IRIS
SIDOTI, Antonina
 Distribuzione geografica
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Continente #
EU - Europa 7.413
NA - Nord America 6.139
AS - Asia 3.519
SA - Sud America 1.268
Continente sconosciuto - Info sul continente non disponibili 441
AF - Africa 98
OC - Oceania 9
Totale 18.887
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Nazione #
US - Stati Uniti d'America 5.987
RU - Federazione Russa 3.524
SG - Singapore 1.519
BR - Brasile 1.075
CN - Cina 964
IT - Italia 828
IE - Irlanda 799
SE - Svezia 788
HK - Hong Kong 408
DE - Germania 368
UA - Ucraina 206
VN - Vietnam 200
GB - Regno Unito 191
FR - Francia 185
PL - Polonia 167
FI - Finlandia 154
IN - India 93
CA - Canada 66
AR - Argentina 55
BD - Bangladesh 46
MX - Messico 46
BE - Belgio 43
TR - Turchia 42
EC - Ecuador 40
NL - Olanda 40
ID - Indonesia 37
CO - Colombia 35
ZA - Sudafrica 31
IQ - Iraq 28
AT - Austria 27
JP - Giappone 24
UZ - Uzbekistan 24
CZ - Repubblica Ceca 22
PK - Pakistan 20
VE - Venezuela 19
CL - Cile 17
MA - Marocco 17
PY - Paraguay 15
ES - Italia 14
IL - Israele 13
LT - Lituania 10
MY - Malesia 10
PH - Filippine 10
AZ - Azerbaigian 9
JM - Giamaica 9
EG - Egitto 8
TH - Thailandia 8
CR - Costa Rica 7
KE - Kenya 7
TN - Tunisia 7
GR - Grecia 6
OM - Oman 6
SA - Arabia Saudita 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
TT - Trinidad e Tobago 5
AL - Albania 4
AO - Angola 4
AU - Australia 4
DO - Repubblica Dominicana 4
EU - Europa 4
GE - Georgia 4
GT - Guatemala 4
HR - Croazia 4
LV - Lettonia 4
NZ - Nuova Zelanda 4
PA - Panama 4
PT - Portogallo 4
UY - Uruguay 4
BO - Bolivia 3
CH - Svizzera 3
HN - Honduras 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
SN - Senegal 3
BH - Bahrain 2
BY - Bielorussia 2
EE - Estonia 2
IR - Iran 2
KH - Cambogia 2
KR - Corea 2
MT - Malta 2
NI - Nicaragua 2
NO - Norvegia 2
PR - Porto Rico 2
RS - Serbia 2
TW - Taiwan 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
Totale 18.434
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Città #
Moscow 1.057
Ashburn 918
Singapore 830
Dublin 796
Dallas 664
Chandler 622
Nyköping 411
Jacksonville 410
Hong Kong 404
Beijing 380
San Jose 294
Messina 262
The Dalles 231
Warsaw 157
Los Angeles 128
Princeton 125
Lauterbourg 114
Medford 113
Munich 106
New York 105
São Paulo 94
Ann Arbor 92
Cambridge 90
Des Moines 90
Council Bluffs 85
Bremen 73
Dearborn 72
Boardman 66
Ho Chi Minh City 65
Lancaster 63
Buffalo 57
Santa Clara 49
Orem 45
Redondo Beach 39
Hanoi 38
Wilmington 38
Brussels 37
Woodbridge 37
Tianjin 36
Turku 36
Rome 32
Rio de Janeiro 31
Brooklyn 30
Belo Horizonte 27
Milan 27
Montreal 25
Helsinki 24
Catania 23
Frankfurt am Main 23
Guangzhou 23
Chicago 22
Jinan 22
London 22
Amsterdam 21
Tashkent 21
Chennai 20
Düsseldorf 20
Houston 20
Jakarta 20
Manchester 20
Atlanta 19
Brasília 19
Mexico City 19
Pune 19
San Francisco 19
Tokyo 19
San Mateo 18
Seattle 18
Denver 17
Shanghai 17
Hyderabad 16
Ningbo 16
Padova 16
Porto Alegre 16
Shenyang 16
Stockholm 16
Baghdad 15
Phoenix 15
Quito 15
Boston 14
Johannesburg 14
Shenzhen 14
Toronto 14
Dong Ket 13
São José dos Campos 13
Guayaquil 12
Nanjing 12
Vienna 12
Naples 11
Ribeirão Preto 11
Washington 11
Fortaleza 10
Norwalk 10
Nuremberg 10
Salvador 10
Campinas 9
Dhaka 9
Istanbul 9
Olomouc 9
Zhengzhou 9
Totale 10.363
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 350
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 264
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 240
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 238
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 235
The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades 217
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 211
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 208
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 208
A mixture of postbiotics/tyndallized probiotics reduces trimethylamine (TMA) in trimethylaminuria models: Evidence from in vitro and in vivo studies 203
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 202
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 198
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 194
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 189
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 187
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 184
Aged fingerprints for DNA profile: First report of successful typing 184
Age dependent switching role of ciclyn D1 in breast cancer 183
Advances in Bioinformatics, Biostatistics and Omic Sciences 182
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 179
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 177
Costameric proteins in human skeletal muscle during muscular inactivity. 177
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 176
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 175
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 173
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 170
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 169
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 164
A genetic dissection of antipsychotic induced movement disorders 164
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 162
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 160
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 159
Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder 159
Distribution and localization of vinculin-talin-integrin system and dystrophin-glycoprotein complex in human skeletal muscle - Immunohistochemical study using confocal laser scanning microscopy 158
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 156
A rare case of TMAU associated with suspected Currarino triad 156
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 154
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 153
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 152
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 152
Genes involved in pruning and inflammation are enriched in a large mega-sample of patients affected by Schizophrenia and Bipolar Disorder and controls 150
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 149
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 149
Editome landscape of CCM-derived endothelial cells 148
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 148
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 148
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 147
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 146
Chloride-sulphate exchange chemically measured in human erythrocyte ghosts 145
The serotonin transporter and the activity regulated cytoskeleton-associated protein genes in antidepressant response and resistance: 5-HTTLPR and other variants 145
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 144
A HORMONE RECEPTORS, CCND1 AND PROLIFERATION IN POSTMENOPAUSAL WOMEN 143
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 142
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 141
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 141
Genes Involved in Neurodevelopment, Neuroplasticity, and Bipolar Disorder: CACNA1C, CHRNA1, and MAPK1 141
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 141
Effetti del NiCl2 sugli eritrociti umani e sullo scambio anionico Cl-/HCO3- 138
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 137
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 135
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 134
Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients. 133
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 133
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 129
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 129
Sulphate influx in the erythrocytes of normotensive, diabetic and hypertensive patients 127
Sulphydryl groups involved in Na+-Li+ exchange in human erythrocytes 127
Oxidative Stress and the Neurovascular Unit 127
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 126
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 125
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 119
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 118
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 117
Molecular analysis of CCM genes promoter regions 116
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 115
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 113
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 112
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 111
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 111
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 111
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases 110
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 109
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 109
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 108
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 107
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 105
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 104
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 104
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 104
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 101
Le basi genetiche delle malattie cardiovascolari: Genetica e malattie cardiovascolari: Ipertensione arteriosa 101
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 101
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 101
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 100
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 100
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia 99
Krit-1 mutations in 100 patients with cerebral cavernomas. 98
Sarcoglycans and integrins in muscular inactivity 97
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 95
Totale 14.963
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Categoria #
all - tutte 62.760
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 62.760
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022933 0 98 37 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
2026/2027371 229 142 0 0 0 0 0 0 0 0 0 0
Totale 18.887