Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis by Hake, L., Süßmuth, K., Komlosi, K., Kopp, J., Drerup, C., Metze, D., Traupe, H., Hausser, I., Eckl, K.M., Hennies, H.C., Fischer, J., Oji, V.

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Acral lamellar Ichthyosis – expanding the phenotype of temperature‐sensitive keratinization disorders by Almeida, H., Has, C., Fischer, J., Hausser, I.

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At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders – a case series by Toberer, F., Happle, R., Schneiderbauer, R., Hausser, I., Kröhl, V., Epple, A., Moog, U., Enk, A.H., Lonsdorf, A.S.

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Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profile by Perusquía-Ortiz, A.M., Oji, V., Sauerland, M.C., Tarinski, T., Zaraeva, I., Seller, N., Metze, D., Aufenvenne, K., Hausser, I., Traupe, H.

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Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis by Dahlqvist, J, Klar, J, Hausser, I, Anton-Lamprecht, I, Pigg, M Hellström, Gedde-Dahl, T, Gånemo, A, Vahlquist, A, Dahl, N

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Familial cervical artery dissections: Clinical, morphologic and genetic studies by Martin, J.J, Hausser, I, Lyrer, P

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Heterozygous carriers of Pseudoxanthoma elasticum were not found among patients with cervical artery dissections by Morcher, Marion, Hausser, Ingrid, Brandt, Tobias, Grond-Ginsbach, Caspar

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The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series by Angwin, C, Byers, P, Dulfer, E, Ghali, N, Harris, Juliette, Hausser, I, McElroy, Abigail, Sobey, G, van Dijk, F S

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Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis by Komlosi, Katalin, Claris, Olivier, Collardeau-Frachon, Sophie, Kopp, Julia, Hausser, Ingrid, Mazereeuw-Hautier, Juliette, Jonca, Nathalie, Zimmer, Andreas D, Sanlaville, Damien, Fischer, Judith

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Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling by Kim, Mi-Ran, Oji, Vinzenz, Valentin, Frederic, Traupe, Heiko, Nofer, Jerzy-Roch, Hausser, Ingrid, Hennies, Hans Christian, Eckl, Katja, Wudy, Stefan A, Sánchez-Guijo, Alberto, Kerschke, Laura, Fischer, Judith, Süßmuth, Kira

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Mouse models for dominant dystrophic epidermolysis bullosa (DDEB) carrying common human point mutations recapitulate the human disease by Smith, B R C, Nystrom, A, Nowell, C J, Hausser, I, Gretzmeier, C, Robertson, S J, Varigos, G A, Has, C, Kern, J S, Pang, K C

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Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing by Laks, Emma, Steif, Adi, Brimhall, Jazmine, Biele, Justina, Wang, Beixi, Masud, Tehmina, Ting, Jerome, Grewal, Diljot, Nielsen, Cydney, Leung, Samantha, Bojilova, Viktoria, Smith, Maia, Golovko, Oleg, Poon, Steven, Eirew, Peter, Kabeer, Farhia, Ruiz de Algara, Teresa, Lee, So Ra, Taghiyar, M. Jafar, Huebner, Curtis, Ngo, Jessica, Chan, Tim, Vatrt-Watts, Spencer, Walters, Pascale, Abrar, Nafis, Chan, Sophia, Martin, Lauren, Scott, R. Wilder, Underhill, T. Michael, Steidl, Christian, Da Costa, Daniel, Ma, Yussanne, Coope, Robin J.N., Corbett, Richard, Pleasance, Stephen, Mar, Colin, Cafferty, Fergus, Chia, Stephen, Hannon, Gregory J., Battistoni, Giorgia, Bressan, Dario, Cannell, Ian, Casbolt, Hannah, Jauset, Cristina, Kovačević, Tatjana, Nugent, Fiona, Pearsall, Isabella, Qosaj, Fatime, Sawicka, Kirsty, Wild, Sophia, Williams, Elena, Aparicio, Samuel, Laks, Emma, Li, Yangguang, Smith, Austin, Ruiz, Teresa, Lee, Maximillian, Bodenmiller, Bernd, Burger, Marcel, Kuett, Laura, Tietscher, Sandra, Windager, Jonas, Boyden, Edward, Alon, Shahar, Cui, Yi, Emenari, Amauche, Goodwin, Dan, Karagiannis, Emmanouil, Sinha, Anubhav, Wassie, Asmamaw T., Caldas, Carlos, Bruna, Alejandra, Lerda, Giulia, Lubling, Yaniv, Harris, Owen, Becker, Robby, Harris, Suvi, Hausser, Jean, Watson, Spencer, Vázquez-García, Ignacio, Tavaré, Simon, Dinh, Khanh, Fisher, Eyal, Kunes, Russell, Walton, Nicolas A., Al Sa’d, Mohammad, Chornay, Nick, Dariush, Ali, Solares, Eduardo Gonzales, Gonzalez-Fernandez, Carlos, Yoldas, Aybuke Kupcu, Millar, Neil, Zhuang, Xiaowei, Fan, Jean, Lee, Hsuan, Duran, Leonardo Sepulveda, Xia, Chenglong, Marra, Marco A., Hansen, Carl, Shah, Sohrab P.

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Association of Vascular Risk Factors With Cervical Artery Dissection and Ischemic Stroke in Young Adults by DEBETTE, Stephanie, METSO, Tiina, MEDEIROS, Elisabeth, SAMSON, Yves, GROND-GINSBACH, Caspar, ENGELTER, Stefan T, THIJS, Vincent, BERETTA, Simone, BEJOT, Yannick, SESSA, Maria, LORENZA MUIESAN, Maria, AMOUYEL, Philippe, PEZZINI, Alessandro, CASTELLANO, Maurizio, ARVEILER, Dominique, TATLISUMAK, Turgut, DALLONGEVILLE, Jean, ABBOUD, Shérine, METSO, Antti, LEYS, Didier, BERSANO, Anna, LOUILLET, Fabien, CASO, Valeria, LAMY, Chantal

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Acute bilateral renal vein thrombosis complicating Netherton syndrome by POHL, M, ZIMMERHACKL, L. B, HAUSSER, I, LUDWIG, H, HILDEBRANDT, F, GORDJANI, N, SUTOR, A. H, ANTON-LAMPRECHT, I, BRANDIS, M

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The natural history, including orofacial features of three patients with Ehlers-Danlos syndrome, dermatosparaxis type (EDS type VIIC) by Malfait, Fransiska, De Coster, Peter, Hausser, Ingrid, van Essen, Anthonie J., Franck, Peter, Colige, Alain, Nusgens, Betty, Martens, Luc, De Paepe, Anne

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CADISP-genetics: an International project searching for genetic risk factors of cervical artery dissections by Debette, S., Metso, T. M., Pezzini, A., Engelter, S. T., Leys, D., Lyrer, P., Metso, A. J., Brandt, T., Kloss, M., Lichy, C., Hausser, I., Touzé, E., Markus, H. S., Abboud, S., Caso, V., Bersano, A., Grau, A., Altintas, A., Amouyel, P., Tatlisumak, T., Dallongeville, J., Grond-Ginsbach, C.

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Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II by DE PAEPE, A, NUYTINCK, L, HAUSSER, I, ANTON-LAMPRECHT, I, NAEYAERT, J.-M

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Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification by HAUSSER, I, ANTON-LAMPRECHT, I

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Mutations in the tropoelastin gene (ELN) were not found in patients with spontaneous cervical artery dissections by GROND-GINSBACH, C, THOMAS-FELES, C, WERNER, I, WEBER, R, WIGGER, F, HAUSSER, I, BRANDT, T

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Mutations in the COL5A1 coding sequence are not common in patients with spontaneous cervical artery dissections by GROND-GINSBACH, C, WEBER, R, HAAS, J, ORBERK, E, KUNZ, S, BUSSE, O, HAUSSER, I, BRANDT, T, WILDEMANN, B

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