IRIS
NOVELLI, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 137.225
EU - Europa 17.451
AS - Asia 17.407
SA - Sud America 2.619
AF - Africa 263
OC - Oceania 47
Continente sconosciuto - Info sul continente non disponibili 39
Totale 175.051
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Nazione #
US - Stati Uniti d'America 136.732
SG - Singapore 8.173
IT - Italia 3.643
CN - Cina 3.030
DE - Germania 2.775
HK - Hong Kong 2.292
BR - Brasile 2.182
RU - Federazione Russa 2.115
UA - Ucraina 1.695
VN - Vietnam 1.475
PL - Polonia 1.308
FR - Francia 1.307
IE - Irlanda 1.281
GB - Regno Unito 926
SE - Svezia 730
FI - Finlandia 638
JP - Giappone 535
KR - Corea 511
NL - Olanda 298
CA - Canada 268
IN - India 267
ID - Indonesia 162
AR - Argentina 160
BD - Bangladesh 151
AT - Austria 150
MX - Messico 133
BE - Belgio 124
ES - Italia 118
TR - Turchia 110
CZ - Repubblica Ceca 108
ZA - Sudafrica 101
IQ - Iraq 100
KG - Kirghizistan 83
PK - Pakistan 68
UZ - Uzbekistan 61
EC - Ecuador 57
CL - Cile 56
TH - Thailandia 52
PH - Filippine 43
LT - Lituania 41
AU - Australia 40
VE - Venezuela 40
MY - Malesia 38
CO - Colombia 36
PY - Paraguay 35
RO - Romania 32
AE - Emirati Arabi Uniti 31
MA - Marocco 31
SA - Arabia Saudita 31
TN - Tunisia 31
CH - Svizzera 30
IL - Israele 30
JM - Giamaica 26
DZ - Algeria 23
EU - Europa 23
IR - Iran 21
KE - Kenya 21
UY - Uruguay 21
PE - Perù 20
EG - Egitto 19
JO - Giordania 19
NP - Nepal 19
TW - Taiwan 18
KZ - Kazakistan 15
PT - Portogallo 14
A2 - ???statistics.table.value.countryCode.A2??? 13
GR - Grecia 12
AL - Albania 11
BG - Bulgaria 11
DK - Danimarca 11
DO - Repubblica Dominicana 11
LB - Libano 11
NO - Norvegia 11
RS - Serbia 11
AZ - Azerbaigian 9
BO - Bolivia 9
NI - Nicaragua 9
OM - Oman 9
BH - Bahrain 8
CR - Costa Rica 8
HU - Ungheria 6
MK - Macedonia 6
NG - Nigeria 6
SI - Slovenia 6
AO - Angola 5
HN - Honduras 5
KW - Kuwait 5
NZ - Nuova Zelanda 5
AM - Armenia 4
BB - Barbados 4
BY - Bielorussia 4
CG - Congo 4
ET - Etiopia 4
GE - Georgia 4
GT - Guatemala 4
HR - Croazia 4
LV - Lettonia 4
SM - San Marino 4
SV - El Salvador 4
SY - Repubblica araba siriana 4
Totale 174.969
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Città #
Woodbridge 38.594
Wilmington 33.301
Houston 31.088
Singapore 4.484
Fairfield 4.231
Ann Arbor 2.919
Ashburn 2.741
Chandler 2.341
Hong Kong 2.266
San Jose 1.898
Seattle 1.661
Cambridge 1.482
Jacksonville 1.391
Beijing 1.301
Dublin 1.189
Kraków 1.177
Rome 1.067
New York 1.025
Medford 948
Santa Clara 692
Dearborn 685
The Dalles 676
Los Angeles 535
Council Bluffs 477
Tokyo 461
Ho Chi Minh City 449
Lawrence 439
Menlo Park 364
Hanoi 337
Moscow 312
Dallas 295
Buffalo 288
Lauterbourg 273
Milan 262
Boardman 254
San Diego 238
Helsinki 222
Munich 218
São Paulo 217
Zhengzhou 189
Mülheim 166
Chicago 164
London 145
Nuremberg 131
Orem 115
Warsaw 113
Jakarta 110
Engelhard 106
Redwood City 104
Frankfurt am Main 98
Atlanta 91
North Bergen 90
Brussels 89
Montreal 87
Dong Ket 85
Palo Alto 85
Redondo Beach 85
Mountain View 84
Norwalk 83
Toronto 81
Brno 78
Brooklyn 75
Phoenix 74
Rio de Janeiro 73
Denver 71
Vienna 69
Guangzhou 68
Seoul 67
Chennai 66
Johannesburg 66
Nanjing 66
Stockholm 66
Amsterdam 63
Falls Church 63
Da Nang 62
San Francisco 56
Hefei 53
Manchester 53
Belo Horizonte 52
Shanghai 51
Lappeenranta 48
Naples 47
Verona 47
Detroit 46
Poplar 46
San Mateo 46
Boston 45
Haiphong 44
Brasília 43
Mumbai 43
Columbus 42
Tashkent 42
Bangkok 41
University Park 40
Ankara 39
Bari 39
Bologna 39
Kunming 39
Florence 38
Baghdad 36
Totale 147.241
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Nome #
Il doping genetico: ipotesi surreale o inquietante realtà? 1.520
Ku70, Ku80, sClusterin: a “cluster” of predicting factors for neoadjuvant chemoradiotherapy treatment response in patients affected by locally advanced rectal cancer 1.208
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 584
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation 583
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 581
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. 538
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
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 534
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 529
Gonadal mosaicism in hereditary angioedema 529
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 523
Awake thoracoscopic biopsy of interstitial lung disease 522
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 521
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 518
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 512
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 511
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 510
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 510
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 506
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 506
Review of nutrient actions on age-related macular degeneration 504
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain 502
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 502
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 502
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 501
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 500
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 497
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 496
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 496
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 496
Human induced pluripotent stem cells for monogenic disease modelling and therapy 496
Design of a novel LOX-1 receptor antagonist mimicking the natural substrate 495
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer 494
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 493
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 493
null 492
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 490
Functional analysis and molecular dynamics simulation of LOX-1 K167N polymorphism reveal alteration of receptor activity. 488
Age-related macular degeneration: insights into inflammatory genes 488
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 488
Effects of TNF-α and IL-1 β on the activation of genes related to inflammatory, immune responses and cell death in immortalized human HaCat keratinocytes 486
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study 486
Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1 486
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 486
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 486
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 485
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 485
Denaturing HPLC in laboratory diagnosis of hereditary angioedema 485
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 485
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 485
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 484
Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1) 484
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 483
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 482
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 480
Advances in exploring the role of micrornas in inflammatory bowel disease 480
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 479
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 479
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 478
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 477
A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene 477
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 475
Androgen- and insulin-related gene signature using a specific low density oligoarray androchip 2 in peripheral blood mononuclear cells in agonists, recreational athletes and sedentary subjects. 475
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 474
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 474
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 473
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene 472
A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism 472
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 471
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study 471
Association of the G289S single nucleotide polymorphism in the HSD17B3 gene with prostate cancer in Italian men 471
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 470
CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa 470
The search for hemizyosity at 22q11 in patients with isolated cleft palate 469
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) 469
Frequency assessment of 25 SNPs in five different populations 469
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 469
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 468
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13 468
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype 467
Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women 467
Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique 466
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 466
Recent advances in exploring the genetic susceptibility to diabetic neuropathy 466
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 465
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 465
Effects of dutasteride on the expression of genes related to androgen metabolism and related pathway in human prostate cancer cell lines 464
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 464
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 464
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome? 464
Randomized comparison of awake nonresectional versus nonawake resectional lung volume reduction surgery. 464
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 460
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2 459
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients 459
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 458
Molecular dynamics simulation of human LOX-1 provides an explanation for the lack of OxLDL binding to the Trp150Ala mutant. 458
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis 458
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 458
Totale 50.713
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Categoria #
all - tutte 411.316
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 411.316
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.250 0 0 0 0 0 0 0 0 0 0 864 386
2021/20225.242 246 593 216 322 176 585 293 271 442 421 393 1.284
2022/20236.243 613 522 158 788 556 1.344 559 384 569 51 499 200
2023/20244.317 381 361 291 104 1.045 888 121 191 67 112 93 663
2024/202513.590 483 3.125 1.428 855 326 607 1.125 775 1.410 1.165 1.258 1.033
2025/202620.099 1.810 1.090 2.421 1.962 1.920 798 2.644 2.561 2.600 2.124 169 0
Totale 177.126