Chen P, Le KM, Li W, Hinrichsen F, Liu X, Braathen RS, Mamia N, Szymanska M, Li Z, Trotta L, Almusa H, Mamia K, Glumoff V, Holland P, Anders S, Kalinichenko A, Kaustio M, Seppänen MRJ, Haapaniemi EM, Varjosalo M, Martelius T, Grönholm J, Saarela J (2026)
Homozygous loss-of-function mutation in SIT1 leads to combined immunodeficiency due to dysregulated T cell receptor signaling
J Allergy Clin Immunol (in press)
DOI 10.1016/j.jaci.2026.03.030, PubMed 42128181

Størdal K, Almaas R, Sanner H, Sletner L, Stene LC (2026)
Incidence and co-occurrence of six autoimmune diseases in childhood: a population-based cohort study in Norway
Lancet Child Adolesc Health, 10 (6), 429-437
DOI 10.1016/S2352-4642(26)00008-8, PubMed 42001894

Hård Af Segerstad EM, Thesen M, Tapia G, Brantsæter AL, Parr CL, Magnus MC, Stene LC, Størdal K, Lund-Blix NA, HEDIMED Investigator Group (2026)
Early-Life Intake of Marine n-3 Fatty Acids, Genetic Fatty Acid Desaturase Variants, and Risk of Celiac Disease
Am J Gastroenterol (in press)
DOI 10.14309/ajg.0000000000004012, PubMed 41914612