IRIS
AMATI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 21.083
EU - Europa 3.620
AS - Asia 2.223
SA - Sud America 330
AF - Africa 39
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 6
Totale 27.310
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Nazione #
US - Stati Uniti d'America 21.013
DE - Germania 1.158
SG - Singapore 976
CN - Cina 429
PL - Polonia 425
IT - Italia 387
RU - Federazione Russa 379
BR - Brasile 268
UA - Ucraina 262
VN - Vietnam 261
FR - Francia 255
GB - Regno Unito 205
KR - Corea 165
IE - Irlanda 162
SE - Svezia 133
HK - Hong Kong 130
FI - Finlandia 114
JP - Giappone 64
NL - Olanda 44
CA - Canada 42
IN - India 32
BD - Bangladesh 31
ID - Indonesia 24
BE - Belgio 21
AR - Argentina 20
IQ - Iraq 20
ZA - Sudafrica 19
MX - Messico 17
CZ - Repubblica Ceca 16
PK - Pakistan 16
AT - Austria 13
CL - Cile 13
TR - Turchia 13
ES - Italia 10
LT - Lituania 10
TW - Taiwan 9
AU - Australia 8
KG - Kirghizistan 8
CO - Colombia 7
EC - Ecuador 7
RO - Romania 7
IR - Iran 6
KE - Kenya 6
UZ - Uzbekistan 6
CH - Svizzera 5
IL - Israele 5
DK - Danimarca 4
KZ - Kazakistan 4
MY - Malesia 4
PE - Perù 4
SA - Arabia Saudita 4
VE - Venezuela 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
EG - Egitto 3
JM - Giamaica 3
MA - Marocco 3
NP - Nepal 3
PY - Paraguay 3
TH - Thailandia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BO - Bolivia 2
CG - Congo 2
EU - Europa 2
PH - Filippine 2
PT - Portogallo 2
TN - Tunisia 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
CI - Costa d'Avorio 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GD - Grenada 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
HR - Croazia 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MQ - Martinica 1
NG - Nigeria 1
NI - Nicaragua 1
NO - Norvegia 1
PW - Palau 1
SC - Seychelles 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
UY - Uruguay 1
Totale 27.310
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Città #
Woodbridge 6.298
Wilmington 4.928
Houston 4.729
Singapore 585
Fairfield 584
Ann Arbor 515
Ashburn 437
Kraków 406
Chandler 352
Seattle 264
Jacksonville 237
Cambridge 231
San Jose 219
Rome 181
Beijing 180
New York 173
Dublin 149
Medford 132
Hong Kong 126
Council Bluffs 107
Dearborn 94
The Dalles 88
Santa Clara 81
Los Angeles 79
Ho Chi Minh City 71
Dong Ket 70
Lawrence 63
Tokyo 55
Helsinki 48
Dallas 43
Moscow 41
Menlo Park 40
Boardman 39
Chicago 37
Buffalo 35
Hanoi 35
Munich 35
Milan 32
San Diego 31
Lauterbourg 30
Mülheim 29
São Paulo 29
London 21
Zhengzhou 21
Norwalk 19
Orem 19
Redwood City 18
Seoul 18
Brussels 17
Frankfurt am Main 17
Jakarta 17
Nuremberg 17
Nürnberg 15
Warsaw 15
Falls Church 14
Guangzhou 14
Mountain View 14
Brno 13
Daejeon 13
Nanjing 13
Johannesburg 12
San Francisco 12
Atlanta 11
Columbus 11
Denver 11
Montreal 11
Palo Alto 11
Toronto 11
Chennai 10
Phoenix 10
Redondo Beach 10
Saint Petersburg 10
Brasília 9
Rio de Janeiro 9
San Mateo 9
Stockholm 9
Haiphong 8
Jinan 8
Miami 8
North Bergen 8
Salt Lake City 8
Turku 8
Belo Horizonte 7
Hefei 7
Manchester 7
Poplar 7
Shanghai 7
Vienna 7
Amsterdam 6
Auburn Hills 6
Baghdad 6
Biên Hòa 6
Brooklyn 6
Islamabad 6
Tampa 6
Verona 6
Boston 5
Catania 5
Detroit 5
Elk Grove Village 5
Totale 22.557
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Nome #
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 588
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 576
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 543
Gene expression profile study in CFTR mutated bronchial cell lines 535
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 534
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 531
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 522
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 519
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 516
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 512
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 510
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 506
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 503
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 502
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 498
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways 498
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 497
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 489
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 483
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 478
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 475
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 475
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 475
Practical guidelines for managing patients with 22q11.2 deletion syndrome. 471
The search for hemizyosity at 22q11 in patients with isolated cleft palate 469
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 468
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 466
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 465
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 461
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 461
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 460
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 458
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 449
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. 449
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. 437
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. 436
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? 436
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome 434
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome 433
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) 429
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome 421
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L) 419
In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction 417
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 405
Gene expression analysis during development by high-throughput methods 401
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist 394
The molecular genetics of the DiGeorge syndrome 394
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding 391
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies 379
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] 378
La bioinformatica come strumento per lo studio dell'espressione genica durante lo sviluppo embrionale 370
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 370
Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot 363
Advances in molecular analysis of congenital heart defects 343
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 343
Epigenetic Modification in Coronary Atherosclerosis 336
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival 323
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes 301
Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients 239
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease 213
Expression profile of HERVs and inflammatory mediators detected in nasal mucosa as a predictive biomarker of COVID-19 severity 150
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 118
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1 117
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 115
Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 103
Low molecular weight heparin -induced miRNA changes in peripheral blood mononuclear cells in pregnancies with unexplained recurrent pregnancy loss 99
Downregulation of circulating hsa-miR-200c-3p correlates with dyslipidemia in patients with stable coronary artery disease 90
Recenti acquisizioni sulla genetica delle cardiopatie congenite 53
Erratum: Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot (Human Mutation (2003) 22 (372-377)) 52
Le Basi Biologiche 44
A gene expression study suggests the possible involvement of IGF2BP2-related ncRNA network in Type 2 Diabetes 17
Totale 27.605
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Categoria #
all - tutte 59.489
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 59.489
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021122 0 0 0 0 0 0 0 0 0 0 0 122
2021/2022734 51 94 31 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
2025/20262.816 217 160 305 299 290 155 343 312 302 269 141 23
Totale 27.605