Author Oji, Vinzenz
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2008 | Journal Article
Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis
Haenssle, H. A.; Finkenrath, A.; Hausser, I.; Oji, V.; Traupe, H.; Hennies, H. C. & Neumann, C. et al. (2008)
Clinical and Experimental Dermatology, 33(5) pp. 578-581. DOI: https://doi.org/10.1111/j.1365-2230.2008.02709.x
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2009 | Journal Article
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup
Oji, V.; Seller, N.; Sandilands, A.; Gruber, R. M.; Gerss, J.; Hueffmeier, U. & Hamm, H. et al. (2009)
British Journal of Dermatology, 160(4) pp. 771-781. DOI: https://doi.org/10.1111/j.1365-2133.2008.08999.x
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2010 | Conference Abstract
A presentation of ichthyosis with severe atopy due to STS and FLG deficiency
Seller, N.; Bohring, A.; Hausser, I.; Steinfeld, R.; Walker, T.; Aufenvenne, K. & Metze, D. et al. (2010)
JDDG Journal der Deutschen Dermatologischen Gesellschaft, 8(11)
Malden: Wiley-blackwell.
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2011 | Journal Article
Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis
Arin, M. J.; Oji, V.; Emmert, S.; Hausser, I.; Traupe, H.; Krieg, T. & Grimberg, G. (2011)
British Journal of Dermatology, 164(2) pp. 442-447. DOI: https://doi.org/10.1111/j.1365-2133.2010.10096.x
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2013 | Conference Abstract
Functional and molecular genetic analyses of 9 newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes
Emmert, S.; Schaefer, A.; Gratchev, A.; Seebode, C.; Hofmann, L.; Schubert, S. & Laspe, P. et al. (2013)
JDDG Journal der Deutschen Dermatologischen Gesellschaft, 11(9)
Hoboken: Wiley-blackwell.
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2013 | Journal Article
Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes
Schaefer, A.; Gratchev, A.; Seebode, C.; Hofmann, L.; Schubert, S.; Laspe, P. & Apel, A. et al. (2013)
Experimental Dermatology, 22(7) pp. 486-489. DOI: https://doi.org/10.1111/exd.12166
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2014 | Conference Abstract
Palmoplantar pustular psoriasis and its genetic background
Moessner, R.; Frambach, Y.; Jacobi, A.; Mueller, M.; Oji, V.; Philipp, S. & Renner, R. et al. (2014)
Experimental Dermatology, 23(3) 41st Annual Meeting of the Arbeitsgemeinschaft-Dermatologische-Forschung (ADF), Cologne, GERMANY.
Hoboken: Wiley-blackwell.
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2014 | Conference Abstract
Palmoplantar pustular psoriasis is associated with a missense variant in CARD14 in European patients
Moessner, R.; Frambach, Y.; Wilsmann-Theis, D.; Loehr, S.; Jacobi, A.; Weyergraf, A. J. & Mueller, M. et al. (2014)
British Journal of Dermatology, 171(6) 7th International Congress of Psoriasis - From Gene to Clinic, London, ENGLAND.
Hoboken: Wiley-blackwell.
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2015 | Journal Article | Letter Note
Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients
Moessner, R.; Frambach, Y.; Wilsmann-Theis, D.; Loehr, S.; Jacobi, A.; Weyergraf, A. J. & Mueller, M. et al. (2015)
Journal of Investigative Dermatology, 135(10) pp. 2538-2541. DOI: https://doi.org/10.1038/jid.2015.186
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2016 | Journal Article
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
Basmanav, F. B. U.; Cau, L.; Tafazzoli, A.; Mechin, M.-C.; Wolf, S.; Romano, M. T. & Valentin, F. et al. (2016)
The American Journal of Human Genetics, 99(6) pp. 1292-1304. DOI: https://doi.org/10.1016/j.ajhg.2016.10.004
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2019 | Journal Article
Analyses of association of psoriatic arthritis and psoriasis vulgaris with functional NCF1 variants
Löhr, S.; Ekici, A. B; Uebe, S.; Büttner, C.; Köhm, M.; Behrens, F. & Böhm, B. et al. (2019)
Rheumatology, 58(5) pp. 915-917. DOI: https://doi.org/10.1093/rheumatology/key448
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2019 | Journal Article
Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights into Disease Pathogenesis
Ralser, D. J.; Takeuchi, H.; Fritz, G.; Basmanav, F. B.; Effern, M.; Sivalingam, S. & El-Shabrawi-Caelen, L. et al. (2019)
Journal of Investigative Dermatology, 139(4) pp. 960-964. DOI: https://doi.org/10.1016/j.jid.2018.10.030
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2020 | Journal Article
Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis
Frey, S.; Sticht, H.; Wilsmann-Theis, D.; Gerschütz, A.; Wolf, K.; Löhr, S. & Haskamp, S. et al. (2020)
Journal of Investigative Dermatology, 140(7) pp. 1451-1455.e13. DOI: https://doi.org/10.1016/j.jid.2019.11.024
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2020 | Journal Article
Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases
Haskamp, S.; Bruns, H.; Hahn, M.; Hoffmann, M.; Gregor, A.; Löhr, S. & Hahn, J. et al. (2020)
The American Journal of Human Genetics, 107(3) pp. 527-538. DOI: https://doi.org/10.1016/j.ajhg.2020.07.001
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2020 | Journal Article |
Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups
Assmann, G.; Köhm, M.; Schuster, V.; Behrens, F.; Mössner, R. ; Magnolo, N. & Oji, V. et al. (2020)
BMC Medical Genetics, 21(1). DOI: https://doi.org/10.1186/s12881-020-01037-7
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2021 | Journal Article
Genetic Analysis of MPO Variants in Four Psoriasis Subtypes in Patients from Germany
Haskamp, S.; Horowitz, J. S.; Oji, V.; Philipp, S.; Sticherling, M.; Schäkel, K. & Schuhmann, S. et al. (2021)
Journal of Investigative Dermatology, 141(8) pp. 2079-2083. DOI: https://doi.org/10.1016/j.jid.2021.01.017
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2023 | Journal Article
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss
Cesarato, N.; Schwieger-Briel, A.; Gossmann, Y.; Henne, S. K; Hillmann, K.; Frommherz, L. H & Wehner, M. et al. (2023)
British Journal of Dermatology, art. ljad314. DOI: https://doi.org/10.1093/bjd/ljad314
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