Schneider, Holm

Activation of canonical Wnt signalling is required for TGF-β-mediated fibrosis

Akhmetshina, A., Palumbo, K., Dees, C., Bergmann, C., Venalis, P., Zerr, P., Horn, A., Kireva, T., Beyer, C., Zwerina, J., et al. (2012) · Nature Communications

TGF-β signaling in diseasesWnt/β-catenin signaling in development and cancer

Cited by 843

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Wright, J. T., Fete, M., Schneider, H., Zinser, M., Koster, M. I., Clarke, A. J., Hadj‐Rabia, S., Tadini, G., Pagnan, N., Visinoni, A. F., et al. (2019) · American Journal of Medical Genetics Part A

dental development and anomaliesGenetic and rare skin diseases.

Cited by 185

Prenatal correction of x-linked hypohidrotic ectodermal dysplasia

Schneider, H., Faschingbauer, F., Schuepbach-Mallepell, S., Körber, I., Wohlfart, S., Dick, A., Wahlbuhl, M., Kowalczyk-Quintas, C., Vigolo, M., Kirby, N., et al. (2018) · New England Journal of Medicine

dental development and anomaliesGenetic and rare skin diseases.

Cited by 183

Prevalence and prevention of severe complications of hypohidrotic ectodermal dysplasia in infancy

Blüschke, G., Nüsken, K.-D., & Schneider, H. (2010) · Early Human Development

dental development and anomaliesGenetic and rare skin diseases.

Cited by 97

Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

Peschel, N., Wright, J. T., Koster, M. I., Clarke, A. J., Tadini, G., Fete, M., Hadj-Rabia, S., Sybert, V. P., Norderyd, J., Maier-Wohlfart, S., et al. (2022) · Genes

dental development and anomaliesGenetic and rare skin diseases.

Cited by 60

Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements

Wohlfart, S., Hammersen, J., & Schneider, H. (2016) · Journal of Human Genetics

dental development and anomaliesGenetic and rare skin diseases.

Cited by 41

Ectodermal dysplasias: New perspectives on the treatment of so far immedicable genetic disorders

Schneider, H. (2022) · Frontiers in Genetics

dental development and anomaliesHair Growth and Disorders

Cited by 26

Sweating ability of patients with p63-associated syndromes

Ferstl, P., Wohlfart, S., & Schneider, H. (2018) · European Journal of Pediatrics

Genetic and rare skin diseases.dental development and anomalies

Cited by 8