| Human melanoma metastases express functional CXCR4 S Scala, P Giuliano, PA Ascierto, C Ieranò, R Franco, M Napolitano, ... Clinical cancer research 12 (8), 2427-2433, 2006 | 157 | 2006 |
| 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 |
| Quality of life in patients with epidermolysis bullosa S Tabolli, F Sampogna, C Di Pietro, A Paradisi, C Uras, P Zotti, ... British Journal of Dermatology 161 (4), 869-877, 2009 | 116 | 2009 |
| Monozygotic twins discordant for recessive dystrophic epidermolysis bullosa phenotype highlight the role of TGF-β signalling in modifying disease severity T Odorisio, M Di Salvio, A Orecchia, G Di Zenzo, E Piccinni, F Cianfarani, ... Human molecular genetics 23 (15), 3907-3922, 2014 | 107 | 2014 |
| The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations PC van den Akker, MF Jonkman, T Rengaw, L Bruckner‐Tuderman, ... Human mutation 32 (10), 1100-1107, 2011 | 105 | 2011 |
| Epidermolysis bullosa-associated squamous cell carcinoma: from pathogenesis to therapeutic perspectives AG Condorelli, E Dellambra, E Logli, G Zambruno, D Castiglia International journal of molecular sciences 20 (22), 5707, 2019 | 104 | 2019 |
| Genotype–phenotype correlation in Italian patients with dystrophic epidermolysis bullosa R Gardella, D Castiglia, P Posteraro, S Bernardini, N Zoppi, M Paradisi, ... Journal of investigative dermatology 119 (6), 1456-1462, 2002 | 101 | 2002 |
| MicroRNA‐155 targets the SKI gene in human melanoma cell lines L Levati, E Pagani, S Romani, D Castiglia, E Piccinni, C Covaciu, ... Pigment cell & melanoma research 24 (3), 538-550, 2011 | 100 | 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 |
| Stromal microenvironment in type VII collagen-deficient skin: The ground for squamous cell carcinoma development L Guerra, T Odorisio, G Zambruno, D Castiglia Matrix Biology 63, 1-10, 2017 | 93 | 2017 |
| The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation MJ Escámez, M García, N Cuadrado‐Corrales, SG Llames, ... British Journal of Dermatology 163 (1), 155-161, 2010 | 83 | 2010 |
| Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene C Has, V Wessagowit, M Pascucci, C Baer, B Didona, C Wilhelm, ... Journal of investigative dermatology 126 (8), 1776-1783, 2006 | 77 | 2006 |
| Pathomechanisms of altered wound healing in recessive dystrophic epidermolysis bullosa F Cianfarani, G Zambruno, D Castiglia, T Odorisio The American journal of pathology 187 (7), 1445-1453, 2017 | 74 | 2017 |
| Hereditary palmoplantar keratodermas. Part I. Non‐syndromic palmoplantar keratodermas: classification, clinical and genetic features L Guerra, M Castori, B Didona, D Castiglia, G Zambruno Journal of the European Academy of Dermatology and Venereology 32 (5), 704-719, 2018 | 67 | 2018 |
| FOXM1 regulates proliferation, senescence and oxidative stress in keratinocytes and cancer cells A Smirnov, E Panatta, AM Lena, D Castiglia, N Di Daniele, G Melino, ... Aging (Albany NY) 8 (7), 1384, 2016 | 67 | 2016 |
| Analysis of candidate genes through a proteomics-based approach in primary cell lines from malignant melanomas and their metastases F Carta, PP Demuro, C Zanini, A Santona, D Castiglia, S D'Atri, ... Melanoma research 15 (4), 235-244, 2005 | 67 | 2005 |
| BRAF Gene Is Somatically Mutated but Does Not Make a Major Contribution to Malignant Melanoma Susceptibility: The Italian Melanoma Intergroup Study M Casula, M Colombino, MP Satta, A Cossu, PA Ascierto, ... Journal of clinical oncology 22 (2), 286-292, 2004 | 65 | 2004 |
| Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization B Drera, D Castiglia, N Zoppi, R Gardella, G Tadini, G Floriddia, ... Clinical genetics 70 (4), 339-347, 2006 | 60 | 2006 |
| A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional … L Ruzzi, P Posteraro, G Zambruno, D Castiglia, M D'Alessio, H Pas, ... Journal of investigative dermatology 116 (1), 182-187, 2001 | 56 | 2001 |
| Family burden in epidermolysis bullosa is high independent of disease type/subtype S Tabolli, C Pagliarello, C Uras, C Di Pietro, G Zambruno, D Castiglia, ... Acta dermato-venereologica 90 (6), 607-611, 2010 | 54 | 2010 |
