Manuela Germeshausen

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

Christoph Klein, Magda Grudzien, Giridharan Appaswamy et al. · Nature Genetics · 2006 · 504 citations

Life Sciences, Genetics, Molecular Genetics +10

c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

Matthias Ballmaier, Manuela Germeshausen, Harald Schulze et al. · Blood · 2001 · 351 citations · Full text

Life Sciences, Genetics, Hematology +13

A Syndrome with Congenital Neutropenia and Mutations in<i>G6PC3</i>

Kaan Boztuǧ, Giridharan Appaswamy, Angel Ashikov et al. · New England Journal of Medicine · 2008 · 349 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: results of a long-term survey

Manuela Germeshausen, Matthias Ballmaier, Karl Welte · Blood · 2006 · 224 citations · Full text

Life Sciences, Genetics, Hematology +11

LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia

Julia Skokowa, Gunnar Cario, Murat Uenalan et al. · Nature Medicine · 2006 · 212 citations

Life Sciences, Hematology, Immunology +14