| 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 |
| Isolation of SPINK6 in human skin: selective inhibitor of kallikrein-related peptidases U Meyer-Hoffert, Z Wu, T Kantyka, J Fischer, T Latendorf, B Hansmann, ... Journal of biological chemistry 285 (42), 32174-32181, 2010 | 113 | 2010 |
| 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 |
| Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytes C Has, C Herz, E Zimina, HY Qu, Y He, ZG Zhang, TT Wen, Y Gache, ... The American journal of pathology 175 (4), 1442-1452, 2009 | 93 | 2009 |
| 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 |
| Highly complex peptide aggregates of the S100 fused-type protein hornerin are present in human skin Z Wu, U Meyer-Hoffert, K Reithmayer, R Paus, B Hansmann, Y He, ... Journal of investigative dermatology 129 (6), 1446-1458, 2009 | 76 | 2009 |
| 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 |
| Research techniques made simple: immunofluorescence antigen mapping in epidermolysis bullosa C Has, Y He Journal of Investigative Dermatology 136 (7), e65-e71, 2016 | 53 | 2016 |
| Crucial role of posttranslational modifications of integrin α3 in interstitial lung disease and nephrotic syndrome EG Yalcin, Y He, D Orhan, C Pazzagli, N Emiralioglu, C Has Human Molecular Genetics 24 (13), 3679-3688, 2015 | 50 | 2015 |
| Kindlin-1 and-2 have overlapping functions in epithelial cells: implications for phenotype modification Y He, P Esser, A Heinemann, L Bruckner-Tuderman, C Has The American journal of pathology 178 (3), 975-982, 2011 | 47 | 2011 |
| Induction of phenotype modifying cytokines by FERMT1 mutations A Heinemann, Y He, E Zimina, M Boerries, H Busch, N Chmel, T Kurz, ... Human Mutation 32 (4), 397-406, 2011 | 45 | 2011 |
| Role of kindlin-2 in fibroblast functions: implications for wound healing Y He, P Esser, V Schacht, L Bruckner-Tuderman, C Has Journal of investigative dermatology 131 (1), 245-256, 2011 | 42 | 2011 |
| Junctional epidermolysis bullosa: allelic heterogeneity and mutation stratification for precision medicine I Condrat, Y He, R Cosgarea, C Has Frontiers in Medicine 5, 363, 2019 | 37 | 2019 |
| Intronic ITGA3 mutation impacts splicing regulation and causes interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa E Tschachler, F Morizot, A Vierkötter, U Ranft, U Krämer, D Sugiri, ... Journal of Investigative Dermatology 136, 1056e1059, 2016 | 36 | 2016 |
| Single amino acid deletion in kindlin-1 results in partial protein degradation which can be rescued by chaperone treatment K Maier, Y He, PR Esser, K Thriene, D Sarca, J Kohlhase, J Dengjel, ... Journal of Investigative Dermatology 136 (5), 920-929, 2016 | 21 | 2016 |
| Natural history of kindler syndrome and propensity for skin cancer–case report and literature review M Saleva, C Has, Y He, S Vassileva, M Balabanova, L Miteva JDDG: Journal der Deutschen Dermatologischen Gesellschaft 16 (3), 338-341, 2018 | 18 | 2018 |
| UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome K Maier, Y He, U Wölfle, PR Esser, T Brummer, C Schempp, ... Human Molecular Genetics 25 (24), 5339-5352, 2016 | 18 | 2016 |
| Homozygous Nonsense Mutation and Additional Deletion of an Amino Acid in BPAG1e Causing Mild Localized Epidermolysis Bullosa Simplex. HE Yinghong, J Leppert, H Steinke, C Has Acta Dermato-Venereologica 97 (5), 2017 | 17 | 2017 |
| RhoA activation by CNFy restores cell–cell adhesion in kindlin‐2‐deficient keratinocytes Y He, T Sonnenwald, A Sprenger, U Hansen, J Dengjel, ... The Journal of pathology 233 (3), 269-280, 2014 | 17 | 2014 |
