IRIS
NOVELLI, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 126.882
EU - Europa 11.660
AS - Asia 2.997
SA - Sud America 63
Continente sconosciuto - Info sul continente non disponibili 36
OC - Oceania 15
AF - Africa 13
Totale 141.666
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Nazione #
US - Stati Uniti d'America 126.832
DE - Germania 2.262
IT - Italia 2.103
UA - Ucraina 1.677
IE - Irlanda 1.270
CN - Cina 1.265
PL - Polonia 1.181
FR - Francia 892
HK - Hong Kong 819
GB - Regno Unito 660
SE - Svezia 639
KR - Corea 491
FI - Finlandia 390
RU - Federazione Russa 284
BE - Belgio 109
VN - Vietnam 107
KG - Kirghizistan 79
NL - Olanda 68
JP - Giappone 61
IN - India 55
BR - Brasile 38
CA - Canada 38
RO - Romania 24
EU - Europa 23
SG - Singapore 21
CL - Cile 20
CH - Svizzera 16
UZ - Uzbekistan 16
A2 - ???statistics.table.value.countryCode.A2??? 13
TR - Turchia 13
AU - Australia 12
IR - Iran 12
IL - Israele 11
AT - Austria 10
ES - Italia 9
GR - Grecia 9
CZ - Repubblica Ceca 8
DK - Danimarca 8
MX - Messico 8
NO - Norvegia 8
IQ - Iraq 7
PT - Portogallo 7
EG - Egitto 6
PK - Pakistan 6
TW - Taiwan 6
BD - Bangladesh 5
MY - Malesia 5
AE - Emirati Arabi Uniti 4
AL - Albania 4
SM - San Marino 4
BG - Bulgaria 3
HU - Ungheria 3
KZ - Kazakistan 3
MA - Marocco 3
NZ - Nuova Zelanda 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
CU - Cuba 2
EC - Ecuador 2
EE - Estonia 2
IS - Islanda 2
PE - Perù 2
PH - Filippine 2
SI - Slovenia 2
ZA - Sudafrica 2
AM - Armenia 1
BO - Bolivia 1
BY - Bielorussia 1
CY - Cipro 1
DM - Dominica 1
GE - Georgia 1
GT - Guatemala 1
ID - Indonesia 1
JO - Giordania 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
QA - Qatar 1
SC - Seychelles 1
Totale 141.666
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Città #
Woodbridge 38.813
Wilmington 33.470
Houston 31.213
Fairfield 4.258
Ann Arbor 2.945
Chandler 2.360
Ashburn 1.908
Seattle 1.655
Cambridge 1.487
Jacksonville 1.396
Dublin 1.180
Kraków 1.177
Medford 954
Hong Kong 808
New York 807
Dearborn 689
Rome 687
Beijing 568
Lawrence 442
Menlo Park 365
San Diego 238
Zhengzhou 179
Mülheim 168
Milan 158
Engelhard 106
Redwood City 105
Palo Alto 86
Dong Ket 85
London 84
Mountain View 84
Brussels 81
Norwalk 81
Boardman 75
Falls Church 62
Nanjing 61
Seoul 58
Hefei 54
Guangzhou 51
San Mateo 46
Verona 43
University Park 40
Detroit 39
Helsinki 39
Saint Petersburg 36
Kunming 35
Shanghai 35
Jinan 30
Nürnberg 30
Toronto 28
Waanrode 27
Hangzhou 25
Bari 24
Castrovillari 24
Chicago 24
Nanchang 23
Bologna 22
Kilburn 22
Hounslow 21
Phoenix 21
Auburn Hills 20
Center 20
Indiana 20
Naples 19
São Paulo 18
Los Angeles 17
Turin 17
Wuhan 17
Hebei 16
Hanoi 14
San Francisco 14
Daejeon 13
Lappeenranta 13
San Jose 13
St. George 13
Brescia 12
Chengdu 12
Fuzhou 12
Monza 12
Mumbai 12
New Bedfont 12
Prescot 12
Redmond 12
Atlanta 11
Changsha 11
Creede 11
Buffalo 10
Caserta 10
Chiswick 10
La Veta 10
Napoli 10
Palermo 10
Tokyo 10
Catania 9
Chongqing 9
Dallas 9
Padova 9
Tappahannock 9
Clearwater 8
Florence 8
Pune 8
Totale 130.144
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Nome #
Il doping genetico: ipotesi surreale o inquietante realtà? 1.132
Ku70, Ku80, sClusterin: a “cluster” of predicting factors for neoadjuvant chemoradiotherapy treatment response in patients affected by locally advanced rectal cancer 1.131
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation 509
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study 503
Gene expression profile study in CFTR mutated bronchial cell lines 485
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome 481
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 467
Gonadal mosaicism in hereditary angioedema 466
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. 462
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2. 457
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 455
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 454
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 453
Awake thoracoscopic biopsy of interstitial lung disease 448
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region 443
Association study of a promoter polymorphism of UFD1L gene with schizophrenia 440
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 439
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 439
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 438
Human induced pluripotent stem cells for monogenic disease modelling and therapy 438
Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation 436
Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22 436
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 436
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 436
Simulative and experimental investigation on the cleavage site that generates the soluble human LOX-1 436
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot 435
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice 435
Functional analysis and molecular dynamics simulation of LOX-1 K167N polymorphism reveal alteration of receptor activity. 434
Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies 432
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 432
Targeted Next Generation Sequencing in patients with Myotonia Congenita 432
Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays 431
The search for hemizyosity at 22q11 in patients with isolated cleft palate 430
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 430
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 429
Association of the G289S single nucleotide polymorphism in the HSD17B3 gene with prostate cancer in Italian men 428
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 428
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 428
Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models 428
Denaturing HPLC in laboratory diagnosis of hereditary angioedema 428
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study 428
Review of nutrient actions on age-related macular degeneration 428
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 426
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2) 426
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study 425
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome 424
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 423
CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa 423
Dynamic changes in gene expression profiles of 22q11 and related orthologous genes during mouse development 423
Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region on 8p 422
Age-period-cohort analysis of 1990-2003 incidence time trends of childhood diabetes in Italy: the RIDI study 422
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 422
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 422
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis 422
Characterization of gene expression induced by RTN-1C in human neuroblastoma cells and in mouse brain 420
Absence of correlation between BMP-4 polymorphism and postmenopausal osteoporosis in Italian women 418
Profiling gene expression in peripheral blood mononuclear cells (PBMC) reflects the changes related to androgen and insulin metabolism pathway in recreational and competitive athletes 418
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 418
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer 418
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign 417
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. 416
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 416
Design of a novel LOX-1 receptor antagonist mimicking the natural substrate 416
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 415
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. 415
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 414
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2 414
Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia 414
Advances in exploring the role of micrornas in inflammatory bowel disease 414
Isolated conotruncal heart defects are really related to microdeletion of chromosome 22q11? 414
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 414
Somatic and gonadal mosaicism in Hutchinson-Gilford progeria 413
Frequency assessment of 25 SNPs in five different populations 413
Age-related macular degeneration: insights into inflammatory genes 413
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death 413
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 412
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 412
The up-to-date molecular genetics of cystic fibrosis 412
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 412
Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiency 411
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster 410
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 410
Interleukin-23R Arg381Gln Is Associated With Susceptibility to Crohn's Disease But Not With Phenotype in an Italian Population 409
In vitro restoration of functional SMN protein in human trophoblast cells affected by spinal muscular atrophy by small fragment homologous replacement 409
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line 408
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients 408
Paternal origin of LMNA mutations in Hutchinson-Gilford progeria [1] 407
Primary laminopathy fibroblasts display altered genome organization and apoptosis 406
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 406
Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1 406
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. 405
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 405
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 405
Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit 405
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 404
Therapeutic strategies for the treatment of Spinal Muscular Atrophy (SMA) disease 404
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3 404
Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L) 403
Elbow deformities in a patient with mandibuloacral dysplasia type A 403
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) 403
Totale 44.018
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Categoria #
all - tutte 259.957
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 259.957
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201910.871 0 0 0 0 0 0 0 0 0 3.265 3.837 3.769
2019/202037.213 3.031 3.135 2.772 3.399 3.038 3.873 3.442 3.346 3.093 3.332 2.167 2.585
2020/202123.105 2.482 2.728 2.298 2.876 2.561 2.282 2.897 2.388 661 673 870 389
2021/20225.277 249 593 217 330 176 589 294 272 446 426 394 1.291
2022/20236.300 618 527 158 795 561 1.355 563 393 573 53 503 201
2023/20243.539 383 362 293 107 1.048 897 123 191 67 68 0 0
Totale 143.484