IRIS
NOVELLI, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 145.088
EU - Europa 18.270
AS - Asia 18.117
SA - Sud America 2.758
Continente sconosciuto - Info sul continente non disponibili 2.179
AF - Africa 282
OC - Oceania 50
Totale 186.744
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Nazione #
US - Stati Uniti d'America 144.254
SG - Singapore 8.182
IT - Italia 4.269
CN - Cina 3.127
DE - Germania 2.785
HK - Hong Kong 2.304
BR - Brasile 2.240
RU - Federazione Russa 2.114
UA - Ucraina 1.698
VN - Vietnam 1.487
PL - Polonia 1.317
FR - Francia 1.314
IE - Irlanda 1.270
GB - Regno Unito 970
SE - Svezia 794
FI - Finlandia 637
BD - Bangladesh 611
JP - Giappone 548
KR - Corea 511
CA - Canada 420
NL - Olanda 324
IN - India 276
ID - Indonesia 180
AR - Argentina 163
AT - Austria 152
MX - Messico 151
BE - Belgio 125
ES - Italia 124
TR - Turchia 116
CZ - Repubblica Ceca 108
ZA - Sudafrica 101
IQ - Iraq 100
KG - Kirghizistan 83
EC - Ecuador 78
CO - Colombia 75
PK - Pakistan 73
JM - Giamaica 65
TH - Thailandia 65
UZ - Uzbekistan 61
MY - Malesia 58
CL - Cile 55
PH - Filippine 52
VE - Venezuela 47
AU - Australia 43
CR - Costa Rica 43
LT - Lituania 41
CH - Svizzera 36
IL - Israele 35
PY - Paraguay 35
SA - Arabia Saudita 35
AE - Emirati Arabi Uniti 33
RO - Romania 33
TN - Tunisia 32
MA - Marocco 31
NI - Nicaragua 30
PE - Perù 29
DZ - Algeria 24
EU - Europa 23
NP - Nepal 23
UY - Uruguay 23
KE - Kenya 22
HN - Honduras 21
IR - Iran 21
EG - Egitto 19
JO - Giordania 19
KZ - Kazakistan 19
NG - Nigeria 18
DK - Danimarca 17
TW - Taiwan 17
GT - Guatemala 16
AL - Albania 15
PT - Portogallo 15
SV - El Salvador 14
A2 - ???statistics.table.value.countryCode.A2??? 13
GR - Grecia 13
LB - Libano 13
TT - Trinidad e Tobago 13
DO - Repubblica Dominicana 12
BG - Bulgaria 11
NO - Norvegia 11
RS - Serbia 11
AZ - Azerbaigian 10
BO - Bolivia 10
EE - Estonia 10
OM - Oman 10
BH - Bahrain 9
PR - Porto Rico 9
BB - Barbados 8
HU - Ungheria 8
KW - Kuwait 6
MD - Moldavia 6
MK - Macedonia 6
SI - Slovenia 6
AO - Angola 5
CG - Congo 5
GE - Georgia 5
NZ - Nuova Zelanda 5
SC - Seychelles 5
AM - Armenia 4
BY - Bielorussia 4
Totale 184.494
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Città #
Woodbridge 38.593
Wilmington 33.292
Houston 31.092
Singapore 4.486
Fairfield 4.227
Ashburn 3.577
Ann Arbor 2.919
San Jose 2.590
Chandler 2.335
Hong Kong 2.274
Seattle 1.683
Cambridge 1.484
Jacksonville 1.399
Beijing 1.319
Dublin 1.186
Kraków 1.177
New York 1.128
Rome 1.125
Council Bluffs 1.100
Medford 946
Santa Clara 780
Dearborn 688
The Dalles 678
Los Angeles 652
Tokyo 468
Ho Chi Minh City 449
Lawrence 438
Dallas 346
Hanoi 342
Menlo Park 331
Buffalo 327
Milan 327
Moscow 310
Lauterbourg 270
Boardman 265
San Diego 250
São Paulo 226
Helsinki 222
Munich 215
Chicago 195
Zhengzhou 189
Denver 180
Phoenix 177
Mülheim 166
Atlanta 157
London 146
Nuremberg 132
Orem 124
Warsaw 117
Montreal 115
Toronto 112
Jakarta 109
Engelhard 106
Redwood City 104
Brooklyn 101
Frankfurt am Main 100
North Bergen 96
Brussels 90
Norwalk 86
Dong Ket 85
Palo Alto 85
Redondo Beach 85
Mountain View 84
Brno 77
Naples 77
Rio de Janeiro 75
San Francisco 71
Vienna 69
Guangzhou 68
Nanjing 67
Chennai 66
Johannesburg 66
Seoul 66
Amsterdam 65
Stockholm 65
Da Nang 63
Falls Church 63
Columbus 59
Manchester 58
Florence 56
Brasília 55
Detroit 54
Boston 53
Hefei 53
Belo Horizonte 52
Shanghai 52
Verona 52
Turin 49
Bari 47
Bologna 47
Lappeenranta 47
Bangkok 46
Philadelphia 46
Poplar 46
San Mateo 46
Haiphong 45
Mumbai 45
Charlotte 44
Salt Lake City 43
Tashkent 42
Totale 150.552
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Nome #
Il doping genetico: ipotesi surreale o inquietante realtà? 1.591
Ku70, Ku80, sClusterin: a “cluster” of predicting factors for neoadjuvant chemoradiotherapy treatment response in patients affected by locally advanced rectal cancer 1.223
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign 650
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 604
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation 603
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 597
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 591
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 584
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 552
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 550
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 547
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 547
Gene expression profile study in CFTR mutated bronchial cell lines 545
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 539
Gonadal mosaicism in hereditary angioedema 538
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 533
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 532
Awake thoracoscopic biopsy of interstitial lung disease 529
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 527
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 526
Review of nutrient actions on age-related macular degeneration 525
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 524
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 523
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 522
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 522
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 521
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 521
Design of a novel LOX-1 receptor antagonist mimicking the natural substrate 521
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 520
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 518
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 515
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain 514
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 513
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 512
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 509
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 509
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) 509
Human induced pluripotent stem cells for monogenic disease modelling and therapy 509
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 509
Age-related macular degeneration: insights into inflammatory genes 508
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer 508
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 506
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 506
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 506
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 505
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 504
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 503
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 502
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 501
Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1 501
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 500
Functional analysis and molecular dynamics simulation of LOX-1 K167N polymorphism reveal alteration of receptor activity. 500
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 500
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 500
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 499
Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique 498
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 497
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study 496
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene 496
Denaturing HPLC in laboratory diagnosis of hereditary angioedema 495
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 495
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 495
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 495
Advances in exploring the role of micrornas in inflammatory bowel disease 492
null 492
A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism 492
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 491
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 491
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 490
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 490
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 489
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) 488
Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women 486
Randomized comparison of awake nonresectional versus nonawake resectional lung volume reduction surgery. 486
Association of the G289S single nucleotide polymorphism in the HSD17B3 gene with prostate cancer in Italian men 484
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 484
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. 484
Molecular dynamics simulation of human LOX-1 provides an explanation for the lack of OxLDL binding to the Trp150Ala mutant. 484
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 483
Effects of dutasteride on the expression of genes related to androgen metabolism and related pathway in human prostate cancer cell lines 482
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 482
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome? 482
The search for hemizyosity at 22q11 in patients with isolated cleft palate 481
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype 481
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 481
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 481
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 481
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study 480
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients 480
CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa 479
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 479
Frequency assessment of 25 SNPs in five different populations 478
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 478
Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L) 477
Early subclinical cochlear dysfunction in myotonic dystrophy type 1. 477
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. 476
SMA human iPSC-derived motor neurons show perturbed differentiation and reduced miR-335-5P expression 476
Recent advances in exploring the genetic susceptibility to diabetic neuropathy 476
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 475
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis 475
Totale 52.603
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Categoria #
all - tutte 456.722
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 456.722
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20224.139 0 0 0 280 176 584 293 271 441 419 393 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
2026/20278.021 1.100 1.645 4.141 1.135 0 0 0 0 0 0 0 0
Totale 186.744