Giuliana Giannuzzi

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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

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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