Giannuzzi Giuliana
Professore Associato
Settore scientifico-disciplinare
BIOS-14/A - Genetica
Gruppo scientifico-disciplinare / settore concorsuale
05/BIOS-14 - GENETICA
Competenze e ambito di ricerca
Contacts
Sede di lavoro
Numero di telefono dell'ufficio
E-mail di ateneo
Teaching - Programme courses
Bachelors and masters
A.A. 2025/2026
A.A. 2024/2025
A.A. 2023/2024
A.A. 2022/2023
Research
Publications
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AGAP duplicons associate with structural diversity at Chromosome 10q11.22 / S. Fornezza, V.S. Delvecchio, W.T. Harvey, P.C. Dishuck, E.E. Eichler, G. Giannuzzi. - In: GENOME RESEARCH. - ISSN 1088-9051. - 34:10(2024 Oct), pp. 1487-1499. [10.1101/gr.279454.124]
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Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators? / S. Redaelli, F.R. Grati, V. Tritto, G. Giannuzzi, M.P. Recalcati, E. Sala, N. Villa, F. Crosti, G. Roversi, F. Malvestiti, V. Zanatta, E. Repetti, O. Rodeschini, C. Valtorta, I. Catusi, L. Romitti, E. Martinoli, D. Conconi, L. Dalprà, M. Lavitrano, P. Riva, A. Bentivegna. - In: HGG ADVANCES. - ISSN 2666-2477. - 5:2(2024 Apr 11), pp. 100261.1-100261.8. [10.1016/j.xhgg.2023.100261]
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The pancancer overexpressed NFYC Antisense 1 controls cell cycle mitotic progression through in cis and in trans modes of action / C. Pandini, G. Pagani, M. Tassinari, E. Vitale, E. Bezzecchi, M.K. Saadeldin, V. Doldi, G. Giannuzzi, R. Mantovani, M. Chiara, A. Ciarrocchi, P. Gandellini. - In: CELL DEATH & DISEASE. - ISSN 2041-4889. - 15:3(2024), pp. 206.1-206.14. [10.1038/s41419-024-06576-y]
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Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts / G. Giannuzzi, N. Chatron, K. Mannik, C. Auwerx, S. Pradervand, G. Willemin, K. Hoekzema, X. Nuttle, J. Chrast, M.C. Sadler, E. Porcu, Y. Herault, B. Isidor, B. Gilbert-Dussardier, E.E. Eichler, Z. Kutalik, A. Reymond. - In: NPJ GENOMIC MEDICINE. - ISSN 2056-7944. - 7:1(2022), pp. 38.1-38.10. [10.1038/s41525-022-00308-x]
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Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss / S. Bassani, E. van Beelen, M. Rossel, N. Voisin, A. Morgan, Y. Arribat, N. Chatron, J. Chrast, M. Cocca, B. Delprat, F. Faletra, G. Giannuzzi, N. Guex, R. Machavoine, S. Pradervand, J.J. Smits, J.M. van de Kamp, A. Ziegler, F. Amati, S. Marlin, H. Kremer, H. Locher, T. Maurice, P. Gasparini, G. Girotto, A. Reymond. - In: HUMAN MOLECULAR GENETICS. - ISSN 0964-6906. - 30:19(2021 Sep 15), pp. 1785-1796. [10.1093/hmg/ddab145]