Concepedia

Wenke Seifert

WS

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Publications

15

Citations

1.4K

H-Index

14

Active since

2004

Affiliations

Charité - Universitätsmedizin Berlin(Current)

Max Planck Institute for Molecular Genetics

University of Cologne

Freie Universität Berlin

Max Delbrück Center

Wenke Seifert is an author at Charité - Universitätsmedizin Berlin specializing in life sciences, genetics, and genetic disorders.

ORCID

Publications per year

2004–2022

15

Publications

15

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

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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 · 158 citations · Full text

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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 · 149 citations · Full text

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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 · 145 citations · Full text

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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

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