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2021
Cesarato, Nicole, Wehner, Maria, Ghughunishvili, Mariam, Schmidt, Axel, Axt, Daisy, Thiele, Holger, Lentze, Michael J., Has, Cristina 
ORCID: 0000-0001-6066-507X, Geyer, Matthias ORCID: 0000-0002-7718-5002, Basmanav, Fitnat Buket and Betz, Regina C.
(2021).
Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes.
Am. J. Med. Genet. A, 185 (12).
S. 3900 - 3905.
HOBOKEN:
WILEY.
ISSN 1552-4833
Hotz, Alrun ORCID: 0000-0003-2560-3951, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette ORCID: 0000-0002-3004-0180, Tantcheva-Poor, Iliana, Hellstrom Pigg, Maritta, Has, Cristina ORCID: 0000-0001-6066-507X, Yang, Zhou, Irvine, Alan D., Betz, Regina C., Zambruno, Giovanna, Tadini, Gianluca, Suessmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter ORCID: 0000-0002-3734-753X, Bolling, Maria C., Hannula-Jouppi, Katariina, Zimmer, Andreas D., Alter, Svenja, Vahlquist, Anders and Fischer, Judith ORCID: 0000-0002-8580-8118
(2021).
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients.
Genes, 12 (1).
BASEL:
MDPI.
ISSN 2073-4425
2020
Kuntz, Thomas, Koushk-jalali, Bijan, Tigges, Christian, Silling, Steffi, Oellig, Frank, Has, Cristina, Hampl, Monika, Wieland, Ulrike and Kreuter, Alexander (2020). Human Papillomavirus-induced Cutaneous and Mucosal Lesions in a Patient with Rothmund-Thomson Syndrome. Acta Derm.-Venereol., 100. UPPSALA: ACTA DERMATO-VENEREOLOGICA. ISSN 1651-2057
2019
Tantcheva-Poor, Iliana and Has, Cristina ORCID: 0000-0001-6066-507X
(2019).
Neonate female with Blister Formation shortly after Birth Preparation for the Specialist Examination: Part 34.
Hautarzt, 70.
S. 31 - 34.
HEIDELBERG:
SPRINGER HEIDELBERG.
ISSN 1432-1173
2016
Tantcheva-Poor, Iliana, Oji, Vinzenz ORCID: 0000-0003-1380-4828 and Has, Cristina ORCID: 0000-0001-6066-507X
(2016).
A multistep approach to the diagnosis of rare genodermatoses.
J. Dtsch. Dermatol. Ges., 14 (10).
S. 969 - 986.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 1610-0387
2014
Has, Cristina ORCID: 0000-0001-6066-507X, Kiritsi, Dimitra ORCID: 0000-0002-2331-8981, Mellerio, Jemima E., Franzke, Claus-Werner, Wedgeworth, Emma, Tantcheva-Poor, Iliana, Kernland-Lang, Kristin, Itin, Peter, Simpson, Michael A., Dopping-Hepenstal, Patricia J., Fujimoto, Wataru, McGrath, John A. and Bruckner-Tuderman, Leena
(2014).
The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome.
J. Invest. Dermatol., 134 (3).
S. 845 - 850.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1523-1747