Bodo Grimbacher
Bodo Grimbacher
Professor of Immunology, Albert-Ludwigs University Freiburg, Germany
Verified email at - Homepage
Cited by
Cited by
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor
EO Glocker, D Kotlarz, K Boztug, EM Gertz, AA Schäffer, F Noyan, M Perro, ...
New England Journal of Medicine 361 (21), 2033-2045, 2009
STAT3 Mutations in the Hyper-IgE Syndrome
SM Holland, FR DeLeo, HZ Elloumi, AP Hsu, G Uzel, N Brodsky, ...
New England Journal of Medicine 357 (16), 1608-1619, 2007
Hyper-IgE syndrome with recurrent infections—an autosomal dominant multisystem disorder
B Grimbacher, SM Holland, JI Gallin, F Greenberg, SC Hill, HL Malech, ...
New England Journal of Medicine 340 (9), 692-702, 1999
Common variable immunodeficiency disorders: division into distinct clinical phenotypes
H Chapel, M Lucas, M Lee, J Bjorkander, D Webster, B Grimbacher, ...
Blood, The Journal of the American Society of Hematology 112 (2), 277-286, 2008
Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency
B Grimbacher, A Hutloff, M Schlesier, E Glocker, K Warnatz, R Dräger, ...
Nature immunology 4 (3), 261-268, 2003
A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal Infections
EO Glocker, A Hennigs, M Nabavi, AA Schäffer, C Woellner, U Salzer, ...
New England Journal of Medicine 361 (18), 1727-1735, 2009
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations
D Schubert, C Bode, R Kenefeck, TZ Hou, JB Wing, A Kennedy, ...
Nature medicine 20 (12), 1410-1416, 2014
Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3
CS Ma, GYJ Chew, N Simpson, A Priyadarshi, M Wong, B Grimbacher, ...
The Journal of experimental medicine 205 (7), 1551-1557, 2008
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
U Salzer, HM Chapel, ADB Webster, Q Pan-Hammarström, ...
Nature genetics 37 (8), 820-828, 2005
B-cell biology and development
K Pieper, B Grimbacher, H Eibel
Journal of Allergy and Clinical Immunology 131 (4), 959-971, 2013
An Antibody-Deficiency Syndrome Due to Mutations in the CD19 Gene
MC Van Zelm, I Reisli, M Van Der Burg, D Castaño, CJM Van Noesel, ...
New England Journal of Medicine 354 (18), 1901-1912, 2006
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
C Klein, M Grudzien, G Appaswamy, M Germeshausen, I Sandrock, ...
Nature genetics 39 (1), 86-92, 2007
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
B Gathmann, N Mahlaoui, L Gérard, E Oksenhendler, K Warnatz, ...
Journal of Allergy and Clinical Immunology 134 (1), 116-126. e11, 2014
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
KR Engelhardt, S McGhee, S Winkler, A Sassi, C Woellner, ...
Journal of Allergy and Clinical Immunology 124 (6), 1289-1302. e4, 2009
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
G Lopez-Herrera, G Tampella, Q Pan-Hammarström, P Herholz, ...
The American Journal of Human Genetics 90 (6), 986-1001, 2012
ICOS deficiency is associated with a severe reduction of CXCR5+ CD4 germinal center Th cells
L Bossaller, J Burger, R Draeger, B Grimbacher, R Knoth, A Plebani, ...
The Journal of Immunology 177 (7), 4927-4932, 2006
Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy
D Kotlarz, R Beier, D Murugan, J Diestelhorst, O Jensen, K Boztug, ...
Gastroenterology 143 (2), 347-355, 2012
Genetic linkage of hyper-IgE syndrome to chromosome 4
B Grimbacher, AA Schäffer, SM Holland, J Davis, JI Gallin, HL Malech, ...
The American Journal of Human Genetics 65 (3), 735-744, 1999
B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans
K Warnatz, U Salzer, M Rizzi, B Fischer, S Gutenberger, J Böhm, ...
Proceedings of the National Academy of Sciences 106 (33), 13945-13950, 2009
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study
TI Coulter, A Chandra, CM Bacon, J Babar, J Curtis, N Screaton, ...
Journal of Allergy and Clinical Immunology 139 (2), 597-606. e4, 2017
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