IRIS
STUPPIA, Liborio
 Distribuzione geografica
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Continente #
EU - Europa 9.808
NA - Nord America 9.083
AS - Asia 5.554
SA - Sud America 70
OC - Oceania 44
AF - Africa 17
Continente sconosciuto - Info sul continente non disponibili 14
Totale 24.590
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Nazione #
US - Stati Uniti d'America 9.017
IT - Italia 2.085
CN - Cina 1.985
SG - Singapore 1.556
IE - Irlanda 1.427
UA - Ucraina 1.407
SE - Svezia 1.094
GB - Regno Unito 995
TR - Turchia 903
FR - Francia 788
IN - India 781
DE - Germania 731
FI - Finlandia 387
AT - Austria 349
RU - Federazione Russa 264
VN - Vietnam 101
BR - Brasile 54
NL - Olanda 54
CA - Canada 50
CZ - Repubblica Ceca 49
BE - Belgio 48
IR - Iran 36
PL - Polonia 36
HK - Hong Kong 34
JP - Giappone 34
AU - Australia 32
KR - Corea 21
ES - Italia 19
GR - Grecia 17
BD - Bangladesh 15
IL - Israele 15
RO - Romania 15
MX - Messico 14
EU - Europa 11
NZ - Nuova Zelanda 11
LT - Lituania 8
TW - Taiwan 8
AE - Emirati Arabi Uniti 7
MY - Malesia 7
PK - Pakistan 7
EG - Egitto 6
ID - Indonesia 6
PH - Filippine 6
BG - Bulgaria 5
IQ - Iraq 5
LB - Libano 5
PT - Portogallo 5
SA - Arabia Saudita 5
SK - Slovacchia (Repubblica Slovacca) 5
EC - Ecuador 4
ZA - Sudafrica 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
AR - Argentina 3
CH - Svizzera 3
CO - Colombia 3
QA - Qatar 3
DK - Danimarca 2
HU - Ungheria 2
JO - Giordania 2
KG - Kirghizistan 2
MA - Marocco 2
ME - Montenegro 2
MT - Malta 2
NO - Norvegia 2
OM - Oman 2
PS - Palestinian Territory 2
RS - Serbia 2
UY - Uruguay 2
BO - Bolivia 1
CL - Cile 1
CR - Costa Rica 1
CY - Cipro 1
DZ - Algeria 1
GE - Georgia 1
JM - Giamaica 1
KE - Kenya 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MD - Moldavia 1
NG - Nigeria 1
PE - Perù 1
PF - Polinesia Francese 1
SC - Seychelles 1
SM - San Marino 1
TH - Thailandia 1
TN - Tunisia 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 24.590
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Città #
Chandler 1.684
Jacksonville 1.603
Dublin 1.411
Singapore 1.303
Southend 810
Princeton 638
Dearborn 511
Nanjing 500
Izmir 467
Chieti 386
Ashburn 349
Wilmington 342
Vienna 326
Beijing 314
Santa Clara 283
Cambridge 252
Altamura 225
Nanchang 193
Boardman 189
Ann Arbor 188
Grafing 130
Pescara 126
Helsinki 113
Dong Ket 99
New York 98
Kunming 97
Shenyang 92
Tianjin 84
Los Angeles 81
Rome 81
Hebei 80
Woodbridge 78
Jiaxing 65
Munich 59
Washington 58
Grevenbroich 52
Milan 48
Jinan 47
Hangzhou 46
Brno 44
Augusta 41
Brussels 39
Nuremberg 39
Guangzhou 38
Norwalk 38
Changsha 37
Kocaeli 36
Ningbo 36
San Mateo 34
Seattle 33
Lanzhou 28
Houston 27
Zhengzhou 27
Falls Church 25
Leawood 25
Tortoreto 25
Toronto 23
Teramo 21
Ardabil 20
Orange 19
Romola 19
Changchun 18
Lappeenranta 18
Florence 17
Kraków 17
Montesilvano Marina 17
Hefei 16
Hong Kong 16
Brisbane 15
Frankfurt am Main 15
London 15
Moscow 15
Istanbul 14
Mumbai 14
Auburn Hills 13
Düsseldorf 13
Pune 13
Chicago 12
Jesi 12
Shanghai 12
Atessa 11
Bangalore 11
Camerino 11
Espoo 11
Bologna 10
Fuzhou 10
Naples 10
Taizhou 10
Viterbo 10
Bari 9
Hanover 9
Monmouth Junction 9
Redmond 9
San Vito Chietino 9
Serra 9
Amsterdam 8
Andover 8
Bellante 8
Chengdu 8
Council Bluffs 8
Totale 14.652
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Nome #
Association of COMT, BDNF and 5-HTT functional polymorphisms with personality characteristics 309
Genetic variants identified in novel candidate genes for anorexia nervosa and analysis of molecular pathways for diagnostic applications 203
A Neural "Tuning Curve" for Multisensory Experience and Cognitive-Perceptual Schizotypy 166
A variant on promoter of the cannabinoid receptor 1 gene (CNR1) moderates the effect of valence on working memory 156
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 136
Wnt Signaling Behaves as a "Master Regulator" in the Osteogenic and Adipogenic Commitment of Human Amniotic Fluid Mesenchymal Stem Cells 136
The modulating role of ADRA2B in emotional working memory: Attending the negative but remembering the positive 135
Widening of a Y-chromosome interval 6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to RBM1 and DAZ genes 134
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 134
Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer 133
Nuove mutazioni del Gene IRF6 associate alla sindrome di Van der Woude 129
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 125
Role of the C1858T polymorphism of protein tyrosine phosphatase non-receptor type 22 (PTPN22) in children and adolescents with type 1 diabetes 125
Music in DNA: From Williams Syndrome to Musical Genes 122
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 120
Acute Effects of Modafinil on Brain Resting State Networks in Young Healthy Subjects 119
5HTR2A and COMT genes in attention-deficit/hyperactivity disorder: a preliminary study 118
Butyrylcholinesterase and Acetylcholinesterase polymorphisms in Multiple Sclerosis patients: implication in peripheral inflammation 118
Omics sciences and precision medicine in thyroid cancer 117
Aging and the Combined effects of ADRA2B and CB1 deletions on Affective Working Memory 116
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 115
The role of depression and emotion regulation on parenting stress in a sample of mothers with cancer 115
Microarray expression profiling of human dental pulp from single subject. 113
Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in Italy 113
Associations between the Antioxidant Network and Emotional Intelligence: A Preliminary Study 113
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 113
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells. 112
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 111
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 110
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 109
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 108
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 108
Inside the granulosa transcriptome 108
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 106
Y chromosome haplogroups and susceptibility to AZFc microdeletion in an Italian population. 105
TNF-α gene polymorphisms and juvenile idiopathic arthritis: Influence on disease outcome and therapeutic response 104
Molecular analysis of a genetic variants panel related to nutrients and metabolism: association with susceptibility to Gestational Diabetes and cardiometabolic risk in affected women 104
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 104
Multiparametric analysis of the leukocytes of Down patients. Effect of ZnS04 therapy 103
null 103
X/Y translocation in a family with Leri-Weill dyschondrosteosis 102
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 102
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 102
Transcriptome modifications in human gingival fibroblasts exposed to 2-hydroxyethyl methacrylate 102
VALUTAZIONE DEI PROFILI D’ESPRESSIONE GENICA ALL’INTERNO DELLA POLPA DENTARIA UMANA 101
Valutazione della macrostruttura e della nanostruttura di un nuovo tipo di impianti dentali. 101
Gene symbol: BRCA1 disease: Breast/ovarian cancer 101
Dentin sialophosphoprotein expression during human matrix development. 101
Serum Steroid Profiling by Liquid Chromatography-Tandem Mass Spectrometry for the Rapid Confirmation and Early Treatment of Congenital Adrenal Hyperplasia: A Neonatal Case Report 101
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 101
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 100
Complete sequence of human mitochondrial DNA obtained by combining multiple displacement amplification and next-generation sequencing on a single oocyte 100
Nutrigenetics, epigenetics and gestational diabetes: consequences in mother and child. 100
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 98
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification. 98
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 98
MBL2 and FCN2 gene polymorphisms in a cohort of Italian children with rheumatic fever: A case-control study 98
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 97
VALUTAZIONE MEDIANTE TECNICA MICROARRAY DELL’ESPRESSIONE GENICA DI PAPILLE PRELEVATE DA GEMME DI TERZO MOLARE 96
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 96
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 96
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 96
Different approaches to the study of apoptosis. 95
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 95
The ADRA2B gene in the production of false memories for affective information in healthy female volunteers 95
Nutrigenetic variants and cardio-metabolic risk in women with or without gestational diabetes 95
Dynactin pathway-related gene expression is altered by aging, but not by vitrification 95
Cardiomyocytes derived from human cardiopoieticamniotic fluids 95
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 94
Spectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region 94
Psychological aspects, risk and protective factors related to BRCA genetic testing: a review of the literature 94
Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome. 93
Characterization of novel genes in AZF regions 93
Association between 5-HTT genotype and sexual behavior traits in healthy female subjects 93
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 93
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 92
Cyclooxygenase-1 haplotype C50T/A-842G does not affect platelet response to aspirin 92
VALUTAZIONE DEL COMPORTAMENTO DI OSTEOBLASTI DERIVANTI DA CELLULE STAMINALI DI LIQUIDO AMNIOTICO SU DIFFERENTI SUPERFICI IMPLANTARI 92
Influence of APOE and RNF219 on behavioral and cognitive features of female patients affected by mild cognitive impairment or Alzheimer's disease 92
Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats 92
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 92
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 91
The Infector Stigma: Centralizing Health Policies in an Age of Global Migration Flows 91
SEM analysis of oral lichen planus before and after treatment with 13 cis-retinoic acid. 91
Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation. 90
SHOX mutations detected by FISH and direct sequencing in patients with short stature 90
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 90
An Epigenetic Approach to Pancreatic Cancer Treatment: the Prospective Role of Histone Deacetylase Inhibitors 90
Age-Dependent Modifications of AMPA Receptor Subunit Expression Levels and Related Cognitive Effects in 3xTg-AD Mice 90
Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits 90
Human second trimester amniotic fluid cells are able to create embryoid body-like structures in vitro and to show typical expression profiles of embryonic and primordial germ cells 90
A protective genetic variant for adverse environments? The role of childhood traumas and serotonin transporter gene on resilience and depressive severity in a high-risk population 89
Cyclooxygenase-1 haplotype C50T/A-842G does not affect platelet response to aspirin. 89
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 89
Valutazione morfostrutturale al SEM di cellule staminali da follicolo dentario su differenti scaffold di titanio. 89
Association BDNF Val66Met genotype and personality traits in healthy female subjects 89
MRAP2 regulates endometrial receptivity and function 89
Air and surface measurements of SARS-CoV-2 inside a bus during normal operation 89
Human height genes and cancer. 89
ISOXAZOLE DERIVATIVES AND THEIR USE AS CYCLOOXYGENASE INHIBITORS 88
Totale 10.694
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Categoria #
all - tutte 104.138
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 104.138
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.086 0 0 0 0 0 0 0 363 116 203 383 21
2020/20212.410 274 30 304 35 147 430 80 61 405 312 159 173
2021/20221.659 42 26 30 298 141 168 48 104 122 69 191 420
2022/20234.836 373 674 285 514 500 980 291 352 561 62 131 113
2023/20242.715 177 92 151 80 146 887 432 181 67 110 89 303
2024/20253.891 400 1.153 970 308 264 265 373 158 0 0 0 0
Totale 25.670