Kaan Boztuǧ

Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor

Erik‐Oliver Glocker, Daniel Kotlarz, Kaan Boztuǧ et al. · New England Journal of Medicine · 2009 · 1.4K citations · Full text

Gene Therapy for Wiskott-Aldrich Syndrome—Long-Term Efficacy and Genotoxicity

Christian Braun, Kaan Boztuǧ, Anna Paruzynski et al. · Science Translational Medicine · 2014 · 543 citations · Full text

Stem-Cell Gene Therapy for the Wiskott–Aldrich Syndrome

Kaan Boztuǧ, Manfred Schmidt, Adrian Schwarzer et al. · New England Journal of Medicine · 2010 · 532 citations · Full text

Cell Therapy, Immunology, Blood Cell +24

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Christoph Klein, Magda Grudzien, Giridharan Appaswamy et al. · Nature Genetics · 2006 · 501 citations

Hax1 Deficiency, Mendelian Disorder, Genetic Disorder +7

Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy

Daniel Kotlarz, Rita Beier, Dhaarini Murugan et al. · Gastroenterology · 2012 · 462 citations · Full text

Inflammation, Cytokine, Mucosal Immunology +8