Sfoglia per Autore
New insights into centromere organization and evolution from the white-cheeked gibbon and marmoset
2009 A. Cellamare, C. Catacchio, C. Alkan, G. Giannuzzi, F. Antonacci, M. Cardone, G. Della Valle, M. Malig, M. Rocchi, E. Eichler, M. Ventura
Characterization of Missing Human Genome Sequences and Copy-number Polymorphic Insertions
2010 J. Kidd, N. Sampas, F. Antonacci, T. Graves, R. Fulton, H. Hayden, C. Alkan, M. Malig, M. Ventura, G. Giannuzzi, J. Kallicki, P. Anderson, A. Tsalenko, N. Yamada, P. Tsang, R. Kaul, R. Wilson, L. Bruhn, E. Eichler
Analysis of high-identity segmental duplications in the grapevine genome
2011 G. Giannuzzi, P. D'Addabbo, M. Gasparro, M. Martinelli, F. Carelli, D. Antonacci, M. Ventura
Centromere Evolution: Digging into Mammalian Primary Constriction
2012 G. Giannuzzi, C. Catacchio, M. Ventura
Read-depth Methodology for the Analysis of Recent Segmental Duplications in the Grapevine Genome
2013 G. Giannuzzi, M. Cardone, M. Ventura, D. Antonacci
Hominoid fission of chromosome 14/15 and the role of segmental duplications
2013 G. Giannuzzi, M. Pazienza, J. Huddleston, F. Antonacci, M. Malig, L. Vives, E. Eichler, M. Ventura
Evolutionary dynamism of the primate LRRC37 gene family
2013 G. Giannuzzi, P. Siswara, M. Malig, C. Bekpen, T. Marques-Bonet, P. NISC Comparative Sequencing, J. Mullikin, M. Ventura, E. Eichler
Novel H3K4me3 marks are enriched at human- and chimpanzee-specific cytogenetic structures
2014 G. Giannuzzi, E. Migliavacca, A. Reymond
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
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
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
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
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
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
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
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
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