Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. by Salzer, U, Chapel, H, Webster, A, Pan-Hammarström, Q, Schmitt-Graeff, A, Schlesier, M, Peter, H, Rockstroh, J, Schneider, P, Schäffer, A, Hammarström, L, Grimbacher, B

Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency by Bronson, P, Chang, D, Bhangale, T, Seldin, M, Ortmann, W, Ferreira, R, Urcelay, E, Pereira, L, Martin, J, Plebani, A, Lougaris, V, Friman, V, Freiberger, T, Litzman, J, Thon, V, Pan-Hammarström, Q, Hammarström, L, Graham, R, Behrens, T

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. by Salzer, U, Bacchelli, C, Buckridge, S, Pan-Hammarström, Q, Jennings, S, Lougaris, V, Bergbreiter, A, Hagena, T, Birmelin, J, Plebani, A, Webster, A, Peter, H, Suez, D, Chapel, H, McLean-Tooke, A, Spickett, G, Anover-Sombke, S, Ochs, H, Urschel, S, Belohradsky, B, Ugrinovic, S, Kumararatne, D, Lawrence, T, Holm, A, Franco, J

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases. by Rioux, J, Goyette, P, Vyse, T, Hammarström, L, Fernando, M, Green, T, De Jager, P, Foisy, S, Wang, J, de Bakker, P, Leslie, S, McVean, G, Padyukov, L, Alfredsson, L, Annese, V, Hafler, D, Pan-Hammarström, Q, Matell, R, Sawcer, S, Compston, A, Cree, B, Mirel, D, Daly, M, Behrens, T, Klareskog, L

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity by Lopez-Herrera, G, Tampella, G, Pan-Hammarström, Q, Herholz, P, Trujillo-Vargas, C, Phadwal, K, Simon, A, Moutschen, M, Etzioni, A, Mory, A, Srugo, I, Melamed, D, Hultenby, K, Liu, C, Baronio, M, Vitali, M, Philippet, P, Dideberg, V, Aghamohammadi, A, Rezaei, N, Enright, V, Du, L, Salzer, U, Eibel, H, Pfeifer, D

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. by Lopez-Herrera, G, Tampella, G, Pan-Hammarström, Q, Herholz, P, Trujillo-Vargas, C, Phadwal, K, Simon, A, Moutschen, M, Etzioni, A, Mory, A, Srugo, I, Melamed, D, Hultenby, K, Liu, C, Baronio, M, Vitali, M, Philippet, P, Dideberg, V, Aghamohammadi, A, Rezaei, N, Enright, V, Du, L, Salzer, U, Eibel, H, Pfeifer, D

DELETERIOUS LRBA MUTATIONS IN A NOVEL SYNDROME OF IMMUNE DEFICIENCY AND AUTOIMMUNITY by Lopez-Herrera, G, Tampella, G, Pan-Hammarstrom, Q, Herholz, P, Trujillo-Vargas, C, Phadwal, K, Simon, A, Moutschen, M, Etzioni, A, Mory, A, Srugo, I, Melamed, D, Hultenby, K, Liu, C, Baronio, M, Vitali, M, Philippet, P, Dideberg, V, Aghamohammadi, A, Rezai, N, Enright, V, Du, L, Salzer, U, Eibel, H, Pfeifer, D