Journal: Wellcome open research
Published: November 01, 2023
Showing 1-12 of 34

Last Updated: 09/26/2026