ROCCHI, Mariano
 Distribuzione geografica
Continente #
NA - Nord America 21.511
EU - Europa 4.292
AS - Asia 1.652
SA - Sud America 9
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 6
Totale 27.482
Nazione #
US - Stati Uniti d'America 21.493
CN - Cina 1.488
DE - Germania 1.154
SE - Svezia 988
UA - Ucraina 640
GB - Regno Unito 441
FI - Finlandia 402
IT - Italia 300
RU - Federazione Russa 172
SG - Singapore 75
BE - Belgio 49
IE - Irlanda 46
FR - Francia 42
IN - India 41
CA - Canada 16
VN - Vietnam 14
NL - Olanda 12
CZ - Repubblica Ceca 8
LU - Lussemburgo 7
EU - Europa 6
AU - Australia 5
ES - Italia 5
RO - Romania 5
BR - Brasile 4
HK - Hong Kong 4
IR - Iran 4
AR - Argentina 3
AT - Austria 3
BG - Bulgaria 3
JP - Giappone 3
PL - Polonia 3
SA - Arabia Saudita 3
TR - Turchia 3
CH - Svizzera 2
DZ - Algeria 2
JO - Giordania 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
LK - Sri Lanka 2
MX - Messico 2
PH - Filippine 2
TH - Thailandia 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
DK - Danimarca 1
EE - Estonia 1
GE - Georgia 1
GR - Grecia 1
HU - Ungheria 1
ID - Indonesia 1
KE - Kenya 1
KZ - Kazakistan 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
NG - Nigeria 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PE - Perù 1
PT - Portogallo 1
SI - Slovenia 1
TN - Tunisia 1
VE - Venezuela 1
Totale 27.482
Città #
Fairfield 3.644
Woodbridge 2.537
Houston 1.804
Chandler 1.591
Ashburn 1.532
Jacksonville 1.478
Seattle 1.434
Cambridge 1.266
Wilmington 1.188
Ann Arbor 866
Nyköping 696
Lawrence 386
Roxbury 384
Nanjing 381
Beijing 258
Des Moines 258
Boardman 251
Princeton 225
New York 212
Bari 189
Inglewood 146
San Diego 143
Los Angeles 111
Shenyang 102
Nanchang 101
Brooklyn 93
Dearborn 93
Hebei 88
Jiaxing 75
London 73
Changsha 67
Tianjin 65
Singapore 47
Dublin 45
Falls Church 45
Brussels 44
Guangzhou 41
Pune 34
Jinan 31
Hefei 28
Kilburn 27
Helsinki 24
Ningbo 23
Zhengzhou 23
Paris 22
Indiana 19
Redwood City 18
Shanghai 17
Norwalk 16
Tappahannock 16
Washington 16
Kunming 14
Hounslow 13
Taizhou 13
Auburn Hills 12
Munich 12
Dong Ket 11
Wuhan 11
Prescot 10
Acton 9
Chiswick 9
Toronto 9
San Francisco 8
Brno 7
Haikou 7
Islington 7
Strasbourg 7
Cerignola 6
Shenzhen 6
Boydton 5
Chicago 5
Fuzhou 5
Jinhua 5
Milan 5
Southwark 5
Waanrode 5
Wandsworth 5
Wuxi 5
Baotou 4
Corigliano Calabro 4
Edinburgh 4
Hangzhou 4
Hong Kong 4
Marseille 4
New Bedfont 4
Phoenix 4
Seelze 4
Berkeley 3
Catania 3
Chengdu 3
Chongqing 3
Hanoi 3
Leawood 3
Montreal 3
Parma 3
Rome 3
San Mateo 3
Sofia 3
Trani 3
Triggiano 3
Totale 22.564
Nome #
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 147
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 136
Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia 132
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 132
Molecular cytogenetic study of instability at 1q21∼q32 in adult acute lymphoblastic leukemia 131
Downregulated expression of genes mapping on chromosome 9 in chronic myeloid leukemia cases bearing genomic deletions on der(9) 128
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 126
The 14/15 association as a paradigmatic example of tracing karyotype evolution in New World monkeys 125
A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11) 125
The human skeletal muscle glycogenin gene: cDNA, tissue expression and chromosomal localization 121
Evolutionary new centromeres in primates 120
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications 118
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints 117
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 117
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 115
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 115
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma 112
Pericentric chromosome 8 inversion associated with the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases 112
Insertion of telomeric repeats at intrachromosomal break sites during primate evolution 111
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 111
Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia 111
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 110
Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis 108
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 107
null 107
The genome of the vervet (Chlorocebus aethiops sabaeus) 107
null 106
A computational reconstruction of Papio phylogeny using Alu insertion polymorphisms 105
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 105
Characterization of chimpanzee-hamster hybrids by chromosome painting 104
Inverted duplications: how many of them are mosaic? 102
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 102
Epigenetic origin of evolutionary novel centromeres 102
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 101
Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements 101
An analysis of segmental duplications and genome assembly in the mouse 101
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patient 100
null 100
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs. 100
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 100
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 99
"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 99
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 98
Preparation of human partial chromosome paints from somatic cell hybrids 98
The comparative genomics and complex population history of Papio baboons 98
Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia 97
Cloning and comparative mapping of a human chromosome 4-specific alpha satellite DNA sequence 96
Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25 96
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 96
Evolutionary history of chromosome 20 95
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 95
The common marmoset genome provides insight into primate biology and evolution 95
Rapid emergence of independent "chromosomal lineages" in silvered-leaf monkey triggered by Y/autosome translocation 94
The interplay between genome organization and nuclear architecture of primate evolutionary neo-centromeres 93
A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbons 93
De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s 93
Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data 92
Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees 92
t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring 92
A panel of radiation hybrids and YAC clones specific for human chromosome 5 92
Characterization of a highly repeated DNA sequence family in five species of the genus Eulemur 92
Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini 91
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) 91
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 90
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 90
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 90
A novel type of c-myc translocation in a T lymphoma cell line 90
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 90
Establishment and phenotypic characterization of the first human pulmonary blastoma cell line 90
Alu insertion polymorphisms as evidence for population structure in baboons 90
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2 89
A novel translocation t(14;15)(q32;q24) bearing deletion on der(14) in Philadelphia-positive chronic myeloid leukemia 89
Immunohistochemical analysis of cyclin D1 shows deregulated expression in multiple myeloma with the t(11;14) 88
Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago 88
Ordered mapping of three alpha satellite DNA subsets on human chromosome 22 88
MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9) 88
Assignment of the carnitine/acylcarnitine translocase gene (CACT) to human chromosome band 3p21.31 by in situ hybridization 88
null 88
Submicroscopic deletions in an acute myelocytic leukemia case with a four-way t(8;11;16;21) 88
Recurrent sites for new centromere seeding 88
Suppression of chimpanzee NORS in hamster/chimpanzee hybrid: report on cell line R48-26 87
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19 87
Papio baboon species indicative Alu elements 87
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13 86
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags database 86
Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p11.2 duplication 86
A prenatally detected inv dup(15). 86
A genome-wide survey of structural variation between human and chimpanzee 86
Characterization of der(9) deletions in CML patients 85
Assignment of the oxoglutarate carrier gene (SLC25A4) to human chromosome 17p13.3 85
A novel X-linked member of the human zinc finger protein gene family: isolation mapping and expression 85
Evolutionary molecular cytogenetics of catarrhine primates: past, present and future 85
Mapping of the Human Voltage-Dependent Anion Channel Isoforms 1 and 2 Reconsidered 85
Progressive proximal expansion of the primate X chromosome centromere 85
Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini RID E-6420-2011 85
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome 84
Assignment of the human erythrocyte acylphosphatase gene (ACYP1) to chromosome band 14q24.3 84
Subchromosomal painting libraries (SCPLs) from somatic cell hybrids 84
Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia 84
Tracking the complex flow of chromosome rearrangements from the Hominoidea Ancestor to extant Hylobates and Nomascus Gibbons by high-resolution synteny mapping 84
Totale 9.925
Categoria #
all - tutte 112.719
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 112.719


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207.143 0 471 283 775 835 579 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
2024/2025191 122 69 0 0 0 0 0 0 0 0 0 0
Totale 27.630