The information published in this page are entirely managed by GIULIANA GIANNUZZI who is completely responsible for it.
Giuliana Giannuzzi obtained a PhD in Genetics and Molecular Evolution from the University of Bari, Italy in 2010. During her PhD, she spent one year as visiting scientist at the University of Washington, Seattle. She did a postdoc at the University of Lausanne and Swiss Institute of Bioinformatics (2012-2020). She joined the Italian National Research Council as Researcher in 2020.
Interest areas:
Human Genetics, Cytogenetics, Genomics
Contacts
Phone: (+39) 02 26422705
International Ids
Orcid ID: 0000-0002-4030-0601
Research products
Maggiolini, Flavia Angela Maria; Mercuri, Ludovica; Antonacci, Francesca; Anaclerio, Fabio; Calabrese, Francesco Maria; Lorusso, Nicola; L'Abbate, Alberto; Sorensen, Melanie; Giannuzzi, Giuliana; Eichler, Evan E.; Catacchio, Claudia Rita; Ventura, Mario
Evolutionary Dynamics of the POTE Gene Family in Human and Nonhuman Primates
(2020) in Genes (Basel)
Giannuzzi, Giuliana; Schmidt, Paul J.; Porcu, Eleonora; Willemin, Gilles; Munson, Katherine M.; Nuttle, Xander; Earl, Rachel; Chrast, Jacqueline; Hoekzema, Kendra; Risso, Davide; Mannik, Katrin; De Nittis, Pasquelena; Baratz, Ethan D.; Herault, Yann; Gao, Xiang; Philpott, Caroline C.; Bernier, Raphael A.; Kutalik, Zoltan; Fleming, Mark D.; Eichler, Evan E.; Reymond, Alexandre; Attanasio, Catia; De Nittis, Pasquelena; Martin, Sandra; Jacquemont, Sebastien; Bottani, Armand; Gerard, Marion; Weber, Sacha; Jacquette, Aurelia; Lesne, Fabien; Isidor, Bertrand; Le Caignec, Cedric; Nizon, Mathilde; Vincent-Delorme, Catherine; Gilbert-Dussardier, Brigitte; Curro, Aurora; Renieri, Alessandra; Giachino, Daniela; Brusco, Alfredo; Reymond, Alexandre
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals
(2019) in American journal of human genetics
Delaneau, O.; Zazhytska, M.; Borel, C.; Giannuzzi, G.; Rey, G.; Howald, C.; Kumar, S.; Ongen, H.; Popadin, K.; Marbach, D.; Ambrosini, G.; Bielser, D.; Hacker, D.; Romano, L.; Ribaux, P.; Wiederkehr, M.; Falconnet, E.; Bucher, P.; Bergmann, S.; Antonarakis, S. E.; Reymond, A.; Dermitzakis, E. T.
yyy HUMAN GENOMICS Chromatin three-dimensional interactions mediate genetic effects on gene expression
(2019) in Science (N. Y., N.Y.)
Moyses-Oliveira, Mariana; Giannuzzi, Giuliana; Fish, Richard J.; Rosenfeld, Jill A.; Petit, Florence; Soares, Maria de Fatima; Kulikowski, Leslie Domenici; Di-Battista, Adriana; Zamariolli, Malu; Xia, Fan; Liehr, Thomas; Kosyakova, Nadezda; Carvalheira, Gianna; Parker, Michael; Seaby, Eleanor G.; Ennis, Sarah; Gilbert, Rodney D.; Hagelstrom, R. Tanner; Cremona, Maria L.; Li, Wenhui L.; Malhotra, Alka; Chandrasekhar, Anjana; Perry, Denise L.; Taft, Ryan J.; McCarrier, Julie; Basel, Donald G.; Andrieux, Joris; Stumpp, Taiza; Antunes, Fernanda; Pereira, Gustavo Jose; Neerman-Arbez, Marguerite; Meloni, Vera Ayres; Drummond-Borg, Margaret; Melaragno, Maria Isabel; Reymond, Alexandre
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
(2018) in Human mutation
Loviglio, Maria Nicla; Arbogast, Thomas; Jonch, Aia Elise; Collins, Stephan C.; Popadin, Konstantin; Bonnet, Camille S.; Giannuzzi, Giuliana; Maillard, Anne M.; Jacquemont, Sebastien; Yalcin, Binnaz; Katsanis, Nicholas; Golzio, Christelle; Reymond, Alexandre
The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs
(2017) in American journal of human genetics
Loviglio, M. N.; Leleu, M.; Maennik, K.; Passeggeri, M.; Giannuzzi, G.; van der Werf, I.; Waszak, S. M.; Zazhytska, M.; Roberts-Caldeira, I.; Gheldof, N.; Migliavacca, E.; Alfaiz, A. A.; Hippolyte, L.; Maillard, A. M.; Van Dijck, A.; Kooy, R. F.; Sanlaville, D.; Rosenfeld, J. A.; Shaffer, L. G.; Andrieux, J.; Marshall, C.; Scherer, S. W.; Shen, Y.; Gusella, J. F.; Thorsteinsdottir, U.; Thorleifsson, G.; Dermitzakis, E. T.; Deplancke, B.; Beckmann, J. S.; Rougemont, J.; Jacquemont, S.; Reymond, A.
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
(2017) in Molecular psychiatry
Chiatante, Giorgia; Giannuzzi, Giuliana; Calabrese, Francesco Maria; Eichler, Evan E.; Ventura, Mario
Centromere Destiny in Dicentric Chromosomes: New Insights from the Evolution of Human Chromosome 2 Ancestral Centromeric Region
(2017) in Molecular biology and evolution
Nuttle, Xander; Giannuzzi, Giuliana; Duyzend, Michael H.; Schraiber, Joshua G.; Narvaiza, Inigo; Sudmant, Peter H.; Penn, Osnat; Chiatante, Giorgia; Malig, Maika; Huddleston, John; Benner, Chris; Camponeschi, Francesca; Ciofi-Baffoni, Simone; Stessman, Holly A. F.; Marchetto, Maria C. N.; Denman, Laura; Harshman, Lana; Baker, Carl; Raja, Archana; Penewit, Kelsi; Janke, Nicolette; Tang, W. Joyce; Ventura, Mario; Banci, Lucia; Antonacci, Francesca; Akey, Joshua M.; Amemiya, Chris T.; Gage, Fred H.; Reymond, Alexandre; Eichler, Evan E.
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility
(2016) in Nature (Lond.)
Cardone, Maria Francesca; D'Addabbo, Pietro; Alkan, Can; Bergamini, Carlo; Catacchio, Claudia Rita; Anaclerio, Fabio; Chiatante, Giorgia; Marra, Annamaria; Giannuzzi, Giuliana; Perniola, Rocco; Ventura, Mario; Antonacci, Donato
Inter-varietal structural variation in grapevine genomes
(2016) in Plant journal (Print)
Migliavacca, Eugenia; Golzio, Christelle; Maennik, Katrin; Blumenthal, Ian; Oh, Edwin C.; Harewood, Louise; Kosmicki, Jack A.; Loviglio, Maria Nicla; Giannuzzi, Giuliana; Hippolyte, Loyse; Maillard, Anne M.; Alfaiz, Ali Abdullah; van Haelst, Mieke M.; Andrieux, Joris; Gusella, James F.; Daly, Mark J.; Beckmann, Jacques S.; Jacquemont, Sebastien; Talkowski, Michael E.; Katsanis, Nicholas; Reymond, Alexandre
A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology
(2015) in American journal of human genetics