IRIS
D'ANGELO, Rosalia
 Distribuzione geografica
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Continente #
EU - Europa 6.422
NA - Nord America 5.957
AS - Asia 2.986
SA - Sud America 1.000
Continente sconosciuto - Info sul continente non disponibili 411
AF - Africa 95
OC - Oceania 11
Totale 16.882
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Nazione #
US - Stati Uniti d'America 5.711
RU - Federazione Russa 2.928
SG - Singapore 1.281
IT - Italia 911
BR - Brasile 841
CN - Cina 806
IE - Irlanda 656
SE - Svezia 654
HK - Hong Kong 356
DE - Germania 323
PL - Polonia 163
FR - Francia 162
VN - Vietnam 160
UA - Ucraina 159
GB - Regno Unito 151
FI - Finlandia 127
CA - Canada 97
IN - India 83
AR - Argentina 46
BD - Bangladesh 46
MX - Messico 39
BE - Belgio 38
TR - Turchia 37
NL - Olanda 35
ID - Indonesia 32
CO - Colombia 29
EC - Ecuador 28
ZA - Sudafrica 28
AT - Austria 24
CZ - Repubblica Ceca 24
JP - Giappone 24
IL - Israele 21
IQ - Iraq 19
VE - Venezuela 19
PK - Pakistan 18
UZ - Uzbekistan 18
HN - Honduras 16
MA - Marocco 15
CR - Costa Rica 14
ES - Italia 14
GT - Guatemala 14
JM - Giamaica 14
CL - Cile 13
PY - Paraguay 13
PH - Filippine 11
PR - Porto Rico 11
SC - Seychelles 11
GP - Guadalupe 10
LT - Lituania 9
TH - Thailandia 9
TT - Trinidad e Tobago 9
EG - Egitto 8
AU - Australia 7
SA - Arabia Saudita 7
SV - El Salvador 7
AE - Emirati Arabi Uniti 6
CW - ???statistics.table.value.countryCode.CW??? 6
KE - Kenya 6
NI - Nicaragua 6
DZ - Algeria 5
EU - Europa 5
GR - Grecia 5
MY - Malesia 5
NP - Nepal 5
OM - Oman 5
PE - Perù 5
PT - Portogallo 5
TN - Tunisia 5
AZ - Azerbaigian 4
ET - Etiopia 4
HR - Croazia 4
JO - Giordania 4
UY - Uruguay 4
AO - Angola 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
DK - Danimarca 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
RS - Serbia 2
SN - Senegal 2
TW - Taiwan 2
Totale 16.458
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Città #
Ashburn 873
Moscow 861
Singapore 715
Dublin 653
Dallas 573
Chandler 522
San Jose 406
Hong Kong 350
Nyköping 340
Beijing 311
Jacksonville 307
Messina 265
The Dalles 191
Council Bluffs 186
Warsaw 154
Los Angeles 117
Princeton 102
Medford 98
Munich 98
New York 98
Lauterbourg 91
Ann Arbor 81
São Paulo 79
Des Moines 71
Bremen 70
Cambridge 68
Boardman 59
Santa Clara 54
Ho Chi Minh City 52
Rome 49
Buffalo 47
Dearborn 43
Lancaster 42
Orem 39
Redondo Beach 39
Turku 38
Woodbridge 37
Milan 36
Brussels 32
Wilmington 31
Hanoi 28
Tianjin 28
Phoenix 27
Brooklyn 25
Montreal 25
Houston 24
Belo Horizonte 22
Catania 22
Rio de Janeiro 22
Atlanta 20
Chennai 20
Frankfurt am Main 20
Manchester 20
North Bergen 20
Pune 19
Amsterdam 18
Helsinki 18
Jakarta 18
London 18
Tokyo 18
Brasília 17
Chicago 17
Düsseldorf 16
Jinan 16
Mexico City 16
San Francisco 16
San Mateo 16
Seattle 16
Shenyang 16
Toronto 16
Columbus 15
Denver 15
Naples 15
Tashkent 15
Guangzhou 14
Shanghai 14
Shenzhen 14
Dong Ket 13
Ningbo 13
Stockholm 13
São José dos Campos 13
Washington 13
Boston 12
Johannesburg 12
Turin 12
Nanjing 11
Quito 11
San José 11
Vienna 11
Florence 10
Guatemala City 10
Norwalk 10
Porto Alegre 10
Bologna 9
Hyderabad 9
Istanbul 9
Nuremberg 9
Olomouc 9
Padova 9
Palermo 9
Totale 9.222
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 360
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 274
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 266
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 254
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 249
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. 240
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 229
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 221
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 219
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 216
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 210
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 208
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 204
Aged fingerprints for DNA profile: First report of successful typing 199
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 196
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 194
Age dependent switching role of ciclyn D1 in breast cancer 192
Advances in Bioinformatics, Biostatistics and Omic Sciences 191
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 190
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 190
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 184
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 182
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 182
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 181
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 180
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 177
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 176
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 173
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 169
A rare case of TMAU associated with suspected Currarino triad 168
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 167
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 163
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 163
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 160
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 160
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 159
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 159
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 158
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 157
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 157
Editome landscape of CCM-derived endothelial cells 156
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 156
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 155
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 153
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 153
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 152
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 152
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 149
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 147
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 145
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 142
Oxidative Stress and the Neurovascular Unit 138
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 136
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 135
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 134
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 132
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 131
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 128
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 128
From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases 127
GENETICS OF CAVERNOMAS: A CASE REPORT 125
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 124
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 121
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 120
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 120
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 119
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 118
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 118
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 118
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 118
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 117
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 117
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 115
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 113
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 112
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 111
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 110
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 109
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 109
Sarcoglycans and integrins in muscular inactivity 108
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 107
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 107
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 106
Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy 106
Krit-1 mutations in 100 patients with cerebral cavernomas. 105
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 105
Genetics of suicide, from genes to behaviour 102
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 101
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 100
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 100
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 99
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity 97
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 96
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 95
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 95
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 95
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 92
NOVEL GENES INVOLVED IN ETIOPATHOGENESIS OF RETINITIS PIGMENTOSA ORPHANFORMS 92
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 91
Sarcoglycans in human smooth muscle: a clsm and molecular study 91
Totale 15.030
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Categoria #
all - tutte 56.979
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 56.979
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022660 0 0 0 0 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
2026/20271.480 161 283 454 452 130 0 0 0 0 0 0 0
Totale 16.882