| Integrin α3 Mutations with Kidney, Lung, and Skin Disease C Has, G Spartà, D Kiritsi, L Weibel, A Moeller, V Vega-Warner, A Waters, ... New England Journal of Medicine 366 (16), 1508-1514, 2012 | 277 | 2012 |
| Losartan ameliorates dystrophic epidermolysis bullosa and uncovers new disease mechanisms A Nyström, K Thriene, V Mittapalli, JS Kern, D Kiritsi, J Dengjel, ... EMBO molecular medicine 7 (9), 1211-1228, 2015 | 173 | 2015 |
| Laminin 332 in junctional epidermolysis bullosa D Kiritsi, C Has, L Bruckner-Tuderman Cell adhesion & migration 7 (1), 135-141, 2013 | 145 | 2013 |
| Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history C Has, D Castiglia, M del Rio, M Garcia Diez, E Piccinni, D Kiritsi, ... Human mutation 32 (11), 1204-1212, 2011 | 143 | 2011 |
| The role of TGFβ in wound healing pathologies D Kiritsi, A Nyström Mechanisms of ageing and development 172, 51-58, 2018 | 128 | 2018 |
| Injury-driven stiffening of the dermis expedites skin carcinoma progression VR Mittapalli, J Madl, S Löffek, D Kiritsi, JS Kern, W Römer, A Nyström, ... Cancer research 76 (4), 940-951, 2016 | 108 | 2016 |
| Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity M Pigors, D Kiritsi, S Krümpelmann, N Wagner, Y He, M Podda, ... Human molecular genetics 20 (9), 1811-1819, 2011 | 107 | 2011 |
| Monoallelic mutations in the translation initiation codon of KLHL24 cause skin fragility Y He, K Maier, J Leppert, I Hausser, A Schwieger-Briel, L Weibel, ... The American Journal of Human Genetics 99 (6), 1395-1404, 2016 | 95 | 2016 |
| Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa D Kiritsi, JS Kern, H Schumann, J Kohlhase, C Has, L Bruckner-Tuderman Journal of medical genetics 48 (7), 450-457, 2011 | 95 | 2011 |
| Forty‐two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large … JS Kern, G Grüninger, R Imsak, ML Müller, H Schumann, D Kiritsi, ... British Journal of Dermatology 161 (5), 1089-1097, 2009 | 95 | 2009 |
| Bullous pemphigoid in infants: characteristics, diagnosis and treatment A Schwieger-Briel, C Moellmann, B Mattulat, F Schauer, D Kiritsi, ... Orphanet journal of rare diseases 9, 1-12, 2014 | 88 | 2014 |
| Dynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partner W Nishie, D Kiritsi, A Nyström, SC Hofmann, L Bruckner-Tuderman The American journal of pathology 179 (2), 829-837, 2011 | 82 | 2011 |
| Therapeutic options for CTLA-4 insufficiency D Egg, IC Rump, N Mitsuiki, J Rojas-Restrepo, ME Maccari, C Schwab, ... Journal of Allergy and Clinical Immunology 149 (2), 736-746, 2022 | 77 | 2022 |
| Loss of desmoglein 1 associated with palmoplantar keratoderma, dermatitis and multiple allergies C Has, T Jakob, Y He, D Kiritsi, I Hausser, L Bruckner‐Tuderman British Journal of Dermatology 172 (1), 257-261, 2015 | 76 | 2015 |
| Genotype, clinical course, and therapeutic decision making in 76 infants with severe generalized junctional epidermolysis bullosa J Hammersen, C Has, N Naumann-Bartsch, D Stachel, D Kiritsi, S Söder, ... Journal of Investigative Dermatology 136 (11), 2150-2157, 2016 | 73 | 2016 |
| Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination D Kiritsi, Y He, AMG Pasmooij, M Onder, R Happle, MF Jonkman, ... The Journal of clinical investigation 122 (5), 1742-1746, 2012 | 70 | 2012 |
| Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations H Schumann, D Kiritsi, M Pigors, I Hausser, J Kohlhase, J Peters, H Ott, ... British Journal of Dermatology 169 (1), 115-124, 2013 | 69 | 2013 |
| Impaired lymphoid extracellular matrix impedes antibacterial immunity in epidermolysis bullosa A Nyström, O Bornert, T Kühl, C Gretzmeier, K Thriene, J Dengjel, ... Proceedings of the National Academy of Sciences 115 (4), E705-E714, 2018 | 62 | 2018 |
| Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals D Kiritsi, I Cosgarea, CW Franzke, H Schumann, V Oji, J Kohlhase, ... The Journal of investigative dermatology 130 (6), 1741-1746, 2010 | 58 | 2010 |
| Mechanisms of natural gene therapy in dystrophic epidermolysis bullosa D Kiritsi, M Garcia, R Brander, C Has, R Meijer, MJ Escámez, J Kohlhase, ... Journal of Investigative Dermatology 134 (8), 2097-2104, 2014 | 56 | 2014 |
