IRIS
SIDOTI, Antonina
 Distribuzione geografica
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Continente #
EU - Europa 3.009
NA - Nord America 2.741
AS - Asia 366
SA - Sud America 10
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 1
Totale 6.138
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Nazione #
US - Stati Uniti d'America 2.731
IE - Irlanda 798
SE - Svezia 783
IT - Italia 574
CN - Cina 312
DE - Germania 204
UA - Ucraina 198
PL - Polonia 136
GB - Regno Unito 110
FI - Finlandia 93
BE - Belgio 42
FR - Francia 24
IN - India 22
RU - Federazione Russa 14
VN - Vietnam 14
NL - Olanda 12
CA - Canada 8
JP - Giappone 7
CO - Colombia 5
CZ - Repubblica Ceca 5
EU - Europa 4
NZ - Nuova Zelanda 4
SG - Singapore 4
AU - Australia 3
BR - Brasile 3
AT - Austria 2
CL - Cile 2
ES - Italia 2
HK - Hong Kong 2
LT - Lituania 2
MT - Malta 2
MX - Messico 2
PH - Filippine 2
PT - Portogallo 2
CH - Svizzera 1
EG - Egitto 1
GR - Grecia 1
IL - Israele 1
IQ - Iraq 1
IR - Iran 1
LU - Lussemburgo 1
MD - Moldavia 1
NO - Norvegia 1
RO - Romania 1
Totale 6.138
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Città #
Dublin 796
Chandler 636
Nyköping 420
Jacksonville 411
Beijing 181
Messina 177
Ashburn 152
Warsaw 136
Princeton 126
Medford 114
Ann Arbor 96
Cambridge 91
Des Moines 87
Bremen 74
Dearborn 72
Lancaster 65
New York 47
Boardman 45
Wilmington 38
Woodbridge 37
Brussels 36
Jinan 22
Rome 19
San Mateo 18
Pune 17
Catania 16
Padova 16
Shenyang 16
Ningbo 15
Milan 14
Dong Ket 13
Seattle 11
Norwalk 10
Nanjing 9
Tianjin 9
Washington 9
Clearwater 6
Hangzhou 6
Taizhou 6
Zhengzhou 6
Amsterdam 5
Houston 5
Ottawa 5
Waanrode 5
Ancona 4
Enna 4
Ferrandina 4
Genova 4
Hefei 4
Helsinki 4
Jiaxing 4
Nanchang 4
Novokuznetsk 4
Prague 4
Rosolini 4
Salerno 4
Taiyuan 4
Termoli 4
Torino 4
Turin 4
Auburn Hills 3
Changsha 3
Falls Church 3
Fuzhou 3
Hebei 3
Lago 3
Los Angeles 3
Mineo 3
Mountain View 3
Napoli 3
Paris 3
San Giovanni La Punta 3
Stockholm 3
Tappahannock 3
Terni 3
Vicosa 3
Whakatane 3
Alcamo 2
Atlanta 2
Belvedere Spinello 2
Cagliari 2
Chicago 2
Dallas 2
Edinburgh 2
Foligno 2
Guangzhou 2
Haikou 2
Lanzhou 2
Lappeenranta 2
Lisbon 2
London 2
Manila 2
Melbourne 2
Milazzo 2
Montalbano 2
Odesa 2
Perugia 2
Phoenix 2
Piazza Armerina 2
Pietà 2
Totale 4.256
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 289
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 103
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 102
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 94
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 94
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 91
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 88
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 82
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 80
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 80
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 77
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 73
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 72
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 70
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 70
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 69
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 68
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 67
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 66
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin 65
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 64
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 61
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 61
Molecular analysis of CCM genes promoter regions 59
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 58
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 57
The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades 56
Effetti del NiCl2 sugli eritrociti umani e sullo scambio anionico Cl-/HCO3- 53
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 53
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 53
The serotonin transporter and the activity regulated cytoskeleton-associated protein genes in antidepressant response and resistance: 5-HTTLPR and other variants 53
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 52
A HORMONE RECEPTORS, CCND1 AND PROLIFERATION IN POSTMENOPAUSAL WOMEN 51
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 51
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia 51
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 51
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 50
Chloride-sulphate exchange chemically measured in human erythrocyte ghosts 50
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 50
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 50
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 50
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 50
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 50
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 49
Effetti contrastanti di alcuni ossidanti sul trasporto di litio in globuli rossi umani 49
Age dependent switching role of ciclyn D1 in breast cancer 49
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 49
Investigating the role of imprinted genes in pediatric sporadic brain arteriovenous malformations 49
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 48
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 48
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 48
The interaction of haemoglobin, magnesium, organic phosphates and band 3 protein in nucleated and anucleated erythrocytes 48
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 48
Distribution of delta 32 mutated allele of ccr5 gene in a healthy sicilian population 47
Distribution and localization of vinculin-talin-integrin system and dystrophin-glycoprotein complex in human skeletal muscle - Immunohistochemical study using confocal laser scanning microscopy 47
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 47
Sarcoglycans and airway epithelium: nucleotide sequence and immunohistochemical analysis. 47
A genetic dissection of antipsychotic induced movement disorders 47
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 47
Le basi genetiche delle malattie cardiovascolari: Genetica e malattie cardiovascolari: Ipertensione arteriosa 46
Krit-1 mutations in 100 patients with cerebral cavernomas. 46
null 46
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 46
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 46
Sulphate influx in the erythrocytes of normotensive, diabetic and hypertensive patients 45
Advances in Bioinformatics, Biostatistics and Omic Sciences 45
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 45
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 44
CCR5Δ32 POLYMORPHISM ASSOCIATED WITH A SLOWER RATE DISEASE PROGRESSION IN A COHORT OF RR-MS SICILIAN PATIENTS 44
Case-control association study of 36 single-nucleotide polymorphisms within 10 candidate genes for major depression and bipolar disorder 44
Sulphydryl groups involved in Na+-Li+ exchange in human erythrocytes 43
Sarcoglycans and integrins in muscular inactivity 43
Fmo3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis 43
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 42
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 42
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 40
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 40
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 40
HIV nef protein is a potential candidate vaccine against AIDS 39
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 39
null 38
Sarcoglycans in human smooth muscle: a clsm and molecular study 38
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 38
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 38
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 38
Oxidative Stress and the Neurovascular Unit 38
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 37
Aged fingerprints for DNA profile: First report of successful typing 37
Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients. 36
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 36
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 35
VIRUS 35
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 35
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 35
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 35
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 35
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 34
Costameric proteins in human skeletal muscle during muscular inactivity. 34
A rare case of TMAU associated with suspected Currarino triad 34
The molecular interaction between the glutamatergic, noradrenergic, dopaminergic and serotoninergic systems informs a detailed genetic perspective on depressive phenotypes. 33
Totale 5.428
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Categoria #
all - tutte 22.970
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 22.970
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019197 0 0 0 0 0 0 0 0 0 172 11 14
2019/2020819 114 53 6 63 7 75 90 71 9 161 142 28
2020/2021828 128 26 106 42 83 75 37 57 47 125 63 39
2021/2022941 4 98 37 19 14 10 54 50 16 242 101 296
2022/20232.463 182 213 122 207 225 227 29 162 997 6 79 14
2023/2024497 54 95 31 66 59 134 11 37 2 8 0 0
Totale 6.447