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The Journal of Allergy and Clinical Immunology|March 29, 2013
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndromeGulbu Uzel, Elizabeth P Sampaio, Monica G Lawrence, et al.
Cell Reports|May 14, 2020
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin LesionsMarta Martin-Fernandez, María Bravo García-Morato, Conor Gruber, et al.
Msphere|January 20, 2017
The Case for Adopting the "Species Complex" Nomenclature for the Etiologic Agents of CryptococcosisKyung J Kwon-Chung, John E Bennett, Brian L Wickes, et al.
Elife|October 27, 2022
Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seqSara E Vazquez, Sabrina A Mann, Aaron Bodansky, et al.
Cell Reports|January 28, 2023
Network analysis of large-scale ImmGen and Tabula Muris datasets highlights metabolic diversity of tissue mononuclear phagocytesAnastasiia Gainullina, Denis A Mogilenko, Li-Hao Huang, et al.
Science Translational Medicine|June 7, 2019
Lymphocyte-driven regional immunopathology in pneumonitis caused by impaired central immune toleranceElise M N Ferré, Timothy J Break, Peter D Burbelo, et al.
Science (New York, N.Y.)|September 16, 2021
Response to Comments on "Aberrant type 1 immunity drives susceptibility to mucosal fungal infections"Timothy J Break, Vasileios Oikonomou, Nicolas Dutzan, et al.
JCI Insight|September 27, 2022
Immunogenetics associated with severe coccidioidomycosisAmy P Hsu, Agnieszka Korzeniowska, Cynthia C Aguilar, et al.
Science (New York, N.Y.)|January 15, 2021
Aberrant type 1 immunity drives susceptibility to mucosal fungal infectionsTimothy J Break, Vasileios Oikonomou, Nicolas Dutzan, et al.
JCI Insight|September 3, 2016
Redefined clinical features and diagnostic criteria in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophyElise M N Ferre, Stacey R Rose, Sergio D Rosenzweig, et al.
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