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Clinical Immunology (Orlando, Fla.)|January 3, 2023
Genetically encoded Runx3 and CD4<sup>+</sup> intestinal epithelial lymphocyte deficiencies link SKG mouse and human predisposition to spondyloarthropathyZaied Ahmed Bhuyan, M Arifur Rahman, Muralidhara Rao Maradana, et al.
Plos One|March 7, 2017
Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucomaTiger Zhou, Emmanuelle Souzeau, Shiwani Sharma, et al.
Investigative Ophthalmology & Visual Science|March 11, 2017
Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle GlaucomaTiger Zhou, Emmanuelle Souzeau, Owen M Siggs, et al.
Nature Genetics|April 28, 2006
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressivaEileen M Shore, Meiqi Xu, George J Feldman, et al.
Human Molecular Genetics|February 3, 2009
Common variants in the region around Osterix are associated with bone mineral density and growth in childhoodNicholas J Timpson, Jon H Tobias, J Brent Richards, et al.
The Lancet. Rheumatology|November 15, 2021
Humoral and cellular immunogenicity to a second dose of COVID-19 vaccine BNT162b2 in people receiving methotrexate or targeted immunosuppression: a longitudinal cohort studySatveer K Mahil, Katie Bechman, Antony Raharja, et al.
Journal of Medical Genetics|April 11, 2013
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearmHou-Feng Zheng, Emma L Duncan, Laura M Yerges-Armstrong, et al.
BMC Medical Genomics|July 25, 2018
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritisElisabeth De Smit, Samuel W Lukowski, Lisa Anderson, et al.
The Lancet. Rheumatology|July 14, 2021
The effect of methotrexate and targeted immunosuppression on humoral and cellular immune responses to the COVID-19 vaccine BNT162b2: a cohort studySatveer K Mahil, Katie Bechman, Antony Raharja, et al.
Bone|June 9, 2018
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genesCelia L Gregson, Felicity Newell, Paul J Leo, et al.
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