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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Daniela Perotti

Department of Preventive and Predictive Medicine

Unit of Molecular Bases of Genetic Risk and Genetic Testing

Fondazione IRCCS Istituto Nazionale dei Tumori

Milano

Italy

[email]@istitutotumori.mi.it

Name/email consistency: high

 
 
 
 
 
Daniela Perotti,  
 

Affiliations

  • Department of Preventive and Predictive Medicine, Unit of Molecular Bases of Genetic Risk and Genetic Testing, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy. 2008 - 2012
  • Department of Experimental Oncology and Laboratories, Istituto Nazionale Tumori, Milan, Italy. 2004 - 2005

References

  1. A novel WT1 mutation in familial wilms tumor. Melchionda, F., Spreafico, F., Ciceri, S., Lima, M., Collini, P., Pession, A., Massimino, M., Radice, P., Perotti, D. Pediatr. Blood. Cancer. (2013) [Pubmed]
  2. First evidence of vertical paternal transmission of osteopatia striata with cranial sclerosis. Ciceri, S., Cattaneo, E., Fossati, C., Radice, P., Selicorni, A., Perotti, D. Am. J. Med. Genet. A. (2013) [Pubmed]
  3. Loss of heterozygosity analysis at different chromosome regions in Wilms tumor confirms 1p allelic loss as a marker of worse prognosis: a study from the Italian Association of Pediatric Hematology and Oncology. Spreafico, F., Gamba, B., Mariani, L., Collini, P., D'Angelo, P., Pession, A., Di Cataldo, A., Indolfi, P., Nantron, M., Terenziani, M., Morosi, C., Radice, P., Perotti, D. J. Urol. (2013) [Pubmed]
  4. WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features. Zicari, A.M., Tarani, L., Perotti, D., Papetti, L., Nicita, F., Liberati, N., Spalice, A., Salvatori, G., Guaraldi, F., Duse, M. Ital. J. Pediatr. (2012) [Pubmed]
  5. Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse. Perotti, D., Spreafico, F., Torri, F., Gamba, B., D'Adamo, P., Pizzamiglio, S., Terenziani, M., Catania, S., Collini, P., Nantron, M., Pession, A., Bianchi, M., Indolfi, P., D'Angelo, P., Fossati-Bellani, F., Verderio, P., Macciardi, F., Radice, P. Genes. Chromosomes. Cancer. (2012) [Pubmed]
  6. Telomere maintenance in Wilms tumors: first evidence for the presence of alternative lengthening of telomeres mechanism. Venturini, L., Daidone, M.G., Motta, R., Collini, P., Spreafico, F., Terenziani, M., Piva, L., Radice, P., Perotti, D., Zaffaroni, N. Genes. Chromosomes. Cancer. (2011) [Pubmed]
  7. Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex. Spreafico, F., Notarangelo, L.D., Schumacher, R.F., Savoldi, G., Gamba, B., Terenziani, M., Collini, P., Fasoli, S., Giordano, L., Luisa, B., Porta, F., Massimino, M., Radice, P., Perotti, D. Am. J. Med. Genet. A. (2011) [Pubmed]
  8. Is WTX a suitable target for cancer therapy?. Perotti, D., Radice, P. Pediatr. Blood. Cancer. (2011) [Pubmed]
  9. Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies. Carella, M., Spreafico, F., Palumbo, O., Storlazzi, C.T., Tabano, S., Miozzo, M., Miglionico, L., Calvano, S., Sindici, G., Gamba, B., Impera, L., Collini, P., Zelante, L., Radice, P., Perotti, D. Am. J. Med. Genet. A. (2010) [Pubmed]
  10. A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor. Terenziani, M., Sardella, M., Gamba, B., Testi, M.A., Spreafico, F., Ardissino, G., Fedeli, F., Fossati-Bellani, F., Radice, P., Perotti, D. Pediatr. Nephrol. (2009) [Pubmed]
  11. Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors. Perotti, D., Gamba, B., Sardella, M., Spreafico, F., Terenziani, M., Collini, P., Pession, A., Nantron, M., Fossati-Bellani, F., Radice, P. Oncogene. (2008) [Pubmed]
  12. Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer. Murrell, A., Ito, Y., Verde, G., Huddleston, J., Woodfine, K., Silengo, M.C., Spreafico, F., Perotti, D., De Crescenzo, A., Sparago, A., Cerrato, F., Riccio, A. PLoS. One. (2008) [Pubmed]
  13. Treatment of high-risk relapsed Wilms tumor with dose-intensive chemotherapy, marrow-ablative chemotherapy, and autologous hematopoietic stem cell support: experience by the Italian Association of Pediatric Hematology and Oncology. Spreafico, F., Bisogno, G., Collini, P., Jenkner, A., Gandola, L., D'Angelo, P., Casazza, G., Piva, L., Luksch, R., Perotti, D., Pession, A., Fagioli, F., Dallorso, S. Pediatr. Blood. Cancer. (2008) [Pubmed]
  14. Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome. Uccini, S., Perotti, D., Colarossi, C., Stoppacciaro, A., Sardella, M., Mannarino, O., Collini, P., Casieri, P., Cozzi, D., Amoroso, L., Spreafico, F., Radice, P., Dominici, C. Pediatr. Blood. Cancer. (2008) [Pubmed]
  15. The IGF signalling pathway in Wilms tumours--a report from the ENCCA Renal Tumours Biology-driven drug development workshop. Maschietto, M., Charlton, J., Perotti, D., Radice, P., Geller, J.I., Pritchard-Jones, K., Weeks, M. Oncotarget. (2014) [Pubmed]
  16. Response Re: Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor. Spreafico, F., Terenziani, M., Testa, S., Perotti, D., Collini, P., Piva, L., Ardissino, G. Pediatr. Blood. Cancer. (2014) [Pubmed]
  17. Long-term renal outcome in adolescent and young adult patients nephrectomized for unilateral Wilms tumor. Spreafico, F., Terenziani, M., Testa, S., Perotti, D., Collini, P., Piva, L., Ardissino, G. Pediatr. Blood. Cancer. (2014) [Pubmed]
  18. Is Wilms tumor a candidate neoplasia for treatment with WNT/β-catenin pathway modulators?--A report from the renal tumors biology-driven drug development workshop. Perotti, D., Hohenstein, P., Bongarzone, I., Maschietto, M., Weeks, M., Radice, P., Pritchard-Jones, K. Mol. Cancer. Ther. (2013) [Pubmed]
  19. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome. Calvello, M., Tabano, S., Colapietro, P., Maitz, S., Pansa, A., Augello, C., Lalatta, F., Gentilin, B., Spreafico, F., Calzari, L., Perotti, D., Larizza, L., Russo, S., Selicorni, A., Sirchia, S.M., Miozzo, M. Epigenetics. (2013) [Pubmed]
  20. WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities. Perotti, D., Mondini, P., Terenziani, M., Spreafico, F., Collini, P., Fossati-Bellani, F., Radice, P. J. Pediatr. Hematol. Oncol. (2005) [Pubmed]
  21. Wilms tumor in monozygous twins: clinical, pathological, cytogenetic and molecular case report. Perotti, D., Vecchi, G.D., Lualdi, E., Testi, M.A., Sozzi, G., Collini, P., Spreafico, F., Terenziani, M., Fossati-Bellani, F., Radice, P. J. Pediatr. Hematol. Oncol. (2005) [Pubmed]
  22. Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14. Perotti, D., De Vecchi, G., Testi, M.A., Lualdi, E., Modena, P., Mondini, P., Ravagnani, F., Collini, P., Di Renzo, F., Spreafico, F., Terenziani, M., Sozzi, G., Fossati-Bellani, F., Radice, P. Hum. Mutat. (2004) [Pubmed]
 
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