IRIS
SIDOTI, Antonina
 Distribuzione geografica
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Continente #
EU - Europa 7.392
NA - Nord America 5.546
AS - Asia 3.455
SA - Sud America 1.260
AF - Africa 100
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 4
Totale 17.766
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Nazione #
US - Stati Uniti d'America 5.425
RU - Federazione Russa 3.558
SG - Singapore 1.516
BR - Brasile 1.071
CN - Cina 924
IE - Irlanda 806
SE - Svezia 793
IT - Italia 770
HK - Hong Kong 407
DE - Germania 370
UA - Ucraina 207
VN - Vietnam 198
GB - Regno Unito 187
FR - Francia 183
PL - Polonia 166
FI - Finlandia 155
IN - India 94
AR - Argentina 54
CA - Canada 47
MX - Messico 46
BE - Belgio 43
TR - Turchia 42
BD - Bangladesh 39
EC - Ecuador 39
NL - Olanda 37
CO - Colombia 35
ID - Indonesia 34
ZA - Sudafrica 31
IQ - Iraq 28
AT - Austria 27
UZ - Uzbekistan 24
JP - Giappone 23
CZ - Repubblica Ceca 22
PK - Pakistan 21
MA - Marocco 19
VE - Venezuela 18
CL - Cile 16
PY - Paraguay 15
ES - Italia 14
IL - Israele 13
LT - Lituania 10
AZ - Azerbaigian 9
PH - Filippine 9
EG - Egitto 8
JM - Giamaica 7
KE - Kenya 7
TN - Tunisia 7
GR - Grecia 6
OM - Oman 6
SA - Arabia Saudita 6
TH - Thailandia 6
CI - Costa d'Avorio 5
CR - Costa Rica 5
DZ - Algeria 5
ET - Etiopia 5
JO - Giordania 5
MY - Malesia 5
NP - Nepal 5
PE - Perù 5
AO - Angola 4
AU - Australia 4
DO - Repubblica Dominicana 4
EU - Europa 4
GE - Georgia 4
HR - Croazia 4
KG - Kirghizistan 4
LV - Lettonia 4
NZ - Nuova Zelanda 4
PA - Panama 4
PT - Portogallo 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
BO - Bolivia 3
CH - Svizzera 3
KW - Kuwait 3
KZ - Kazakistan 3
LB - Libano 3
LU - Lussemburgo 3
MD - Moldavia 3
MN - Mongolia 3
PS - Palestinian Territory 3
SN - Senegal 3
TT - Trinidad e Tobago 3
BH - Bahrain 2
BY - Bielorussia 2
HN - Honduras 2
IR - Iran 2
KH - Cambogia 2
KR - Corea 2
MT - Malta 2
NI - Nicaragua 2
NO - Norvegia 2
RS - Serbia 2
TW - Taiwan 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
CG - Congo 1
Totale 17.752
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Città #
Moscow 1.067
Ashburn 857
Singapore 836
Dublin 804
Dallas 678
Chandler 629
Nyköping 416
Jacksonville 413
Hong Kong 403
Beijing 377
Messina 256
The Dalles 235
San Jose 215
Warsaw 156
Princeton 126
Los Angeles 121
Lauterbourg 115
Medford 114
Munich 106
New York 97
Ann Arbor 96
São Paulo 94
Cambridge 91
Des Moines 89
Bremen 73
Dearborn 72
Boardman 68
Lancaster 65
Ho Chi Minh City 63
Buffalo 55
Orem 44
Hanoi 39
Redondo Beach 39
Wilmington 38
Brussels 37
Woodbridge 37
Tianjin 36
Turku 36
Rio de Janeiro 31
Brooklyn 29
Council Bluffs 29
Rome 29
Belo Horizonte 27
Santa Clara 25
Frankfurt am Main 24
Helsinki 24
Milan 24
Catania 23
Guangzhou 23
Jinan 22
Amsterdam 21
Tashkent 21
Chennai 20
Düsseldorf 20
Jakarta 20
Manchester 20
Brasília 19
London 19
Mexico City 19
Pune 19
Houston 18
San Mateo 18
Seattle 18
Tokyo 18
Hyderabad 17
Montreal 17
Shanghai 17
Chicago 16
Ningbo 16
Padova 16
Porto Alegre 16
Shenyang 16
Stockholm 16
Baghdad 15
Quito 15
San Francisco 15
Boston 14
Denver 14
Johannesburg 14
Phoenix 14
Shenzhen 14
Dong Ket 13
São José dos Campos 13
Atlanta 12
Toronto 12
Vienna 12
Guayaquil 11
Nanjing 11
Ribeirão Preto 11
Fortaleza 10
Norwalk 10
Nuremberg 10
Salvador 10
Washington 10
Campinas 9
Dhaka 9
Istanbul 9
Olomouc 9
Zhengzhou 9
Baku 8
Totale 10.133
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 347
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 260
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 235
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 234
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 232
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 208
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 203
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 203
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 193
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 192
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 191
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 185
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 183
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 181
Age dependent switching role of ciclyn D1 in breast cancer 179
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 179
Advances in Bioinformatics, Biostatistics and Omic Sciences 178
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 177
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 174
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 171
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 171
Aged fingerprints for DNA profile: First report of successful typing 171
Costameric proteins in human skeletal muscle during muscular inactivity. 168
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 168
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 165
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 162
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 161
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 159
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 157
A genetic dissection of antipsychotic induced movement disorders 156
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 155
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 154
Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder 154
A rare case of TMAU associated with suspected Currarino triad 153
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 150
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 149
Distribution and localization of vinculin-talin-integrin system and dystrophin-glycoprotein complex in human skeletal muscle - Immunohistochemical study using confocal laser scanning microscopy 149
Genes involved in pruning and inflammation are enriched in a large mega-sample of patients affected by Schizophrenia and Bipolar Disorder and controls 147
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 146
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 146
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 146
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 146
Editome landscape of CCM-derived endothelial cells 145
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 145
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 145
Chloride-sulphate exchange chemically measured in human erythrocyte ghosts 144
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 144
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 143
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 142
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 139
The serotonin transporter and the activity regulated cytoskeleton-associated protein genes in antidepressant response and resistance: 5-HTTLPR and other variants 139
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 139
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 139
A HORMONE RECEPTORS, CCND1 AND PROLIFERATION IN POSTMENOPAUSAL WOMEN 138
Genes Involved in Neurodevelopment, Neuroplasticity, and Bipolar Disorder: CACNA1C, CHRNA1, and MAPK1 138
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 138
Effetti del NiCl2 sugli eritrociti umani e sullo scambio anionico Cl-/HCO3- 137
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 134
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 132
Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients. 131
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 129
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 129
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 128
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 127
Sulphate influx in the erythrocytes of normotensive, diabetic and hypertensive patients 126
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 125
Sulphydryl groups involved in Na+-Li+ exchange in human erythrocytes 124
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 123
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 122
Oxidative Stress and the Neurovascular Unit 120
The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades 116
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 115
Molecular analysis of CCM genes promoter regions 115
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 115
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 113
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 112
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 109
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 108
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 108
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 108
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 107
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 106
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 106
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 105
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 104
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 101
Le basi genetiche delle malattie cardiovascolari: Genetica e malattie cardiovascolari: Ipertensione arteriosa 100
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 100
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 99
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia 99
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 99
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 99
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 98
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 98
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 96
Krit-1 mutations in 100 patients with cerebral cavernomas. 95
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 94
Sarcoglycans and integrins in muscular inactivity 94
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 93
Investigating the role of imprinted genes in pediatric sporadic brain arteriovenous malformations 93
Totale 14.408
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Categoria #
all - tutte 57.481
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 57.481
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021227 0 0 0 0 0 0 0 0 0 125 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
2025/20268.471 397 572 792 619 701 1.872 1.093 1.005 1.082 338 0 0
Totale 18.199