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Annals of the Rheumatic Diseases|August 17, 2022
Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosusLingxiao Xu, Jian Zhao, Qing Sun, et al.
Neuro-Oncology Advances|July 10, 2020
Expression profiling of the adhesion G protein-coupled receptor GPR133 (ADGRD1) in glioma subtypesJoshua D Frenster, Michael Kader, Scott Kamen, et al.
Vaccines|April 27, 2024
Impact of Recombinant VSV-HIV Prime, DNA-Boost Vaccine Candidates on Immunogenicity and Viremia on SHIV-Infected Rhesus MacaquesAlice Berger, Jannie Pedersen, Monika M Kowatsch, et al.
Clinical Chemistry and Laboratory Medicine|April 22, 2010
The European Register of Specialists in Clinical Chemistry and Laboratory Medicine: guide to the Register, version 3-2010Janet McMurray, Simone Zérah, Michael Hallworth, et al.
Arthritis Research & Therapy|February 20, 2024
Longitudinal patterns and predictors of response to standard-of-care therapy in lupus nephritis: data from the Accelerating Medicines Partnership Lupus NetworkPeter M Izmirly, Mimi Y Kim, Philip M Carlucci, et al.
Arthritis Care & Research|October 6, 2025
Serum Soluble Mediator Signatures of Lupus Nephritis: Histologic Features and Response to TreatmentAndrea Fava, Catriona A Wagner, Carla J Guthridge, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|April 17, 2025
Approaches to optimally target frailty screening among people with HIV in clinical care: findings from the Centers for AIDS Research Network of Integrated Clinical Systems (CNICS)Heidi M Crane, Stephanie A Ruderman, Robin M Nance, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 20, 2020
Brain functional network integrity sustains cognitive function despite atrophy in presymptomatic genetic frontotemporal dementiaKamen A Tsvetanov, Stefano Gazzina, P Simon Jones, et al.
Nature Genetics|January 31, 2017
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseasesJian Zhao, Jianyang Ma, Yun Deng, et al.
Nature Communications|February 20, 2024
Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNAAdam Benjamin Rohrlach, Maïté Rivollat, Patxuka de-Miguel-Ibáñez, et al.
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