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Donata Orioli

Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor
1995 · Martin Gassmann, Franca Casagranda, et al. · Nature · 1,160
Nuk Controls Pathfinding of Commissural Axons in the Mammalian Central Nervous System
1996 · Mark Henkemeyer, Donata Orioli, et al. · Cell · 536
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Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation.
1996 · D. Orioli, M. Henkemeyer, et al. · The EMBO Journal · 330
From Structure to Phenotype: Impact of Collagen Alterations on Human Health
2018 · Lavinia Arseni, Anita Lombardi, et al. · International Journal of Molecular Sciences · 198
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The eph receptor family:axonal guidance by contact repulsion
1997 · D. Orioli, R. Klein · Trends in Genetics · 183
Epigenetic Regulation of Skin Cells in Natural Aging and Premature Aging Diseases
2018 · Donata Orioli, Elena Dellambra · Cells · 152
The role of CSA in the response to oxidative DNA damage in human cells
2007 · M D'Errico, E Parlanti, et al. · Oncogene · 143
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage
2009 · Tiziana Nardo, Roberta Oneda, et al. · Proceedings of the National Academy of Sciences · 141
Rab17 Regulates Membrane Trafficking through Apical Recycling Endosomes in Polarized Epithelial Cells
1998 · Paola Zacchi, Harald Stenmark, et al. · The Journal of Cell Biology · 140
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Trichothiodystrophy: From basic mechanisms to clinical implications
2009 · M. Stefanini, E. Botta, et al. · DNA repair · 127
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome
2018 · Nadege Calmels, Elena Botta, et al. · Journal of Medical Genetics · 87
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GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy
2016 · Christiane Kuschal, Elena Botta, et al. · The American Journal of Human Genetics · 74
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Similarities and Differences in the Way Transmembrane-Type Ligands Interact with the Elk Subclass of Eph Receptors
1996 · Riccardo Brambilla, Katja Brückner, et al. · Molecular and Cellular Neuroscience · 70
Heterogeneity and overlaps in nucleotide excision repair disorders
2019 · Debora Ferri, Donata Orioli, et al. · Clinical Genetics · 61
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype
2019 · Arjan F. Theil, Elena Botta, et al. · The American Journal of Human Genetics · 59
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Retinoic acid-induced growth arrest and differentiation of neuroblastoma cells are counteracted by N-myc and enhanced by max overexpressions.
1996 · F A Peverali, D Orioli, et al. · PubMed · 54
Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy
2021 · Elena Botta, Arjan F Theil, et al. · Human Molecular Genetics · 51
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In Vivo Destabilization and Functional Defects of the Xeroderma Pigmentosum C Protein Caused by a Pathogenic Missense Mutation
2007 · Gentaro Yasuda, Ryotaro Nishi, et al. · Molecular and Cellular Biology · 49
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
2015 · Cristina Tintori, Giuseppina La Sala, et al. · Journal of Medicinal Chemistry · 38
Overexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells
2016 · Barbara Pascucci, Mariarosaria D’Errico, et al. · Oncotarget · 31
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin
2015 · Lavinia Arseni, Manuela Lanzafame, et al. · Proceedings of the National Academy of Sciences · 30
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in theXPDgene
2008 · Elena Botta, Tiziana Nardo, et al. · Human Mutation · 30
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XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression
2012 · D. Orioli, E. Compe, et al. · Human Molecular Genetics · 26
Cockayne Syndrome Type A Protein Protects Primary Human Keratinocytes from Senescence
2018 · Sonia Cordisco, Lavinia Tinaburri, et al. · Journal of Investigative Dermatology · 23
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes
2015 · Manuela Lanzafame, Elena Botta, et al. · Experimental Dermatology · 20
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Works count: 47
Citation count: 3,939
H-index: 23
I10-index: 31
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