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Mostrati risultati da 1 a 20 di 48
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Evolutionary structural dynamics of macaque chromosome 6 neocentromere 1-gen-2006 Ventura, Mario; Antonacci, Francesca; Cardone, M. F.; Stanyon, R.; D'Addabbo, Pietro; Cellamare, A.; Sprague, L. J.; Eichler, E. E.; Archidiacono, Nicoletta; Rocchi, M.
Evolutionary formation of new centromeres in macaque 1-gen-2007 Ventura, Mario; Antonacci, Francesca; Cardone, Mf; Stanyon, R; D'Addabbo, Pietro; Cellamare, A; Sprague, Lj; Eichler, Ee; Archidiacono, Nicoletta; Rocchi, Mariano
Discovery and characterization of Human/Great-Ape inversion polymorphisms 1-gen-2008 Antonacci, Francesca; Kidd, Jm; Marques Bonet, T; Ventura, Mario; Siswara, P; Jiang, Z; Eichler, E. E.
Mapping and sequencing of structural variation from eight human genomes 1-gen-2008 Kidd, Jm; Cooper, Gm; Donahue, Wf; Hayden, Hs; Sampas, N; Graves, T; Hansen, N; Teague, B; Alkan, C; Antonacci, Francesca; Haugen, E; Zerr, T; Yamada, Na; Tsang, P; Newman, Tl; Tüzün, E; Cheng, Z; Ebling, Hm; Tusneem, N; David, R; Gillett, W; Phelps, Ka; Weaver, M; Saranga, D; Brand, A; Tao, W; Gustafson, E; Mckernan, K; Chen, L; Malig, M; Smith, Jd; Korn, Jm; Mccarroll, Sa; Altshuler, Da; Peiffer, Da; Dorschner, M; Stamatoyannopoulos, J; Schwartz, D; Nickerson, Da; Mullikin, Jc; Wilson, Rk; Bruhn, L; Olson, Mv; Kaul, R; Smith, Dr; Eichler, Ee
Mapping of 5q35 chromosomal rearrangements within a genomically unstable region 1-gen-2008 Buysse, K; Crepel, A; Menten, B; Pattyn, F; Antonacci, Francesca; Veltman, Ja; Larsen, La; Tümer, Z; de Klein, A; van de Laar, I; Devriendt, K; Mortier, G; Speleman, F.
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics 1-gen-2008 Vandesompele, J; Michels, E; De Preter, K; Menten, B; Schramm, A; Eggert, A; Ambros, Pf; Combaret, V; Francotte, N; Antonacci, Francesca; De Paepe, A; Laureys, G; Speleman, F; Van Roy, N.
Evolutionary toggling of the MAPT 17q21.31 inversion region. 1-gen-2008 Zody, Mc; Jiang, Z; Fung, Hc; Antonacci, Francesca; Hillier, Lw; Cardone, Mf; Graves, Ta; Kidd, Jm; Cheng, Z; Abouelleil, A; Chen, L; Wallis, J; Glasscock, J; Wilson, Rk; Reily, Ad; Duckworth, J; Ventura, Mario; Hardy, J; Warren, Wc; Eichler, Ee
Unusual 8p inverted duplication deletion with telomere capture from 8q.(*First two authors contributed equally to this work) 1-gen-2009 Buysse, K; Antonacci, Francesca; Callewaert, B; Loeys, B; Fränkel, U; Siu, V; Mortier, G; Speleman, F; Menten, B.
Programmed loss of millions of base pairs from a vertebrate genome 1-gen-2009 Smith, Jj; Antonacci, Francesca; Eichler, Ee; Amemiya, Ct
New Insights into Centromere Organization and Evolution from the White-cheeked Gibbon and Marmoset 1-gen-2009 Cellamare, A; Catacchio, CLAUDIA RITA; Alkan, C; Giannuzzi, G; Antonacci, Francesca; Cardone, Mf; Della Valle, G; Malig, M; Rocchi, Mariano; Eichler, Ee; Ventura, Mario
Personalized copy number and segmental duplication maps using next-generation sequencing 1-gen-2009 Alkan, C; Kidd, Jm; Marques Bonet, T; Aksay, G; Antonacci, Francesca; Hormozdiari, F; Kitzman, Jo; Baker, C; Malig, M; Mutlu, O; Sahinalp, Sc; Gibbs, Ra; Eichler, Ee
Characterization of six human disease-associated inversion polymorphisms 1-gen-2009 Antonacci, Francesca; Kidd, Jm; Marques Bonet, T; Ventura, Mario; Siswara, P; Jiang, Zs; Eichler, Ee
Death and Resurrection of the Human IRGM Gene 1-gen-2009 Bekpen, C; Marques Bonet, T; Alkan, C; Antonacci, Francesca; Leogrande, Mb; Ventura, Mario; Kidd, Jm; Siswara, P; Howard, Jc; Eichler, Ee
Characterization of missing human genome sequences and copy-number polymorphic insertions 1-gen-2010 Kidd, Jm; Sampas, N; Antonacci, Francesca; Graves, T; Fulton, R; Hayden, Hs; Alkan, C; Malig, M; Ventura, Mario; Giannuzzi, G; Kallicki, J; Anderson, P; Tsalenko, A; Yamada, Na; Tsang, P; Kaul, R; Wilson, Rk; Bruhn, L; Eichler, Ee
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk 1-gen-2010 Antonacci, Francesca; Kidd, Jm; Marques Bonet, T; Teague, B; Ventura, Mario; Girirajan, S; Alkan, C; Campbell, Cd; Vives, L; Malig, M; Rosenfeld, Ja; Ballif, Bc; Shaffer, Lg; Graves, Ta; Wilson, Rk; Schwartz, Dc; Eichler, Ee
Copy Number Variation Analysis in Single-Suture Craniosynostosis: Multiple Rare Variants Including RUNX2 Duplication in Two Cousins With Metopic Craniosynostosis 1-gen-2010 Mefford, Hc; Shafer, N; Antonacci, Francesca; Tsai, Jm; Park, Ss; Hing, Av; Rieder, Mj; Smyth, Md; Speltz, Ml; Eichler, Ee; Cunningham, Ml
Diversity of Human Copy Number Variation and Multicopy Genes. 1-gen-2010 Sudmant, Ph; Kitzman, Jo; Antonacci, Francesca; Alkan, C; Malig, M; Tsalenko, A; Sampas, N; Bruhn, L; Shendure, J; 1000 Genomes, Project; Eichler, Ee
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. 1-gen-2010 Girirajan, S; Rosenfeld, Ja; Cooper, Gm; Antonacci, F; Siswara, P; Itsara, A; Vives, L; Walsh, T; Mccarthy, Se; Baker, C; Mefford, Hc; Kidd, Jm; Browning, Sr; Browning, Bl; Dickel, De; Levy, Dl; Ballif, Bc; Platky, K; Farber, Dm; Gowans, Gc; Wetherbee, Jj; Asamoah, A; Weaver, Dd; Mark, Pr; Dickerson, J; Garg, Bp; Ellingwood, Sa; Smith, R; Banks, Vc; Smith, W; Mcdonald, Mt; Hoo, Jj; French, Bn; Hudson, C; Johnson, Jp; Ozmore, Jr; Moeschler, Jb; Surti, U; Escobar, Lf; El Khechen, D; Gorski, Jl; Kussmann, J; Salbert, B; Lacassie, Y; Biser, A; McDonald McGinn, Dm; Zackai, Eh; Deardorff, Ma; Shaikh, Th; Haan, E; Friend, Kl; Fichera, M; Romano, C; Gécz, J; Delisi, Le; Sebat, J; King, Mc; Shaffer, Lg; Eichler, Ee
Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses 1-gen-2011 Hurle, B; Marques Bonet, T; Antonacci, Francesca; Hughes, I; Ryan, Jf; NISC Comparative Sequencing, Program; Eichler, Ee; Ornitz, Dm; Green, Ed
Genome-wide characterization of centromeric satellites from multiple mammalian genomes. 1-gen-2011 Alkan, C; Cardone, Mf; Catacchio, CLAUDIA RITA; Antonacci, Francesca; O'Brien, Sj; Ryder, Oa; Purgato, S; Zoli, M; Della Valle, G; Eichler, Ee; Ventura, Mario
Mostrati risultati da 1 a 20 di 48
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