• Contact
• How to Find Us
• Organisations
• Media

Most important publications

Mohammadi J, C Liu, Aghamohammadi A, Bergbreiter A, Du L, Lu J, Rezaei N, Amirzargar AA, Moin M, Salzer U, Pan-Hammarström Q, Hammarström L. Novel Mutations in TACI (TNFRSF13B) Causing Common 5 Variable Immunodeficiency J Clin Immunol, DOI 10.1007/s10875-009-9317-5.

Salzer U*, Bacchelli C*, Buckridge S, Pan-Hammarström Q, Jennings S, Lougaris V, Hagena T, Birmelin J, Plebani A, Webster ADB, Peter HH, Suez D, Chapel H, Maclean-Tooke A, Spickett GP, Anover-Sombke S, Ochs HD, Urschel S, Belohradsky BH, Kumararatne DS, Lawrence TC, Holm AM, Franco JL, Schulze I, Schneider P, Hammarström L, Thrasher AJ, Gaspar HB, Grimbacher B Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease causing from disease modifying TNFRSF13B variants in common variable immunodeficiency. Blood 2009 113:1967-1976.

Zhang L, Radigan L, Salzer U, Behrens TW, Grimbacher B, Diaz G, Bussel J, Cunningham-Rundles C. Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: Clinical and immunologic outcomes in heterozygotes. J Allergy Clin Immunol. 2007, 120:1178-1185.

Salzer U, Birmelin J, Bacchelli C, Witte T, Buchegger-Podbielski U, Buckridge S, Rzepka R, Gaspar HB, Thrasher AJ, Schmidt RE, Melchers I, Grimbacher B. Sequence Analysis of TNFRSF13b, Encoding TACI, in Patients with Systemic Lupus Erythematosus. J Clin Immunol. 2007, 27:372-377.

Pan-Hammarström Q*, Salzer U*, Du L, Björkander J, Cunningham-Rundles C, Nelson DL, Bacchelli C, Gaspar HB, Offer S, Behrens TW, Grimbacher B and Hammarström L Reexamining the role of TACI coding variants in common variable immunodefiency and selective IgA deficiency Nat Genet. 2007, 39:429-430.

Salzer U, Chapel HM, Webster AD, Pan-Hammarstrom Q, Schmitt-Graeff A,Schlesier M, Peter HH, Rockstroh JK, Schneider P, Schaffer AA, Hammarstrom L, Grimbacher B. Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Nat Genet. 2005, 37:820-828.

Warnatz K*, Salzer U*, Rizzi M, Fischer B, Gutenberger S, Böhm J, Pan-Hammarström Q, Hammarström L, Rakhmanov M, Schlesier M, Grimbacher B, Peter HH, Eibel H. BAFF-R deficiency is associated with an adult onset antibody deficiency syndrome in humans. Proc Natl Acad Sci U S A., in press.

Litzman J, Freiberger T, Grimbacher B, Gathmann B, Salzer U, Pavlík T, Vlček J, Postránecká V, Travnickova Z, Thon V. Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency. Clin Exp Immunol 2008, 153:324-330.

Salzer U, Hagena T, Webster ADB and Grimbacher B. Sequence analysis of XIAP in male patients with common variable immunodeficiency. Int Arch Allergy Immunol 2008, 147:147-151.

Salzer U, Neumann C, Thiel J, Woellner C, Pan-Hammarstrom Q, Lougaris V, Hagena T, Jung J, Birmelin J, Du L, Metin A, Webster ADB, Plebani A, Moschese V, Hammarstrom L, Schaffer AA, Grimbacher B. Screening of functional and positional candidate genes in families with common variable immunodeficiency. BMC Immunology 2008, 9:3.

Losi CG, Salzer U, Gatta R, Lougaris V, Cattaneo G, Meini A, Soresina A, Grimbacher B, Plebani A. Mutational Analysis of Human BLyS in Patients with Common Variable Immunodeficiency. J Clin Immunol. 2006, 26:396-399.

Roscioli T, Cliffe ST, Bloch DB, Bell CG, Mullan G, Taylor PJ, Sarris M, Wang J, Donald JA, Kirk EP, Ziegler JB, Salzer U, McDonald GB, Wong M, Robert Lindeman R, Buckley MF. Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease. Nat Genet. 2006, 38:620-622.

Warnatz K, Bossaller L*, Salzer U*, Skrabl-Baumgartner A, Schwinger W, van der Burg M, van Dongen JJ, Orlowska-Volk M, Knoth R, Durandy A, Draeger R, Schlesier M, Peter HH, Grimbacher B. Human ICOS-deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency. Blood. 2006, 107:3045-3052. *equal contribution

Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH,Litzman J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B. ICOS deficiency in patients with common variable immunodeficiency. Clin Immunol. 2004, 113:234-240.

• deutsch