Author Oji, Vinzenz

1 to 18 of 18 Items
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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.
    ​Details  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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.
    ​Details  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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.
    ​Details  WoS 
  • 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.
    ​Details  WoS 
  • 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 
    ​Details  DOI  PMID  PMC  WoS 
  • 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 
    ​Details  DOI  WoS 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 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 
    ​Details  DOI 
  • 2024 | Journal Article
    ​ ​Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations​
    Hotz, A.; Fölster-Holst, R.; Oji, V.; Bourrat, E.; Frank, J.; Marrakchi, S. & Ennouri, M. et al.​ (2024) 
    Genes, 15(3) pp. 288​.​ DOI: https://doi.org/10.3390/genes15030288 
    ​Details  DOI 

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