IRIS
SIDOTI, Antonina
 Distribuzione geografica
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Continente #
EU - Europa 7.513
NA - Nord America 7.198
AS - Asia 3.538
SA - Sud America 1.279
Continente sconosciuto - Info sul continente non disponibili 441
AF - Africa 101
OC - Oceania 9
Totale 20.079
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Nazione #
US - Stati Uniti d'America 7.003
RU - Federazione Russa 3.524
SG - Singapore 1.522
BR - Brasile 1.080
CN - Cina 971
IT - Italia 921
IE - Irlanda 799
SE - Svezia 788
HK - Hong Kong 411
DE - Germania 368
UA - Ucraina 206
VN - Vietnam 200
GB - Regno Unito 198
FR - Francia 185
PL - Polonia 167
FI - Finlandia 154
IN - India 94
CA - Canada 86
AR - Argentina 55
BD - Bangladesh 49
MX - Messico 46
BE - Belgio 43
TR - Turchia 42
EC - Ecuador 41
NL - Olanda 40
ID - Indonesia 37
CO - Colombia 36
ZA - Sudafrica 31
IQ - Iraq 28
AT - Austria 27
JP - Giappone 25
UZ - Uzbekistan 24
CZ - Repubblica Ceca 22
VE - Venezuela 22
PK - Pakistan 20
CL - Cile 18
MA - Marocco 17
JM - Giamaica 16
PY - Paraguay 15
ES - Italia 14
IL - Israele 13
CR - Costa Rica 11
LT - Lituania 10
MY - Malesia 10
PH - Filippine 10
AZ - Azerbaigian 9
EG - Egitto 8
TH - Thailandia 8
KE - Kenya 7
SA - Arabia Saudita 7
TN - Tunisia 7
TT - Trinidad e Tobago 7
GR - Grecia 6
GT - Guatemala 6
OM - Oman 6
AE - Emirati Arabi Uniti 5
CI - Costa d'Avorio 5
DZ - Algeria 5
ET - Etiopia 5
JO - Giordania 5
NP - Nepal 5
PE - Perù 5
AL - Albania 4
AO - Angola 4
AU - Australia 4
DO - Repubblica Dominicana 4
EU - Europa 4
GE - Georgia 4
HN - Honduras 4
HR - Croazia 4
LV - Lettonia 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
PA - Panama 4
PT - Portogallo 4
UY - Uruguay 4
BO - Bolivia 3
CH - Svizzera 3
KG - Kirghizistan 3
KW - Kuwait 3
KZ - Kazakistan 3
LB - Libano 3
LU - Lussemburgo 3
MD - Moldavia 3
MN - Mongolia 3
PS - Palestinian Territory 3
SC - Seychelles 3
SN - Senegal 3
BH - Bahrain 2
BY - Bielorussia 2
EE - Estonia 2
IR - Iran 2
KH - Cambogia 2
KR - Corea 2
MT - Malta 2
NO - Norvegia 2
PR - Porto Rico 2
RS - Serbia 2
SV - El Salvador 2
TW - Taiwan 2
Totale 19.621
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Città #
Moscow 1.057
Ashburn 1.040
Singapore 831
Dublin 796
Dallas 673
Chandler 622
San Jose 465
Jacksonville 412
Nyköping 411
Hong Kong 407
Beijing 385
Messina 263
Council Bluffs 252
The Dalles 231
Warsaw 157
Los Angeles 137
Princeton 126
Lauterbourg 114
Medford 113
New York 113
Munich 106
São Paulo 94
Ann Arbor 92
Cambridge 91
Des Moines 90
Bremen 73
Dearborn 72
Boardman 66
Ho Chi Minh City 65
Lancaster 63
Buffalo 60
Santa Clara 60
Orem 47
Rome 44
Redondo Beach 39
Wilmington 39
Hanoi 38
Woodbridge 38
Brussels 37
Tianjin 36
Turku 36
Brooklyn 35
Milan 32
Phoenix 31
Rio de Janeiro 31
Belo Horizonte 28
Atlanta 26
Houston 26
Montreal 26
Chicago 25
Catania 24
Helsinki 24
Frankfurt am Main 23
Guangzhou 23
Brasília 22
Jinan 22
London 22
San Francisco 22
Amsterdam 21
Tashkent 21
Chennai 20
Denver 20
Düsseldorf 20
Jakarta 20
Manchester 20
Tokyo 20
Mexico City 19
Pune 19
Seattle 19
Columbus 18
San Mateo 18
Boston 17
Shanghai 17
Toronto 17
Hyderabad 16
Naples 16
Ningbo 16
Padova 16
Porto Alegre 16
Shenyang 16
Stockholm 16
Baghdad 15
Quito 15
Johannesburg 14
Shenzhen 14
Dong Ket 13
Guayaquil 13
São José dos Campos 13
Washington 13
Nanjing 12
Vienna 12
Ribeirão Preto 11
Fortaleza 10
Norwalk 10
Nuremberg 10
Salvador 10
Campinas 9
Dhaka 9
Istanbul 9
Olomouc 9
Totale 10.972
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 359
A mixture of postbiotics/tyndallized probiotics reduces trimethylamine (TMA) in trimethylaminuria models: Evidence from in vitro and in vivo studies 282
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 272
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 260
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 247
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 245
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 224
The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades 220
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 216
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 215
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 215
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 207
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 203
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 201
Aged fingerprints for DNA profile: First report of successful typing 195
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 192
Age dependent switching role of ciclyn D1 in breast cancer 190
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 190
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 189
Advances in Bioinformatics, Biostatistics and Omic Sciences 188
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 184
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 182
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 182
Costameric proteins in human skeletal muscle during muscular inactivity. 182
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 180
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 180
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 178
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 173
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 172
A genetic dissection of antipsychotic induced movement disorders 172
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 170
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 169
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 167
Distribution and localization of vinculin-talin-integrin system and dystrophin-glycoprotein complex in human skeletal muscle - Immunohistochemical study using confocal laser scanning microscopy 166
Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder 164
A rare case of TMAU associated with suspected Currarino triad 164
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 163
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 161
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 161
Genes involved in pruning and inflammation are enriched in a large mega-sample of patients affected by Schizophrenia and Bipolar Disorder and controls 159
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 158
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 157
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 156
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 156
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 156
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 155
Editome landscape of CCM-derived endothelial cells 154
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 154
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 154
Chloride-sulphate exchange chemically measured in human erythrocyte ghosts 153
Genes Involved in Neurodevelopment, Neuroplasticity, and Bipolar Disorder: CACNA1C, CHRNA1, and MAPK1 152
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 151
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 151
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 150
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 149
The serotonin transporter and the activity regulated cytoskeleton-associated protein genes in antidepressant response and resistance: 5-HTTLPR and other variants 149
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 147
A HORMONE RECEPTORS, CCND1 AND PROLIFERATION IN POSTMENOPAUSAL WOMEN 146
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 145
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 143
Effetti del NiCl2 sugli eritrociti umani e sullo scambio anionico Cl-/HCO3- 142
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 141
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 140
Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients. 139
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 136
Sulphate influx in the erythrocytes of normotensive, diabetic and hypertensive patients 135
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 135
Sulphydryl groups involved in Na+-Li+ exchange in human erythrocytes 134
Oxidative Stress and the Neurovascular Unit 133
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 132
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 130
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 129
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 127
Molecular analysis of CCM genes promoter regions 124
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 123
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 122
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 120
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases 119
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 119
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 118
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 117
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 117
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 116
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 116
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 116
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 115
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 114
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 113
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 111
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 110
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 109
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 108
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 108
Sarcoglycans and integrins in muscular inactivity 107
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 106
New evaluation methods of read mapping by 17 aligners on simulated and empirical NGS data: an updated comparison of DNA- and RNA-Seq data from Illumina and Ion Torrent technologies 106
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 105
Le basi genetiche delle malattie cardiovascolari: Genetica e malattie cardiovascolari: Ipertensione arteriosa 104
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia 104
Krit-1 mutations in 100 patients with cerebral cavernomas. 103
Totale 15.778
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Categoria #
all - tutte 66.807
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 66.807
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022798 0 0 0 19 14 10 54 50 16 242 100 293
2022/20232.428 180 207 120 200 223 223 29 158 990 6 78 14
2023/2024641 53 95 30 66 59 133 11 37 2 27 17 111
2024/20253.121 71 29 87 208 117 117 103 667 746 190 277 509
2025/20268.859 392 565 780 611 693 1.854 1.088 994 1.075 398 164 245
2026/20271.563 229 516 509 309 0 0 0 0 0 0 0 0
Totale 20.079