IRIS
AMATI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 21.499
EU - Europa 3.675
AS - Asia 2.275
SA - Sud America 340
Continente sconosciuto - Info sul continente non disponibili 301
AF - Africa 39
OC - Oceania 9
Totale 28.138
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Nazione #
US - Stati Uniti d'America 21.413
DE - Germania 1.159
SG - Singapore 979
CN - Cina 433
IT - Italia 425
PL - Polonia 425
RU - Federazione Russa 381
BR - Brasile 272
UA - Ucraina 262
VN - Vietnam 262
FR - Francia 255
GB - Regno Unito 205
KR - Corea 165
IE - Irlanda 162
SE - Svezia 143
HK - Hong Kong 131
FI - Finlandia 114
JP - Giappone 64
BD - Bangladesh 62
CA - Canada 48
NL - Olanda 46
IN - India 33
ID - Indonesia 25
AR - Argentina 21
BE - Belgio 21
IQ - Iraq 20
MX - Messico 20
ZA - Sudafrica 19
PK - Pakistan 17
CZ - Repubblica Ceca 16
TR - Turchia 15
AT - Austria 13
CL - Cile 13
ES - Italia 11
LT - Lituania 10
CO - Colombia 9
EC - Ecuador 9
TW - Taiwan 9
AU - Australia 8
KG - Kirghizistan 8
RO - Romania 7
IR - Iran 6
KE - Kenya 6
UZ - Uzbekistan 6
CH - Svizzera 5
DK - Danimarca 5
IL - Israele 5
JM - Giamaica 5
KZ - Kazakistan 5
MY - Malesia 5
TH - Thailandia 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
PE - Perù 4
PH - Filippine 4
SA - Arabia Saudita 4
AL - Albania 3
EG - Egitto 3
MA - Marocco 3
NP - Nepal 3
PY - Paraguay 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BO - Bolivia 2
CG - Congo 2
EU - Europa 2
HN - Honduras 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
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GD - Grenada 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HR - Croazia 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MQ - Martinica 1
NG - Nigeria 1
NO - Norvegia 1
PW - Palau 1
SC - Seychelles 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
UY - Uruguay 1
Totale 27.843
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Città #
Woodbridge 6.298
Wilmington 4.929
Houston 4.730
Singapore 586
Fairfield 584
Ann Arbor 515
Ashburn 467
Kraków 406
Chandler 352
San Jose 286
Seattle 267
Jacksonville 237
Cambridge 231
Rome 184
New York 181
Beijing 180
Council Bluffs 159
Dublin 149
Medford 132
Hong Kong 127
Dearborn 94
The Dalles 89
Santa Clara 88
Los Angeles 86
Ho Chi Minh City 71
Dong Ket 70
Lawrence 63
Tokyo 55
Dallas 51
Helsinki 48
Buffalo 41
Moscow 41
Menlo Park 40
Milan 40
Boardman 39
Chicago 38
Hanoi 35
Munich 35
San Diego 34
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
Columbus 16
Phoenix 16
Nürnberg 15
Warsaw 15
Falls Church 14
Guangzhou 14
Mountain View 14
Atlanta 13
Brno 13
Daejeon 13
Nanjing 13
Denver 12
Johannesburg 12
Montreal 12
San Francisco 12
Miami 11
Palo Alto 11
Toronto 11
Chennai 10
North Bergen 10
Redondo Beach 10
Saint Petersburg 10
Brasília 9
Haiphong 9
Rio de Janeiro 9
San Mateo 9
Stockholm 9
Brooklyn 8
Detroit 8
Jinan 8
Salt Lake City 8
Turku 8
Amsterdam 7
Belo Horizonte 7
Hefei 7
Manchester 7
Poplar 7
Shanghai 7
Tampa 7
Turin 7
Verona 7
Vienna 7
Auburn Hills 6
Baghdad 6
Biên Hòa 6
Boston 6
Islamabad 6
Pittsburgh 6
Totale 22.798
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Nome #
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 595
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 582
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 578
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 542
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 539
Gene expression profile study in CFTR mutated bronchial cell lines 538
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 529
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 524
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 523
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 519
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 517
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 511
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 510
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 509
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways 509
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 508
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 503
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 498
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 491
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 485
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 481
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 479
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 479
Practical guidelines for managing patients with 22q11.2 deletion syndrome. 476
The search for hemizyosity at 22q11 in patients with isolated cleft palate 474
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 472
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 469
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 469
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 469
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 468
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 467
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 460
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. 459
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 452
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? 447
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. 446
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. 442
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome 439
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) 437
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome 435
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome 426
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L) 426
In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction 420
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 411
Gene expression analysis during development by high-throughput methods 408
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding 401
The molecular genetics of the DiGeorge syndrome 400
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist 398
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies 384
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] 380
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 378
La bioinformatica come strumento per lo studio dell'espressione genica durante lo sviluppo embrionale 376
Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot 367
Advances in molecular analysis of congenital heart defects 349
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 347
Epigenetic Modification in Coronary Atherosclerosis 342
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival 329
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes 314
Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients 251
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease 242
Expression profile of HERVs and inflammatory mediators detected in nasal mucosa as a predictive biomarker of COVID-19 severity 159
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 132
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1 121
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 120
Downregulation of circulating hsa-miR-200c-3p correlates with dyslipidemia in patients with stable coronary artery disease 116
Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 111
Low molecular weight heparin -induced miRNA changes in peripheral blood mononuclear cells in pregnancies with unexplained recurrent pregnancy loss 107
Recenti acquisizioni sulla genetica delle cardiopatie congenite 56
Erratum: Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot (Human Mutation (2003) 22 (372-377)) 56
Le Basi Biologiche 50
A gene expression study suggests the possible involvement of IGF2BP2-related ncRNA network in Type 2 Diabetes 31
Totale 28.138
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Categoria #
all - tutte 62.393
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 62.393
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022589 0 0 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
2025/20262.897 217 160 305 299 290 155 343 312 302 269 141 104
2026/2027452 122 179 151 0 0 0 0 0 0 0 0 0
Totale 28.138