IRIS
AMATI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 19.559
EU - Europa 2.942
AS - Asia 603
SA - Sud America 5
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 23.119
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Nazione #
US - Stati Uniti d'America 19.551
DE - Germania 1.091
PL - Polonia 406
UA - Ucraina 257
IT - Italia 244
FR - Francia 210
CN - Cina 170
GB - Regno Unito 165
RU - Federazione Russa 165
KR - Corea 163
IE - Irlanda 159
SG - Singapore 155
SE - Svezia 123
VN - Vietnam 72
FI - Finlandia 58
BE - Belgio 18
CZ - Repubblica Ceca 16
NL - Olanda 10
JP - Giappone 7
KG - Kirghizistan 7
CA - Canada 6
HK - Hong Kong 6
IN - India 6
IR - Iran 6
RO - Romania 5
BR - Brasile 4
DK - Danimarca 4
CH - Svizzera 3
IL - Israele 3
PK - Pakistan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AT - Austria 2
AU - Australia 2
EU - Europa 2
GR - Grecia 2
IQ - Iraq 2
ZA - Sudafrica 2
CL - Cile 1
DM - Dominica 1
EE - Estonia 1
EG - Egitto 1
ES - Italia 1
MX - Messico 1
NO - Norvegia 1
PH - Filippine 1
PT - Portogallo 1
SC - Seychelles 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 23.119
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Città #
Woodbridge 6.297
Wilmington 4.928
Houston 4.722
Fairfield 584
Ann Arbor 514
Kraków 406
Chandler 352
Ashburn 307
Seattle 262
Jacksonville 236
Cambridge 231
Dublin 147
New York 134
Medford 132
Rome 130
Singapore 129
Dearborn 94
Beijing 75
Dong Ket 70
Lawrence 63
Menlo Park 40
Boardman 39
San Diego 31
Mülheim 30
Moscow 25
Milan 24
Santa Clara 22
Zhengzhou 20
Norwalk 19
Redwood City 18
Seoul 16
Nürnberg 15
Brno 14
Brussels 14
Falls Church 14
London 14
Mountain View 14
Daejeon 13
Nanjing 12
Palo Alto 11
Saint Petersburg 10
Guangzhou 9
San Mateo 9
Los Angeles 8
Munich 8
Buffalo 7
Hefei 7
Auburn Hills 6
Jinan 6
Shanghai 6
Verona 6
Kunming 5
University Park 5
Kilburn 4
Mainz 4
Parma 4
San Francisco 4
Toronto 4
Cascina 3
Chicago 3
Detroit 3
Hebei 3
Helsinki 3
Hounslow 3
Islamabad 3
Monza 3
Nuremberg 3
São Paulo 3
Tehran 3
Turin 3
Acton 2
Baghdad 2
Braunschweig 2
Changsha 2
Chengdu 2
Council Bluffs 2
Creede 2
Del Norte 2
Delhi 2
Engelhard 2
Enterprise 2
Esbjerg 2
Florence 2
Fuzhou 2
Gijzenzele 2
Griesstatt 2
Hangzhou 2
Ho Chi Minh City 2
Hong Kong 2
Jena 2
Johannesburg 2
Latina 2
Leawood 2
Noblesville 2
Phoenix 2
Portland 2
San Jose 2
San Marcos 2
Sgurgola 2
Stockholm 2
Totale 20.426
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Nome #
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 507
Gene expression profile study in CFTR mutated bronchial cell lines 488
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 484
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 469
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 467
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 462
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 459
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 451
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 443
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 443
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways 442
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 441
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 441
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 440
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 440
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 438
The search for hemizyosity at 22q11 in patients with isolated cleft palate 434
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 432
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 431
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 429
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 425
Practical guidelines for managing patients with 22q11.2 deletion syndrome. 422
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 420
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 418
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 418
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 418
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 416
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 411
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 411
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 407
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 407
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 403
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome 402
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 398
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome 395
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? 391
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. 383
In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction 379
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. 372
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L) 372
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome 368
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. 367
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) 361
Gene expression analysis during development by high-throughput methods 358
The molecular genetics of the DiGeorge syndrome 356
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome 356
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] 354
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding 349
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 336
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist 332
Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot 324
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies 321
La bioinformatica come strumento per lo studio dell'espressione genica durante lo sviluppo embrionale 314
Advances in molecular analysis of congenital heart defects 291
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 290
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes 241
Epigenetic Modification in Coronary Atherosclerosis 241
Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival 234
Expression profiles of the SARS-CoV-2 host invasion genes in nasopharyngeal and oropharyngeal swabs of COVID-19 patients 150
Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study 51
Low molecular weight heparin -induced miRNA changes in peripheral blood mononuclear cells in pregnancies with unexplained recurrent pregnancy loss 42
An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease 40
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 39
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1 39
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 25
Recenti acquisizioni sulla genetica delle cardiopatie congenite 21
Expression profile of HERVs and inflammatory mediators detected in nasal mucosa as a predictive biomarker of COVID-19 severity 21
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors 15
Downregulation of Circulating Hsa-miR-200c-3p Correlates with Dyslipidemia in Patients with Stable Coronary Artery Disease 12
Le Basi Biologiche 8
Erratum: Mutations of ZFPM2/FOG2 Gene in Sporadic Cases of Tetralogy of Fallot (Human Mutation (2003) 22 (372-377)) 6
Totale 23.371
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Categoria #
all - tutte 42.099
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 42.099
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.124 0 476 445 518 490 594 490 522 442 483 281 383
2020/20213.223 353 375 309 430 268 308 404 316 120 87 131 122
2021/2022734 51 94 31 32 29 86 38 34 60 49 48 182
2022/2023885 83 81 21 129 78 181 54 65 92 5 64 32
2023/2024426 39 14 28 10 35 146 18 23 7 11 11 84
2024/2025247 91 156 0 0 0 0 0 0 0 0 0 0
Totale 23.371