Kaan Boztug
Kaan Boztug
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
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
Stem-cell gene therapy for the Wiskott–Aldrich syndrome
K Boztug, M Schmidt, A Schwarzer, PP Banerjee, IA Díez, RA Dewey, ...
New England Journal of Medicine 363 (20), 1918-1927, 2010
Gene therapy for Wiskott-Aldrich syndrome—long-term efficacy and genotoxicity
CJ Braun, K Boztug, A Paruzynski, M Witzel, A Schwarzer, M Rothe, ...
Science translational medicine 6 (227), 227ra33-227ra33, 2014
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
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
A syndrome with congenital neutropenia and mutations in G6PC3
K Boztug, G Appaswamy, A Ashikov, AA Schäffer, U Salzer, J Diestelhorst, ...
New England Journal of Medicine 360 (1), 32-43, 2009
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
CS Ma, N Wong, G Rao, DT Avery, J Torpy, T Hambridge, J Bustamante, ...
Journal of Allergy and Clinical Immunology 136 (4), 993-1006. e1, 2015
Inherited DOCK2 deficiency in patients with early-onset invasive infections
K Dobbs, C Domínguez Conde, SY Zhang, S Parolini, M Audry, J Chou, ...
New England Journal of Medicine 372 (25), 2409-2422, 2015
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27
E Salzer, S Daschkey, S Choo, M Gombert, E Santos-Valente, S Ginzel, ...
haematologica 98 (3), 473, 2013
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses
S Spencer, S Köstel Bal, W Egner, H Lango Allen, SI Raza, CA Ma, ...
Journal of Experimental Medicine 216 (9), 1986-1998, 2019
CD55 deficiency, early-onset protein-losing enteropathy, and thrombosis
A Ozen, WA Comrie, RC Ardy, C Domínguez Conde, B Dalgic, ÖF Beser, ...
New England Journal of Medicine 377 (1), 52-61, 2017
Interferon-independent, human immunodeficiency virus type 1 gp120-mediated induction of CXCL10/IP-10 gene expression by astrocytes in vivo and in vitro
VC Asensio, J Maier, R Milner, K Boztug, C Kincaid, M Moulard, ...
Journal of virology 75 (15), 7067-7077, 2001
Early-onset inflammatory bowel disease and common variable immunodeficiency–like disease caused by IL-21 deficiency
E Salzer, A Kansu, H Sic, P Májek, A Ikincioğullari, FE Dogu, ...
Journal of Allergy and Clinical Immunology 133 (6), 1651-1659. e12, 2014
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ
E Salzer, E Santos-Valente, S Klaver, SA Ban, W Emminger, ...
Blood, The Journal of the American Society of Hematology 121 (16), 3112-3116, 2013
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency
OK Alkhairy, R Perez-Becker, GJ Driessen, H Abolhassani, ...
Journal of Allergy and Clinical Immunology 136 (3), 703-712. e10, 2015
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity
KL Willmann, S Klaver, F Doğu, E Santos-Valente, W Garncarz, I Bilic, ...
Nature communications 5 (1), 5360, 2014
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia
K Boztug, PM Järvinen, E Salzer, T Racek, S Mönch, W Garncarz, ...
Nature genetics 46 (9), 1021-1027, 2014
RASGRP1 deficiency causes immunodeficiency with impaired cytoskeletal dynamics
E Salzer, D Cagdas, M Hons, EM Mace, W Garncarz, ÖY Petronczki, ...
Nature immunology 17 (12), 1352-1360, 2016
Interleukin-2-inducible T-cell kinase (ITK) deficiency-clinical and molecular aspects
S Ghosh, K Bienemann, K Boztug, A Borkhardt
Journal of Clinical Immunology 34, 892-899, 2014
Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2
J Jung, G Bohn, A Allroth, K Boztug, G Brandes, I Sandrock, AA Schäffer, ...
Blood 108 (1), 362-369, 2006
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