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Basmanav, F. Buket U., Cau, Laura 
ORCID: 0000-0002-2480-536X, Tafazzoli, Aylar, Mechin, Marie-Claire, Wolf, Sabrina, Romano, Maria Teresa, Valentin, Frederic, Wiegmann, Henning, Huchenq, Anne, Kandil, Rima, Bartels, Natalie Garcia, Kilic, Arzu, George, Susannah, Ralser, Damian J., Bergner, Stefan, Ferguson, David J. P., Oprisoreanu, Ana-Maria ORCID: 0000-0002-9409-0830, Wehner, Maria, Thiele, Holger, Altmueller, Janine, Nuerenberg, Peter, Swan, Daniel ORCID: 0000-0001-8978-8129, Houniet, Darren, Buechner, Aline, Weibel, Lisa, Wagner, Nicola, Grimalt, Ramon, Bygum, Anette ORCID: 0000-0002-3004-0180, Serre, Guy, Blume-Peytavi, Ulrike, Sprecher, Eli, Schoch, Susanne, Oji, Vinzenz ORCID: 0000-0003-1380-4828, Hamm, Henning, Farrant, Paul, Simon, Michel ORCID: 0000-0003-3655-6329 and Betz, Regina C.
(2016).
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.
Am. J. Hum. Genet., 99 (6).
S. 1292 - 1305.
CAMBRIDGE:
CELL PRESS.
ISSN 1537-6605
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
Jansen, Patrick A. M., van den Bogaard, Ellen H. ORCID: 0000-0003-4846-0287, Kersten, Ferry F. J., Oostendorp, Corien ORCID: 0000-0003-3992-4262, van Vlijmen-Willems, Ivonne M. J. J., Oji, Vinzenz ORCID: 0000-0003-1380-4828, Traupe, Heiko, Hennies, Hans C., Schalkwijk, Joost ORCID: 0000-0002-1308-1319 and Zeeuwen, Patrick L. J. M.
(2012).
Cystatin M/E knockdown by lentiviral delivery of shRNA impairs epidermal morphogenesis of human skin equivalents.
Exp. Dermatol., 21 (11).
S. 889 - 892.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 0906-6705
Busch, Jutta, Frank, Valeska, Bachmann, Nadine, Otsuka, Atoshi, Oji, Vinzenz ORCID: 0000-0003-1380-4828, Metze, Dieter, Shah, Krati, Danda, Sumita, Watzer, Bernhard, Traupe, Heiko, Bolz, Hanno J., Kabashima, Kenji ORCID: 0000-0002-0773-0554 and Bergmann, Carsten
(2012).
Mutations in the Prostaglandin Transporter SLCO2A1 Cause Primary Hypertrophic Osteoarthropathy with Digital Clubbing.
J. Invest. Dermatol., 132 (10).
S. 2473 - 2477.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 0022-202X
Blaydon, Diana C., Nitoiu, Daniela, Eckl, Katja-Martina, Cabral, Rita M., Bland, Philip, Hausser, Ingrid, van Heel, David A., Rajpopat, Shefali, Fischer, Judith ORCID: 0000-0002-8580-8118, Oji, Vinzenz ORCID: 0000-0003-1380-4828, Zvulunov, Alex, Traupe, Heiko, Hennies, Hans Christian and Kelsell, David P.
(2011).
Mutations in CSTA, Encoding Cystatin A, Underlie Exfoliative Ichthyosis and Reveal a Role for This Protease Inhibitor in Cell-Cell Adhesion.
Am. J. Hum. Genet., 89 (4).
S. 564 - 572.
CAMBRIDGE:
CELL PRESS.
ISSN 0002-9297
Oji, Vinzenz ORCID: 0000-0003-1380-4828, Tadini, Gianluca, Akiyama, Masashi, Bardon, Claudine Blanchet, Bodemer, Christine, Bourrat, Emmanuelle, Coudiere, Philippe, DiGiovanna, John J., Elias, Peter, Fischer, Judith ORCID: 0000-0002-8580-8118, Fleckman, Philip, Gina, Michal, Harper, John, Hashimoto, Takashi, Hausser, Ingrid, Hennies, Hans Christian, Hohl, Daniel, Hovnanian, Alain ORCID: 0000-0003-3412-7512, Ishida-Yamamoto, Akemi, Jacyk, Witold K., Leachman, Sancy, Leigh, Irene, Mazereeuw-Hautier, Juliette, Milstone, Leonard, Morice-Picard, Fanny, Paller, Amy S., Richard, Gabriele, Schmuth, Matthias ORCID: 0000-0002-4064-1334, Shimizu, Hiroshi, Sprecher, Eli, Van Steensel, Maurice, Taieb, Alain, Toro, Jorge R., Vabres, Pierre ORCID: 0000-0001-8693-3183, Vahlquist, Anders, Williams, Mary and Traupe, Heiko
(2010).
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Soreze 2009.
J. Am. Acad. Dermatol., 63 (4).
S. 607 - 642.
NEW YORK:
MOSBY-ELSEVIER.
ISSN 0190-9622