IRIS
D'ANGELO, Rosalia
 Distribuzione geografica
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Continente #
EU - Europa 6.199
NA - Nord America 4.566
AS - Asia 2.879
SA - Sud America 980
AF - Africa 83
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 5
Totale 14.719
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Nazione #
US - Stati Uniti d'America 4.471
RU - Federazione Russa 2.915
SG - Singapore 1.264
BR - Brasile 830
CN - Cina 767
IT - Italia 736
IE - Irlanda 655
SE - Svezia 652
HK - Hong Kong 350
DE - Germania 319
PL - Polonia 162
FR - Francia 158
UA - Ucraina 157
VN - Vietnam 156
GB - Regno Unito 138
FI - Finlandia 127
IN - India 81
AR - Argentina 44
BE - Belgio 38
CA - Canada 38
MX - Messico 38
BD - Bangladesh 37
TR - Turchia 36
NL - Olanda 32
ID - Indonesia 29
CO - Colombia 28
EC - Ecuador 28
ZA - Sudafrica 27
AT - Austria 24
CZ - Repubblica Ceca 24
JP - Giappone 22
IQ - Iraq 19
UZ - Uzbekistan 18
PK - Pakistan 17
VE - Venezuela 16
MA - Marocco 15
ES - Italia 14
PY - Paraguay 13
CL - Cile 11
PH - Filippine 10
LT - Lituania 9
EG - Egitto 8
IL - Israele 8
KE - Kenya 6
SA - Arabia Saudita 6
TH - Thailandia 6
DZ - Algeria 5
EU - Europa 5
GR - Grecia 5
JM - Giamaica 5
NP - Nepal 5
OM - Oman 5
PT - Portogallo 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CR - Costa Rica 4
ET - Etiopia 4
HR - Croazia 4
JO - Giordania 4
PE - Perù 4
UY - Uruguay 4
AO - Angola 3
AU - Australia 3
CI - Costa d'Avorio 3
DO - Repubblica Dominicana 3
GE - Georgia 3
IR - Iran 3
KZ - Kazakistan 3
LV - Lettonia 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
BY - Bielorussia 2
CH - Svizzera 2
HN - Honduras 2
HU - Ungheria 2
KH - Cambogia 2
KR - Corea 2
KW - Kuwait 2
LB - Libano 2
LU - Lussemburgo 2
MD - Moldavia 2
MT - Malta 2
NO - Norvegia 2
PA - Panama 2
RS - Serbia 2
SN - Senegal 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
DJ - Gibuti 1
GA - Gabon 1
GT - Guatemala 1
Totale 14.708
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Città #
Moscow 862
Singapore 711
Ashburn 704
Dublin 653
Dallas 563
Chandler 522
Hong Kong 344
Nyköping 340
Jacksonville 305
Beijing 304
Messina 257
San Jose 192
The Dalles 191
Warsaw 153
Los Angeles 101
Princeton 101
Medford 98
Munich 98
Lauterbourg 91
New York 86
Ann Arbor 81
São Paulo 79
Bremen 70
Des Moines 69
Cambridge 67
Boardman 57
Ho Chi Minh City 50
Dearborn 43
Buffalo 42
Lancaster 41
Redondo Beach 39
Turku 38
Orem 37
Woodbridge 36
Brussels 32
Wilmington 30
Hanoi 28
Tianjin 28
Rome 26
Milan 25
Council Bluffs 23
Rio de Janeiro 22
Belo Horizonte 21
Brooklyn 21
Catania 21
Santa Clara 21
Chennai 20
Frankfurt am Main 20
Manchester 20
Pune 19
Amsterdam 18
Helsinki 18
Jakarta 18
Düsseldorf 16
Houston 16
Jinan 16
Mexico City 16
Shenyang 16
Tokyo 16
London 15
Montreal 15
San Mateo 15
Seattle 15
Tashkent 15
Guangzhou 14
Shanghai 14
Shenzhen 14
Brasília 13
Dong Ket 13
Ningbo 13
San Francisco 13
Stockholm 13
São José dos Campos 13
Atlanta 12
Johannesburg 12
Denver 11
Phoenix 11
Quito 11
Vienna 11
Boston 10
Chicago 10
Nanjing 10
Norwalk 10
Porto Alegre 10
Toronto 10
Hyderabad 9
Nuremberg 9
Olomouc 9
Padova 9
Washington 9
Baghdad 8
Guayaquil 8
Istanbul 8
Lappeenranta 8
Medellín 8
Prague 8
Curitiba 7
Dhaka 7
Guarulhos 7
Limeira 7
Totale 8.396
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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
Altered platelet magnesium and plasma and urinary soluble form of intercellular adhesion molecule I (sICAM-1) concentrations in insulin dependent diabetes mellitus (IDDM) patients with microalbuminuria. 229
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 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
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
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 155
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
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
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 Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 140
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 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
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 138
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
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
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 125
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
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 118
GENETICS OF CAVERNOMAS: A CASE REPORT 117
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 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
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
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
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 93
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 93
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 91
Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy 91
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases 90
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 89
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 89
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 87
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 87
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 87
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 86
NOVEL GENES INVOLVED IN ETIOPATHOGENESIS OF RETINITIS PIGMENTOSA ORPHANFORMS 86
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 85
FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 84
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 84
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 83
Genetics of suicide, from genes to behaviour 83
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 80
Sarcoglycans in human smooth muscle: a clsm and molecular study 80
Totale 13.607
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Categoria #
all - tutte 47.831
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 47.831
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021184 0 0 0 0 0 0 0 0 0 91 59 34
2021/2022794 3 86 32 13 14 10 33 45 14 221 71 252
2022/20232.027 147 166 98 170 194 185 27 138 817 5 68 12
2023/2024550 43 85 26 57 47 127 3 23 2 22 17 98
2024/20252.626 64 26 73 183 96 97 99 546 617 158 241 426
2025/20266.996 322 474 656 467 601 1.488 949 827 908 304 0 0
Totale 15.110