GIANNUZZI, GIULIANA
GIANNUZZI, GIULIANA
Dipartimento di Bioscienze
The pancancer overexpressed NFYC Antisense 1 controls cell cycle mitotic progression through in cis and in trans modes of action
2024 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
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
2023 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
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts
2022 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
Alpha satellite insertions and the evolutionary landscape of centromeres
2021 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
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
2021 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
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
2021 N. Voisin, R.E. Schnur, S. Douzgou, S.M. Hiatt, C.F. Rustad, N.J. Brown, D.L. Earl, B. Keren, O. Levchenko, S. Geuer, S. Verheyen, D. Johnson, Y.A. Zarate, M. Hancarova, D.J. Amor, E.M. Bebin, J. Blatterer, A. Brusco, G. Cappuccio, J. Charrow, N. Chatron, G.M. Cooper, T. Courtin, E. Dadali, J. Delafontaine, E. Del Giudice, M. Doco, G. Douglas, A. Eisenkolbl, T. Funari, G. Giannuzzi, U. Gruber-Sedlmayr, N. Guex, D. Heron, O.L. Holla, A.C.E. Hurst, J. Juusola, D. Kronn, A. Lavrov, C. Lee, S. Lorrain, E. Merckoll, A. Mikhaleva, J. Norman, S. Pradervand, D. Prchalova, L. Rhodes, V.R. Sanders, Z. Sedlacek, H.A. Seebacher, E.A. Sellars, F. Sirchia, T. Takenouchi, A.J. Tanaka, H. Taska-Tench, E. Tonne, K. Tveten, G. Vitiello, M. Vlckova, T. Uehara, C. Nava, B. Yalcin, K. Kosaki, D. Donnai, S. Mundlos, N. Brunetti-Pierri, W.K. Chung, A. Reymond
Alpha satellite insertion close to an ancestral centromeric region
2021 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
The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms
2020 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. Portnoã¯, F. Prieur, M. Rio, J. Siffroi, S. Valence, J.C. Taylor, A.O.M. Wilkie, P. Edery, A. Reymond, D. Sanlaville, C. Schluth-Bolard
Evolutionary dynamics of the POTE gene family in human and nonhuman primates
2020 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
Chromatin three-dimensional interactions mediate genetic effects on gene expression
2019 O. Delaneau, M. Zazhytska, C. Borel, G. Giannuzzi, G. Rey, C. Howald, S. Kumar, H. Ongen, K. Popadin, D. Marbach, G. Ambrosini, D. Bielser, D. Hacker, L. Romano, P. Ribaux, M. Wiederkehr, E. Falconnet, P. Bucher, S. Bergmann, S. Antonarakis, A. Reymond, E. Dermitzakis
The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism patients
2019 G. Giannuzzi, P.J. Schmidt, E. Porcu, G. Willemin, K.M. Munson, X. Nuttle, R. Earl, J. Chrast, K. Hoekzema, D. Risso, K. Männik, P. De Nittis, E.D. Baratz, Y. Herault, X. Gao, C.C. Philpott, R.A. Bernier, Z. Kutalik, M.D. Fleming, E.E. Eichler, A. Reymond
The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism individuals
2019 G. Giannuzzi, P. Schmidt, K. Porcu Männik, P. De Nittis, E. Baratz
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
2018 M. Moysés-Oliveira, G. Giannuzzi, R. Fish, J. Rosenfeld, F. Petit, M. Soares, L. Kulikowski, A. Di-Battista, M. Zamariolli, F. Xia, T. Liehr, N. Kosyakova, G. Carvalheira, M. Parker, E. Seaby, S. Ennis, R. Gilbert, R. Hagelstrom, M. Cremona, W. Li, A. Malhotra, A. Chandrasekhar, D. Perry, R. Taft, J. Mccarrier, D. Basel, J. Andrieux, T. Stumpp, F. Antunes, G. Pereira, M. Neerman-Arbez, V. Meloni, M. Drummond-Borg, M. Melaragno, A. Reymond
Centromere destiny in dicentric chromosomes : New insights from the evolution of human chromosome 2 ancestral centromeric region
2017 G. Chiatante, G. Giannuzzi, F.M. Calabrese, E.E. Eichler, M. Ventura
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs
2017 M. Loviglio, T. Arbogast, A. Jønch, S. Collins, K. Popadin, C. Bonnet, G. Giannuzzi, A. Maillard, S. Jacquemont, B. Yalcin, N. Katsanis, C. Golzio, A. Reymond
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
2017 M. Loviglio, M. Leleu, K. Männik, M. Passeggeri, G. Giannuzzi, I. van der Werf, S. Waszak, M. Zazhytska, I. Roberts-Caldeira, N. Gheldof, E. Migliavacca, A. Alfaiz, L. Hippolyte, A. Maillard, 2.C. 16p11., C. 2p15, A. Van Dijck, R. Kooy, D. Sanlaville, J. Rosenfeld, L. Shaffer, J. Andrieux, C. Marshall, S. Scherer, Y. Shen, J. Gusella, U. Thorsteinsdottir, G. Thorleifsson, E. Dermitzakis, B. Deplancke, J. Beckmann, J. Rougemont, S. Jacquemont, A. Reymond
Inter-varietal structural variation in grapevine genomes
2016 M.F. Cardone, P. D'Addabbo, C. Alkan, C. Bergamini, C.R. Catacchio, F. Anaclerio, G. Chiatante, A. Marra, G. Giannuzzi, R. Perniola, M. Ventura, D. Antonacci
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility
2016 X. Nuttle, G. Giannuzzi, M.H. Duyzend, J.G. Schraiber, I. Narvaiza, P.H. Sudmant, O. Penn, G. Chiatante, M. Malig, J. Huddleston, C. Benner, F. Camponeschi, S. Ciofi Baffoni, H.A.F. Stessman, M.C.N. Marchetto, L. Denman, L. Harshman, C. Baker, A. Raja, K. Penewit, N. Janke, W. Joyce Tang, M. Ventura, L. Banci, F. Antonacci, J.M. Akey, C.T. Amemiya, F.H. Gage, A. Reymond, E.E. Eichler
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology
2015 E. Migliavacca, C. Golzio, K. Männik, I. Blumenthal, E. Oh, L. Harewood, J. Kosmicki, M. Loviglio, G. Giannuzzi, L. Hippolyte, A. Maillard, A. Alfaiz, 2.E.C. 16p11., M. van Haelst, J. Andrieux, J. Gusella, M. Daly, J. Beckmann, S. Jacquemont, M. Talkowski, N. Katsanis, A. Reymond
Novel H3K4me3 marks are enriched at human- and chimpanzee-specific cytogenetic structures
2014 G. Giannuzzi, E. Migliavacca, A. Reymond