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

Marcella Zollino

Istituto di Genetica Medica

Università Cattolica Sacro Cuore

Policlinico A. Gemelli



Name/email consistency: high



  • Istituto di Genetica Medica, Università Cattolica Sacro Cuore, Policlinico A. Gemelli, Italy. 1999 - 2011
  • Department of Medical Genetics, Università Cattolica Sacro Cuore, Italy. 2008


  1. Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndrome. Zollino, M., Gurrieri, F., Orteschi, D., Marangi, G., Leuzzi, V., Neri, G. Eur. J. Hum. Genet. (2011) [Pubmed]
  2. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review. Zollino, M., Murdolo, M., Marangi, G., Pecile, V., Galasso, C., Mazzanti, L., Neri, G. Am. J. Med. Genet. C. Semin. Med. Genet (2008) [Pubmed]
  3. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16. Zollino, M., Lecce, R., Murdolo, M., Orteschi, D., Marangi, G., Selicorni, A., Midro, A., Sorge, G., Zampino, G., Memo, L., Battaglia, D., Petersen, M., Pandelia, E., Gyftodimou, Y., Faravelli, F., Tenconi, R., Garavelli, L., Mazzanti, L., Fischetto, R., Cavalli, P., Savasta, S., Rodriguez, L., Neri, G. Hum. Genet. (2007) [Pubmed]
  4. A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome. Zollino, M., Lecce, R., Selicorni, A., Murdolo, M., Mancuso, I., Marangi, G., Zampino, G., Garavelli, L., Ferrarini, A., Rocchi, M., Opitz, J.M., Neri, G. Eur. J. Hum. Genet. (2004) [Pubmed]
  5. Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked trait. Zollino, M., Colosimo, C., Zuffardi, O., Rossi, E., Tosolini, A., Walsh, C.A., Neri, G. Am. J. Med. Genet. A (2003) [Pubmed]
  6. Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2. Zollino, M., Lecce, R., Fischetto, R., Murdolo, M., Faravelli, F., Selicorni, A., Buttè, C., Memo, L., Capovilla, G., Neri, G. Am. J. Hum. Genet. (2003) [Pubmed]
  7. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. Zollino, M., Di Stefano, C., Zampino, G., Mastroiacovo, P., Wright, T.J., Sorge, G., Selicorni, A., Tenconi, R., Zappalà, A., Battaglia, A., Di Rocco, M., Palka, G., Pallotta, R., Altherr, M.R., Neri, G. Am. J. Med. Genet. (2000) [Pubmed]
  8. Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome. Zollino, M., Tiziano, F., Di Stefano, C., Neri, G. Am. J. Med. Genet. (1999) [Pubmed]
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