“…In recent years, we have reported on the association of various immune response related genes with the susceptibility to both BD and VKH including STAT4, STAT3, JAK2, CD40 [7] , [8] , [9] , [40] . In the present study, the selection of the candidate locus/gene was primarily based on GWAS data in patients with psoriasis, psoriatic arthritis (PsA) [24] and psoriasis vulgaris (PsV) [23] , previously described associations for inflammatory diseases [17] , [25] , [41] , [42] , as well as the involvement of the gene products in the control of the immune and inflammatory response [43] , [44] , [45] .…”