IRIS
ROCCHI, Mariano
 Distribuzione geografica
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Continente #
NA - Nord America 21.806
EU - Europa 4.966
AS - Asia 2.658
SA - Sud America 351
AF - Africa 27
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 6
Totale 29.821
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Nazione #
US - Stati Uniti d'America 21.762
CN - Cina 1.534
DE - Germania 1.180
SE - Svezia 986
SG - Singapore 898
RU - Federazione Russa 740
UA - Ucraina 643
GB - Regno Unito 451
FI - Finlandia 409
IT - Italia 326
BR - Brasile 318
BE - Belgio 50
HK - Hong Kong 50
IE - Irlanda 47
FR - Francia 42
IN - India 42
ID - Indonesia 27
CA - Canada 23
NL - Olanda 18
AT - Austria 15
MX - Messico 14
VN - Vietnam 14
AR - Argentina 10
BD - Bangladesh 10
TR - Turchia 10
CZ - Repubblica Ceca 9
JP - Giappone 8
UZ - Uzbekistan 8
ZA - Sudafrica 8
EC - Ecuador 7
LU - Lussemburgo 7
AU - Australia 6
ES - Italia 6
EU - Europa 6
RO - Romania 6
VE - Venezuela 6
AZ - Azerbaigian 5
IQ - Iraq 5
MA - Marocco 5
PK - Pakistan 5
PL - Polonia 5
IR - Iran 4
JM - Giamaica 4
KE - Kenya 4
LT - Lituania 4
PY - Paraguay 4
SA - Arabia Saudita 4
TN - Tunisia 4
AL - Albania 3
BG - Bulgaria 3
DZ - Algeria 3
JO - Giordania 3
KZ - Kazakistan 3
LK - Sri Lanka 3
NP - Nepal 3
OM - Oman 3
PE - Perù 3
AM - Armenia 2
CH - Svizzera 2
CL - Cile 2
DK - Danimarca 2
GE - Georgia 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
MD - Moldavia 2
NG - Nigeria 2
PH - Filippine 2
PS - Palestinian Territory 2
PT - Portogallo 2
TH - Thailandia 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
EE - Estonia 1
GR - Grecia 1
GT - Guatemala 1
HU - Ungheria 1
KW - Kuwait 1
LV - Lettonia 1
MN - Mongolia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
RS - Serbia 1
SI - Slovenia 1
UY - Uruguay 1
Totale 29.821
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Città #
Fairfield 3.637
Woodbridge 2.532
Houston 1.800
Chandler 1.591
Ashburn 1.528
Jacksonville 1.471
Seattle 1.430
Cambridge 1.263
Wilmington 1.185
Ann Arbor 863
Nyköping 696
Singapore 472
Lawrence 386
Roxbury 384
Nanjing 380
Boardman 274
Beijing 263
Des Moines 258
Princeton 225
New York 212
Bari 190
Inglewood 146
San Diego 142
Los Angeles 116
Shenyang 102
Nanchang 99
Brooklyn 93
Dearborn 93
Hebei 88
London 80
Jiaxing 75
Changsha 68
Santa Clara 67
Tianjin 65
Moscow 57
Hong Kong 49
Dublin 46
Brussels 45
Falls Church 45
Guangzhou 44
Pune 34
Helsinki 32
Jinan 32
Hefei 29
Jakarta 27
Kilburn 27
Ningbo 23
São Paulo 23
Paris 22
Zhengzhou 22
Indiana 19
Nuremberg 19
Redwood City 18
Norwalk 16
Shanghai 16
Tappahannock 16
Washington 16
Kunming 14
Hounslow 13
Taizhou 13
Toronto 13
Auburn Hills 12
Munich 12
Dong Ket 11
Wuhan 11
Prescot 10
Acton 9
Chiswick 9
Council Bluffs 8
San Francisco 8
Tashkent 8
Brno 7
Haikou 7
Islington 7
Rio de Janeiro 7
Rome 7
Shenzhen 7
Strasbourg 7
Vienna 7
Belo Horizonte 6
Cerignola 6
Tokyo 6
Baku 5
Boydton 5
Campinas 5
Chicago 5
Fortaleza 5
Fuzhou 5
Jinhua 5
Mexico City 5
Milan 5
Phoenix 5
Ribeirão Preto 5
Southwark 5
Waanrode 5
Wandsworth 5
Wuxi 5
Amsterdam 4
Baghdad 4
Baotou 4
Totale 23.263
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Nome #
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome 170
Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients 149
A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma 145
A computational reconstruction of Papio phylogeny using Alu insertion polymorphisms 144
A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11) 144
Characterization of a recurrent translocation t(2;3)(p15–22;q26) occurring in acute myeloid leukaemia 140
Molecular cytogenetic study of instability at 1q21∼q32 in adult acute lymphoblastic leukemia 140
Downregulated expression of genes mapping on chromosome 9 in chronic myeloid leukemia cases bearing genomic deletions on der(9) 137
The 14/15 association as a paradigmatic example of tracing karyotype evolution in New World monkeys 137
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene 135
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications 131
A novel chromosomal translocation t(3;7)(q26;q21)in myeloid leukemia resulting in overexpression of EVI1 131
The human skeletal muscle glycogenin gene: cDNA, tissue expression and chromosomal localization 128
Evolutionary new centromeres in primates 125
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints 125
The genome of the vervet (Chlorocebus aethiops sabaeus) 122
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia 121
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma 119
Insertion of telomeric repeats at intrachromosomal break sites during primate evolution 119
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1 119
Molecular cytogenetic findings supporting the evidence of a biclonal origin in acute myeloid leukemia 118
Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma 118
Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis 116
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 115
Pericentric chromosome 8 inversion associated with the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases 115
Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes 114
"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 114
Epigenetic origin of evolutionary novel centromeres 114
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patient 113
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 111
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 110
Rapid emergence of independent "chromosomal lineages" in silvered-leaf monkey triggered by Y/autosome translocation 110
A panel of partial chromosome paints and YAC probes specific for human chromosome 2 109
Inverted duplications: how many of them are mosaic? 109
Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements 109
An analysis of segmental duplications and genome assembly in the mouse 109
Characterization of chimpanzee-hamster hybrids by chromosome painting 108
Alu insertion polymorphisms as evidence for population structure in baboons 108
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs. 107
null 107
A panel of radiation hybrids and YAC clones specific for human chromosome 5 107
null 106
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene 106
null 106
The common marmoset genome provides insight into primate biology and evolution 106
Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia 105
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 105
Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia 104
A novel translocation t(14;15)(q32;q24) bearing deletion on der(14) in Philadelphia-positive chronic myeloid leukemia 104
Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia 104
A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbons 103
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) 103
Papio baboon species indicative Alu elements 103
Preparation of human partial chromosome paints from somatic cell hybrids 102
Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25 102
Characterization of a highly repeated DNA sequence family in five species of the genus Eulemur 101
null 100
Evolutionary history of chromosome 20 100
Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia 100
Cloning and comparative mapping of a human chromosome 4-specific alpha satellite DNA sequence 99
Assignment of the carnitine/acylcarnitine translocase gene (CACT) to human chromosome band 3p21.31 by in situ hybridization 99
A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient 99
Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases 99
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 98
The interplay between genome organization and nuclear architecture of primate evolutionary neo-centromeres 98
Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia 98
Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data 97
Immunohistochemical analysis of cyclin D1 shows deregulated expression in multiple myeloma with the t(11;14) 97
Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees 97
De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s 97
Evolutionary history of chromosome 11 featuring four distinct centromere repositioning events in Catarrhini 97
t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring 96
A genome-wide survey of structural variation between human and chimpanzee 96
CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia 95
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology 95
Evolutionary molecular cytogenetics of catarrhine primates: past, present and future 95
A novel type of c-myc translocation in a T lymphoma cell line 95
Recurrent sites for new centromere seeding 95
Progressive proximal expansion of the primate X chromosome centromere 95
A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization 95
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2 94
Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14) 94
Establishment and phenotypic characterization of the first human pulmonary blastoma cell line 94
Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago 93
MIRN199B downregulation in chronic myeloid leukaemia is associated with deletions on der(9) 93
A human short-chain dehydrogenase/reductase gene: structure, chromosomal localization, tissue expression and subcellular localization of its product 93
Ordered mapping of three alpha satellite DNA subsets on human chromosome 22 92
Assignment of the oxoglutarate carrier gene (SLC25A4) to human chromosome 17p13.3 92
A prenatally detected inv dup(15). 92
X pentasomy: a case and review 92
Submicroscopic deletions in an acute myelocytic leukemia case with a four-way t(8;11;16;21) 92
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19 92
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer 92
Characterization of der(9) deletions in CML patients 91
Suppression of chimpanzee NORS in hamster/chimpanzee hybrid: report on cell line R48-26 91
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13 91
Reciprocal translocations: a trap for cytogenetists? 91
A novel X-linked member of the human zinc finger protein gene family: isolation mapping and expression 91
Genome sequence, comparative analysis, and population genetics of the domestic horse 91
A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative 91
Totale 10.756
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Categoria #
all - tutte 133.285
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 133.285
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.235 0 0 0 0 0 0 0 0 0 456 556 223
2020/20214.195 417 378 419 311 319 222 339 362 371 598 186 273
2021/20222.941 119 634 13 86 181 179 264 110 153 155 499 548
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
2024/20252.597 122 97 512 176 132 415 344 490 237 72 0 0
Totale 29.975