Georg Bohn

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

A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14

Georg Bohn, Anna Allroth, Gudrun Brandes et al. · Nature Medicine · 2006 · 209 citations

Primary Immunodeficiency, Autoimmune Disease, Immunodeficiencies +8

p14–MP1-MEK1 signaling regulates endosomal traffic and cellular proliferation during tissue homeostasis

David Teis, Nicole Taub, R Kurzbauer et al. · The Journal of Cell Biology · 2006 · 205 citations · Full text

A family of γ‐like calcium channel subunits

Norbert Klugbauer, Shuiping Dai, Verena Specht et al. · FEBS Letters · 2000 · 199 citations

Perturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21

Anindita Roy, Gillian Cowan, Adam J. Mead et al. · Proceedings of the National Academy of Sciences · 2012 · 165 citations · Full text