IRIS
STUPPIA, Liborio
 Distribuzione geografica
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Continente #
EU - Europa 9.242
NA - Nord America 8.093
AS - Asia 4.015
OC - Oceania 34
Continente sconosciuto - Info sul continente non disponibili 14
SA - Sud America 13
AF - Africa 3
Totale 21.414
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Nazione #
US - Stati Uniti d'America 8.058
CN - Cina 1.885
IT - Italia 1.833
IE - Irlanda 1.436
UA - Ucraina 1.414
SE - Svezia 1.102
GB - Regno Unito 974
TR - Turchia 892
IN - India 744
FR - Francia 740
DE - Germania 655
AT - Austria 327
FI - Finlandia 280
SG - Singapore 258
RU - Federazione Russa 257
VN - Vietnam 101
CZ - Repubblica Ceca 52
BE - Belgio 42
PL - Polonia 35
CA - Canada 30
IR - Iran 29
AU - Australia 28
NL - Olanda 26
GR - Grecia 17
KR - Corea 16
IL - Israele 15
JP - Giappone 15
ES - Italia 14
HK - Hong Kong 14
EU - Europa 11
RO - Romania 11
BR - Brasile 9
TW - Taiwan 8
ID - Indonesia 6
PK - Pakistan 6
LB - Libano 5
MX - Messico 5
MY - Malesia 5
NZ - Nuova Zelanda 5
PT - Portogallo 5
SK - Slovacchia (Repubblica Slovacca) 5
AE - Emirati Arabi Uniti 4
PH - Filippine 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
BG - Bulgaria 3
IQ - Iraq 3
CH - Svizzera 2
CO - Colombia 2
DK - Danimarca 2
JO - Giordania 2
MT - Malta 2
RS - Serbia 2
CL - Cile 1
CY - Cipro 1
EC - Ecuador 1
EG - Egitto 1
GE - Georgia 1
HU - Ungheria 1
KE - Kenya 1
NO - Norvegia 1
PF - Polinesia Francese 1
SA - Arabia Saudita 1
SC - Seychelles 1
SM - San Marino 1
Totale 21.414
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Città #
Chandler 1.702
Jacksonville 1.613
Dublin 1.420
Southend 810
Princeton 643
Dearborn 514
Nanjing 503
Izmir 470
Ashburn 355
Wilmington 344
Chieti 335
Vienna 318
Beijing 308
Cambridge 253
Altamura 227
Nanchang 193
Ann Arbor 190
Boardman 190
Singapore 150
Grafing 130
Dong Ket 101
New York 98
Kunming 97
Shenyang 92
Tianjin 84
Hebei 80
Woodbridge 78
Jiaxing 66
Rome 65
Pescara 63
Washington 58
Grevenbroich 52
Los Angeles 47
Brno 46
Jinan 44
Milan 42
Augusta 41
Hangzhou 39
Norwalk 38
Changsha 36
Kocaeli 36
Ningbo 36
Brussels 34
San Mateo 34
Seattle 34
Guangzhou 33
Helsinki 31
Lanzhou 29
Munich 29
Houston 27
Zhengzhou 26
Falls Church 25
Leawood 25
Tortoreto 25
Ardabil 20
Orange 19
Changchun 17
Kraków 17
Teramo 17
Hefei 16
Brisbane 15
Moscow 14
Auburn Hills 13
Düsseldorf 13
Pune 13
Toronto 13
Bangalore 12
Jesi 12
Montesilvano Marina 12
Atessa 11
Bellante 11
London 11
Bari 10
Chicago 10
Taizhou 10
Viterbo 10
Bologna 9
Frankfurt am Main 9
Fuzhou 9
Hanover 9
Monmouth Junction 9
Mumbai 9
Redmond 9
San Vito Chietino 9
Serra 9
Istanbul 8
Redwood City 8
Roseto Degli Abruzzi 8
Sartrouville 8
Taranto 8
Torino 8
Vasto 8
Amsterdam 7
Campobasso 7
Catania 7
Edinburgh 7
Guardiagrele 7
L'aquila 7
Nuremberg 7
Simi Valley 7
Totale 12.848
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Nome #
Association of COMT, BDNF and 5-HTT functional polymorphisms with personality characteristics 237
A variant on promoter of the cannabinoid receptor 1 gene (CNR1) moderates the effect of valence on working memory 146
A Neural "Tuning Curve" for Multisensory Experience and Cognitive-Perceptual Schizotypy 145
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 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 130
Wnt Signaling Behaves as a "Master Regulator" in the Osteogenic and Adipogenic Commitment of Human Amniotic Fluid Mesenchymal Stem Cells 128
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 125
The modulating role of ADRA2B in emotional working memory: Attending the negative but remembering the positive 123
Music in DNA: From Williams Syndrome to Musical Genes 116
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 113
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 111
5HTR2A and COMT genes in attention-deficit/hyperactivity disorder: a preliminary study 110
Acute Effects of Modafinil on Brain Resting State Networks in Young Healthy Subjects 110
Nuove mutazioni del Gene IRF6 associate alla sindrome di Van der Woude 109
The role of depression and emotion regulation on parenting stress in a sample of mothers with cancer 109
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 109
Microarray expression profiling of human dental pulp from single subject. 106
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 106
Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in Italy 106
Aging and the Combined effects of ADRA2B and CB1 deletions on Affective Working Memory 105
Role of the C1858T polymorphism of protein tyrosine phosphatase non-receptor type 22 (PTPN22) in children and adolescents with type 1 diabetes 104
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 102
Butyrylcholinesterase and Acetylcholinesterase polymorphisms in Multiple Sclerosis patients: implication in peripheral inflammation 102
Y chromosome haplogroups and susceptibility to AZFc microdeletion in an Italian population. 101
Molecular analysis of a genetic variants panel related to nutrients and metabolism: association with susceptibility to Gestational Diabetes and cardiometabolic risk in affected women 101
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 101
BRCA1 AND BRCA2 MUTATION IN BREAST/OVARIAN CANCER PATIENTS FROM CENTRAL ITALY 100
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 99
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 99
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 99
Associations between the Antioxidant Network and Emotional Intelligence: A Preliminary Study 98
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 97
X/Y translocation in a family with Leri-Weill dyschondrosteosis 96
VALUTAZIONE DEI PROFILI D’ESPRESSIONE GENICA ALL’INTERNO DELLA POLPA DENTARIA UMANA 96
Transcriptome modifications in human gingival fibroblasts exposed to 2-hydroxyethyl methacrylate 96
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells. 95
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 95
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 95
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 94
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 93
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 93
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 93
Role of THRB, ARG1, and ADRB2 Genetic Variants on Bronchodilators Response in Asthmatic Children. 93
Dentin sialophosphoprotein expression during human matrix development. 92
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 91
Nutrigenetic variants and cardio-metabolic risk in women with or without gestational diabetes 91
Nutrigenetics, epigenetics and gestational diabetes: consequences in mother and child. 91
Inside the granulosa transcriptome 91
VALUTAZIONE MEDIANTE TECNICA MICROARRAY DELL’ESPRESSIONE GENICA DI PAPILLE PRELEVATE DA GEMME DI TERZO MOLARE 90
Complete sequence of human mitochondrial DNA obtained by combining multiple displacement amplification and next-generation sequencing on a single oocyte 90
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 90
The ADRA2B gene in the production of false memories for affective information in healthy female volunteers 90
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 90
VALUTAZIONE DEL COMPORTAMENTO DI OSTEOBLASTI DERIVANTI DA CELLULE STAMINALI DI LIQUIDO AMNIOTICO SU DIFFERENTI SUPERFICI IMPLANTARI 89
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 88
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 88
Spectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region 88
Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats 88
Biological insight into the extracellular vesicles in women with and without gestational diabetes 88
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 87
Psychological aspects, risk and protective factors related to BRCA genetic testing: a review of the literature 87
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 86
SHOX mutations detected by FISH and direct sequencing in patients with short stature 86
Characterization of novel genes in AZF regions 86
Age-Dependent Modifications of AMPA Receptor Subunit Expression Levels and Related Cognitive Effects in 3xTg-AD Mice 86
MBL2 and FCN2 gene polymorphisms in a cohort of Italian children with rheumatic fever: A case-control study 86
Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits 86
Multiparametric analysis of the leukocytes of Down patients. Effect of ZnS04 therapy 85
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 85
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 85
SEM analysis of oral lichen planus before and after treatment with 13 cis-retinoic acid. 85
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification. 84
ISOXAZOLE DERIVATIVES AND THEIR USE AS CYCLOOXYGENASE INHIBITORS 84
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 84
Valutazione della macrostruttura e della nanostruttura di un nuovo tipo di impianti dentali. 84
TNF-α gene polymorphisms and juvenile idiopathic arthritis: Influence on disease outcome and therapeutic response 84
Gene symbol: BRCA1 disease: Breast/ovarian cancer 84
Cyclooxygenase-1 haplotype C50T/A-842G does not affect platelet response to aspirin 83
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 83
Genetic determinants of blood pressure responses to caffeine drinking 83
Influence of APOE and RNF219 on behavioral and cognitive features of female patients affected by mild cognitive impairment or Alzheimer's disease 83
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 83
Dynactin pathway-related gene expression is altered by aging, but not by vitrification 82
Cardiomyocytes derived from human cardiopoieticamniotic fluids 82
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 81
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 81
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 81
Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation. 80
Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome. 80
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 80
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 80
An Epigenetic Approach to Pancreatic Cancer Treatment: the Prospective Role of Histone Deacetylase Inhibitors 80
Different approaches in the molecular analysis of the SHOX gene dysfunctions 80
Association between 5-HTT genotype and sexual behavior traits in healthy female subjects 80
Serum Steroid Profiling by Liquid Chromatography-Tandem Mass Spectrometry for the Rapid Confirmation and Early Treatment of Congenital Adrenal Hyperplasia: A Neonatal Case Report 80
Genetic determinants of cognitive responses to caffeine drinking identified from a double-blind, randomized, controlled trial 79
Amniotic fluid stem cells: A novel source for modeling of human genetic diseases 79
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 79
Genetic variants identified in novel candidate genes for anorexia nervosa and analysis of molecular pathways for diagnostic applications 78
Reduced thromboxane biosynthesis in carriers of toll-like receptor 4 polymorphisms in vivo. 78
Totale 9.545
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Categoria #
all - tutte 78.974
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 78.974
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.836 0 258 27 137 365 389 566 366 118 204 385 21
2020/20212.448 276 32 310 36 148 441 85 61 406 313 165 175
2021/20221.675 42 26 32 301 142 168 53 104 123 69 192 423
2022/20234.887 375 680 288 522 505 986 293 358 565 63 135 117
2023/20242.752 178 93 153 81 151 898 433 182 70 112 91 310
2024/2025427 403 24 0 0 0 0 0 0 0 0 0 0
Totale 22.405