IRIS
NOVELLI, GIUSEPPE
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 133.281
EU - Europa 15.058
AS - Asia 13.810
SA - Sud America 2.419
AF - Africa 193
Continente sconosciuto - Info sul continente non disponibili 38
OC - Oceania 23
Totale 164.822
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 132.933
SG - Singapore 6.899
IT - Italia 3.164
DE - Germania 2.705
CN - Cina 2.444
HK - Hong Kong 2.203
BR - Brasile 2.059
UA - Ucraina 1.688
PL - Polonia 1.298
IE - Irlanda 1.267
RU - Federazione Russa 1.020
FR - Francia 969
GB - Regno Unito 861
VN - Vietnam 705
SE - Svezia 695
FI - Finlandia 506
KR - Corea 500
NL - Olanda 250
CA - Canada 189
IN - India 177
AR - Argentina 144
AT - Austria 143
JP - Giappone 139
BE - Belgio 121
MX - Messico 115
ID - Indonesia 111
CZ - Repubblica Ceca 102
BD - Bangladesh 97
TR - Turchia 88
ZA - Sudafrica 88
ES - Italia 84
KG - Kirghizistan 83
IQ - Iraq 68
UZ - Uzbekistan 46
PK - Pakistan 45
CL - Cile 44
EC - Ecuador 43
LT - Lituania 37
PY - Paraguay 32
RO - Romania 28
AE - Emirati Arabi Uniti 26
VE - Venezuela 26
CH - Svizzera 25
CO - Colombia 25
IL - Israele 25
MA - Marocco 25
EU - Europa 23
IR - Iran 20
TN - Tunisia 19
UY - Uruguay 18
AU - Australia 17
EG - Egitto 17
PE - Perù 17
SA - Arabia Saudita 15
MY - Malesia 14
A2 - ???statistics.table.value.countryCode.A2??? 13
JO - Giordania 13
KZ - Kazakistan 13
TW - Taiwan 13
DZ - Algeria 11
GR - Grecia 11
JM - Giamaica 11
KE - Kenya 10
NO - Norvegia 10
PT - Portogallo 10
AL - Albania 9
BG - Bulgaria 9
DK - Danimarca 9
PH - Filippine 9
BO - Bolivia 8
DO - Repubblica Dominicana 8
LB - Libano 8
AZ - Azerbaigian 7
BH - Bahrain 7
OM - Oman 7
MK - Macedonia 6
NP - Nepal 6
CR - Costa Rica 5
HU - Ungheria 5
TH - Thailandia 5
AO - Angola 4
GE - Georgia 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
RS - Serbia 4
SM - San Marino 4
AM - Armenia 3
ET - Etiopia 3
GY - Guiana 3
SC - Seychelles 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BY - Bielorussia 2
CG - Congo 2
CU - Cuba 2
EE - Estonia 2
GA - Gabon 2
GD - Grenada 2
Totale 164.783
Salva come PNG Salva come JPEG
Città #
Woodbridge 38.593
Wilmington 33.300
Houston 31.068
Fairfield 4.229
Singapore 3.393
Ann Arbor 2.918
Ashburn 2.421
Chandler 2.341
Hong Kong 2.191
Seattle 1.657
Cambridge 1.481
Jacksonville 1.389
Beijing 1.255
Kraków 1.177
Dublin 1.176
Rome 1.000
New York 963
Medford 948
Dearborn 685
Santa Clara 659
Los Angeles 499
The Dalles 468
Lawrence 439
Menlo Park 364
Dallas 288
Buffalo 274
Council Bluffs 254
Boardman 248
San Diego 237
Milan 227
Munich 218
Ho Chi Minh City 211
São Paulo 199
Moscow 189
Zhengzhou 189
Mülheim 166
Hanoi 139
Chicago 130
London 129
Nuremberg 127
Warsaw 108
Engelhard 106
Redwood City 104
Helsinki 96
Brussels 88
Dong Ket 85
Palo Alto 85
Redondo Beach 85
Mountain View 84
Norwalk 81
Brno 78
Tokyo 78
Jakarta 77
Montreal 71
Rio de Janeiro 71
Brooklyn 69
Guangzhou 66
Toronto 66
Denver 65
Seoul 65
Vienna 65
Nanjing 64
Stockholm 64
Atlanta 63
Phoenix 63
Falls Church 62
Johannesburg 60
San Francisco 54
Hefei 53
Chennai 52
Frankfurt am Main 52
Belo Horizonte 50
Orem 50
San Jose 48
San Mateo 46
Amsterdam 45
Poplar 45
Shanghai 44
Verona 44
Boston 42
Brasília 42
Lappeenranta 42
Columbus 40
Manchester 40
University Park 40
Bari 39
North Bergen 39
Ankara 38
Kunming 38
Detroit 37
Naples 37
Saint Petersburg 36
Curitiba 35
Florence 33
Mexico City 33
Jinan 32
Bologna 30
Nürnberg 30
Salt Lake City 30
Turin 30
Totale 141.254
Salva come PNG Salva come JPEG
Nome #
Il doping genetico: ipotesi surreale o inquietante realtà? 1.402
Ku70, Ku80, sClusterin: a “cluster” of predicting factors for neoadjuvant chemoradiotherapy treatment response in patients affected by locally advanced rectal cancer 1.189
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 568
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 566
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 563
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation 562
Gene expression profile study in CFTR mutated bronchial cell lines 522
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 516
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 513
Gonadal mosaicism in hereditary angioedema 509
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 508
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 500
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 500
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 499
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 495
Awake thoracoscopic biopsy of interstitial lung disease 495
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 494
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 493
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 492
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 489
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 489
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 488
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 486
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 483
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 481
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 480
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 479
Review of nutrient actions on age-related macular degeneration 479
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 478
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 477
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain 476
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 475
Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1 475
Functional analysis and molecular dynamics simulation of LOX-1 K167N polymorphism reveal alteration of receptor activity. 474
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 473
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 473
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study 473
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) 472
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer 472
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 471
Human induced pluripotent stem cells for monogenic disease modelling and therapy 471
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 470
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 469
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 469
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 467
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 467
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 467
Targeted Next Generation Sequencing in patients with Myotonia Congenita 467
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 466
Advances in exploring the role of micrornas in inflammatory bowel disease 466
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 465
Denaturing HPLC in laboratory diagnosis of hereditary angioedema 465
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 465
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 465
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 464
Design of a novel LOX-1 receptor antagonist mimicking the natural substrate 464
Age-related macular degeneration: insights into inflammatory genes 464
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 463
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. 459
CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa 458
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 458
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 458
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 458
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study 457
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 456
Association of the G289S single nucleotide polymorphism in the HSD17B3 gene with prostate cancer in Italian men 456
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 456
The search for hemizyosity at 22q11 in patients with isolated cleft palate 455
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) 455
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 455
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 455
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 455
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 455
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 454
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 454
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 454
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 452
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 452
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis 452
Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women 451
Frequency assessment of 25 SNPs in five different populations 451
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 450
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 449
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 448
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2 448
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients 447
Somatic and gonadal mosaicism in Hutchinson-Gilford progeria 447
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 447
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 447
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 446
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 446
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome? 446
HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons syndrome/toxic epidermal necrolysis susceptibility in a population from Mozambique 445
Genetic factors in systemic lupus erythematosus: Contribution to disease phenotype 445
Effects of dutasteride on the expression of genes related to androgen metabolism and related pathway in human prostate cancer cell lines 444
Profiling gene expression in peripheral blood mononuclear cells (PBMC) reflects the changes related to androgen and insulin metabolism pathway in recreational and competitive athletes 444
Early subclinical cochlear dysfunction in myotonic dystrophy type 1. 444
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13 444
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 443
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype 443
Totale 48.762
Salva come PNG Salva come JPEG
Categoria #
all - tutte 388.873
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 388.873
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202110.090 0 0 0 0 0 2.266 2.879 2.371 655 669 864 386
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
2025/20269.858 1.810 1.090 2.421 1.962 1.920 655 0 0 0 0 0 0
Totale 166.885