Carlos Rose, MD

Simonds, M. M., Schlefman, A. R., McCahan, S. M., Sullivan, K. E., Rose, C. D., & Brescia, A. M. C. (2021). The culture microenvironment of juvenile idiopathic arthritis synovial fibroblasts is favorable for endochondral bone formation through BMP4 and repressed by chondrocytes. Pediatric Rheumatology, 19(1). doi:10.1186/s12969-021-00556-8

Simonds, M. M., Schlefman, A. R., McCahan, S. M., Sullivan, K. E., Rose, C. D., & Brescia, A. M. C. (2020). Juvenile idiopathic arthritis fibroblast-like synoviocytes influence chondrocytes to alter BMP antagonist expression demonstrating an interaction between the two prominent cell types involved in endochondral bone formation. Pediatric Rheumatology, 18(1). doi:10.1186/s12969-020-00483-0

Rose, C. D., Fawcett, P. T., Gibney, K., Doughty, R. A., & Singsen, B. H. (2019). Serial measurements of soluble interleukin 2 receptor levels (sIL2-R) in children with juvenile rheumatoid arthritis treated with oral methotrexate. Pediatrics, 144(1), 471-474. doi:10.1542/peds.2018-3604

Wang, L., Rose, C. D., Foley, K. P., Anton, J., Bader-Meunier, B., Brissaud, P., & Wouters, C. H. (2018). S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome. Rheumatology (United Kingdom), 57(7), 1299-1304. doi:10.1093/rheumatology/key090

Hinks, A., Marion, M. C., Cobb, J., Comeau, M. E., Sudman, M., Ainsworth, H. C., & Juvenile Idiopathic Arthritis Consortium for Immunochip. (2018). Brief Report: The Genetic Profile of Rheumatoid Factor-Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis. Arthritis and Rheumatology, 70(6), 957-962. doi:10.1002/art.40443

Sarens, I. L., Casteels, I., Anton, J., Bader-Meunier, B., Brissaud, P., Chedeville, G., & Wouters, C. H. (2018). Blau Syndrome-Associated Uveitis: Preliminary Results From an International Prospective Interventional Case Series. American Journal of Ophthalmology, 187, 158-166. doi:10.1016/j.ajo.2017.08.017

Brescia, A. M. C., Simonds, M. M., McCahan, S. M., Sullivan, K. E., & Rose, C. D. (2018). Prior to extension, transcriptomes of fibroblast-like synoviocytes from extended and polyarticular juvenile idiopathic arthritis are indistinguishable. Pediatric Rheumatology, 16(1). doi:10.1186/s12969-017-0217-6

McIntosh, L. A., Marion, M. C., Sudman, M., Comeau, M. E., Becker, M. L., Bohnsack, J. F., & Thompson, S. D. (2017). Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci. Arthritis and Rheumatology, 69(11), 2222-2232. doi:10.1002/art.40216

Horton, D. B., Haynes, K., Denburg, M. R., Thacker, M. M., Rose, C. D., Putt, M. E., & Strom, B. L. (2017). Oral glucocorticoid use and osteonecrosis in children and adults with chronic inflammatory diseases: A population-based cohort study. BMJ Open, 7(7). doi:10.1136/bmjopen-2017-016788

Rose, C. D. (2017c). Ethical conduct of research in children: Pediatricians and their IRB (Part 2 of 2). Pediatrics, 139(6). doi:10.1542/peds.2016-3650

Rose, C. D. (2017b). Ethical conduct of research in children: Pediatricians and their irb (part 1 of 2). Pediatrics, 139(5). doi:10.1542/peds.2016-3648

Brescia, A. C., Simonds, M. M., Sullivan, K. E., & Rose, C. D. (2017). Secretion of pro-inflammatory cytokines and chemokines and loss of regulatory signals by fibroblast-like synoviocytes in juvenile idiopathic arthritis. Proteomics - Clinical Applications, 11(5-6). doi:10.1002/prca.201600088

Rose, C. D. (2017a). Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity. Pediatric Dermatology, 34(2), 216-218. doi:10.1111/pde.13021

Schlefman, A. R., Brescia, A. C., Leffler, M. G., & Rose, C. D. (2017). Unilateral Periorbital Swelling in Two Previously Healthy Females. Global Pediatric Health, 4. doi:10.1177/2333794X17733860

Wouters, C. H., & Rose, C. D. (2016). Childhood Sarcoidosis. In Handbook of Systemic Autoimmune Diseases (Vol 11, bll 427-449). doi:10.1016/B978-0-444-63596-9.00020-7

Horton, D. B., Strom, B. L., Putt, M. E., Rose, C. D., Sherry, D. D., & Sammons, J. S. (2016). Epidemiology of clostridium difficile infection-associated reactive arthritis in children: An underdiagnosed, potentially morbid condition. JAMA Pediatrics, 170(7). doi:10.1001/jamapediatrics.2016.0217

Dugan, J., Griffiths, E., Snow, P., Rosenzweig, H., Lee, E., Brown, B., & Davey, M. P. (2015). Blau syndrome-associated Nod2 mutation alters expression of full-length NOD2 and limits responses to muramyl dipeptide in knock-in mice. Journal of Immunology, 194(1), 349-357. doi:10.4049/jimmunol.1402330

Rose, C. D., Pans, S., Casteels, I., Anton, J., Bader-Meunier, B., Brissaud, P., & Wouters, C. H. (2015). Blau syndrome: Cross-sectional data from a multicentre study of clinical, radiological and functional outcomes. Rheumatology (United Kingdom), 54(6), 1008-1016. doi:10.1093/rheumatology/keu437

Horton, D. B., Scott, F. I., Haynes, K., Putt, M. E., Rose, C. D., Lewis, J. D., & Strom, B. L. (2015). Antibiotic exposure and juvenile idiopathic arthritis: A case-control study. Pediatrics, 136(2), e333-e343. doi:10.1542/peds.2015-0036