IRIS
D'ANGELO, Rosalia
 Distribuzione geografica
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Continente #
EU - Europa 2.790
NA - Nord America 2.374
AS - Asia 969
SA - Sud America 650
AF - Africa 40
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
Totale 6.833
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Nazione #
US - Stati Uniti d'America 2.343
IT - Italia 677
IE - Irlanda 651
SE - Svezia 641
BR - Brasile 579
SG - Singapore 470
CN - Cina 301
DE - Germania 189
UA - Ucraina 154
PL - Polonia 137
FI - Finlandia 85
GB - Regno Unito 79
BE - Belgio 38
FR - Francia 32
IN - India 32
RU - Federazione Russa 27
NL - Olanda 26
HK - Hong Kong 24
TR - Turchia 22
CZ - Repubblica Ceca 15
ID - Indonesia 15
UZ - Uzbekistan 15
CO - Colombia 14
EC - Ecuador 14
VN - Vietnam 14
AR - Argentina 13
MX - Messico 12
VE - Venezuela 11
CA - Canada 10
PK - Pakistan 10
ZA - Sudafrica 10
JP - Giappone 9
MA - Marocco 9
BD - Bangladesh 8
PY - Paraguay 7
AT - Austria 6
CL - Cile 6
EG - Egitto 6
IQ - Iraq 6
EU - Europa 5
IL - Israele 4
KE - Kenya 4
PT - Portogallo 4
TH - Thailandia 4
AO - Angola 3
AZ - Azerbaigian 3
HR - Croazia 3
IR - Iran 3
JM - Giamaica 3
JO - Giordania 3
LT - Lituania 3
LV - Lettonia 3
NZ - Nuova Zelanda 3
PH - Filippine 3
TN - Tunisia 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BY - Bielorussia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
ES - Italia 2
GE - Georgia 2
GR - Grecia 2
KZ - Kazakistan 2
LU - Lussemburgo 2
MD - Moldavia 2
MT - Malta 2
NO - Norvegia 2
NP - Nepal 2
OM - Oman 2
PE - Perù 2
PS - Palestinian Territory 2
SN - Senegal 2
TW - Taiwan 2
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CI - Costa d'Avorio 1
HN - Honduras 1
HU - Ungheria 1
IM - Isola di Man 1
KG - Kirghizistan 1
KH - Cambogia 1
KR - Corea 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
MN - Mongolia 1
PA - Panama 1
RO - Romania 1
RS - Serbia 1
SA - Arabia Saudita 1
SI - Slovenia 1
Totale 6.833
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Città #
Dublin 649
Chandler 522
Nyköping 340
Jacksonville 304
Singapore 289
Messina 247
Beijing 154
Warsaw 135
Ashburn 119
Princeton 101
Medford 98
Ann Arbor 81
Bremen 70
Cambridge 67
Des Moines 67
Boardman 57
New York 47
Dearborn 43
Lancaster 41
São Paulo 40
Woodbridge 35
Brussels 32
Wilmington 30
Rome 25
Hong Kong 21
Belo Horizonte 18
Catania 18
Helsinki 18
Milan 17
Pune 17
Jinan 16
Shenyang 16
Jakarta 15
San Mateo 15
Amsterdam 13
Dong Ket 13
Los Angeles 13
Rio de Janeiro 13
Tashkent 13
Munich 12
Ningbo 12
Seattle 12
São José dos Campos 12
The Dalles 11
Brasília 10
Norwalk 10
Padova 9
Hyderabad 8
Nanjing 8
Porto Alegre 8
Washington 8
Manaus 7
Prague 7
Zhengzhou 7
Guarulhos 6
Guayaquil 6
Hefei 6
Istanbul 6
Limeira 6
Nuremberg 6
Salvador 6
Tianjin 6
Brno 5
Campinas 5
Canoas 5
Contagem 5
Hebei 5
Ipatinga 5
Newark 5
Quito 5
Shanghai 5
Syracuse 5
Waanrode 5
Ancona 4
Cairo 4
Clearwater 4
Curitiba 4
Ferrandina 4
Genova 4
Guangzhou 4
Hangzhou 4
Hortolândia 4
Houston 4
Lappeenranta 4
Lisbon 4
Moscow 4
Mountain View 4
Nairobi 4
Naples 4
Ottawa 4
Pelotas 4
Ribeirão Preto 4
Rosolini 4
Salerno 4
São Bernardo do Campo 4
Taiyuan 4
Taizhou 4
Termoli 4
Torino 4
Toronto 4
Totale 4.181
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Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 306
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 123
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 121
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 113
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 111
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 109
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 108
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 101
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 101
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 98
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 95
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 94
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 93
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 87
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. 84
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 84
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 83
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 83
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 83
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 83
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 82
GENETICS OF CAVERNOMAS: A CASE REPORT 80
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 78
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 78
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 76
Advances in Bioinformatics, Biostatistics and Omic Sciences 76
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 74
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 74
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 73
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 73
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 72
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 71
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 70
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 68
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 68
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 67
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 66
Age dependent switching role of ciclyn D1 in breast cancer 66
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 65
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 65
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 63
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 63
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 63
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 63
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 62
Aged fingerprints for DNA profile: First report of successful typing 61
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 60
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 60
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 60
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 60
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 59
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 59
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 59
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 59
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 59
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 59
Krit-1 mutations in 100 patients with cerebral cavernomas. 58
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 58
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 58
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 57
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 56
Sarcoglycans and integrins in muscular inactivity 56
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 56
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 56
Editome landscape of CCM-derived endothelial cells 55
A rare case of TMAU associated with suspected Currarino triad 54
Oxidative Stress and the Neurovascular Unit 54
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 53
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 53
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration 52
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 52
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 52
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 52
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 51
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 50
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 50
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 49
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 48
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 48
HORMONE RECEPTORS, CCND1 AND PROLIFERATION EQUIVALENT TYPE OF BREAST CARCINOMAS IN POSTMENOPAUSAL WOMEN 48
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 48
Sarcoglycans in human smooth muscle: a clsm and molecular study 47
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 47
null 46
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 46
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 45
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 45
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 45
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 44
FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 42
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 42
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 41
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 41
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells 39
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 39
Genetic and functional study of CCR5 gene in HIV-1 infection 39
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 39
null 38
Trimethylaminuria: do abnormal chaperons play a pathogenic role? 38
Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy 37
Totale 6.695
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Categoria #
all - tutte 30.089
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 30.089
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020282 0 0 0 0 0 0 0 0 7 131 125 19
2020/2021689 111 26 85 37 73 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
2024/20251.724 64 26 73 183 96 97 99 546 540 0 0 0
Totale 7.212