Vinzenz Oji

Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia

Karl‐Heinz Grzeschik, Dorothea Bornholdt, Frank Oeffner et al. · Nature Genetics · 2007 · 281 citations

Life Sciences, Developmental Biology, Molecular Biology +11

Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease

Vinzenz Oji, Katja‐Martina Eckl, Karin Aufenvenne et al. · The American Journal of Human Genetics · 2010 · 247 citations · Full text

Medicine, Dermatology, Pathology +16

Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length

Katja‐Martina Eckl, Rotem Tidhar, Holger Thiele et al. · Journal of Investigative Dermatology · 2013 · 165 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome

F. Buket Basmanav, Laura Cau, Aylar Tafazzoli et al. · The American Journal of Human Genetics · 2016 · 146 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion

Diana C. Blaydon, Daniela Nitoiu, Katja‐Martina Eckl et al. · The American Journal of Human Genetics · 2011 · 117 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +10