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Publications by Hans Christian Hennies

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , Which Encode Subcomponents C1r and C1s of Complement

American Journal of Human Genetics
Genetics
2016English

Transglutaminase 1 Replacement Therapy Successfully Mitigates the ARCI Phenotype in Full-Thickness Skin Disease Equivalents

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2019English

Full-Thickness Human Skin Models for Congenital Ichthyosis and Related Keratinization Disorders

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2011English

In Vitro Modeling of Ryanodine Receptor 2 Dysfunction Using Human Induced Pluripotent Stem Cells

Cellular Physiology and Biochemistry
Physiology
2011English

Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14

American Journal of Human Genetics
Genetics
2006English

Localization of the Gene Causing Keratolytic Winter Erythema to Chromosome 8p22-P23, and Evidence for a Founder Effect in South African Afrikaans-Speakers

American Journal of Human Genetics
Genetics
1997English

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

American Journal of Human Genetics
Genetics
2009English

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