IRIS
NOVELLI, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 140.235
EU - Europa 18.032
AS - Asia 18.005
SA - Sud America 2.640
Continente sconosciuto - Info sul continente non disponibili 2.170
AF - Africa 265
OC - Oceania 50
Totale 181.397
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Nazione #
US - Stati Uniti d'America 139.584
SG - Singapore 8.178
IT - Italia 4.125
CN - Cina 3.126
DE - Germania 2.776
HK - Hong Kong 2.304
BR - Brasile 2.182
RU - Federazione Russa 2.114
UA - Ucraina 1.697
VN - Vietnam 1.473
PL - Polonia 1.313
FR - Francia 1.306
IE - Irlanda 1.269
GB - Regno Unito 924
SE - Svezia 794
FI - Finlandia 637
BD - Bangladesh 601
JP - Giappone 541
KR - Corea 511
CA - Canada 348
NL - Olanda 317
IN - India 273
ID - Indonesia 163
AR - Argentina 160
AT - Austria 150
MX - Messico 137
BE - Belgio 125
ES - Italia 123
TR - Turchia 109
CZ - Repubblica Ceca 108
IQ - Iraq 100
ZA - Sudafrica 100
KG - Kirghizistan 83
PK - Pakistan 71
EC - Ecuador 61
UZ - Uzbekistan 61
CL - Cile 55
TH - Thailandia 53
MY - Malesia 50
PH - Filippine 44
AU - Australia 43
CO - Colombia 43
JM - Giamaica 41
LT - Lituania 41
VE - Venezuela 41
PY - Paraguay 35
CH - Svizzera 34
AE - Emirati Arabi Uniti 33
RO - Romania 33
IL - Israele 32
TN - Tunisia 32
MA - Marocco 31
SA - Arabia Saudita 31
PE - Perù 29
DZ - Algeria 24
EU - Europa 23
NP - Nepal 22
UY - Uruguay 22
IR - Iran 21
KE - Kenya 20
CR - Costa Rica 19
EG - Egitto 19
JO - Giordania 19
TW - Taiwan 17
KZ - Kazakistan 16
DK - Danimarca 15
NI - Nicaragua 15
PT - Portogallo 15
A2 - ???statistics.table.value.countryCode.A2??? 13
AL - Albania 13
GR - Grecia 13
GT - Guatemala 13
HN - Honduras 13
BG - Bulgaria 11
DO - Repubblica Dominicana 11
LB - Libano 11
NO - Norvegia 11
RS - Serbia 11
SV - El Salvador 10
AZ - Azerbaigian 9
BO - Bolivia 9
OM - Oman 9
TT - Trinidad e Tobago 9
BH - Bahrain 8
HU - Ungheria 7
PR - Porto Rico 7
MK - Macedonia 6
NG - Nigeria 6
SI - Slovenia 6
AO - Angola 5
GE - Georgia 5
KW - Kuwait 5
MD - Moldavia 5
NZ - Nuova Zelanda 5
SC - Seychelles 5
AM - Armenia 4
BB - Barbados 4
BY - Bielorussia 4
CG - Congo 4
ET - Etiopia 4
Totale 179.168
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Città #
Woodbridge 38.592
Wilmington 33.291
Houston 31.084
Singapore 4.484
Fairfield 4.227
Ashburn 2.928
Ann Arbor 2.919
Chandler 2.335
Hong Kong 2.274
San Jose 2.065
Seattle 1.677
Cambridge 1.481
Jacksonville 1.396
Beijing 1.319
Dublin 1.186
Kraków 1.177
New York 1.116
Rome 1.106
Council Bluffs 1.094
Medford 946
Santa Clara 750
Dearborn 686
The Dalles 678
Los Angeles 623
Tokyo 461
Ho Chi Minh City 445
Lawrence 438
Hanoi 340
Menlo Park 331
Dallas 330
Buffalo 321
Milan 315
Moscow 310
Lauterbourg 270
Boardman 261
San Diego 246
Helsinki 222
São Paulo 220
Munich 215
Zhengzhou 189
Chicago 183
Mülheim 166
London 145
Nuremberg 130
Phoenix 123
Orem 121
Atlanta 119
Warsaw 116
Jakarta 108
Engelhard 106
Redwood City 104
Montreal 102
Frankfurt am Main 100
North Bergen 96
Toronto 94
Brussels 90
Brooklyn 88
Dong Ket 85
Palo Alto 85
Redondo Beach 85
Mountain View 84
Norwalk 83
Brno 77
Denver 76
Rio de Janeiro 72
Naples 70
Vienna 69
Guangzhou 68
Nanjing 67
Chennai 66
San Francisco 66
Seoul 66
Johannesburg 65
Stockholm 65
Amsterdam 64
Falls Church 63
Da Nang 62
Manchester 58
Columbus 57
Detroit 53
Florence 53
Hefei 53
Belo Horizonte 52
Shanghai 52
Verona 52
Boston 49
Bologna 47
Lappeenranta 47
Poplar 46
San Mateo 46
Turin 46
Bari 45
Haiphong 44
Mumbai 44
Brasília 43
Bangkok 42
Salt Lake City 42
Tashkent 42
University Park 40
Ankara 39
Totale 148.869
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Nome #
Il doping genetico: ipotesi surreale o inquietante realtà? 1.561
Ku70, Ku80, sClusterin: a “cluster” of predicting factors for neoadjuvant chemoradiotherapy treatment response in patients affected by locally advanced rectal cancer 1.214
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign 641
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 593
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation 592
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 592
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 578
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 577
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 539
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 538
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 537
Gene expression profile study in CFTR mutated bronchial cell lines 537
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 535
Gonadal mosaicism in hereditary angioedema 532
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 526
Awake thoracoscopic biopsy of interstitial lung disease 524
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 521
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 520
Review of nutrient actions on age-related macular degeneration 518
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 518
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 517
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 514
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 514
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 510
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 510
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 509
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 509
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain 508
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 507
Design of a novel LOX-1 receptor antagonist mimicking the natural substrate 507
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 506
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 503
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 502
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) 502
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 501
Human induced pluripotent stem cells for monogenic disease modelling and therapy 500
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 499
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 499
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 499
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer 499
Age-related macular degeneration: insights into inflammatory genes 498
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 498
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 497
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 496
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 496
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 494
Functional analysis and molecular dynamics simulation of LOX-1 K167N polymorphism reveal alteration of receptor activity. 493
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 493
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 493
null 492
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 491
Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1 491
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 489
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 489
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 489
Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique 488
Denaturing HPLC in laboratory diagnosis of hereditary angioedema 488
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study 488
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene 487
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 486
Advances in exploring the role of micrornas in inflammatory bowel disease 486
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 485
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 485
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 485
A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism 482
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 481
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 481
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 481
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 480
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 479
Association of the G289S single nucleotide polymorphism in the HSD17B3 gene with prostate cancer in Italian men 477
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 477
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. 477
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) 477
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 476
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 476
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 476
Randomized comparison of awake nonresectional versus nonawake resectional lung volume reduction surgery. 476
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study 474
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients 474
CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa 473
Frequency assessment of 25 SNPs in five different populations 473
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 473
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 472
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis 472
SMA human iPSC-derived motor neurons show perturbed differentiation and reduced miR-335-5P expression 472
The search for hemizyosity at 22q11 in patients with isolated cleft palate 471
Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women 471
Effects of dutasteride on the expression of genes related to androgen metabolism and related pathway in human prostate cancer cell lines 471
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 471
Recent advances in exploring the genetic susceptibility to diabetic neuropathy 471
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome? 471
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype 470
Molecular dynamics simulation of human LOX-1 provides an explanation for the lack of OxLDL binding to the Trp150Ala mutant. 470
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 470
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13 469
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 468
A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of spinal muscular atrophy (SMA) 468
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 467
Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L) 467
Totale 51.639
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Categoria #
all - tutte 441.998
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 441.998
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224.948 0 593 216 280 176 584 293 271 441 419 393 1.282
2022/20236.224 612 522 157 788 554 1.342 558 380 568 51 492 200
2023/20244.278 380 360 287 104 1.043 886 115 185 63 111 87 657
2024/202513.531 482 3.117 1.424 849 325 606 1.119 761 1.402 1.162 1.252 1.032
2025/202621.908 1.805 1.077 2.409 1.956 1.912 797 2.633 2.552 2.593 2.120 1.196 858
2026/20272.674 1.100 1.574 0 0 0 0 0 0 0 0 0 0
Totale 181.397