| Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor M Gassmann, F Casagranda, D Orioli, H Simon, C Lai, R Klein, G Lemke Nature 378 (6555), 390-394, 1995 | 1351 | 1995 |
| Nuk controls pathfinding of commissural axons in the mammalian central nervous system M Henkemeyer, D Orioli, JT Henderson, TM Saxton, J Roder, T Pawson, ... Cell 86 (1), 35-46, 1996 | 669 | 1996 |
| Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation. D Orioli, M Henkemeyer, G Lemke, R Klein, T Pawson The EMBO journal 15 (22), 6035-6049, 1996 | 429 | 1996 |
| The Eph receptor family: axonal guidance by contact repulsion. D Orioli, R Klein Trends in genetics: TIG 13 (9), 354-359, 1997 | 240 | 1997 |
| Rab17 regulates membrane trafficking through apical recycling endosomes in polarized epithelial cells P Zacchi, H Stenmark, RG Parton, D Orioli, F Lim, A Giner, I Mellman, ... The Journal of cell biology 140 (5), 1039-1053, 1998 | 175 | 1998 |
| From structure to phenotype: impact of collagen alterations on human health L Arseni, A Lombardi, D Orioli International journal of molecular sciences 19 (5), 1407, 2018 | 161 | 2018 |
| The role of CSA in the response to oxidative DNA damage in human cells M D'errico, E Parlanti, M Teson, P Degan, T Lemma, A Calcagnile, ... Oncogene 26 (30), 4336-4343, 2007 | 160 | 2007 |
| A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage T Nardo, R Oneda, G Spivak, B Vaz, L Mortier, P Thomas, D Orioli, ... Proceedings of the National Academy of Sciences 106 (15), 6209-6214, 2009 | 154 | 2009 |
| Trichothiodystrophy: from basic mechanisms to clinical implications M Stefanini, E Botta, M Lanzafame, D Orioli DNA repair 9 (1), 2-10, 2010 | 126 | 2010 |
| Epigenetic regulation of skin cells in natural aging and premature aging diseases D Orioli, E Dellambra Cells 7 (12), 268, 2018 | 103 | 2018 |
| Similarities and differences in the way transmembrane-type ligands interact with the Elk subclass of Eph receptors R Brambilla, K Brückner, D Orioli, AD Bergemann, JG Flanagan, R Klein Molecular and Cellular Neuroscience 8 (2-3), 199-209, 1996 | 88 | 1996 |
| Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome N Calmels, E Botta, N Jia, H Fawcett, T Nardo, Y Nakazawa, ... Journal of medical genetics 55 (5), 329-343, 2018 | 64 | 2018 |
| In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutation G Yasuda, R Nishi, E Watanabe, T Mori, S Iwai, D Orioli, M Stefanini, ... Molecular and cellular biology 27 (19), 6606-6614, 2007 | 64 | 2007 |
| Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions. FA Peverali, D Orioli, L Tonon, P Ciana, G Bunone, M Negri, G Della-Valle Oncogene 12 (2), 457-462, 1996 | 61 | 1996 |
| GTF2E2 mutations destabilize the general transcription factor complex TFIIE in individuals with DNA repair-proficient trichothiodystrophy C Kuschal, E Botta, D Orioli, JJ Digiovanna, S Seneca, K Keymolen, ... The American Journal of Human Genetics 98 (4), 627-642, 2016 | 59 | 2016 |
| Bi-allelic TARS mutations are associated with brittle hair phenotype AF Theil, E Botta, A Raams, DEC Smith, MI Mendes, G Caligiuri, ... The American Journal of Human Genetics 105 (2), 434-440, 2019 | 53 | 2019 |
| Heterogeneity and overlaps in nucleotide excision repair disorders D Ferri, D Orioli, E Botta Clinical genetics 97 (1), 12-24, 2020 | 48 | 2020 |
| Studies on the ATP binding site of Fyn kinase for the identification of new inhibitors and their evaluation as potential agents against tauopathies and tumors C Tintori, G La Sala, G Vignaroli, L Botta, AL Fallacara, F Falchi, M Radi, ... Journal of Medicinal Chemistry 58 (11), 4590-4609, 2015 | 37 | 2015 |
| TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin L Arseni, M Lanzafame, E Compe, P Fortugno, A Afonso-Barroso, ... Proceedings of the National Academy of Sciences 112 (5), 1499-1504, 2015 | 33 | 2015 |
| Genotype–phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD gene E Botta, T Nardo, D Orioli, R Guglielmino, R Ricotti, S Bondanza, ... Human mutation 30 (3), 438-445, 2009 | 31 | 2009 |
