IRIS
D'ANGELO, Rosalia
 Distribuzione geografica
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Continente #
EU - Europa 6.255
NA - Nord America 5.068
AS - Asia 2.963
SA - Sud America 987
Continente sconosciuto - Info sul continente non disponibili 405
AF - Africa 84
OC - Oceania 7
Totale 15.769
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Nazione #
US - Stati Uniti d'America 4.939
RU - Federazione Russa 2.909
SG - Singapore 1.279
BR - Brasile 834
CN - Cina 804
IT - Italia 785
IE - Irlanda 656
SE - Svezia 652
HK - Hong Kong 356
DE - Germania 319
PL - Polonia 163
FR - Francia 160
VN - Vietnam 160
UA - Ucraina 158
GB - Regno Unito 141
FI - Finlandia 127
IN - India 82
CA - Canada 55
AR - Argentina 45
BD - Bangladesh 45
MX - Messico 39
BE - Belgio 38
TR - Turchia 36
NL - Olanda 34
ID - Indonesia 32
CO - Colombia 28
EC - Ecuador 28
ZA - Sudafrica 27
AT - Austria 24
CZ - Repubblica Ceca 24
JP - Giappone 23
IQ - Iraq 19
UZ - Uzbekistan 18
PK - Pakistan 17
VE - Venezuela 17
MA - Marocco 15
ES - Italia 14
PY - Paraguay 13
CL - Cile 12
PH - Filippine 11
LT - Lituania 9
TH - Thailandia 9
CR - Costa Rica 8
EG - Egitto 8
IL - Israele 8
JM - Giamaica 7
SA - Arabia Saudita 7
AE - Emirati Arabi Uniti 6
KE - Kenya 6
DZ - Algeria 5
EU - Europa 5
GR - Grecia 5
MY - Malesia 5
NP - Nepal 5
OM - Oman 5
PT - Portogallo 5
TN - Tunisia 5
AZ - Azerbaigian 4
ET - Etiopia 4
GT - Guatemala 4
HN - Honduras 4
HR - Croazia 4
JO - Giordania 4
PE - Perù 4
TT - Trinidad e Tobago 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
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
AL - Albania 2
BY - Bielorussia 2
CH - Svizzera 2
EE - Estonia 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
PR - Porto Rico 2
RS - Serbia 2
SN - Senegal 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
Totale 15.354
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Città #
Moscow 861
Ashburn 764
Singapore 715
Dublin 653
Dallas 567
Chandler 522
Hong Kong 350
Nyköping 340
Beijing 311
Jacksonville 306
San Jose 275
Messina 264
The Dalles 191
Council Bluffs 164
Warsaw 154
Los Angeles 109
Princeton 101
Medford 98
Munich 98
Lauterbourg 91
New York 90
Ann Arbor 81
São Paulo 79
Des Moines 71
Bremen 70
Cambridge 67
Boardman 57
Ho Chi Minh City 52
Buffalo 44
Santa Clara 44
Dearborn 43
Lancaster 42
Redondo Beach 39
Turku 38
Orem 37
Woodbridge 36
Brussels 32
Wilmington 30
Rome 29
Hanoi 28
Milan 28
Tianjin 28
Montreal 22
Rio de Janeiro 22
Belo Horizonte 21
Brooklyn 21
Catania 21
Chennai 20
Frankfurt am Main 20
Houston 20
Manchester 20
Pune 19
Amsterdam 18
Helsinki 18
Jakarta 18
London 17
Tokyo 17
Düsseldorf 16
Jinan 16
Mexico City 16
San Francisco 16
San Mateo 16
Seattle 16
Shenyang 16
Columbus 15
Tashkent 15
Atlanta 14
Denver 14
Guangzhou 14
Shanghai 14
Shenzhen 14
Brasília 13
Chicago 13
Dong Ket 13
Ningbo 13
Stockholm 13
São José dos Campos 13
Johannesburg 12
Phoenix 12
Toronto 12
Nanjing 11
Quito 11
Vienna 11
Boston 10
Norwalk 10
Porto Alegre 10
Washington 10
Hyderabad 9
Nuremberg 9
Olomouc 9
Padova 9
Baghdad 8
Guayaquil 8
Istanbul 8
Lappeenranta 8
Medellín 8
Naples 8
Prague 8
Curitiba 7
Dhaka 7
Totale 8.798
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 351
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 266
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 243
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 240
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 237
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. 232
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 213
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 210
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 209
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 204
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 199
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 198
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 195
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 189
Aged fingerprints for DNA profile: First report of successful typing 187
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 185
Age dependent switching role of ciclyn D1 in breast cancer 185
Advances in Bioinformatics, Biostatistics and Omic Sciences 183
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 179
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 178
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 178
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 178
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 173
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 171
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 165
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 161
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 160
A rare case of TMAU associated with suspected Currarino triad 158
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 157
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 155
Absence of mutations at SERPINI1 gene in a cohort of 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 154
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 152
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 150
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 150
Editome landscape of CCM-derived endothelial cells 149
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 149
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 149
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 148
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 146
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 145
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 145
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 144
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 143
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 142
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 141
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 138
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 135
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 134
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 130
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 127
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 127
Oxidative Stress and the Neurovascular Unit 127
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 120
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 120
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 119
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 118
GENETICS OF CAVERNOMAS: A CASE REPORT 118
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 115
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 114
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 113
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 113
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases 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 112
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 111
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 110
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 110
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 109
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 107
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 107
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 107
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 106
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 105
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 103
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 103
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 102
Krit-1 mutations in 100 patients with cerebral cavernomas. 101
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 101
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 101
Sarcoglycans and integrins in muscular inactivity 98
Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy 98
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 96
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 96
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 95
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 94
Genetics of suicide, from genes to behaviour 92
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 91
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 90
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 89
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 89
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 89
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 89
NOVEL GENES INVOLVED IN ETIOPATHOGENESIS OF RETINITIS PIGMENTOSA ORPHANFORMS 89
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 88
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 87
FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 86
Genetic and functional study of CCR5 gene in HIV-1 infection 85
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 85
Totale 14.136
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Categoria #
all - tutte 53.137
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 53.137
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022791 0 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
2025/20267.288 322 474 656 467 601 1.488 949 827 898 356 123 127
2026/2027367 161 206 0 0 0 0 0 0 0 0 0 0
Totale 15.769