Pubblicazioni
N.B. viene riportato in rosso a partire dal 2000, l’impact factor : in corsivo <3 , normale >3, in grassetto >6
2008 - 2011
1. Stanyon R, Garofalo F, Steinberg ER, Capozzi O, Di Marco S, Nieves M, Archidiacono N, Mudry
MD: Chromosome painting in two genera of South American monkeys: species Identification, conservation, and management. Cytogenet Genome Res in press (2011) I.F. 1.729
2. 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, Ponting CP, Marques-Bonet T, Alkan C, Chen L, Cheng
Z, Kidd JM, Eichler EE, White S, Searle S, Vilella AJ, Chen Y, Flicek P, Ma J, Raney B, Suh B,
Burhans R, Herrero J, Haussler D, Faria R, Fernando O, Darre F, Farre D, Gazave E, Oliva M,
Navarro A, Roberto R, Capozzi O, Archidiacono N, Valle GD, Purgato S, Rocchi M, Konkel MK,
Walker JA, Ullmer B, Batzer MA, Smit AF, Hubley R, Casola C, Schrider DR, Hahn MW, Quesada V,
Puente XS, Ordonez GR, Lopez-Otin C, Vinar T, Brejova B, Ratan A, Harris RS, Miller W, Kosiol C,
Lawson HA, Taliwal V, Martins AL, Siepel A, Roychoudhury A, Ma X, Degenhardt J, Bustamante
CD, Gutenkunst RN, Mailund T, Dutheil JY, Hobolth A, Schierup MH, Ryder OA, Yoshinaga Y, de
Jong PJ, Weinstock GM, Rogers J, Mardis ER, Gibbs RA, Wilson RK: Comparative and demographic analysis of orang-utan genomes. Nature 469:529-33 (2011) I.F. 34.480
3. Rocchi M, Stanyon R, Archidiacono N: Evolutionary new centromeres in primates. Prog Mol
Subcell Biol 48:103-152 (2009) Chapter
4. 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
5. 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. 3.230
6. 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 research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 16:977-85 (2008) I.F. 3.230
7. 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 research 18:1530-7 (2008)
I.F. 11.342
8. 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. 6.626
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2007 - 2004
9. 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. 29.747
10. 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. 11.224
11. 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. 3.327
12. 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 computational biology 3:1807-18 (2007) I.F. 6.236
13. 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. 1.537

14. 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. 2.919
15. 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. 3.327
16. 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. 6.626
17. Rocchi M, Archidiacono N: Genome plasticity in evolution. The Genomic Basis of Disease,
PStankiewicz and JR Lupski Editors, Humana Press pp:153-165 (2006) Chapter
18. Rocchi M, Archidiacono N, Stanyon R: Ancestral genomes reconstruction: An integrated, multidisciplinary approach is needed. Genome Res 16:1441 –1444 (2006) I.F. 11.342
19. 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
20. 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. 1.537
21. 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. 9.872
22. Locke DP, Jiang Z, Pertz LM, Misceo D, Archidiacono N, Eichler EE: Molecular evolution of the human chromosome 15 pericentromeric region. Cytogenet Genome Res 108:73-82 (2005) I.F.
1.729
23. 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. 34.480
24. Ventura M, Weigl S, Carbone L, Cardone MF, Misceo D, Teti M, D'Addabbo P, Wandall A, Bjorck E, de Jong PJ, She X, Eichler EE, Archidiacono N, Rocchi M: Recurrent sites for new centromere seeding. Genome research 14:1696-703 (2004) I.F. 11.342
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2003 – 2000
25. Eder V, Ventura M, Ianigro M, Teti M, Rocchi M, Archidiacono N: Chromosome 6 phylogeny in primates and centromere repositioning. Molecular biology and evolution 20:1506-12 (2003) I.F.
6.050
26. Horvath JE, Gulden CL, Bailey JA, Yohn C, McPherson JD, Prescott A, Roe BA, de Jong PJ,
Ventura M, Misceo D, Archidiacono N, Zhao S, Schwartz S, Rocchi M, Eichler EE: Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications. Molecular biology and evolution 20:1463-79 (2003) I.F. 6.050
27. Locke DP, Archidiacono N, Misceo D, Cardone MF, Deschamps S, Roe B, Rocchi M, Eichler EE:
Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster.
Genome Biol 4:R50 (2003a) I.F
. 6.626
28. Locke DP, Segraves R, Carbone L, Archidiacono N, Albertson DG, Pinkel D, Eichler EE: Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization. Genome Res 13:347-357 (2003b) I.F. 11.342
29. Misceo D, Ventura M, Eder V, Rocchi M, Archidiacono N: Human chromosome 16 conservation in primates. Chromosome Res 11:323-326 (2003) I.F. 3.230
30. Ruault M, Ventura M, Galtier N, Brun ME, Archidiacono N, Roizes G, De Sario A: BAGE genes generated by juxtacentromeric reshuffling in the Hominidae lineage are under selective pressure.
Genomics 81:391-9 (2003) I.F
. 3.327
31. Ventura M, Mudge JM, Palumbo V, Burn S, Blennow E, Pierluigi M, Giorda R, Zuffardi O,
Archidiacono N, Jackson MS, Rocchi M: Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25. Genome Res 13:2059 –2068 (2003) I.F. 11.342
32. Bailey JA, Yavor AM, Viggiano L, Misceo D, Horvath JE, Archidiacono N, Schwartz S, Rocchi M,
Eichler EE: Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22. Am J Hum Genet 70:83-100 (2002) I.F. 12.303
33. Ballarati L, Piccini I, Carbone L, Archidiacono N, Rollier A, Marozzi A, Meneveri R, Ginelli E: Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats. Gene 296:21-
27 (2002) I.F
. 2.416

34. Boniotto M, Ventura M, Cardone MF, Boaretto F, Archidiacono N, Rocchi M, Crovella S: Localization of a new highly repeated DNA sequence of Lemur cafta (Lemuridae, Strepsirhini). Genome /
National Research Council Canada = Genome / Conseil national de recherches Canada
45:973-6 (2002) I.F. 1.815
35. Carbone L, Ventura M, Tempesta S, Rocchi M, Archidiacono N: Evolutionary history of chromosome
10 in primates. Chromosoma 111:267-272 (2002) I.F
. 4.979
36. Cardone MF, Ventura M, Tempesta S, Rocchi M, Archidiacono N: Analysis of chromosome conservation in Lemur catta studied by chromosome paints and BAC/PAC probes. Chromosoma
111:348-356 (2002) I.F. . 4.979
37. Causio F, Gentile E, Fischetto R, Archidiacono N, Magro N: 47,XX + mar karyotype containing genes from the azoospermia factor region. A case report. The Journal of reproductive medicine
47:575-80 (2002)
38. Crosier M, Viggiano L, Guy J, Misceo D, Stones R, Wei W, Hearn T, Ventura M, Archidiacono N,
Rocchi M, Jackson MS: Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms. Genome Res 12:67-80
(2002) I.F. 11.342
39. Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G, Zagaria A, Jimenez
Velasco A, Heiniger A, Scaravaglio P, Torres Gomez A, Roman Gomez J, Archidiacono N, Banfi S,
Rocchi M: A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation.
Proc Natl Acad Sci U S A 99:9882-9887 (2002) I.F. 9.432
40. Ventura M, Boniotto M, Cardone MF, Fulizio L, Archidiacono N, Rocchi M, Crovella S:
Characterization of a highly repeated DNA sequence family in five species of the genus Eulemur.
Gene 275:305-310 (2001a) I.F. 2.721
41. Ventura M, Archidiacono N, Rocchi M: Centromere emergence in evolution. Genome Res 11:595-
599 (2001b) I.F. 11.342
42. Gianfrancesco F, Sanges R, Esposito T, Tempesta S, Rao E, Rappold G, Archidiacono N, Graves
JA, Forabosco A, D'Urso M: Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. Genome Res 11:2095-100
(2001) I.F. 11.342
43. Eichler EE, Johnson ME, Alkan C, Tuzun E, Sahinalp C, Misceo D, Archidiacono N, Rocchi M:
Divergent origins and concerted expansion of two segmental duplications on chromosome 16. J
Hered 92:462-8 (2001) I.F. 2.052
44. Archidiacono N, Marzella R, Spalluto C, Pennacchia M, Viggiano L, Rocchi M: Preparation of human partial chromosome paints from somatic cell hybrids. Methods Mol Biol 123:3-13 (2000) Chapter
45. Causio F, Canale D, Schonauer LM, Fischetto R, Leonetti T, Archidiacono N: Breakpoint of a Y chromosome pericentric inversion in the DAZ gene area. A case report. J Reprod Med 45:591-4
(2000)
46. Ciccodicola A, D'Esposito M, Esposito T, Gianfrancesco F, Migliaccio C, Miano MG, Matarazzo MR,
Vacca M, Franz A, Cuccurese M, Cocchia M, Curci A, Terracciano A, Torino A, Cocchia S,
Mercadante G, Pannone E, Archidiacono N, Rocchi M, Schlessinger D, D'Urso M: Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region. Hum Mol
Genet 9:395-401 (2000) I.F. 7.386
47. Guy J, Spalluto C, McMurray A, Hearn T, Crosier M, Viggiano L, Miolla V, Archidiacono N, Rocchi M,
Scott C, Lee PA, Sulston J, Rogers J, Bentley D, Jackson MS: Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q. Hum Mol Genet 9:2029-42 (2000) I.F
. 7.386
48. Horvath JE, Viggiano L, Loftus BJ, Adams MD, Archidiacono N, Rocchi M, Eichler EE: Molecular structure and evolution of an alpha satellite/non-alpha satellite junction at 16p11. Hum Mol Genet
9:113-23 (2000) I.F. 7.386
49. Marzella R, Viggiano L, Miolla V, Storlazzi CT, Ricco A, Gentile E, Roberto R, Surace C, Fratello A,
Mancini M, Archidiacono N, Rocchi M: Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes. Genomics 63:307-313 (2000)
I.F. 3.327
50. Muller S, Stanyon R, Finelli P, Archidiacono N, Wienberg J: Molecular cytogenetic dissection of human chromosomes 3 and 21 evolution. Proc Natl Acad Sci U S A 97:206-11 (2000) I.F. 9.432
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1999 - 1996
51. Eichler EE, Archidiacono N, Rocchi M: CAGGG repeats and the pericentromeric duplication of the hominoid genome. Genome Res 9:1048-58 (1999)

52. Fogli A, Giglio S, Arrigo G, Lo Nigro C, Zollo M, Viggiano L, Rocchi M, Archidiacono N, Zuffardi O,
Carrozzo R: Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes. Cytogenet Cell Genet 86:225-32 (1999)
53. Jackson MS, Rocchi M, Thompson G, Hearn T, Crosier M, Guy J, Kirk D, Mulligan L, Ricco A,
Piccininni S, Marzella R, Viggiano L, Archidiacono N: Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations. Hum Mol Genet
8:205-15 (1999)
54. Montefalcone G, Tempesta S, Rocchi M, Archidiacono N: Centromere repositioning. Genome Res
9:1184-8 (1999)
55. Vacca M, Matarazzo MR, Jones J, Spalluto C, Archidiacono N, Ma P, Rocchi M, D'Urso M, Chen
EY, D'Esposito M, Mumm S: Evolution of the X-specific block embedded in the human
Xq21.3/Yp11.1 homology region. Genomics 62:293-6 (1999)
56. Viggiano L, Miolla V, Ricco A, Storlazzi CT, Pennacchia M, Fratello A, Mancini M, Marzella R,
Archidiacono N, Rocchi M: Molecular cytogenetic resources specific for chromosome 12. Am J Med
Genet 87:40-4 (1999)
57. Viggiano L, Marzella R, Ricco AS, Storlazzi TC, Fratello A, Varella-Garcia M, Archidiacono N,
Rocchi M: A panel of partial chromosome paints and YAC probes specific for human chromosome 2.
Somat Cell Mol Genet 24:13-21 (1998)
58. Panarello C, Rosanda C, Morerio C, Russo I, Dallorso S, Gambini C, Ricco AS, Storlazzi T,
Archidiacono N, Rocchi M: Lipoblastoma: a case with t(7;8)(q31;q13). Cancer Genet Cytogenet
102:12-4 (1998)
59. de Capoa A, Di Leandro M, Grappelli C, Menendez F, Poggesi I, Giancotti P, Marotta MR, Spano A,
Rocchi M, Archidiacono N, Niveleau A: Computer-assisted analysis of methylation status of individual interphase nuclei in human cultured cells. Cytometry 31:85-92 (1998)
60. Archidiacono N, Storlazzi CT, Spalluto C, Ricco AS, Marzella R, Rocchi M: Evolution of chromosome
Y in primates. Chromosoma 107:241-6 (1998)
61. Zelante L, Dallapiccola B, Calvano S, Memeo E, Gasparini P, Simi P, Rossi S, Finelli P, Rocchi M,
Archidiacono N: Two mosaic-YY males carrying asymmetric Y chromosomes. Clin Genet 51:65-8
(1997)
62. Rocchi M, Storlazzi CT, Marzella R, Ricco AS, Archidiacono N: Evolution of chromosome Y in primates. Eur J Histochem 41 Suppl 2:181-2 (1997)
63. Marzella R, Viggiano L, Ricco AS, Tanzariello A, Fratello A, Archidiacono N, Rocchi M: A panel of radiation hybrids and YAC clones specific for human chromosome 5. Cytogenet Cell Genet 77:232-
7 (1997a)
64. Marzella R, Kokkinaki MA, Kapsetaki M, Ricco A, Argyrokastritis A, Kamakari S, Sarafidou T,
Archidiacono N, Roussou A, Pasparaki A, Rocchi M, Moschonas NK: Map integration at human chromosome 10: molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map. Cytogenet Cell Genet 79:257-
65 (1997b)
65. D'Esposito M, Matarazzo MR, Ciccodicola A, Strazzullo M, Mazzarella R, Quaderi NA, Fujiwara H,
Ko MS, Rowe LB, Ricco A, Archidiacono N, Rocchi M, Schlessinger D, D'Urso M: Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region. Hum Mol Genet 6:1917-23 (1997)
66. Villa A, Strina D, Frattini A, Faranda S, Macchi P, Finelli P, Bozzi F, Susani L, Archidiacono N,
Rocchi M, Vezzoni P: The ZNF75 zinc finger gene subfamily: isolation and mapping of the four members in humans and great apes. Genomics 35:312-20 (1996)
67. Nelis E, Van Broeckhoven C, De Jonghe P, Lofgren A, Vandenberghe A, Latour P, Le Guern E,
Brice A, Mostacciuolo ML, Schiavon F, Palau F, Bort S, Upadhyaya M, Rocchi M, Archidiacono N,
Mandich P, Bellone E, Silander K, Savontaus ML, Navon R, Goldberg-Stern H, Estivill X, Volpini V,
Friedl W, Gal A, et al.: Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. Eur J
Hum Genet 4:25-33 (1996)
68. Muller S, Koehler U, Weinberg J, Marzella R, Finelli P, Antonacci R, Rocchi M, Archidiacono N:
Comparative fluorescence in situ hybridization mapping of primate chromosomes with Alu polymerase chain reaction generated probes from human/rodent somatic cell hybrids. Chromosome
Res 4:38-42 (1996)
69. Meroni G, Franco B, Archidiacono N, Messali S, Andolfi G, Rocchi M, Ballabio A: Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region. Hum Mol Genet 5:423-31 (1996)
70. Finelli P, Antonacci R, Marzella R, Lonoce A, Archidiacono N, Rocchi M: Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19. Genomics
38:325-30 (1996)

71. Casula L, Archidiacono N, Grazia Pau M, Addis M, Mura R, Galanello R, Biddau P, Cao A, Nucaro
A: Cytogenetic and molecular characterization of a variant translocation associated with acute promyelocytic leukemia and involving chromosomes 11, 15 and 17. Leukemia 10:1655-7 (1996)
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1995 - 1992
72. Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R,
Finelli P, Archidiacono N, et al.: Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication. Muscle Nerve 18:628-35 (1995)
73. Archidiacono N, Antonacci R, Marzella R, Finelli P, Lonoce A, Rocchi M: Comparative mapping of human alphoid sequences in great apes using fluorescence in situ hybridization. Genomics 25:477-
84 (1995)
74. Antonacci R, Rocchi M, Archidiacono N, Baldini A: Ordered mapping of three alpha satellite DNA subsets on human chromosome 22. Chromosome Res 3:124-7 (1995a)
75. Antonacci R, Marzella R, Finelli P, Lonoce A, Forabosco A, Archidiacono N, Rocchi M: A panel of subchromosomal painting libraries representing over 300 regions of the human genome. Cytogenet
Cell Genet 68:25-32 (1995b)
76. Uncini A, Di Muzio A, Chiavaroli F, Gambi D, Sabatelli M, Archidiacono N, Antonacci R, Marzella R,
Rocchi M: Hereditary motor and sensory neuropathy with calf hypertrophy is associated with
17p11.2 duplication. Ann Neurol 35:552-8 (1994)
77. Rocchi M, Archidiacono N, Antonacci R, Finelli P, D'Aiuto L, Carbone R, Lindsay E, Baldini A:
Cloning and comparative mapping of recently evolved human chromosome 22-specific alpha satellite DNA. Somat Cell Mol Genet 20:443-8 (1994)
78. Gariboldi M, Maestrini E, Canzian F, Manenti G, De Gregorio L, Rivella S, Chatterjee A, Herman GE,
Archidiacono N, Antonacci R, et al.: Comparative mapping of the actin-binding protein 280 genes in human and mouse. Genomics 21:428-30 (1994)
79. Archidiacono N, Marzella R, Finelli P, Antonacci R, Jones C, Rocchi M: Characterization of chimpanzee-hamster hybrids by chromosome painting. Somat Cell Mol Genet 20:439-42 (1994a)
80. Archidiacono N, Antonacci R, Forabosco A, Rocchi M: Preparation of human chromosomal painting probes from somatic cell hybrids. Methods Mol Biol 33:1-13 (1994b)
81. Antonacci R, Colombo I, Archidiacono N, Volta M, DiDonato S, Finocchiaro G, Rocchi M:
Assignment of the gene encoding the beta-subunit of the electron-transfer flavoprotein (ETFB) to human chromosome 19q13.3. Genomics 19:177-9 (1994)
82. D'Aiuto L, Antonacci R, Marzella R, Archidiacono N, Rocchi M: Cloning and comparative mapping of a human chromosome 4-specific alpha satellite DNA sequence. Genomics 18:230-5 (1993)
83. Marino M, Archidiacono N, Franze A, Rosati M, Rocchi M, Ballabio A, Grimaldi G: A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression. Mamm
Genome 4:252-7 (1993)
84. Meneveri R, Agresti A, Marozzi A, Saccone S, Rocchi M, Archidiacono N, Corneo G, Della Valle G,
Ginelli E: Molecular organization and chromosomal location of human GC-rich heterochromatic blocks. Gene 123:227-34 (1993)
85. Daniele A, Altruda F, Ferrone M, Silengo L, Romeo G, Archidiacono N, Rocchi M: Mapping of human hexokinase 1 gene to 10q11----qter. Hum Hered 42:107-10 (1992) 2
86. Baldini A, Archidiacono N, Carbone R, Bolino A, Shridhar V, Miller OJ, Miller DA, Ward DC, Rocchi
M: Isolation and comparative mapping of a human chromosome 20-specific alpha-satellite DNA clone. Cytogenet Cell Genet 59:12-6 (1992)
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1991 - 1988
87. Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G: Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations. Hum
Genet 86:604-6 (1991)
88. Cianchetti C, Sannio-Fancello G, Fratta AL, Manconi F, Orano A, Pischedda MP, Pruna D, Spinicci
G, Archidiacono N, Filippi G: Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families. Am J Med Genet 40:234-43 (1991)
89. Franze A, Archidiacono N, Rocchi M, Marino M, Grimaldi G: Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome. Genomics 9:728-
36 (1991)
90. Rocchi M, Archidiacono N, Romeo G, Saginati M, Zardi L: Assignment of the gene for human tenascin to the region q32-q34 of chromosome 9. Hum Genet 86:621-3 (1991a)

91. Rocchi M, Archidiacono N, Ward DC, Baldini A: A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization. Genomics 9:517-
23 (1991)
92. Zunino A, Arena G, Rossi O, Archidiacono N, Rocchi M, Romeo G, Abbondandolo A: Chromosomal assignment of human O6-methylguanine-DNA-methyltransferase gene by hamster-human somatic cell hybrids. Mutagenesis 6:395-7 (1991)
93. Wei S, Rocchi M, Archidiacono N, Sacchi N, Romeo G, Gatti RA: Physical mapping of the human chromosome 11q23 region containing the ataxia-telangiectasia locus. Cancer Genet Cytogenet
46:1-8 (1990)
94. Rocchi M, Baldini A, Archidiacono N, Lainwala S, Miller OJ, Miller DA: Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone. Genomics 8:705-9 (1990)
95. Rocchi M, Archidiacono N, Rinaldi A, Filippi G, Bartolucci G, Fancello GS, Siniscalco M: Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivationdependent effect. Am J Hum Genet 46:738-43 (1990)
96. Maestrini E, Rivella S, Tribioli C, Purtilo D, Rocchi M, Archidiacono N, Toniolo D: Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28.
Genomics 8:664-70 (1990)
97. Baldini A, Rocchi M, Archidiacono N, Miller OJ, Miller DA: A human alpha satellite DNA subset specific for chromosome 12. Am J Hum Genet 46:784-8 (1990)
98. Ceccherini I, Lituania M, Cordone MS, Perfumo F, Gusmano R, Callea F, Archidiacono N, Romeo G:
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks. Prenat Diagn 9:751-8 (1989)
99. Cammarata S, Archidiacono N, Romeo G, Benassi G, Guarino M, D'Alessandro R: Prevalence of mental retardation related to fragile X syndrome and other chromosomal abnormalities in the
Republic of San Marino. Dev Med Child Neurol 30:646-9 (1988)
100. de Capoa A, Felli MP, Baldini A, Rocchi M, Archidiacono N, Aleixandre C, Miller OJ, Miller DA:
Relationship between the number and function of human ribosomal genes. Hum Genet 79:301-4
(1988)
101. Romeo G, Devoto M, Archidiacono N, Ferlini A, Roncuzzi L, Melis MA, Paderi E, Ferrari M, Tedeschi
S, Galluzzi G, et al.: Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies. Eur J Pediatr 147:412-5 (1988) 4
102. Rocchi M, Archidiacono N, Filippi G: X-linked mental retardation. I. Martin-Bell syndrome (report of
18 families). J Genet Hum 35:351-79 (1987)
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1987 - 1984
103. Purrello M, Alhadeff B, Whittington E, Buckton KE, Daniel A, Arnaud P, Rocchi M, Archidiacono N,
Filippi G, Siniscalco M: Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Cytogenet Cell Genet
44:32-40 (1987)
104. Furst D, Nave R, Osborn M, Weber K, Bardosi A, Archidiacono N, Ferro M, Romano V, Romeo G:
Nebulin and titin expression in Duchenne muscular dystrophy appears normal. FEBS Lett 224:49-53
(1987)
105. Archidiacono N, Rocchi M, Rinaldi A, Filippi G: X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families). J Genet Hum 35:381-98 (1987) 5
106. de Capoa A, Marlekaj P, Baldini A, Felli MP, Rocchi M, Archidiacono N, Cianfarani S, Spadoni GL,
Boscherini B: Growth hormone-induced regulation of rRNA gene activity in human cultured cells.
Horm Metab Res 18:574-5 (1986)
107. Rocchi M, Roncuzzi L, Santamaria R, Archidiacono N, Dente L, Romeo G: Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1acid glycoprotein to chromosome 9. Hum Genet 74:30-3 (1986)
108. Romeo G, Archidiacono N, Ferlini A, Rocchi M: Rett syndrome: lack of association with fragile site
Xp22 and strategy for genetic mapping of X-linked new mutations. Am J Med Genet Suppl 1:355-9
(1986)
109. Rocchi M, Pecile V, Archidiacono N, Monni G, Dumez Y, Filippi G: Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes. Prenat Diagn
5:229-31 (1985)
110. Dracopoli NC, Rettig WJ, Albino AP, Esposito D, Archidiacono N, Rocchi M, Siniscalco M, Old LJ:
Genes controlling gp25/30 cell-surface molecules map to chromosomes X and Y and escape Xinactivation. Am J Hum Genet 37:199-207 (1985)
111. de Capoa A, Marlekaj P, Baldini A, Rocchi M, Archidiacono N: Cytologic demonstration of differential activity of rRNA gene clusters in different human tissues. Hum Genet 69:212-7 (1985)

112. de Capoa A, Marlekaj P, Baldini A, Archidiacono N, Rocchi M: The transcriptional activity of individual ribosomal DNA gene clusters is modulated by serum concentration. J Cell Sci 74:21-35
(1985)
113. de Capoa A, Baldini A, Marlekaj P, Natoli C, Rocchi M, Archidiacono N, Cianfarani S, Spadoni GL,
Boscherini B: Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs.
Cell Biol Int Rep 9:791-6 (1985)
114. Archidiacono N, Rett A, Rocchi M, Rolando S, Lugaresi E, Romeo G: Rett syndrome and fragile site in Xp22. Lancet 2:1242-3 (1985)
115. Archidiacono N, Pecile V, Rocchi M, Dalpra L, Nocera G, Simoni G: A rare non-heterochromatic 9p+ variant in two amniotic fluid cell cultures. Prenat Diagn 4:231-3 (1984)
116. Pecile V, Archidiacono N, Rocchi M: Treated glass coverslips for in situ culture of amniotic cells: better cell adhesion and growth than on plastic. J Med Genet 21:136-7 (1984a) 2
117. Pecile V, Archidiacono N, Rustico MA, Fiscella C, Rocchi M: A prenatally detected inv dup(15). Am
J Med Genet 18:751-3 (1984)
118. Rocchi M, Cigui I, Archidiacono N, Pecile V, Porcelli G, Filippi G: A young girl with ring(18) mosaicism: cytogenetic studies and PEP A mapping. Clin Genet 26:156-60 (1984)
119. Szabo P, Purrello M, Rocchi M, Archidiacono N, Alhadeff B, Filippi G, Toniolo D, Martini G, Luzzatto
L, Siniscalco M: Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site. Proc Natl Acad Sci
U S A 81:7855-9 (1984)
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1983 - 1974
120. Filippi G, Rinaldi A, Archidiacono N, Rocchi M, Balazs I, Siniscalco M: Brief report: linkage between
G6PD and fragile-X syndrome. Am J Med Genet 15:113-9 (1983 )
121. Filippi G, Pecile V, Archidiacono N, Baragino E, Auber G, Rocchi M: X chromosome replication patterns in a case of X;9 balanced translocation. J Med Genet 20:467-8 (1983)
122. Mostacci C, Ferraro M, Pelliccia F, Archidiacono N, Rocchi M, de Capoa A: Characterization of normal and rearranged human chromosomes by simultaneous Q- and R-banding with chromomycin
A3. Cytogenet Cell Genet 28:3-9 (1980)
123. Rocchi M, Stormi M, Archidiacono N, Filippi G: Extra small metacentric chromosome identified as i(18p). J Med Genet 16:69-73 (1979a) 1
124. Rocchi M, Archidiacono N, Magnani I, Rossella F: [Family studies in cases of pericentric inversion of chromosome 9]. Pathologica 71:404-5 (1979)
125. Rinaldi A, Archidiacono N, Rocchi M, Filippi G: Additional pedigree supporting the frequent origin of
XXYY from consecutive meiotic non-disjunction in paternal gametogenesis. J Med Genet 16:225-6
(1979)
126. Archidiacono N, Tecilazich D, Tonini G, Rocchi M, Filippi G: Trisomy 20p from maternal t(3;20) translocation. J Med Genet 16:229-32 (1979)
127. Archidiacono N, Rocchi M, Valente M, Filippi G: X pentasomy: a case and review. Hum Genet
52:69-77 (1979)
128. Rocchi M, Ferraro M, Archidiacono N, Pelliccia F, Valenti C, De Capoa A: A new translocation involving chromosomes no. 5 and no. 12 t(5;12) (5q15;12p13). J Genet Hum 25:135-9 (1977) 2
129. Ferraro M, Archidiacono N, Pelliccia F, Rocchi M, Rocchi A, de Capoa A: Secondary constrictions and nucleolus organizer regions in man. Exp Cell Res 104:428-30 (1977)
130. Archidiacono N, de Capoa A, Ferraro M, Pelliccia F, Rocchi A, Rocchi M: Nucleolus organizer and
N-band distribution in morphologic and fluorescence variants of human chromosomes. Hum Genet
37:285-9 (1977)
131. de Capoa A, Ferraro M, Archidiacono N, Pelliccia F, Rocchi M, Rocchi A: Nucleolus organizer and satellite association in a variant D-group chromosome. Hum Genet 34:13-6 (1976)
132. Rocchi A, Gigliani F, de Capoa A, Archidiacono N: Labelling of human chromosomes with 3H-AMD.
Humangenetik 24:297-301 (1974)