Karin Beutel

Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11

Udo zur Stadt, Jan Rohr, Wenke Seifert et al. · The American Journal of Human Genetics · 2009 · 415 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes

Yenan T. Bryceson, Daniela Pende, Andrea Maul‐Pavicic et al. · Blood · 2012 · 307 citations · Full text

Medicine, Hematology, Internal Medicine +12

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A

Udo zur Stadt, Karin Beutel, Susanne Kolberg et al. · Human Mutation · 2005 · 281 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

Julia Pagel, Karin Beutel, Kai Lehmberg et al. · Blood · 2012 · 164 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Malignancy‐associated haemophagocytic lymphohistiocytosis in children and adolescents

Kai Lehmberg, Björn Sprekels, Kim E. Nichols et al. · British Journal of Haematology · 2015 · 158 citations · Full text

Medicine, Hematology, Pediatrics +17