Eve L. Coomber
Wellcome Sanger Institute(GB)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomics and Chromatin Dynamics, Genetics and Neurodevelopmental Disorders, Neutrophil, Myeloperoxidase and Oxidative Mechanisms, Genetic Associations and Epidemiology
Most-Cited Works
- → Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders(2016)472 cited
- → An African Salmonella Typhimurium ST313 sublineage with extensive drug-resistance and signatures of host adaptation(2019)135 cited
- → EROS/CYBC1 mutations: Decreased NADPH oxidase function and chronic granulomatous disease(2018)88 cited
- → Interleukin-22 promotes phagolysosomal fusion to induce protection against Salmonella enterica Typhimurium in human epithelial cells(2018)49 cited
- → Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with TRAF3 mutations(2022)39 cited
- → IRF5 Promotes Influenza Virus-Induced Inflammatory Responses in Human Induced Pluripotent Stem Cell-Derived Myeloid Cells and Murine Models(2020)30 cited
- → Screening for functional regulatory variants in open chromatin using GenIE-ATAC(2023)17 cited
- → Screening for functional transcriptional and splicing regulatory variants with GenIE(2020)16 cited
- → A novel mutation in EROS (CYBC1) causes chronic granulomatous disease(2023)16 cited
- → Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data(2019)11 cited