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Autoimmunity Reviews|October 26, 2011
The biological significance of TLR3 variant, L412F, in conferring susceptibility to cutaneous candidiasis, CMV and autoimmunityAmit Nahum, Harjit Dadi, Andrea Bates, et al.European Journal of Immunology|January 9, 2003
Ephrin stimulation modulates T cell chemotaxisNigel Sharfe, Andrew Freywald, Ana Toro, et al.The Journal of Allergy and Clinical Immunology|September 25, 2010
Characterization of ζ-associated protein, 70 kd (ZAP70)-deficient human lymphocytesChaim M Roifman, Harjit Dadi, Raz Somech, et al.Journal of Autoimmunity|September 20, 2015
The effects of RelB deficiency on lymphocyte development and functionNigel Sharfe, Daniele Merico, Ariana Karanxha, et al.Blood|July 26, 2003
Inhibition of acute lymphoblastic and myeloid leukemias by a novel kinase inhibitorThomas Grunberger, Peter Demin, Olga Rounova, et al.The Journal of Allergy and Clinical Immunology|November 19, 2013
Fatal combined immunodeficiency associated with heterozygous mutation in STAT1Nigel Sharfe, Amit Nahum, Andrea Newell, et al.The Journal of Allergy and Clinical Immunology|September 27, 2020
Combined immunodeficiency caused by a novel homozygous NFKB1 mutationAmarilla B Mandola, Nigel Sharfe, Zahra Nagdi, et al.The Journal of Allergy and Clinical Immunology|November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic featuresNigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.Frontiers in Immunology|February 7, 2022
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic VariantOri Scott, Nigel Sharfe, Harjit Dadi, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 5, 2021
DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patientsOri Scott, Harjit Dadi, Linda Vong, et al.Pageof 2