IRIS
AMATI, FRANCESCA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 22.157
EU - Europa 3.710
AS - Asia 2.283
SA - Sud America 355
Continente sconosciuto - Info sul continente non disponibili 301
AF - Africa 41
OC - Oceania 9
Totale 28.856
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 22.057
DE - Germania 1.165
SG - Singapore 979
IT - Italia 437
CN - Cina 433
PL - Polonia 428
RU - Federazione Russa 381
BR - Brasile 282
VN - Vietnam 264
UA - Ucraina 262
FR - Francia 256
GB - Regno Unito 214
KR - Corea 165
IE - Irlanda 163
SE - Svezia 143
HK - Hong Kong 131
FI - Finlandia 114
JP - Giappone 65
BD - Bangladesh 62
CA - Canada 54
NL - Olanda 47
IN - India 34
ID - Indonesia 25
AR - Argentina 22
BE - Belgio 21
MX - Messico 21
IQ - Iraq 20
ZA - Sudafrica 20
PK - Pakistan 18
CZ - Repubblica Ceca 16
TR - Turchia 15
AT - Austria 13
CL - Cile 13
EC - Ecuador 11
ES - Italia 11
LT - Lituania 11
CO - Colombia 9
TW - Taiwan 9
AU - Australia 8
KG - Kirghizistan 8
JM - Giamaica 7
RO - Romania 7
CH - Svizzera 6
IL - Israele 6
IR - Iran 6
KE - Kenya 6
UZ - Uzbekistan 6
VE - Venezuela 6
DK - Danimarca 5
KZ - Kazakistan 5
MY - Malesia 5
PH - Filippine 5
TH - Thailandia 5
AE - Emirati Arabi Uniti 4
PE - Perù 4
SA - Arabia Saudita 4
AL - Albania 3
BO - Bolivia 3
EG - Egitto 3
HN - Honduras 3
MA - Marocco 3
NP - Nepal 3
PY - Paraguay 3
A2 - ???statistics.table.value.countryCode.A2??? 2
CG - Congo 2
CR - Costa Rica 2
EU - Europa 2
GT - Guatemala 2
NG - Nigeria 2
NI - Nicaragua 2
PT - Portogallo 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
CI - Costa d'Avorio 1
CU - Cuba 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GD - Grenada 1
GR - Grecia 1
GY - Guiana 1
HR - Croazia 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MQ - Martinica 1
NO - Norvegia 1
PR - Porto Rico 1
PW - Palau 1
SC - Seychelles 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
UY - Uruguay 1
Totale 28.561
Salva come PNG Salva come JPEG
Città #
Woodbridge 6.298
Wilmington 4.929
Houston 4.732
Ashburn 647
Singapore 586
Fairfield 584
Ann Arbor 515
Kraków 406
Chandler 352
San Jose 289
Seattle 268
Jacksonville 237
Cambridge 231
Rome 189
New York 183
Beijing 180
Council Bluffs 159
Dublin 149
Medford 132
Hong Kong 127
Santa Clara 102
Dearborn 95
Los Angeles 91
The Dalles 89
Ho Chi Minh City 71
Dong Ket 70
Lawrence 63
Tokyo 56
Dallas 53
Chicago 52
Helsinki 48
Boardman 42
Buffalo 41
Milan 41
Moscow 41
Menlo Park 40
Hanoi 36
Munich 35
San Diego 34
São Paulo 33
Lauterbourg 30
Mülheim 29
Denver 24
Phoenix 23
London 21
Zhengzhou 21
Orem 20
Norwalk 19
Nuremberg 18
Redwood City 18
Seoul 18
Atlanta 17
Brussels 17
Frankfurt am Main 17
Jakarta 17
Columbus 16
North Bergen 16
Nürnberg 15
Warsaw 15
Falls Church 14
Guangzhou 14
Mountain View 14
Brno 13
Daejeon 13
Johannesburg 13
Nanjing 13
San Francisco 13
Brooklyn 12
Miami 12
Montreal 12
Toronto 12
Brasília 11
Palo Alto 11
Chennai 10
Redondo Beach 10
Saint Petersburg 10
Haiphong 9
Rio de Janeiro 9
San Mateo 9
Stockholm 9
Detroit 8
Jinan 8
Manchester 8
Salt Lake City 8
Turin 8
Turku 8
Vienna 8
Amsterdam 7
Belo Horizonte 7
Hefei 7
Kingston 7
Philadelphia 7
Poplar 7
Shanghai 7
Tampa 7
Verona 7
Auburn Hills 6
Baghdad 6
Biên Hòa 6
Boston 6
Totale 23.083
Salva come PNG Salva come JPEG
Nome #
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 604
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 594
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 588
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 555
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 553
Gene expression profile study in CFTR mutated bronchial cell lines 545
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 540
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 534
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 533
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 524
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 522
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 522
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 521
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 521
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 518
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways 516
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 514
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 512
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 507
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 499
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 491
Practical guidelines for managing patients with 22q11.2 deletion syndrome. 490
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 490
The search for hemizyosity at 22q11 in patients with isolated cleft palate 483
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 483
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 483
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 478
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 478
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 476
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. 474
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 474
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 473
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 465
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 457
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? 457
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. 456
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. 449
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) 449
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome 447
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L) 444
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome 442
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome 439
In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction 432
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 420
The molecular genetics of the DiGeorge syndrome 415
Gene expression analysis during development by high-throughput methods 413
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding 409
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist 408
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies 397
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] 386
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 385
La bioinformatica come strumento per lo studio dell'espressione genica durante lo sviluppo embrionale 383
Advances in molecular analysis of congenital heart defects 375
Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot 373
Epigenetic Modification in Coronary Atherosclerosis 356
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 354
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival 343
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes 319
Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients 258
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease 249
Expression profile of HERVs and inflammatory mediators detected in nasal mucosa as a predictive biomarker of COVID-19 severity 174
Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome 142
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1 134
Low molecular weight heparin -induced miRNA changes in peripheral blood mononuclear cells in pregnancies with unexplained recurrent pregnancy loss 133
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 130
Downregulation of circulating hsa-miR-200c-3p correlates with dyslipidemia in patients with stable coronary artery disease 122
Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 119
Recenti acquisizioni sulla genetica delle cardiopatie congenite 68
Erratum: Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot (Human Mutation (2003) 22 (372-377)) 61
Le Basi Biologiche 54
A gene expression study suggests the possible involvement of IGF2BP2-related ncRNA network in Type 2 Diabetes 44
Totale 28.856
Salva come PNG Salva come JPEG
Categoria #
all - tutte 64.394
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 64.394
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022558 0 0 0 32 29 86 38 34 60 49 48 182
2022/2023874 83 81 21 129 78 181 54 57 92 5 62 31
2023/2024414 38 13 27 8 33 143 18 23 7 11 11 82
2024/20251.688 90 343 169 89 78 78 89 134 175 227 130 86
2025/20262.897 217 160 305 299 290 155 343 312 302 269 141 104
2026/20271.170 122 179 547 322 0 0 0 0 0 0 0 0
Totale 28.856