Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Süßmuth K, Gruber R, Rodriguez E, Traupe H, Amler S, Sánchez-Guijo A, Valentin F, Tarinski T, Straub N, Metze D, Schneider SW, Hausser I, Baurecht H, Weidinger S, Oji V (2017)
In: J Invest Dermatol, 2017
Type of Publication: Research article (journal)

Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature

Wittkowski H, Hinze C, Häfner-Harms S, Oji V, Masjosthusmann K, Monninger M, Grenzebach U, Foell D (2017)
In: Pediatr Rheumatol Online J, 2017(15(1):19)
Type of Publication: Research article (journal)

16 novel mutations in {PNPLA}1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in {PNPLA}1 that is essential for…

Zimmer A, Kim G, Hotz A, Bourrat E, Hausser I, Has C, Oji V, Stieler K, Vahlquist A, Kunde V, Weber B, Radner F, Leclerc-Mercier S, Schlipf N, Demmer P, Küsel J, Fischer J (2017)
In: British Journal of Dermatology, 2017
Type of Publication: Research article (journal)

Expanding the Clinical and Genetic Spectrum of {KRT}1, {KRT}2 and {KRT}10 Mutations in Keratinopathic Ichthyosis

Hotz A, Oji V, Bourrat E, Jonca N, Mazereeuw-Hautier J, Betz R, Blume-Peytavi U, Stieler K, Morice-Picard F, Schönbuchner I, Markus S, Schlipf N, Fischer J (2016)
In: Acta Dermato Venereologica, 96(4)
Type of Publication: Research article (journal)

Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in {IL}36RN in German patients

Löhr S, Uebe S, Behrens F, Böhm B, Köhm M, Traupe H, Oji V, Burkhardt H, Reis A, Hüffmeier U (2016)
In: British Journal of Dermatology, 175(3)
Type of Publication: Research article (journal)

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Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination Süßmuth K, Gruber R, Rodriguez E, Traupe H, Amler S, Sánchez-Guijo A, Valentin F, Tarinski T, Straub N, Metze D, Schneider SW, Hausser I, Baurecht H, Weidinger S, Oji V (2017) In: J Invest Dermatol, 2017 Type of Publication: Research article (journal)
The genetic basis in most patients with pustular skin disease remains elusive Mössner R, Wilsmann-Theis D, Oji V, Gkogkolou P, Löhr S*, Schulz P, Körber A, Christoph -Prinz J, Renner R, Schäkel K, Vogelsang L, Peters K-P, Philipp S, Reich K, Ständer H, Jacobi J, Weyergraf A, Kingo K, Kõks S, Gerdes S, Steinz K, Schill T, Griewank K G, Müller M, Frey S, Ebertsch L, Uebe S, Sticherling M, Sticht H, Hüffmeier U (2017) In: British Journal of Dermatology, Epub Type of Publication: Research article (journal)
Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature Wittkowski H, Hinze C, Häfner-Harms S, Oji V, Masjosthusmann K, Monninger M, Grenzebach U, Foell D (2017) In: Pediatr Rheumatol Online J, 2017(15(1):19) Type of Publication: Research article (journal)
Guideline (S1) for diagnostics and management of the ichthyoses (update) Oji V, Preil ML, Kleinow B, Wehr G, Fischer J, Hennies HC, Hausser I, Aufenvenne K, Stieler K, Tantcheva-Poór I, Weidinger S, Emmert S, Hamm H, Perusquia-Ortiz AM, Diem A, Giehl K, Fölster-Holst R, Höger P, Ott H, Traupe H (2017) In: J Dtsch Dermatol Ges, 2017 Type of Publication: Research article (journal)
16 novel mutations in {PNPLA}1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in {PNPLA}1 that is essential for… Zimmer A, Kim G, Hotz A, Bourrat E, Hausser I, Has C, Oji V, Stieler K, Vahlquist A, Kunde V, Weber B, Radner F, Leclerc-Mercier S, Schlipf N, Demmer P, Küsel J, Fischer J (2017) In: British Journal of Dermatology, 2017 Type of Publication: Research article (journal)
Diminished Protein-Bound $\upomega$-Hydroxylated Ceramides In The Skin Of Ichthyosis Patients With 12r-Lox Or Elox-3 Deficiency Dick A, Tantcheva-Po{ó}}r I, Oji V, Giehl K, Fischer J, Krieg P, Schneider H, Rauh M (2017) In: British Journal of Dermatology, 2017 Type of Publication: Research article (journal)
Expanding the Clinical and Genetic Spectrum of {KRT}1, {KRT}2 and {KRT}10 Mutations in Keratinopathic Ichthyosis Hotz A, Oji V, Bourrat E, Jonca N, Mazereeuw-Hautier J, Betz R, Blume-Peytavi U, Stieler K, Morice-Picard F, Schönbuchner I, Markus S, Schlipf N, Fischer J (2016) In: Acta Dermato Venereologica, 96(4) Type of Publication: Research article (journal)
Association of Cole disease with novel heterozygous mutations in the somatomedin-B domains of {theENPP}1gene: necessary, but not always sufficient Schlipf N, Traupe H, Gilaberte Y, Peitsch W, Hausser I, Oji V, Schmieder A, Schneider S, Demmer P, Rösler B, Fischer J (2016) In: British Journal of Dermatology, 174(5) Type of Publication: Research article (journal)
Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in {IL}36RN in German patients Löhr S, Uebe S, Behrens F, Böhm B, Köhm M, Traupe H, Oji V, Burkhardt H, Reis A, Hüffmeier U (2016) In: British Journal of Dermatology, 175(3) Type of Publication: Research article (journal)
Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen Tantcheva-Po{ó}}r I, Oji V, Has C (2016) In: {JDDG}: Journal der Deutschen Dermatologischen Gesellschaft, 14(10) Type of Publication: Research article (journal)