IRIS
SIDOTI, Antonina
 Distribuzione geografica
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Continente #
NA - Nord America 4.759
EU - Europa 3.715
AS - Asia 2.704
SA - Sud America 1.164
AF - Africa 76
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12.430
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Nazione #
US - Stati Uniti d'America 4.659
SG - Singapore 1.188
BR - Brasile 1.017
IE - Irlanda 802
SE - Svezia 792
IT - Italia 742
CN - Cina 691
HK - Hong Kong 391
DE - Germania 352
UA - Ucraina 206
GB - Regno Unito 167
PL - Polonia 163
FI - Finlandia 155
VN - Vietnam 150
RU - Federazione Russa 96
FR - Francia 63
IN - India 60
AR - Argentina 44
BE - Belgio 43
CA - Canada 41
MX - Messico 37
NL - Olanda 33
EC - Ecuador 31
TR - Turchia 30
ZA - Sudafrica 28
ID - Indonesia 26
AT - Austria 23
CO - Colombia 23
CZ - Repubblica Ceca 22
UZ - Uzbekistan 22
BD - Bangladesh 21
JP - Giappone 20
IQ - Iraq 18
PK - Pakistan 15
VE - Venezuela 14
MA - Marocco 13
CL - Cile 12
PY - Paraguay 11
ES - Italia 10
IL - Israele 9
LT - Lituania 8
AZ - Azerbaigian 7
EG - Egitto 7
JM - Giamaica 6
CI - Costa d'Avorio 5
CR - Costa Rica 5
GR - Grecia 5
KE - Kenya 5
PE - Perù 5
TN - Tunisia 5
DZ - Algeria 4
EU - Europa 4
JO - Giordania 4
KG - Kirghizistan 4
LV - Lettonia 4
NP - Nepal 4
NZ - Nuova Zelanda 4
PH - Filippine 4
TH - Thailandia 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
AO - Angola 3
AU - Australia 3
BO - Bolivia 3
CH - Svizzera 3
DO - Repubblica Dominicana 3
GE - Georgia 3
HR - Croazia 3
LB - Libano 3
LU - Lussemburgo 3
MN - Mongolia 3
PA - Panama 3
PT - Portogallo 3
SN - Senegal 3
TT - Trinidad e Tobago 3
AL - Albania 2
BY - Bielorussia 2
IR - Iran 2
KH - Cambogia 2
KR - Corea 2
KW - Kuwait 2
KZ - Kazakistan 2
MD - Moldavia 2
MT - Malta 2
NO - Norvegia 2
OM - Oman 2
PS - Palestinian Territory 2
SA - Arabia Saudita 2
TW - Taiwan 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CG - Congo 1
DJ - Gibuti 1
HN - Honduras 1
HU - Ungheria 1
IM - Isola di Man 1
LA - Repubblica Popolare Democratica del Laos 1
Totale 12.422
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Città #
Dublin 800
Dallas 674
Chandler 629
Singapore 561
Ashburn 538
Nyköping 416
Jacksonville 412
Hong Kong 387
Beijing 357
Messina 255
The Dalles 176
Warsaw 153
Princeton 126
Medford 114
Los Angeles 111
Munich 106
Ann Arbor 96
Cambridge 91
Des Moines 87
New York 85
São Paulo 85
Bremen 73
Dearborn 72
Boardman 68
Lancaster 65
Buffalo 53
Ho Chi Minh City 49
Redondo Beach 39
Wilmington 38
Brussels 37
Woodbridge 37
Turku 36
Hanoi 35
Rio de Janeiro 29
Rome 29
Brooklyn 27
Moscow 27
Tianjin 26
Belo Horizonte 25
Helsinki 24
Catania 23
Jinan 22
Milan 21
Düsseldorf 20
Tashkent 19
Amsterdam 18
Brasília 18
Jakarta 18
Pune 18
San Mateo 18
Seattle 18
London 17
Santa Clara 17
Hyderabad 16
Montreal 16
Ningbo 16
Padova 16
Porto Alegre 16
Shenyang 16
Stockholm 15
Tokyo 15
Boston 14
Johannesburg 14
San Francisco 14
Chicago 13
Dong Ket 13
Houston 13
Phoenix 13
São José dos Campos 13
Denver 12
Mexico City 12
Quito 12
Vienna 12
Atlanta 11
Frankfurt am Main 11
Ribeirão Preto 11
Baghdad 10
Chennai 10
Fortaleza 10
Guayaquil 10
Norwalk 10
Salvador 10
Toronto 10
Washington 10
Campinas 9
Manchester 9
Nanjing 9
Olomouc 9
Zhengzhou 9
Council Bluffs 8
Lappeenranta 8
Lauterbourg 8
Nuremberg 8
Orem 8
Baku 7
Canoas 7
Contagem 7
Guangzhou 7
Hangzhou 7
Istanbul 7
Totale 7.816
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 327
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 179
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 171
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 158
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 154
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 148
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 147
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 145
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 142
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 141
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 137
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 131
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 128
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 127
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 127
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 126
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 123
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 119
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 118
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 118
Advances in Bioinformatics, Biostatistics and Omic Sciences 117
Age dependent switching role of ciclyn D1 in breast cancer 116
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 115
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 115
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 114
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 113
Costameric proteins in human skeletal muscle during muscular inactivity. 113
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 112
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 112
A genetic dissection of antipsychotic induced movement disorders 111
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 111
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 110
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 110
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 107
The serotonin transporter and the activity regulated cytoskeleton-associated protein genes in antidepressant response and resistance: 5-HTTLPR and other variants 106
Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder 105
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 104
Distribution and localization of vinculin-talin-integrin system and dystrophin-glycoprotein complex in human skeletal muscle - Immunohistochemical study using confocal laser scanning microscopy 101
Aged fingerprints for DNA profile: First report of successful typing 101
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 100
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 99
Editome landscape of CCM-derived endothelial cells 99
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 99
A rare case of TMAU associated with suspected Currarino triad 99
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 98
A HORMONE RECEPTORS, CCND1 AND PROLIFERATION IN POSTMENOPAUSAL WOMEN 98
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 98
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 98
Chloride-sulphate exchange chemically measured in human erythrocyte ghosts 97
Effetti del NiCl2 sugli eritrociti umani e sullo scambio anionico Cl-/HCO3- 95
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 95
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 95
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 94
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 93
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 93
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 92
Molecular analysis of CCM genes promoter regions 92
Genes involved in pruning and inflammation are enriched in a large mega-sample of patients affected by Schizophrenia and Bipolar Disorder and controls 91
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 91
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 89
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 89
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 88
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 88
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 88
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 88
The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades 87
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 87
Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients. 86
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 85
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 84
Possible protective role of the ABCA4 gene c.1268A>G missense variant in Stargardt disease and syndromic retinitis pigmentosa in a Sicilian family: Preliminary data 84
Sulphydryl groups involved in Na+-Li+ exchange in human erythrocytes 83
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 83
Genes Involved in Neurodevelopment, Neuroplasticity, and Bipolar Disorder: CACNA1C, CHRNA1, and MAPK1 83
Oxidative Stress and the Neurovascular Unit 83
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 82
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 81
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia 81
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 81
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 81
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 80
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 80
Le basi genetiche delle malattie cardiovascolari: Genetica e malattie cardiovascolari: Ipertensione arteriosa 79
Sulphate influx in the erythrocytes of normotensive, diabetic and hypertensive patients 78
Sarcoglycans and integrins in muscular inactivity 77
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 77
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 76
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 76
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 75
Krit-1 mutations in 100 patients with cerebral cavernomas. 74
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 74
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 73
Investigating the role of imprinted genes in pediatric sporadic brain arteriovenous malformations 73
Distribution of delta 32 mutated allele of ccr5 gene in a healthy sicilian population 72
VIRUS 72
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 72
Sarcoglycans and airway epithelium: nucleotide sequence and immunohistochemical analysis. 71
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 71
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 71
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 70
Totale 10.247
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Categoria #
all - tutte 49.173
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 49.173
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021443 0 0 0 0 0 75 37 57 47 125 63 39
2021/2022941 4 98 37 19 14 10 54 50 16 242 101 296
2022/20232.449 182 210 121 203 224 225 29 159 997 6 79 14
2023/2024646 54 95 31 66 59 134 11 37 2 28 17 112
2024/20253.146 71 29 87 215 117 118 103 670 752 195 278 511
2025/20263.132 397 572 792 619 701 51 0 0 0 0 0 0
Totale 12.860