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Journal of Autoimmunity|November 19, 2022
NFκB pathway dysregulation due to reduced RelB expression leads to severe autoimmune disorders and declining immunityNigel Sharfe, Ilan Dalal, Zahra Naghdi, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2025
Autosomal-dominant Roquin-1 immunodeficiency and hyperinflammationAmit Nahum, Nigel Sharfe, Daniele Merico, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
The Journal of Allergy and Clinical Immunology|August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)Harjit Dadi, Tyler A Jones, Daniele Merico, et al.
Frontiers in Immunology|June 13, 2017
Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in ZAP70 and RNF168Ivan K Chinn, Robert P Sanders, Asbjørg Stray-Pedersen, et al.
Blood|October 26, 2013
IL-21 signalling via STAT3 primes human naive B cells to respond to IL-2 to enhance their differentiation into plasmablastsLucinda J Berglund, Danielle T Avery, Cindy S Ma, et al.
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