Wenke Seifert

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 · 411 citations · Full text

Impaired Binding, Mendelian Disorder, Autoimmune Disease +11

Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin

Hans Christian Hennies, Uwe Kornak, Haikuo Zhang et al. · Nature Genetics · 2008 · 156 citations · Full text

Biology, Gerodermia Osteodysplastica, Somatic Variant +8

Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity

Wenke Seifert, Jirko Kühnisch, Tanja Maritzen et al. · Journal of Biological Chemistry · 2011 · 146 citations · Full text

Cohen Syndrome Pathology, Protein Function, Mendelian Disorder +12

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

Denise Horn, Johannes Kapeller, Núria Rivera‐Bruguès et al. · Human Mutation · 2010 · 138 citations · Full text

Cohen Syndrome-associated Protein COH1 Physically and Functionally Interacts with the Small GTPase RAB6 at the Golgi Complex and Directs Neurite Outgrowth

Wenke Seifert, Jirko Kühnisch, Tanja Maritzen et al. · Journal of Biological Chemistry · 2014 · 89 citations · Full text

Protein Function, Signal Transduction, Signaling Pathway +9