Jensen, B., James, R., Hong, Y., Omoyinmi, E., Pilkington, C., Sebire, N. J., . . . Eleftheriou, D. (2020). A case of Myhre syndrome mimicking juvenile scleroderma. Pediatr Rheumatol Online J, 18 (1), 72. doi:10.1186/s12969-020-00466-1

Rowczenio, D. M., Youngstein, T., Trojer, H., Omoyinmi, E., Baginska, A., Brogan, P., . . . Lachmann, H. J. (2020). British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature. Rheumatology. doi:10.1093/rheumatology/kez334

Hong, Y., Keylock, A., Jensen, B., Jacques, T. S., Ogunbiyi, O., Omoyinmi, E., . . . Eleftheriou, D. (2020). Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene. Neurology: Genetics, 6 (4), e448. doi:10.1212/NXG.0000000000000448

Vignesh, P., Singhal, M., Suri, D., Kakkar, N., Omoyinmi, E., Brogan, P., & Singh, S. (2020). Extensive Oral Scarring and Bilateral Subclavian Artery Stenosis in Pediatric-Onset Behçet's Disease. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 26 (5), e91-e92. doi:10.1097/RHU.0000000000000924

Standing, A. S., Hong, Y., Paisan-Ruiz, C., Omoyinmi, E., Medlar, A., Stanescu, H., . . . Brogan, P. A. (2020). TRAP1 chaperone protein mutations and autoinflammation. Life Sci Alliance, 3 (2). doi:10.26508/lsa.201900376

McCreary, D., Omoyinmi, E., Hong, Y., Mulhern, C., Papadopoulou, C., Casimir, M., . . . Eleftheriou, D. (2019). Development and Validation of a Targeted Next-Generation Sequencing Gene Panel for Children With Neuroinflammation. JAMA Network Open, 2 (10), e1914274. doi:10.1001/jamanetworkopen.2019.14274

Garg, S., Wynne, K., Omoyinmi, E., Eleftheriou, D., & Brogan, P. (2019). Efficacy and safety of anakinra for undifferentiated autoinflammatory diseases in children: a retrospective case review. Rheumatol Adv Pract, 3 (1), rkz004. doi:10.1093/rap/rkz004

Melo Gomes, S., Dias, C., Omoyinmi, E., Compeyrot-Lacassagne, S., Klein, N., Sebire, N. J., & Brogan, P. (2019). Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome. Pediatrics. doi:10.1542/peds.2018-1741

Mulhern, C. M., Hong, Y., Omoyinmi, E., Jacques, T., D'Arco, F., Hemingway, C., . . . Eleftheriou, D. (2019). Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation. Journal of Allergy and Clinical Immunology. doi:10.1016/j.jaci.2019.05.026

Papadopoulou, C., Hong, Y., Omoyinmi, E., Brogan, P. A., & Eleftheriou, D. (2019). Janus kinase 1/2 inhibition with baricitinib in the treatment of juvenile dermatomyositis. Brain. doi:10.1093/brain/awz005