Alrun Hotz

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients

Maritta Hellström Pigg, Anette Bygum, Agneta Gånemo et al. · Acta Dermato Venereologica · 2016 · 89 citations · Full text

Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis

Alrun Hotz, Vinzenz Oji, E. Bourrat et al. · Acta Dermato Venereologica · 2015 · 65 citations · Full text

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +12

Microdeletion 5q14.3 and anomalies of brain development

Alrun Hotz, Yorck Hellenbroich, Jürgen Sperner et al. · American Journal of Medical Genetics Part A · 2013 · 50 citations

Epidemiology of inherited epidermolysis bullosa in Germany

Cristina Has, Moritz Hess, Waltraud Anemüller et al. · Journal of the European Academy of Dermatology and Venereology · 2022 · 42 citations

Sixteen novel mutations in <i>PNPLA1</i> in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in <i>PNPLA1</i> that is essential for proper human skin barrier function

Andreas Zimmer, G.J. Kim, Alrun Hotz et al. · British Journal of Dermatology · 2017 · 30 citations