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Annals of the Rheumatic Diseases|February 25, 2025
A coding single nucleotide polymorphism in the interleukin-6 receptor enhances IL-6 signalling in CD4 T cells and predicts treatment response to tocilizumab in giant cell arteritisRobert Zorc, Christopher Redmond, McKella Sylvester, et al.
Open Forum Infectious Diseases|July 30, 2024
Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) SyndromeMary Czech, Jennifer Cuellar-Rodriguez, Bhavisha A Patel, et al.
Blood Advances|April 1, 2026
American Society of Hematology 2026 Guidelines for the Diagnosis and Management of Severe Acquired Aplastic AnemiaPhillip Scheinberg, Debra A O'Neal, Ana Lisa Basquiera, et al.
Arthritis Care & Research|July 13, 2026
Development of a Disease Activity Index for the Assessment of VEXAS Syndrome (VEXAS-DAI)Kevin Byram, Heřman Mann, Danielle Hammond, et al.
Blood Advances|January 19, 2018
Heterozygous <i>RTEL1</i> variants in bone marrow failure and myeloid neoplasmsJudith C W Marsh, Fernanda Gutierrez-Rodrigues, James Cooper, et al.
British Journal of Haematology|September 21, 2022
Clinical outcomes and immune responses to SARS-CoV-2 vaccination in severe aplastic anaemiaRoma V Rajput, Xiaoyang Ma, Kristin L Boswell, et al.
The New England Journal of Medicine|October 27, 2020
Somatic Mutations in <i>UBA1</i> and Severe Adult-Onset Autoinflammatory DiseaseDavid B Beck, Marcela A Ferrada, Keith A Sikora, et al.
Blood|November 25, 2025
Somatic genetic rescue in ZCCHC8-associated telomere biology disordersSophie De Tocqueville, Flavia Donaires, Nicholas F DeCleene, et al.
Blood|July 6, 2022
Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesisMarcela A Ferrada, Sinisa Savic, Daniela Ospina Cardona, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 29, 2021
Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXASMarcela A Ferrada, Keith A Sikora, Yiming Luo, et al.
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