IRIS
STUPPIA, Liborio
 Distribuzione geografica
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Continente #
EU - Europa 8.846
NA - Nord America 8.017
AS - Asia 3.731
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 14
SA - Sud America 12
AF - Africa 2
Totale 20.638
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Nazione #
US - Stati Uniti d'America 7.984
CN - Cina 1.868
IT - Italia 1.778
IE - Irlanda 1.441
UA - Ucraina 1.414
SE - Svezia 1.105
GB - Regno Unito 972
TR - Turchia 889
IN - India 740
FR - Francia 733
DE - Germania 610
AT - Austria 326
FI - Finlandia 265
VN - Vietnam 101
BE - Belgio 42
RU - Federazione Russa 35
PL - Polonia 33
CA - Canada 28
IR - Iran 27
NL - Olanda 22
SG - Singapore 18
GR - Grecia 17
JP - Giappone 14
IL - Israele 13
KR - Corea 13
ES - Italia 12
HK - Hong Kong 12
EU - Europa 11
RO - Romania 11
AU - Australia 10
BR - Brasile 8
CZ - Repubblica Ceca 7
TW - Taiwan 7
PK - Pakistan 6
MX - Messico 5
MY - Malesia 5
NZ - Nuova Zelanda 5
SK - Slovacchia (Repubblica Slovacca) 5
PH - Filippine 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AE - Emirati Arabi Uniti 3
AL - Albania 3
BG - Bulgaria 3
ID - Indonesia 3
LB - Libano 3
CH - Svizzera 2
CO - Colombia 2
DK - Danimarca 2
IQ - Iraq 2
MT - Malta 2
RS - Serbia 2
CL - Cile 1
CY - Cipro 1
EC - Ecuador 1
GE - Georgia 1
HU - Ungheria 1
KE - Kenya 1
NO - Norvegia 1
PF - Polinesia Francese 1
PT - Portogallo 1
SA - Arabia Saudita 1
SC - Seychelles 1
SM - San Marino 1
Totale 20.638
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Città #
Chandler 1.705
Jacksonville 1.613
Dublin 1.426
Southend 810
Princeton 643
Dearborn 514
Nanjing 503
Izmir 470
Ashburn 357
Wilmington 344
Chieti 338
Vienna 318
Beijing 306
Cambridge 253
Altamura 227
Nanchang 193
Ann Arbor 190
Boardman 131
Grafing 130
Dong Ket 101
New York 98
Kunming 97
Shenyang 92
Tianjin 84
Hebei 80
Woodbridge 78
Jiaxing 66
Rome 60
Washington 58
Grevenbroich 52
Pescara 52
Los Angeles 45
Jinan 44
Augusta 41
Hangzhou 39
Norwalk 38
Changsha 36
Kocaeli 36
Milan 36
Ningbo 36
Seattle 35
Brussels 34
San Mateo 34
Guangzhou 29
Lanzhou 29
Houston 27
Zhengzhou 26
Falls Church 25
Leawood 25
Tortoreto 25
Ardabil 20
Helsinki 20
Orange 19
Changchun 17
Kraków 17
Hefei 16
Pune 14
Teramo 14
Auburn Hills 13
Düsseldorf 13
Toronto 13
Bangalore 12
Jesi 12
Atessa 11
Bellante 11
London 11
Bari 10
Montesilvano Marina 10
Singapore 10
Taizhou 10
Viterbo 10
Bologna 9
Fuzhou 9
Monmouth Junction 9
Mumbai 9
Redmond 9
San Vito Chietino 9
Serra 9
Redwood City 8
Roseto Degli Abruzzi 8
Sartrouville 8
Taranto 8
Torino 8
Vasto 8
Campobasso 7
Edinburgh 7
Frankfurt am Main 7
Guardiagrele 7
Istanbul 7
L'aquila 7
Simi Valley 7
Andover 6
Catania 6
Chandigarh 6
Chicago 6
Fairfield 6
Florence 6
Hanover 6
Chengdu 5
Francavilla Al Mare 5
Totale 12.524
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Nome #
Association of COMT, BDNF and 5-HTT functional polymorphisms with personality characteristics 198
A variant on promoter of the cannabinoid receptor 1 gene (CNR1) moderates the effect of valence on working memory 144
A Neural "Tuning Curve" for Multisensory Experience and Cognitive-Perceptual Schizotypy 142
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 133
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 128
Wnt Signaling Behaves as a "Master Regulator" in the Osteogenic and Adipogenic Commitment of Human Amniotic Fluid Mesenchymal Stem Cells 127
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 122
The modulating role of ADRA2B in emotional working memory: Attending the negative but remembering the positive 121
Music in DNA: From Williams Syndrome to Musical Genes 113
The role of depression and emotion regulation on parenting stress in a sample of mothers with cancer 108
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 108
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 107
5HTR2A and COMT genes in attention-deficit/hyperactivity disorder: a preliminary study 107
Nuove mutazioni del Gene IRF6 associate alla sindrome di Van der Woude 107
Acute Effects of Modafinil on Brain Resting State Networks in Young Healthy Subjects 106
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 106
Microarray expression profiling of human dental pulp from single subject. 105
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 105
Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in Italy 103
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 101
Aging and the Combined effects of ADRA2B and CB1 deletions on Affective Working Memory 101
Role of the C1858T polymorphism of protein tyrosine phosphatase non-receptor type 22 (PTPN22) in children and adolescents with type 1 diabetes 101
Y chromosome haplogroups and susceptibility to AZFc microdeletion in an Italian population. 99
Butyrylcholinesterase and Acetylcholinesterase polymorphisms in Multiple Sclerosis patients: implication in peripheral inflammation 99
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 99
Molecular analysis of a genetic variants panel related to nutrients and metabolism: association with susceptibility to Gestational Diabetes and cardiometabolic risk in affected women 98
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 97
BRCA1 AND BRCA2 MUTATION IN BREAST/OVARIAN CANCER PATIENTS FROM CENTRAL ITALY 96
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 96
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 96
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 96
VALUTAZIONE DEI PROFILI D’ESPRESSIONE GENICA ALL’INTERNO DELLA POLPA DENTARIA UMANA 95
Transcriptome modifications in human gingival fibroblasts exposed to 2-hydroxyethyl methacrylate 95
X/Y translocation in a family with Leri-Weill dyschondrosteosis 94
Associations between the Antioxidant Network and Emotional Intelligence: A Preliminary Study 94
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells. 93
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 93
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 91
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 91
Nutrigenetics, epigenetics and gestational diabetes: consequences in mother and child. 91
Role of THRB, ARG1, and ADRB2 Genetic Variants on Bronchodilators Response in Asthmatic Children. 91
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 90
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 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
Inside the granulosa transcriptome 90
VALUTAZIONE MEDIANTE TECNICA MICROARRAY DELL’ESPRESSIONE GENICA DI PAPILLE PRELEVATE DA GEMME DI TERZO MOLARE 89
The ADRA2B gene in the production of false memories for affective information in healthy female volunteers 89
Nutrigenetic variants and cardio-metabolic risk in women with or without gestational diabetes 89
Dentin sialophosphoprotein expression during human matrix development. 89
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 88
VALUTAZIONE DEL COMPORTAMENTO DI OSTEOBLASTI DERIVANTI DA CELLULE STAMINALI DI LIQUIDO AMNIOTICO SU DIFFERENTI SUPERFICI IMPLANTARI 87
Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats 87
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 87
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 86
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 86
Spectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region 86
MBL2 and FCN2 gene polymorphisms in a cohort of Italian children with rheumatic fever: A case-control study 86
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 85
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 85
SHOX mutations detected by FISH and direct sequencing in patients with short stature 85
Psychological aspects, risk and protective factors related to BRCA genetic testing: a review of the literature 85
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 84
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification. 84
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 84
Characterization of novel genes in AZF regions 84
Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits 84
Biological insight into the extracellular vesicles in women with and without gestational diabetes 84
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 83
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 83
Valutazione della macrostruttura e della nanostruttura di un nuovo tipo di impianti dentali. 83
Age-Dependent Modifications of AMPA Receptor Subunit Expression Levels and Related Cognitive Effects in 3xTg-AD Mice 83
SEM analysis of oral lichen planus before and after treatment with 13 cis-retinoic acid. 83
ISOXAZOLE DERIVATIVES AND THEIR USE AS CYCLOOXYGENASE INHIBITORS 82
Genetic determinants of blood pressure responses to caffeine drinking 82
TNF-α gene polymorphisms and juvenile idiopathic arthritis: Influence on disease outcome and therapeutic response 82
Gene symbol: BRCA1 disease: Breast/ovarian cancer 82
Multiparametric analysis of the leukocytes of Down patients. Effect of ZnS04 therapy 81
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 81
Influence of APOE and RNF219 on behavioral and cognitive features of female patients affected by mild cognitive impairment or Alzheimer's disease 81
Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation. 80
Cyclooxygenase-1 haplotype C50T/A-842G does not affect platelet response to aspirin 80
Dynactin pathway-related gene expression is altered by aging, but not by vitrification 80
Cardiomyocytes derived from human cardiopoieticamniotic fluids 80
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 80
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 79
Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome. 79
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 79
Genetic determinants of cognitive responses to caffeine drinking identified from a double-blind, randomized, controlled trial 79
Different approaches in the molecular analysis of the SHOX gene dysfunctions 79
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 79
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 78
An Epigenetic Approach to Pancreatic Cancer Treatment: the Prospective Role of Histone Deacetylase Inhibitors 78
Serum Steroid Profiling by Liquid Chromatography-Tandem Mass Spectrometry for the Rapid Confirmation and Early Treatment of Congenital Adrenal Hyperplasia: A Neonatal Case Report 77
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 76
Reduced thromboxane biosynthesis in carriers of toll-like receptor 4 polymorphisms in vivo. 76
VALUTAZIONE DELL’ESPRESIONE GENICA DEL PROCOLLAGENE E DELLE METALLOPROTEINASI NELLA POLPA DENTARIA 76
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 76
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 76
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 76
Totale 9.289
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Categoria #
all - tutte 69.230
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 69.230
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019727 0 0 0 0 0 0 0 0 0 0 32 695
2019/20203.974 1.138 258 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
2022/20234.911 375 680 288 529 510 991 294 359 569 63 136 117
2023/20242.372 178 94 153 81 151 905 434 185 70 112 9 0
Totale 21.622