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Ausgewählte Publikationen

Schneider, H., Schweikl, C., Faschingbauer, F., Hadj-Rabia, S., Schneider, P.: A causal treatment for X-linked hypohidrotic ectodermal dysplasia: Long-term results of short-term perinatal ectodysplasin A1 replacement. Int. J. Mol. Sci. 24, 7155 ff. (2023)

Meyer, J.M., Vávrová, K., Radner, F.P.W., Schneider, H., Dick, A., Elias, P.M., Mauro, T.M.: ALOX12B and PNPLA1 have distinct roles in lipid lamellar organization. J. Invest. Dermatol. 143, 332-335 (2023)

Schneider, H., Hadj-Rabia, S., Faschingbauer, F., Bodemer, C., Grange, D.K., Norton, M., Cavalli, R., Tadini, G., Stepan, H., Clarke, A., Guillén Navarro, E., Maier-Wohlfart, S., Bouroubi, A., Porte, F.: Protocol for the phase 2 EDELIFE trial investigating the efficacy and safety of intra-amniotic ER004 administration to male subjects with X-linked hypohidrotic ectodermal dysplasia. Genes 14, 153 ff. (2023)

Has, C., Hess, M., Anemüller, W., Blume-Peytavi, U., Emmert, S., Fölster-Holst, R., Frank, J., Giehl, K., Günther, C., Hammersen, J., Hillmann, K., Höflein, B., Höger, P.H., Mai, T.A., Oji, V., Schneider, H., Süßmuth, K., Tantcheva-Póor, I., Zirn, B., Fischer, J., Reimer-Taschenbrecker, A.: Epidemiology of inherited Epidermolysis bullosa in Germany. J. Eur. Acad. Dermatol. Venereol. 37, 402-410 (2023)

Schneider, H., Faschingbauer, F.: Genetisch bedingte Stillschwierigkeiten. Deutsche Hebammen-Zeitschrift 75, 56-63 (2023)

Morhart, P., Kehl, S., Schuh, W., Hermes, K., Meltendorf, S., Neubert, A., Schneider, M., Brunner-Weinzierl, M., Schneider, H., Lingel, H.: Age-related differences in immune reactions to SARS-CoV-2 spike and nucleocapsid antigens. In vivo 37, 70-78 (2023)

Maier-Wohlfart, S., Aicher, C., Peschel, N., Willershausen, I., Meißner, U., Gölz, L., Schneider, H.: Congenital nail disorders among children with suspected ectodermal dysplasia. Genes 13, 2119 ff. (2022)

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., Fete, T., Pagnan, N., Visinoni, A.F., Schneider, H.: Molecular pathway-based classification of ectodermal dysplasias: first five-yearly update. Genes 13, 2327 ff. (2022)

Schneider, H.: Ectodermal dysplasias: New perspectives on the treatment of so far immedicable genetic disorders. Front. Genet. 13, 1000744 ff. (2022)

Morhart, P., Mardin, C., Rauh, M., Jüngert, J., Hammersen, J., Kehl, S., Schuh, W., Maier-Wohlfart, S., Hermes, K., Neubert, A., Schneider, M., Hein, A., Wölfle, J., Schneider, H.: Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant. Eur. J. Pediatr. 181, 413–418 (2022)

Leo, B., Schneider, H., Hammersen, J.: Reproductive decision-making in women with X-linked hypohidrotic ectodermal dysplasia. J. Eur. Acad. Dermatol. Venereol. 36, 1863–1870 (2022)

Schneider, F., Runer, A., Burkert, F., Seilern Und Aspang, J., Reider, S., Schneider, H., Pocecco, E.: Digital workout versus team training: the impact of the COVID-19 pandemic on athletes. Sports Med. Int. Open 6, E18–E24 (2022)

Hein, A., Kehl, S., Häberle, L., Tiemann, C., Peuker, R., Mereutanu, D., Stumpfe, F.M., Faschingbauer, F., Meyer-Schlinkmann, K., Koch, M.C., Kainer, F., Dammer, U., Zoche, H., Kladt, C., Schrauder, M., Weingärtler, S., Hanf, V., Hartmann, A., Rübner, M., Schneider, H., Lelieveld, J., Beckmann, M.W., Wurmthaler, L.A., Fasching, P.A., Schneider, M.O.: Prevalence of SARS-CoV-2 in pregnant women assessed by RT-PCR in Franconia, Germany: First results of the SCENARIO study (SARS-CoV-2 prEvalence in pregNAncy and at biRth In FrancOnia). Geburtsh. Frauenheilk. 82, 226-234 (2022)

Goekdere, S., Schneider, H., Hehr, U., Schneider, P., Maier-Wohlfart, S.: Functional and clinical analysis of five EDA variants associated with ectodermal dysplasia but with a hard-to-predict significance. Front. Genet. 13, 934395 ff. (2022)

Schweikl, C., Maier-Wohlfart, S., Schneider, H., Park, J.: Ectodysplasin A1 deficiency leads to osteopetrosis-like changes in bones of the skull associated with diminished osteoclastic activity. Int. J. Mol. Sci. 23, 12189 ff. (2022)

De Rosa, L., Enzo, E., Zardi, G., Bodemer, C., Magnoni, C., Schneider, H., De Luca, M.: Hologene 5: a phase II/III clinical trial of combined cell and gene therapy of junctional epidermolysis bullosa. Front. Genet. 12, 705019 ff. (2021)

Körber, L., Schneider, H., Fleischer, N., Wohlfart, S.: No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia. Orphanet J. Rare Dis. 16, 98 (2021)

Schuepbach-Mallepell, S., Kowalczyk-Quintas, C., Dick, A., Eslami, M., Vigolo, M., Headon, D.J., Cheeseman, M., Schneider, H., Schneider, P.: Methods for the administration of EDAR pathway modulators in mice. Methods Mol. Biol. 2248, 167-183 (2021)

Hennig, V., Schuh, W., Rauh, M., Neubert, A., Mielenz, D., Schneider, H.: Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia. Orphanet J. Rare Dis. 16, 373 ff. (2021)

Meyer, J.M., Crumrine, D., Schneider, H., Dick, A., Schmuth, M, Gruber, R., Radner, F.W.P., Grond, S., Wakefield, J., Mauro, T.M., Elias, P.M.: Unbound corneocyte lipid envelopes in 12R-lipoxygenase deficiency support a specific role in lipid-protein crosslinking. Am. J. Pathol. 191, 921-929 (2021)

Schneider, H., De Luca, M.: Gene and protein replacement therapy of genetic muscle, bone and skin disorders. Front. Genet. 12, 771611 (2021)

Kossel, C.S., Wahlbuhl, M., Schuepbach-Mallepell, S., Park, J., Kowalczyk-Quintas, C., Seeling, M., von der Mark, K., Schneider, P., Schneider, H.: Correction of vertebral bone development in ectodysplasin A1-deficient mice by prenatal treatment with a replacement protein. Front. Genet. 12, 709736 (2021)

Schuh, W., Baus, L., Steinmetz, T., Schulz, S.R., Weckwerth, L., Roth, E., Hauke, M., Krause, S., Morhart, P., Rauh, M., Hoffmann, M., Vesper, N., Reth, M. Schneider, H., Jäck, H.M., Mielenz, D.: A surrogate cell-based SARS-CoV-2 spike blocking assay. Eur. J. Immunol. 51, 2665–2676 (2021)

Schneider, H.: Vorgeburtlicher Proteinersatz zur Behandlung der ektodermalen Dysplasie. Spectrum Dermatologie 1/21, 16-17 (2021)

Wohlfart, S., Meiller, R., Hammersen, J., Park, J., Menzel-Severing, J., Melichar, V., Huttner, K., Johnson, R., Porte, F., Schneider, H.: Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study. Orphanet J. Rare Dis. 15, 7 ff. (2020)

Krieg, P., Dick, A., Latzko, S., Rosenberger, S., Meyer, J., Crumrine, D., Hielscher, T., Elias, P.M., Rauh, M., Schneider, H.: Conditional Alox12b knockout: degradation of the corneocyte lipid envelope in a mouse model of autosomal recessive congenital ichthyoses. J. Invest. Dermatol. 140, 249-253 (2020)

Heller, S., Kölsch, U., Magg, T., Krüger, R., Scheuern, A., Schneider, H., Eichinger, A., Wahn, V., Unterwalder, N., Lorenz, M., Schwarz, K., Meisel, C., Schulz, A., Hauck, F., von Bernuth, H.: T-cell impairment is predictive for a severe clinical course in NEMO-deficiency. J. Clin. Immunol. 40, 421-434 (2020)

Körber, I., Klein, O., Morhart, P., Faschingbauer, F., Grange, D., Clarke, A., Bodemer, C., Maynard, J., Maitz, S., Huttner, K., Kirby, N., Durand, C., Schneider, H.: Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects. Br. J. Clin. Pharmacol. 86, 2063-2069 (2020)  

Sagar, R., Almeida-Porada, G., Blakemore, K., Chan, J.K.Y., Choolani, M., Götherström, C., Jaulent, A., MacKenzie, T.C., Mattar, C., Porada, C.D., Peranteau, W.H., Schneider, H., Shaw, S., Waddington, S.N., Westgren, M., David, A.L.: Fetal and maternal safety considerations for in utero therapy clinical trials: iFeTiS consensus statement. Mol. Ther. 28, 2316-2319 (2020)

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., Bergendal, B., Abbott, B., Fete, T., Stanford, C., Butcher, C., D‘Souza, R.N., Sybert, V.P., Morasso, M.I.: Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway. Am. J. Med. Genet. Part A 179, 442-447 (2019)

Hammersen, J., Wohlfart, S., Goecke, T.W., Köninger, A., Stepan, H., Gallinat, R., Morris, S., Bücher, K., Clarke, A., Wünsche, S., Beckmann, M.W., Schneider, H./ Faschingbauer, F. (joined senior authors): Reliability of prenatal detection of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography. Prenat. Diagn. 39, 796-805 (2019)

Wohlfart, S., Schneider, H.: Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia. Clin. Genet. 95, 427-432 (2019)

Margolis, C.A., Schneider, P., Huttner, K., Kirby, N., Houser, T.P., Wildman, L., Grove, G., Schneider, H., Casal, M.L.: Prenatal treatment of X-linked hypohidrotic ectodermal dysplasia using recombinant ectodysplasin in a canine model. J. Pharmacol. Exp. Ther. 370, 806-813 (2019)

Ferstl, P., Wohlfart, S., Schneider, H.: Sweating ability of patients with EEC and AEC syndrome. Eur. J. Pediatr. 177, 1727-1731 (2018)

Schneider, H., Faschingbauer, F., Schuepbach-Mallepell, S., Körber, I., Wohlfart, S., Dick, A., Wahlbuhl, M., Kowalczyk-Quintas, C., Vigolo, M., Kirby, N., Tannert, C., Rompel, O., Rascher, W., Beckmann, M.W., Schneider, P.: Prenatal correction of X-linked hypohidrotic ectodermal dysplasia. N. Engl. J. Med. 378, 1604-1610 (2018)

Wahlbuhl, M., Schuepbach-Mallepell, S., Kowalczyk-Quintas, C., Dick, A., Fahlbusch, F.B., Schneider, P., Schneider, H.: Attenuation of mammary gland dysplasia and feeding difficulties in Tabby mice by fetal therapy. J. Mammary Gland Biol. Neoplasia 23, 125-138 (2018)

Hadj-Rabia, S., Schneider, H., Navarro, E., Klein, O., Kirby, N., Huttner, K., Wolf, L., Orin, M., Wohlfart, S., Bodemer, C., Grange, D.: Automatic recognition of the XLHED phenotype from facial images. Am. J. Med. Genet. Part A 173, 2408-2414 (2017)

Schneider, H.: Unconditionally? Daring to have ordinary children in an age of technical perfection. Imago Hom. 24, 11-13 (2017)

Wahlbuhl-Becker, M., Faschingbauer, F., Beckmann, M.W., Schneider, H.: Hypohidrotic ectodermal dysplasia: Breastfeeding complications due to impaired breast development. Geburtsh. Frauenheilk. 77, 377-382 (2017)

Podzus, J., Kowalczyk-Quintas, C., Schuepbach-Mallepell, S., Willen, L., Staehlin, G., Vigolo, M., Tardivel, A., Headon, D., Kirby, N., Mikkola, M., Schneider, H., Schneider, P.: Ectodysplasin A in biological fluids and diagnosis of ectodermal dysplasia. J. Dent. Res. 96, 217-224 (2017)

Wohlfart, S., Hammersen, J., Schneider, H.: Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in four independent cases of rare genomic rearrangements. J. Hum. Genet. 61, 891-897 (2016)

Wohlfart, S. Söder, S., Smahi, A., Schneider, H.: A novel missense mutation in the gene EDARADD associated with an unusual phenotype of hypohidrotic ectodermal dysplasia. Am. J. Med. Genet. Part A 170, 249-253 (2016)

Wünsche, S., Jüngert, J., Faschingbauer, F., Mommsen, H., Goecke, T., Schwanitz, K., Stepan, H., Schneider, H.: Non-invasive prenatal diagnosis of hypohidrotic ectodermal dysplasia by tooth germ sonography. Ultraschall Med. 36, 381-385 (2015)

Kaercher, T., Dietz, J., Jacobi, C., Berz, R., Schneider, H.: Diagnosis of X-linked hypohidrotic ectodermal dysplasia by meibography and infrared thermography of the eye. Curr. Eye Res. 40, 884-890 (2015)

Hermes, K., Schneider, P., Krieg, P., Dang, A., Huttner, K., Schneider, H.: Prenatal therapy in developmental disorders: drug targeting via intra-amniotic injection to treat X-linked hypohidrotic ectodermal dysplasia. J. Invest. Dermatol. 134, 2985-2987 (2014)

Kowalczyk-Quintas, C., Willen, L., Dang, A., Sarrasin, H., Tardivel, A., Hermes, K., Schneider, H., Gaide, O., Donzé, O., Kirby, N., Headon, D.J., Schneider, P.: Generation and characterization of function blocking anti-ectodysplasin A (EDA) monoclonal antibodies that induce ectodermal dysplasia. J. Biol. Chem. 289, 4273-4285 (2014)

Burger, K., Schneider, A.T., Wohlfart, S., Kiese-wetter, F., Huttner, K., Johnson, R., Schneider, H.: Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia. Am J. Med. Genet. Part A, 164, 2424-2432 (2014)

Salinas, C.F., Irvine, A.D., Itin, P.H., Di Giovanna, J., Schneider, H., Clarke, A.J., Sternesky McGovern, L., Fete, M.: Second International Conference on a classification of ectodermal dysplasias: Development of a multiaxis model. Am J. Med. Genet. Part A, 164, 2482-2489 (2014)

Dietz, J., Kaercher, T., Schneider, A.T., Zimmermann, T., Huttner, K., Johnson, R., Schneider, H.: Early respiratory and ocular involvement in X-linked hypohidrotic ectodermal dysplasia. Eur. J. Pediatr. 172, 1023-1031 (2013)

Hammersen, J., Neukam, V., Nüsken, K.-D., Schneider, H.: Systematic evaluation of exertional hyperthermia in children with hypohidrotic ectodermal dysplasia: an observational study. Pediatr. Res. 70, 297-301 (2011)

Schneider, H., Hammersen, J., Preisler-Adams, S., Huttner, K., Rascher, W., Bohring, A.: Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia. J. Med. Genet. 48, 426-432 (2011)