ROCCHI, Mariano
 Distribuzione geografica
Continente #
NA - Nord America 21.805
EU - Europa 4.669
AS - Asia 2.235
SA - Sud America 22
AF - Africa 8
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 6
Totale 28.752
Nazione #
US - Stati Uniti d'America 21.777
CN - Cina 1.540
DE - Germania 1.159
SE - Svezia 988
UA - Ucraina 640
SG - Singapore 590
RU - Federazione Russa 491
GB - Regno Unito 450
FI - Finlandia 408
IT - Italia 320
BE - Belgio 50
IE - Irlanda 47
FR - Francia 42
IN - India 41
CA - Canada 23
NL - Olanda 16
BR - Brasile 15
VN - Vietnam 14
HK - Hong Kong 13
CZ - Repubblica Ceca 9
LU - Lussemburgo 7
AU - Australia 6
ES - Italia 6
EU - Europa 6
MX - Messico 5
PL - Polonia 5
RO - Romania 5
TR - Turchia 5
IR - Iran 4
JP - Giappone 4
LT - Lituania 4
AR - Argentina 3
AT - Austria 3
BG - Bulgaria 3
LK - Sri Lanka 3
SA - Arabia Saudita 3
AL - Albania 2
CH - Svizzera 2
DK - Danimarca 2
DZ - Algeria 2
JO - Giordania 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
MA - Marocco 2
NG - Nigeria 2
PH - Filippine 2
PT - Portogallo 2
TH - Thailandia 2
VE - Venezuela 2
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
EC - Ecuador 1
EE - Estonia 1
GE - Georgia 1
GR - Grecia 1
HU - Ungheria 1
ID - Indonesia 1
KE - Kenya 1
KZ - Kazakistan 1
LV - Lettonia 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
OM - Oman 1
PE - Perù 1
SI - Slovenia 1
TN - Tunisia 1
Totale 28.752
Città #
Fairfield 3.644
Woodbridge 2.537
Houston 1.804
Chandler 1.591
Ashburn 1.533
Jacksonville 1.478
Seattle 1.434
Cambridge 1.266
Wilmington 1.188
Ann Arbor 866
Nyköping 696
Singapore 469
Lawrence 386
Roxbury 384
Nanjing 382
Boardman 274
Beijing 263
Des Moines 258
Princeton 225
New York 212
Bari 190
Inglewood 146
San Diego 143
Los Angeles 112
Shenyang 102
Nanchang 101
Brooklyn 93
Dearborn 93
Hebei 88
London 79
Jiaxing 75
Changsha 68
Santa Clara 67
Tianjin 65
Dublin 46
Brussels 45
Falls Church 45
Guangzhou 44
Pune 34
Jinan 32
Helsinki 30
Hefei 29
Kilburn 27
Zhengzhou 24
Ningbo 23
Paris 22
Indiana 19
Redwood City 18
Shanghai 17
Norwalk 16
Tappahannock 16
Washington 16
Kunming 14
Hong Kong 13
Hounslow 13
Taizhou 13
Toronto 13
Auburn Hills 12
Munich 12
Dong Ket 11
Wuhan 11
Prescot 10
Acton 9
Chiswick 9
San Francisco 8
Brno 7
Haikou 7
Islington 7
Shenzhen 7
Strasbourg 7
Cerignola 6
Boydton 5
Chicago 5
Fuzhou 5
Jinhua 5
Milan 5
Phoenix 5
Rome 5
Southwark 5
Waanrode 5
Wandsworth 5
Wuxi 5
Amsterdam 4
Baotou 4
Chengdu 4
Corigliano Calabro 4
Edinburgh 4
Frankfurt am Main 4
Hangzhou 4
Marseille 4
New Bedfont 4
Romola 4
Seelze 4
Berkeley 3
Casoria 3
Catania 3
Chongqing 3
Clifton 3
Hanoi 3
Lanzhou 3
Totale 23.124
Nome #
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 155
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 142
A computational reconstruction of Papio phylogeny using Alu insertion polymorphisms 141
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 137
Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia 135
Molecular cytogenetic study of instability at 1q21∼q32 in adult acute lymphoblastic leukemia 134
Downregulated expression of genes mapping on chromosome 9 in chronic myeloid leukemia cases bearing genomic deletions on der(9) 133
A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11) 131
The 14/15 association as a paradigmatic example of tracing karyotype evolution in New World monkeys 129
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 128
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications 126
The human skeletal muscle glycogenin gene: cDNA, tissue expression and chromosomal localization 126
Evolutionary new centromeres in primates 124
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints 124
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 121
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 120
Insertion of telomeric repeats at intrachromosomal break sites during primate evolution 118
Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia 117
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 117
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma 116
Pericentric chromosome 8 inversion associated with the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases 114
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 113
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 113
Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis 112
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 111
The genome of the vervet (Chlorocebus aethiops sabaeus) 110
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 109
Characterization of chimpanzee-hamster hybrids by chromosome painting 107
null 107
null 106
Inverted duplications: how many of them are mosaic? 106
Epigenetic origin of evolutionary novel centromeres 106
null 106
An analysis of segmental duplications and genome assembly in the mouse 106
"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 105
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 105
Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements 105
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patient 103
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 103
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 103
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs. 103
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 102
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 102
A panel of radiation hybrids and YAC clones specific for human chromosome 5 101
null 100
Preparation of human partial chromosome paints from somatic cell hybrids 100
The common marmoset genome provides insight into primate biology and evolution 100
Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia 99
Cloning and comparative mapping of a human chromosome 4-specific alpha satellite DNA sequence 98
Rapid emergence of independent "chromosomal lineages" in silvered-leaf monkey triggered by Y/autosome translocation 98
Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25 98
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 98
Alu insertion polymorphisms as evidence for population structure in baboons 98
Characterization of a highly repeated DNA sequence family in five species of the genus Eulemur 98
A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbons 97
Evolutionary history of chromosome 20 97
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 97
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 97
The interplay between genome organization and nuclear architecture of primate evolutionary neo-centromeres 96
Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees 96
De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s 96
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) 96
Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data 95
A novel translocation t(14;15)(q32;q24) bearing deletion on der(14) in Philadelphia-positive chronic myeloid leukemia 95
t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring 95
Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini 95
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 94
Papio baboon species indicative Alu elements 94
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2 93
Assignment of the carnitine/acylcarnitine translocase gene (CACT) to human chromosome band 3p21.31 by in situ hybridization 93
A novel type of c-myc translocation in a T lymphoma cell line 93
Establishment and phenotypic characterization of the first human pulmonary blastoma cell line 93
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 92
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 92
Recurrent sites for new centromere seeding 92
MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9) 91
Submicroscopic deletions in an acute myelocytic leukemia case with a four-way t(8;11;16;21) 91
Characterization of der(9) deletions in CML patients 90
Immunohistochemical analysis of cyclin D1 shows deregulated expression in multiple myeloma with the t(11;14) 90
Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago 90
Ordered mapping of three alpha satellite DNA subsets on human chromosome 22 90
A prenatally detected inv dup(15). 90
Progressive proximal expansion of the primate X chromosome centromere 90
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13 89
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database 89
Assignment of the oxoglutarate carrier gene (SLC25A4) to human chromosome 17p13.3 89
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19 89
A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient 89
A genome-wide survey of structural variation between human and chimpanzee 89
Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini RID E-6420-2011 89
Suppression of chimpanzee NORS in hamster/chimpanzee hybrid: report on cell line R48-26 88
Subchromosomal painting libraries (SCPLs) from somatic cell hybrids 88
null 88
X pentasomy: a case and review 88
A novel X-linked member of the human zinc finger protein gene family: isolation mapping and expression 88
Mapping of the Human Voltage-Dependent Anion Channel Isoforms 1 and 2 Reconsidered 88
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 87
Assignment of the human erythrocyte acylphosphatase gene (ACYP1) to chromosome band 14q24.3 87
Reciprocal translocations: a trap for cytogenetists? 87
Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p11.2 duplication 87
Totale 10.328
Categoria #
all - tutte 125.389
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 125.389


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20204.200 0 0 0 0 0 0 1.008 914 1.041 457 557 223
2020/20214.208 418 379 420 312 320 222 340 363 372 601 187 274
2021/20222.945 119 634 13 86 182 180 264 110 154 156 499 548
2022/20234.184 693 310 211 429 565 541 55 489 687 23 89 92
2023/20241.321 151 242 83 97 110 331 40 74 13 25 5 150
2024/20251.464 122 97 512 176 132 415 10 0 0 0 0 0
Totale 28.903