IRIS
D'ANGELO, Rosalia
 Distribuzione geografica
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Continente #
NA - Nord America 3.888
EU - Europa 3.185
AS - Asia 2.246
SA - Sud America 904
AF - Africa 64
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 5
Totale 10.298
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Nazione #
US - Stati Uniti d'America 3.806
SG - Singapore 997
BR - Brasile 787
IT - Italia 711
IE - Irlanda 651
SE - Svezia 651
CN - Cina 574
HK - Hong Kong 334
DE - Germania 301
PL - Polonia 159
UA - Ucraina 156
FI - Finlandia 127
GB - Regno Unito 121
VN - Vietnam 115
RU - Federazione Russa 84
FR - Francia 61
IN - India 48
BE - Belgio 38
AR - Argentina 37
CA - Canada 35
MX - Messico 32
NL - Olanda 29
TR - Turchia 26
CZ - Repubblica Ceca 24
EC - Ecuador 24
ZA - Sudafrica 24
AT - Austria 20
ID - Indonesia 20
JP - Giappone 19
BD - Bangladesh 18
CO - Colombia 17
UZ - Uzbekistan 17
VE - Venezuela 12
IQ - Iraq 11
PK - Pakistan 11
ES - Italia 10
MA - Marocco 10
CL - Cile 9
PY - Paraguay 9
EG - Egitto 7
LT - Lituania 7
IL - Israele 6
EU - Europa 5
GR - Grecia 5
JM - Giamaica 5
AE - Emirati Arabi Uniti 4
CR - Costa Rica 4
DZ - Algeria 4
JO - Giordania 4
KE - Kenya 4
NP - Nepal 4
PE - Perù 4
PH - Filippine 4
PT - Portogallo 4
TH - Thailandia 4
TN - Tunisia 4
UY - Uruguay 4
AO - Angola 3
AZ - Azerbaigian 3
CI - Costa d'Avorio 3
HR - Croazia 3
IR - Iran 3
LV - Lettonia 3
NZ - Nuova Zelanda 3
AU - Australia 2
BY - Bielorussia 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
GE - Georgia 2
HU - Ungheria 2
KH - Cambogia 2
KR - Corea 2
KZ - Kazakistan 2
LB - Libano 2
LU - Lussemburgo 2
MD - Moldavia 2
MT - Malta 2
NO - Norvegia 2
OM - Oman 2
PS - Palestinian Territory 2
SA - Arabia Saudita 2
SN - Senegal 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
DJ - Gibuti 1
HN - Honduras 1
IM - Isola di Man 1
KG - Kirghizistan 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
MN - Mongolia 1
MY - Malesia 1
NG - Nigeria 1
NR - Nauru 1
PA - Panama 1
Totale 10.295
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Città #
Dublin 649
Dallas 560
Chandler 522
Singapore 474
Ashburn 428
Nyköping 340
Hong Kong 328
Jacksonville 305
Beijing 289
Messina 256
Warsaw 150
The Dalles 141
Princeton 101
Medford 98
Munich 98
Los Angeles 92
Ann Arbor 81
New York 75
São Paulo 75
Bremen 70
Cambridge 67
Des Moines 67
Boardman 57
Dearborn 43
Lancaster 41
Buffalo 40
Redondo Beach 39
Turku 38
Ho Chi Minh City 37
Woodbridge 35
Brussels 32
Wilmington 30
Moscow 26
Rome 26
Hanoi 22
Milan 22
Catania 21
Tianjin 21
Belo Horizonte 20
Brooklyn 20
Rio de Janeiro 20
Helsinki 18
Pune 18
Düsseldorf 16
Jakarta 16
Jinan 16
Shenyang 16
Amsterdam 15
San Mateo 15
Seattle 15
London 14
Montreal 14
Santa Clara 14
Tashkent 14
Brasília 13
Dong Ket 13
Ningbo 13
São José dos Campos 13
Tokyo 13
Johannesburg 12
San Francisco 12
Stockholm 12
Atlanta 11
Houston 11
Mexico City 11
Vienna 11
Boston 10
Chennai 10
Norwalk 10
Phoenix 10
Porto Alegre 10
Quito 10
Denver 9
Frankfurt am Main 9
Manchester 9
Olomouc 9
Padova 9
Toronto 9
Washington 9
Chicago 8
Guayaquil 8
Hyderabad 8
Lappeenranta 8
Nanjing 8
Orem 8
Prague 8
Guangzhou 7
Lauterbourg 7
Limeira 7
Manaus 7
Nuremberg 7
Ribeirão Preto 7
Salvador 7
Zhengzhou 7
Ankara 6
Campinas 6
Canoas 6
Columbus 6
Contagem 6
Fortaleza 6
Totale 6.473
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 327
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 180
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 171
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. 166
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 159
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 154
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 148
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 147
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 145
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 142
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 141
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 137
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 128
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 127
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 127
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 127
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 123
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 119
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 118
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 118
Advances in Bioinformatics, Biostatistics and Omic Sciences 117
Age dependent switching role of ciclyn D1 in breast cancer 116
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 115
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 115
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 114
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 114
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 112
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 111
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 110
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 110
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 108
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 104
Aged fingerprints for DNA profile: First report of successful typing 101
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 100
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 99
Editome landscape of CCM-derived endothelial cells 99
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 99
A rare case of TMAU associated with suspected Currarino triad 99
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 98
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 98
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 98
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 95
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 95
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 94
GENETICS OF CAVERNOMAS: A CASE REPORT 94
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 93
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 93
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 92
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 91
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 90
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 89
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 89
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 89
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 88
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 88
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 87
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 85
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 84
Oxidative Stress and the Neurovascular Unit 84
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 83
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 82
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 81
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 81
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 81
Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners 80
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 80
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 79
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 78
Sarcoglycans and integrins in muscular inactivity 77
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 76
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 76
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 75
Krit-1 mutations in 100 patients with cerebral cavernomas. 74
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 74
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 74
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 72
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 72
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 71
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 71
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 70
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 70
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 70
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 68
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 68
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 68
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 67
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 65
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 65
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 65
Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies 64
Sarcoglycans in human smooth muscle: a clsm and molecular study 64
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 63
FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 63
The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment 62
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 60
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 60
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 59
Genetic and functional study of CCR5 gene in HIV-1 infection 58
HORMONE RECEPTORS, CCND1 AND PROLIFERATION EQUIVALENT TYPE OF BREAST CARCINOMAS IN POSTMENOPAUSAL WOMEN 58
NOVEL GENES INVOLVED IN ETIOPATHOGENESIS OF RETINITIS PIGMENTOSA ORPHANFORMS 57
Totale 9.742
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Categoria #
all - tutte 41.000
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 41.000
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021357 0 0 0 0 0 58 36 43 36 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
2025/20262.572 322 474 656 467 601 52 0 0 0 0 0 0
Totale 10.686