D'ANGELO, Rosalia
 Distribuzione geografica
Continente #
EU - Europa 2.608
NA - Nord America 2.267
AS - Asia 393
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
AF - Africa 1
Totale 5.286
Nazione #
US - Stati Uniti d'America 2.257
IE - Irlanda 647
SE - Svezia 644
IT - Italia 589
CN - Cina 265
DE - Germania 178
UA - Ucraina 147
PL - Polonia 135
GB - Regno Unito 76
FI - Finlandia 70
SG - Singapore 64
BE - Belgio 37
FR - Francia 33
IN - India 28
NL - Olanda 15
VN - Vietnam 14
CZ - Repubblica Ceca 12
RU - Federazione Russa 11
CA - Canada 8
JP - Giappone 8
CO - Colombia 5
EU - Europa 5
IR - Iran 3
NZ - Nuova Zelanda 3
PH - Filippine 3
PK - Pakistan 3
AT - Austria 2
AU - Australia 2
CL - Cile 2
ES - Italia 2
HK - Hong Kong 2
MT - Malta 2
MX - Messico 2
PT - Portogallo 2
EG - Egitto 1
GR - Grecia 1
IL - Israele 1
IQ - Iraq 1
KR - Corea 1
LT - Lituania 1
LU - Lussemburgo 1
MD - Moldavia 1
NO - Norvegia 1
RO - Romania 1
Totale 5.286
Città #
Dublin 645
Chandler 529
Nyköping 344
Jacksonville 304
Messina 208
Beijing 152
Warsaw 135
Ashburn 118
Princeton 101
Medford 98
Ann Arbor 81
Bremen 71
Cambridge 67
Des Moines 67
Boardman 58
New York 47
Dearborn 43
Lancaster 41
Woodbridge 35
Singapore 32
Brussels 31
Wilmington 30
Pune 17
Catania 16
Jinan 16
Rome 16
Shenyang 16
San Mateo 15
Dong Ket 13
Ningbo 12
Milan 11
Seattle 11
Norwalk 10
Hyderabad 9
Padova 9
Amsterdam 8
Nanjing 8
Washington 8
Munich 7
Los Angeles 6
Tianjin 6
Brno 5
Hebei 5
Hefei 5
Waanrode 5
Zhengzhou 5
Ancona 4
Clearwater 4
Ferrandina 4
Genova 4
Hangzhou 4
Helsinki 4
Houston 4
Mountain View 4
Prague 4
Rosolini 4
Salerno 4
Taizhou 4
Termoli 4
Torino 4
Turin 4
Auburn Hills 3
Falls Church 3
Fuzhou 3
Islamabad 3
Jiaxing 3
Lago 3
Lappeenranta 3
Novokuznetsk 3
Ottawa 3
Paris 3
San Giovanni La Punta 3
Shanghai 3
Taiyuan 3
Tappahannock 3
Terni 3
Toronto 3
Whakatane 3
Abbiategrasso 2
Alcamo 2
Ardabil 2
Atlanta 2
Belvedere Spinello 2
Cagliari 2
Changsha 2
Dallas 2
Durham 2
Edinburgh 2
Enna 2
Foligno 2
Fort Worth 2
Guangzhou 2
Lanzhou 2
Lisbon 2
Manila 2
Milazzo 2
Mineo 2
Montalbano 2
Nanchang 2
Napoli 2
Totale 3.631
Nome #
LA TRIMETILAMINURIA TMAU (FISH ODOUR SYNDROME): UNA MALATTIARARA, MONOGENICA. REGOLAZIONE DEL GENE FMO3 IMPLICATO NELLA SUAMANIFESTAZIONE 290
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome 104
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study. 104
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study 95
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population 94
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions 92
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: A case-control study. 90
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance 83
CCR5Δ32 Polymorphism Associated with a Slower Rate DiseaseProgression in a Cohort of RR-MS Sicilian Patients 81
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens 80
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? 80
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype 75
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin 75
Screening genetico dei geni CCM in pazienti italiani affetti da angioma cavernoso cerebrale: un caso familiare 72
IL SUBCOMPLESSO DEI SARCOGLICANI NEL MUSCOLO LISCIO UMANO 70
Analisi di riarrangiamenti genomici in pazienti portatori di angiomi cavernosi cerebrali 70
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations 70
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations 70
Sarcoglycan subcomplex in normal human smooth muscle: An immunohistochemical and molecular study 67
GENETICS OF CAVERNOMAS: A CASE REPORT 66
FMO3 allelic variants in a Mediterranean population frequency and linkage analysis. 65
A MOLECULAR- GENETIC ANALYSIS OF FLAVIN-CONTAINING MONOOXYGENASE3 GENE (FMO3) IN AN ITALIAN CHILD WITH A TMAURIA LIKE-PHENOTYPE 65
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa 64
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. 62
A stable deletion/insertion polymorphism 9.1 Kb in mediterranean population 61
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations 58
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations 56
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis 55
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies 54
POLIMORFISMI DELLA GLIOSSALASI I E DELLA PARAOXONASI I IN INDIVIDUI SANI ED INDIVIDUI AFFETTI DA SCLEROSI MULTIPLA.FATTORI DI SUSCETTIBILITA'? 53
Analisi Mutazionale in 95 pazienti italiani affetti da angioma cavernoso cerebrale. 53
Distribuzione dell'allele mutato Δ32 del gene CCR5 nella popolazione sana del bacino del mediterraneo. 53
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells 53
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU 53
Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas 52
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 52
Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation 52
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study 52
Glyoxalase I A111E, paraoxonase 1 q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis? 51
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 51
Age dependent switching role of ciclyn D1 in breast cancer 51
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report 51
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation 51
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 51
Is α- sarcoglycan a member of sarcoglycan complex in human smooth muscle? 50
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells 50
Advances in Bioinformatics, Biostatistics and Omic Sciences 50
p53 subcellular compartmentalization, cell cycle and apoptotic pattern in non small cell lung cancer (NSLC) 49
Recettore delle chemochine CCR5 e mobilizzazione del calcio intracellulare in linfociti umani: correlazione genotipo-fenotipo 49
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 49
Sporadic Cerebral Cavernous Malformations: Report of Further Mutations of CCM Genes in 40 Italian Patients 48
Dati preliminari sulla caratterizzazione molecolare dei casi di melanoma familiare di origine siciliana. 47
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes 47
Krit-1 mutations in 100 patients with cerebral cavernomas. 46
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New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype? 46
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa 45
Sarcoglycans and integrins in muscular inactivity 44
Distribution of Δ32-CCR5 polymorphism in a mediterranean basin population. 44
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria. 44
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing? 43
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations 42
Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM). 42
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells 42
Oxidative Stress and the Neurovascular Unit 42
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 41
Distribuzione dell'allele mutato delta 32 del gene CCR5 nella popolazione siciliana 41
KRIT 1: Una nuova proteina sulle vie di segnalazione delle integrine 40
FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor 40
NOVEL PDCD10 PROMOTER VARIANTS IN PATIENTS WITH CEREBRAL CAVERNOUSMALFORMATIONS 39
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HORMONE RECEPTORS, CCND1 AND PROLIFERATION EQUIVALENT TYPE OF BREAST CARCINOMAS IN POSTMENOPAUSAL WOMEN 38
Sarcoglycans in human smooth muscle: a clsm and molecular study 38
Aged fingerprints for DNA profile: First report of successful typing 38
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 37
Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: A causative mutation? 36
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis 36
Mutazioni del gene KRIT1 in 106 pazienti Italiani affetti da Angioma Cavernoso Cerebrale 36
A rare case of TMAU associated with suspected Currarino triad 36
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling 36
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline 36
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function? 36
Hormone receptors, CCND1 and proliferation equivalent type of breast carcinomas in postmenopausal women 35
La Trimetilaminuria (TMAU) o “ Fish odour syndrome”: Regolazione dell' espressione del gene FMO3 35
Plasma, erythrocyte and platelet magnesium levels in type 1 diabetic patients with microalbuminuria and clinical proteinuria 34
Quantification of trimethylamine (TMA) and trimethylamine oxide (TMAO) for diagnostic and targeted diet purposes. 34
Immunohistochemical and molecular study of sarcoglycan subcomplex in normal human smooth muscle 33
Genetic and functional study of CCR5 gene in HIV-1 infection 32
FMO3 allelic variants in Sicily and Sardinia islands population frequency and linkage analysis. 32
Pedigree analysis of a family affected by hereditary cerebral cavernous malformations novel candidate genes detected by whole genome sequencing 32
Distribution of the mutated delta32 allele of the CCR5 gene in a Sicilian population 32
Editome landscape of CCM-derived endothelial cells 31
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Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs 31
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis 28
PON I and GLO I Gene Polymorphisms and Their Association with Breast Cancer: A Case-Control Study in a Population from Southern Italy 28
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 27
Raman Spectroscopic Study of Amyloid Deposits in Gelatinous Drop-like Corneal Dystrophy 26
Trimethylaminuria: do abnormal chaperons play a pathogenic role? 24
Totale 5.310
Categoria #
all - tutte 22.501
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 22.501


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020557 0 40 6 52 8 48 64 57 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
2022/20232.041 147 169 99 174 195 187 27 141 817 5 68 12
2023/2024553 43 85 26 57 47 127 3 23 2 24 17 99
2024/202579 65 14 0 0 0 0 0 0 0 0 0 0
Totale 5.584