Giannuzzi Giuliana

RICERCATORE A TEMPO DETERMINATO (Lettera B)
SSD
BIO/18 - GENETICA
Settore concorsuale
05/I1 - GENETICA

Contatti

Sede di lavoro

Via Celoria, 26 - Corpo C
20133 MILANO (MI)

E-mail di ateneo
Ricerca

Pubblicazioni

Pubblicazioni
  • 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]
  • Alpha satellite insertions and the evolutionary landscape of centromeres / G. Giannuzzi, G. A Logsdon, N. Chatron, D. E Miller, J. Reversat, K. M Munson, K. Hoekzema, M. Bonnet-Dupeyron, P. Rollat-Farnier, C. A Baker, D. Sanlaville, E. E Eichler, C. Schluth-Bolard, A. Reymond. - (2021 Mar 12).
  • The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms / N. Chatron, G. Giannuzzi, P. Rollat-Farnier, F. Diguet, E. Porcu, T. Yammine, K. Uguen, Z. Bellil, J. Lauer Zillhardt, A. Sorlin, F. Ader, A. Afenjar, J. Andrieux, C. Bardel, E. Calpena, S. Chantot-Bastaraud, P. Callier, N. Chelloug, E. Chopin, M. Cordier, C. Dubourg, L. Faivre, F. Girard, S. Heide, Y. Herenger, S. Jaillard, B. Keren, S.J.L. Knight, J. Lespinasse, L. Lohmann, N. Marle, R. Maroofian, A. Masurel-Paulet, M. Mathieu-Dramard, C. Metay, A.T. Pagnamenta, M. Portnoï, F. Prieur, M. Rio, J. Siffroi, S. Valence, J.C. Taylor, A.O.M. Wilkie, P. Edery, A. Reymond, D. Sanlaville, C. Schluth-Bolard. - (2020 Jul 17). [10.1101/2020.07.17.206771]
  • Evolutionary dynamics of the POTE gene family in human and nonhuman primates / F.A.M. Maggiolini, L. Mercuri, F. Antonacci, F. Anaclerio, F.M. Calabrese, N. Lorusso, A. L'abbate, M. Sorensen, G. Giannuzzi, E.E. Eichler, C.R. Catacchio, M. Ventura. - In: GENES. - ISSN 2073-4425. - 11:2(2020), pp. 213.1-213.24. [10.3390/genes11020213]
  • The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism individuals / G. Giannuzzi, P. Schmidt, K. Porcu Männik, P. De Nittis, E. Baratz. - In: AMERICAN JOURNAL OF HUMAN GENETICS. - ISSN 0002-9297. - 105:5(2019), pp. 947-958. [10.1016/j.ajhg.2019.09.023]