See‐Tarn Woon

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency

Manfred Fliegauf, Vanessa L. Bryant, Natalie Frede et al. · The American Journal of Human Genetics · 2015 · 243 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +13

A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes

Paul Bastard, Kuang‐Chih Hsiao, Qian Zhang et al. · The Journal of Experimental Medicine · 2022 · 67 citations · Full text

Life Sciences, Genetics, Immunology +17

Epistatic interactions between mutations of TACI (<i>TNFRSF13B</i>) and <i>TCF3</i> result in a severe primary immunodeficiency disorder and systemic lupus erythematosus

Rohan Ameratunga, Wikke Koopmans, See‐Tarn Woon et al. · Clinical & Translational Immunology · 2017 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

First Identified Case of Fatal Fulminant Necrotizing Eosinophilic Myocarditis Following the Initial Dose of the Pfizer-BioNTech mRNA COVID-19 Vaccine (BNT162b2, Comirnaty): an Extremely Rare Idiosyncratic Hypersensitivity Reaction

Rohan Ameratunga, See‐Tarn Woon, Mary N. Sheppard et al. · Journal of Clinical Immunology · 2022 · 55 citations · Full text

Medicine, Internal Medicine, Pathology +10

Common Variable Immunodeficiency Disorders, T-Cell Responses to SARS-CoV-2 Vaccines, and the Risk of Chronic COVID-19

Rohan Ameratunga, Hilary Longhurst, Richard Steele et al. · The Journal of Allergy and Clinical Immunology In Practice · 2021 · 49 citations · Full text

Life Sciences, Immunology, Infectious Diseases +17