<"79">Camerlingo R, Franco R, Tirino V, Cantile M, Rocchi M, La Rocca A, Martucci N, Botti G, Rocco G, Pirozzi G: Establishment and phenotypic characterization of the first human pulmonary blastoma cell line. Lung Cancer (2011) I.F. 3.140

<"80">Locke DP, Hillier LW, Warren WC, Worley KC, Nazareth LV, Muzny DM, Yang SP, Wang Z, Chinwalla AT, Minx P, Mitreva M, Cook L, Delehaunty KD, Fronick C, Schmidt H, Fulton LA, Fulton RS, Nelson JO, Magrini V, Pohl C, Graves TA, Markovic C, Cree A, Dinh HH, Hume J, Kovar CL, Fowler GR, Lunter G, Meader S, Heger A, et al.: Comparative and demographic analysis of orang-utan genomes. Nature 469:529-33 (2011) I.F. 34.480

<"75">Albano F, Anelli L, Zagaria A, Coccaro N, Casieri P, Rossi AR, Vicari L, Liso V, Rocchi M, Specchia G: Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements. Mol Cancer 9:120 (2010) I.F. 4.160

<"76">Albano F, Anelli L, Zagaria A, Coccaro N, D'Addabbo P, Liso V, Rocchi M, Specchia G: Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia. Oncogene 29:2509-2516 (2010) I.F. 7.135

<"77">Guastadisegni MC, Lonoce A, Impera L, Di Terlizzi F, Fugazza G, Aliano S, Grasso R, Cluzeau T, Raynaud S, Rocchi M, Storlazzi CT: CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia. Leukemia 24:1516-9 (2010) I.F. 8.296

<"78">Storlazzi CT, Lonoce A, Guastadisegni MC, Trombetta D, D'Addabbo P, Daniele G, L'Abbate A, Macchia G, Surace C, Kok K, Ullmann R, Purgato S, Palumbo O, Carella M, Ambros PF, Rocchi M: Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure. Genome Res 20:1198-1206 (2010) I.F. 11.342

Albano F, Anelli L, Zagaria A, Liso V, Rocchi M, Specchia G: MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9). Br J Haematol 144:271-3 (2009) I.F. 4,490

<"64">Albano F, Anelli L, Zagaria A, Pannunzio A, Liso V, Rocchi M, Specchia G: Downregulated expression of genes mapping on chromosome 9 in chronic myeloid leukemia cases bearing genomic deletions on der(9). Leukemia 23:813-816 (2009) I.F. 8.634

<"65">Capozzi O, Purgato S, D'Addabbo P, Archidiacono N, Battaglia P, Baroncini A, Capucci A, Stanyon R, Della Valle G, Rocchi M: Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago. Genome Res 19:778-784 (2009) I.F. 11.342

<"66">Carbone L, D'Addabbo P, Cardone MF, Teti MG, Misceo D, Vessere GM, de Jong PJ, Rocchi M: A satellite-like sequence, representing a "clone gap" in the human genome, was likely involved in the seeding of a novel centromere in macaque. Chromosoma 118:269-277 (2009) I.F. 4.337

<"67">Cellamare A, Catacchio CR, Alkan C, Giannuzzi G, Antonacci F, Cardone MF, Della Valle G, Malig M, Rocchi M, Eichler EE, Ventura M: New insights into centromere organization and evolution from the white-cheeked gibbon and marmoset. Mol Biol Evol 26:1889-1900 (2009) I.F. 9.872

<"68">Costa V, Casamassimi A, Roberto R, Gianfrancesco F, Matarazzo M, D'Urso M, D'Esposito M, Rocchi M, Ciccodicola A: DDX11L: a novel transcript family emerging from human subtelomeric regions. BMC Genomics 10:250 (2009) I.F. 3.926

<"69">Dencic-Fekete M, Dordevic V, Storlazzi CT, Jankovic G, Bogdanovic A, Jovanovic J, Rocchi M, Todoric-Zivanovic B, Strnad M, Gotic M: t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia. Int J Hematol 89:508-512 (2009) I.F. 1.491

<"70">Girirajan S, Chen L, Graves T, Marques-Bonet T, Ventura M, Fronick C, Fulton L, Rocchi M, Fulton RS, Wilson RK, Mardis ER, Eichler EE: Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites. Genome Research 19:178-190 (2009) I.F. 11.342

<"71">Klajn A, Ferrai C, Stucchi L, Prada I, Podini P, Baba T, Rocchi M, Meldolesi J, D'Alessandro R: The rest repression of the neurosecretory phenotype is negatively modulated by BHC80, a protein of the BRAF/HDAC complex. J Neurosci 29:6296-6307 (2009) I.F. 7.178

<"72">Misceo D, Rocchi M, van der Hagen CB, Frengen E: A partial trisomy 1q patient with a deletion 1q22 and an insertion 1(q42q44) into 1q22. Am J Med Genet A 149A:290-293 (2009) I.F. 2.440

<"73">Rocchi M, Stanyon R, Archidiacono N: Evolutionary new centromeres in primates. Prog Mol Subcell Biol 48:103-152 (2009)

<"74">Wade CM, Giulotto E, Sigurdsson S, Zoli M, Gnerre S, Imsland F, Lear TL, Adelson DL, Bailey E, Bellone RR, Blocker H, Distl O, Edgar RC, Garber M, Leeb T, Mauceli E, MacLeod JN, Penedo MC, Raison JM, Sharpe T, Vogel J, Andersson L, Antczak DF, Biagi T, Binns MM, Chowdhary BP, Coleman SJ, Della Valle G, Fryc S, Guerin G, et al.: Genome sequence, comparative analysis, and population genetics of the domestic horse. Science 326:865-867 (2009) I.F. 28.103

<"47">Albano F, Anelli L, Zagaria A, Lonoce A, La Starza R, Liso V, Rocchi M, Specchia G: Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia. Leuk Res 32:347-51 (2008) I.F. 2.561

<"48">Albano F, Pannunzio A, Anelli L, Zagaria A, Liso V, Rocchi M, Specchia G: Genomic and molecular switching in relapsed acute promyelocytic leukemia. Leukemia 22:1469-1472 (2008) I.F. 6.924

<"49">Albano F, Zagaria A, Anelli L, Pannunzio A, Manodoro F, Coccaro N, Russo Rossi A, Liso V, Rocchi M, Specchia G: The double deceit generated by an insertion mechanism in chronic myeloid leukemia with t(9;9;22). Ann Hematol 87:923-926 (2008) I.F. 2.342

<"50">Capozzi O, Purgato S, Verdun di Cantogno L, Grosso E, Ciccone R, Zuffardi O, Della Valle G, Rocchi M: Evolutionary and clinical neocentromeres:  two faces of the same coin? Chromosoma 117:339-344 (2008) I.F. 4.337

<"51">Cardone MF, Jiang Z, D'Addabbo P, Archidiacono N, Rocchi M, Eichler EE, Ventura M: Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication. Genome Biol 9:R28 (2008) I.F. 6.589

<"52">Guastadisegni MC, Lonoce A, Impera L, Albano F, D'Addabbo P, Caruso S, Vasta I, Panagopoulos I, Leszl A, Basso G, Rocchi M, Storlazzi CT: Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation. Mol Cancer 7:80 (2008) I.F. 3.690

<"53">Impera L, Albano F, Lo Cunsolo C, Funes S, Iuzzolino P, Laveder F, Panagopoulos I, Rocchi M, Storlazzi CT: A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma. Oncogene 27:6187-6190 (2008) I.F. 6.440

<"54">Impera L, Albano F, Mancini M, Aventin A, Rocchi M, Storlazzi CT: Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia. Cancer Genet Cytogenet 181:131-137 (2008) I.F. 1.559

<"55">Lomiento M, Jiang Z, D'Addabbo P, Eichler EE, Rocchi M: Evolutionary-new centromeres preferentially emerge within gene deserts. Genome Biol 9:R173 (2008) I.F. 6.589

<"56">Misceo D, Bjorgo K, Ormerod E, Ringen O, Rocchi M, van der Hagen CB, Frengen E: A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient. Am J Med Genet A 146A:3230-3233 (2008) I.F. 2.440

<"57">Misceo D, Capozzi O, Roberto R, Dell'Oglio MP, Rocchi M, Stanyon R, Archidiacono N: Tracking the complex flow of chromosome rearrangements from the Hominoidea ancestor to extant Hylobates and Nomascus gibbons by high-resolution synteny mapping. Genome Res 18:1530-1537 (2008) I.F. 11.342

<"58">Qiu H, Taudien S, Herlyn H, Schmitz J, Zhou Y, Chen G, Roberto R, Rocchi M, Platzer M, Wojnowski L: CYP3 phylogenomics: evidence for positive selection of CYP3A4 and CYP3A7. Pharmacogenet Genomics 18:53-66 (2008) I.F. 4.409

<"59">Roberto R, Misceo D, D'Addabbo P, Archidiacono N, Rocchi M: Refinement of macaque synteny arrangement with respect to the official rheMac2 macaque sequence assembly. Chromosome Res 16:977-985 (2008) I.F. 3.469

<"60">Stanyon R, Rocchi M, Capozzi O, Roberto R, Misceo D, Ventura M, Cardone M, Bigoni F, Archidiacono N: Primate chromosome evolution: ancestral karyotypes, marker order and neocentromeres. Chromosome Res 16:17-39 (2008) I.F. 3.469

<"61">Storlazzi CT, Albano F, Guastadisegni MC, Impera L, Muhlematter D, Meyer-Monard S, Wuillemin W, Rocchi M, Jotterand M: Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia. Blood Cells Mol Dis 40:452-455 (2008) I.F. 2.555

<"62">Surace C, Pedeutour F, Trombetta D, Burel-Vandenbos F, Rocchi M, Storlazzi CT: Episomal amplification of MYCN in a case of medulloblastoma. Virchows Arch 452:491-497 (2008) I.F. 2.029

<"32">Albano F, Anelli L, Zagaria A, Archidiacono N, Liso V, Specchia G, Rocchi M: "Home-brew" FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia. Cancer Genet Cytogenet 174:121-126 (2007) I.F. 1.559

<"34">Alkan C, Ventura M, Archidiacono N, Rocchi M, Sahinalp SC, Eichler EE: Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data. PLoS Comput Biol 3:1807-1818 (2007) I.F. 6.236

<"35">Bodega B, Cardone MF, Muller S, Neusser M, Orzan F, Rossi E, Battaglioli E, Marozzi A, Riva P, Rocchi M, Meneveri R, Ginelli E: Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2). BMC Evol Biol 7:39 (2007) I.F. 4.091

<"36">Bosch N, Caceres M, Cardone MF, Carreras A, Ballana E, Rocchi M, Armengol L, Estivill X: Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events. Hum Mol Genet 16:2572-82 (2007) I.F. 7.806

<"37">Cardone MF, Lomiento M, Teti MG, Misceo D, Roberto R, Capozzi O, D'Addabbo P, Ventura M, Rocchi M, Archidiacono N: Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini. Genomics 90:35-43 (2007) I.F. 3.613

<"38">De Gregori M, Ciccone R, Magini P, Pramparo T, Gimelli S, Messa J, Novara F, Vetro A, Rossi E, Maraschio P, Bonaglia MC, Anichini C, Ferrero GB, Silengo M, Fazzi E, Zatterale A, Fischetto R, Previdere C, Belli S, Turci A, Calabrese G, Bernardi F, Meneghelli E, Riegel M, Rocchi M, Guerneri S, Lalatta F, Zelante L, Romano C, Fichera M, et al.: Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 cases. J Med Genet (2007) I.F. 5.535

<"39">Gibbs RA, Rogers J, Katze MG, Bumgarner R, Weinstock GM, Mardis ER, Remington KA, Strausberg RL, Venter JC, Wilson RK, Batzer MA, Bustamante CD, Eichler EE, Hahn MW, Hardison RC, Makova KD, Miller W, Milosavljevic A, Palermo RE, Siepel A, Sikela JM, Attaway T, Bell S, Bernard KE, Buhay CJ, Chandrabose MN, Dao M, Davis C, Delehaunty KD, Ding Y, et al.: Evolutionary and biomedical insights from the rhesus macaque genome. Science 316:222-234 (2007) I.F. 26.372

<"40">Giorda R, Ciccone R, Gimelli G, Pramparo T, Beri S, Bonaglia MC, Giglio S, Genuardi M, Argente J, Rocchi M, Zuffardi O: Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Hum Mutat 28:459-468 (2007) I.F. 6.273

<"41">Marques-Bonet T, Sanchez-Ruiz J, Armengol L, Khaja R, Bertranpetit J, Rocchi M, Gazave E, Lopez-Bigas N, Navarro A: On the association between chromosomal rearrangements and genic evolution in humans and chimpanzees. Genome Biol 8:R230 (2007) I.F. 6.589

<"42">Minervini CF, Marsano RM, Casieri P, Fanti L, Caizzi R, Pimpinelli S, Rocchi M, Viggiano L: Heterochromatin protein 1 interacts with 5'UTR of transposable element ZAM in a sequence-specific fashion. Gene 393:1-10 (2007) I.F. 2.871

<"43">Roberto R, Capozzi O, Wilson RK, Mardis ER, Lomiento M, Tuzun E, Cheng Z, Mootnick AR, Archidiacono N, Rocchi M, Eichler EE: Molecular refinement of gibbon genome rearrangement. Genome Res 17:249-257 (2007) I.F. 11.342

<"44">Storlazzi CT, Albano F, Dencic-Fekete M, Djordjevic V, Rocchi M: Late-appearing pseudocentric fission event during chronic myeloid leukemia progression. Cancer Genet Cytogenet 174:61-67 (2007) I.F. 1.559

<"45">Storlazzi CT, Albano F, Lo Cunsolo C, Doglioni C, Guastadisegni MC, Impera L, Lonoce A, Funes S, Macri E, Iuzzolino P, Panagopoulos I, Specchia G, Rocchi M: Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma. Leukemia 17:2221-2225 (2007) I.F. 6.924

<"46">Ventura M, Antonacci F, Cardone MF, Stanyon R, D'Addabbo P, Cellamare A, Sprague LJ, Eichler EE, Archidiacono N, Rocchi M: Evolutionary formation of new centromeres in macaque. Science 316:243-246 (2007) I.F. 26.372

<"17">Albano F, Specchia G, Anelli L, Zagaria A, Archidiacono N, Liso V, Rocchi M: Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia. Ann Hematol 85:129-131 (2006) I.F. 2.254

<"18">Blasi P, Palmerio F, Aiello A, Rocchi M, Malaspina P, Novelletto A: SSADH Variation in Primates: Intra- and Interspecific Data on a Gene with a Potential Role in Human Cognitive Functions. J Mol Evol 63:54-68 (2006) I.F. 2.767

<"19">Bodega B, Cardone MF, Rocchi M, Meneveri R, Marozzi A, Ginelli E: The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution. Genomics 88:564-571 (2006) I.F. 3.558

<"20">Carbone L, Nergadze SG, Magnani E, Misceo D, Francesca Cardone M, Roberto R, Bertoni L, Attolini C, Francesca Piras M, de Jong P, Raudsepp T, Chowdhary BP, Guerin G, Archidiacono N, Rocchi M, Giulotto E: Evolutionary movement of centromeres in horse, donkey, and zebra. Genomics 87:777-782 (2006) I.F. 3.558

<"21">Cardone MF, Alonso A, Pazienza M, Ventura M, Montemurro G, Carbone L, de Jong PJ, Stanyon R, D'Addabbo P, Archidiacono N, She X, Eichler EE, Warburton PE, Rocchi M: Independent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigs. Genome Biol 7:R91 (2006) I.F. 7.172

<"22">Ciccone R, Mattina T, Giorda R, Bonaglia MC, Rocchi M, Pramparo T, Zuffardi O: Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture. J Med Genet 43:e19 (2006) I.F. 5.008

<"23">Rocchi M, Archidiacono N: Genome Plasticity in Evolution. The Genomic Basis of Disease, PStankiewicz and JR Lupski Editors, Humana Press  pp:153-165 (2006)

<"24">Rocchi M, Archidiacono N, Stanyon R: Ancestral genomes reconstruction: An integrated, multi-disciplinary approach is needed. Genome Res 16:1441-1444 (2006) I.F. 10.256

<"25">She X, Liu G, Ventura M, Zhao S, Misceo D, Roberto R, Cardone MF, Rocchi M, Green ED, Archidiacono N, Eichler EE: A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. Genome Res 16:576-583 (2006) I.F. 11.342

<"26">Storlazzi CT, Albano F, Locunsolo C, Lonoce A, Funes S, Guastadisegni MC, Cimarosto L, Impera L, D'Addabbo P, Panagopoulos I, Specchia G, Rocchi M: t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene. Leukemia 20:2190-2192 (2006) I.F. 6.146

<"27">Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strombeck B, D'Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Muhlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Sole F, Van Roy N, Johansson B, Rocchi M: MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Hum Mol Genet 15:933-942 (2006) I.F. 8.099

<"28">Todoric-Zivanovic B, Marisavljevic D, Surace C, Cemerikic V, Markovic O, Krtolica K, Tatomirovic Z, Cikota B, Magic Z, Rocchi M: A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1). Cancer Genet Cytogenet 166:180-185 (2006) 2

<"29">Trubia M, Albano F, Cavazzini F, Cambrin GR, Quarta G, Fabbiano F, Ciambelli F, Magro D, M. HJ, Mancini M, Diverio D, Pelicci PG, L. CF, Mecucci C, Specchia G, Rocchi M, Liso V, Cuneo A: Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia. Leukemia 20:48-54 (2006) I.F. 6.146

<"30">Van Roy N, Vandesompele J, Menten B, Nilsson H, De Smet E, Rocchi M, De Paepe A, Pahlman S, Speleman F: Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1. Genes Chromosomes Cancer 45:107-117 (2006) I.F. 3.900

<"31">Zagaria A, Anelli L, Albano F, Vicari L, Schiavone EM, Annunziata M, Pane F, Liso V, Rocchi M, Specchia G: Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia. Cancer Genet Cytogenet 167:97-102 (2006) I.F. 1.544

<"1">Albano F, Specchia G, Anelli L, Liso A, Zagaria A, Santoro A, Mirto S, Liso V, Rocchi M: Submicroscopic deletions in an acute myeloid leukemia case with a four-way t(8;11;16;21). Leuk Res 29:855-8 (2005) I.F. 2.372

<"2">Anelli L, Albano F, Zagaria A, Liso A, Cuneo A, Mancini M, Liso V, Rocchi M, Specchia G: Pericentric chromosome 8 inversion associated with the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases. Ann Hematol 84:245-9 (2005) I.F. 2.193

<"3">Cheng Z, Ventura M, She X, Khaitovich P, Graves T, Osoegawa K, Church D, DeJong P, Wilson RK, Paabo S, Rocchi M, Eichler EE: A genome-wide comparison of recent chimpanzee and human segmental duplications. Nature 437:88-93 (2005) I.F. 29.273

<"4">Ciccone R, Giorda R, Gregato G, Guerrini R, Giglio S, Carrozzo R, Bonaglia MC, Priolo E, Lagana C, Tenconi R, Rocchi M, Pramparo T, Zuffardi O, Rossi E: Reciprocal translocations: a trap for cytogenetists? Hum Genet 117:571-582 (2005) I.F. 4.331

<"5">Consortium, ..., Rocchi M, Archidiacono N, Ventura M, ... Initial sequence of the chimpanzee genome and comparison with the human genome. Nature 437:69-87 (2005) I.F. 29.273

<"6">De Gregori M, Pramparo T, Memo L, Gimelli G, Messa J, Rocchi M, Patricelli MG, Ciccone R, Giorda R, Zuffardi O: Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement? Hum Genet 18:207-213 (2005) I.F. 4.331

<"7">Giambra V, Fruscalzo A, Giufre M, Martinez-Labarga C, Favaro M, Rocchi M, Frezza D: Evolution of human IgH3'EC duplicated structures: both enhancers HS1,2 are polymorphic with variation of transcription factor's consensus sites. Gene 346:105-114 (2005) I.F. 2.694

<"8">Horvath JE, Gulden CL, Vallente RU, Eichler MY, Ventura M, McPherson JD, Graves TA, Wilson RK, Schwartz S, Rocchi M, Eichler EE: Punctuated duplication seeding events during the evolution of human chromosome 2p11. Genome Res 15:914-27 (2005) I.F. 10.139

<"9">Jackson MS, Oliver K, Loveland J, Humphray JS, Dunham I, Rocchi M, Viggiano V, P. Park JP, Hurles M, Santibanez-Koref M: Evidence for widespread reticulate evolution within human duplicons. Am J Hum Genet 77:824-840 (2005) I.F. 12.649

<"10">Marzella R, Carrozzo C, Chiarappa P, Miolla V, Rocchi M: Panels of somatic cell hybrids specific for chimpanzee, gorilla, orangutan, and baboon. Cytogenet Genome Res 108:223-228 (2005) I.F. 2.076

<"11">Misceo D, Cardone MF, Carbone L, D'Addabbo P, de Jong PJ, Rocchi M, Archidiacono N: Evolutionary history of chromosome 20. Mol Biol Evol 22:360-366 (2005) I.F. 6.233

<"12">Newman TL, Tuzun E, Morrison VA, Hayden KE, Ventura M, McGrath SD, Rocchi M, Eichler EE: A genome-wide survey of structural variation between human and chimpanzee. Genome Res 15:1344-1356 (2005) I.F. 11.342

<"13">Pramparo T, Grosso S, Messa J, Zatterale A, Bonaglia MC, Chessa L, Balestri P, Rocchi M, Zuffardi O, Giorda R: Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy. Hum Genet 118:76-81 (2005) I.F. 4.331

<"14">Schueler MG, Dunn JM, Bird CP, Ross MT, Viggiano L, Rocchi M, Willard HF, Green ED: Progressive proximal expansion of the primate X chromosome centromere. Proc Natl Acad Sci U S A 102:10563-10568 (2005) I.F. 10.231

<"15">Specchia G, Albano F, Anelli L, Zagaria A, Liso A, Pannunzio A, Archidiacono N, Liso V, Rocchi M: Molecular cytogenetic study of instability at 1q21 approximately q32 in adult acute lymphoblastic leukemia. Cancer Genet Cytogenet 156:54-58 (2005) I.F. 1.640

<"16">Surace C, Storlazzi CT, Engellau J, Domanski HA, Gustafson P, Panagopoulos I, D'Addabbo P, Rocchi M, Mandahl N, Mertens F: Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma. Virchows Arch 447:869-874 (2005) I.F. 2.224