Eve Coomber | Senior Research Assistant

Coomber, Eve

Eve works in the Human Complex Traits team lead by Nicole Soranzo.

Publications

  • EROS/CYBC1 mutations: Decreased NADPH oxidase function and chronic granulomatous disease.

    Thomas DC, Charbonnier LM, Schejtman A, Aldhekri H, Coomber EL et al.

    The Journal of allergy and clinical immunology 2019;143;2;782-785.e1

  • Large-scale discovery of novel genetic causes of developmental disorders.

    Deciphering Developmental Disorders Study

    Nature 2015;519;7542;223-8

  • Induction by sodium butyrate of cytomegalovirus replication in human endothelial cells.

    Radsak K, Fuhrmann R, Franke RP, Schneider D, Kollert A et al.

    Archives of virology 1989;107;1-2;151-8

  • Interleukin-22 promotes phagolysosomal fusion to induce protection against Salmonella enterica Typhimurium in human epithelial cells.

    Forbester JL, Lees EA, Goulding D, Forrest S, Yeung A et al.

    Proceedings of the National Academy of Sciences of the United States of America 2018;115;40;10118-10123

  • Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

    Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L et al.

    Nature neuroscience 2016;19;4;571-7

  • EROS/CYBC1 mutations: Decreased NADPH oxidase function and chronic granulomatous disease.

    Thomas DC, Charbonnier LM, Schejtman A, Aldhekri H, Coomber EL et al.

    The Journal of allergy and clinical immunology 2019;143;2;782-785.e1

  • Interleukin-22 promotes phagolysosomal fusion to induce protection against Salmonella enterica Typhimurium in human epithelial cells.

    Forbester JL, Lees EA, Goulding D, Forrest S, Yeung A et al.

    Proceedings of the National Academy of Sciences of the United States of America 2018;115;40;10118-10123

  • Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

    Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L et al.

    Nature neuroscience 2016;19;4;571-7

  • Large-scale discovery of novel genetic causes of developmental disorders.

    Deciphering Developmental Disorders Study

    Nature 2015;519;7542;223-8

Career/Research Highlights

Coomber, Eve
Eve's Timeline
2018

Senior Research Assistant
Soranzo Team, Human Complex Traits

2016

Advanced Research Assistant
Pathogen Lab Support, Simon Clare

2013

Advanced Research Assistant
Wellcome Trust Sanger Institute
Hurles Team, Deciphering Developmental Disease

MSci Human Genetics
1st Class Hons University of Nottingham

2012

Hematopoietic Stem Cells
Masters project, Martin Gering

2011

Regeneration, Ageing and Stem cells
Undergraduate project and Summer student, Aziz Aboobaker