DONATO, Luigi
 Distribuzione geografica
Continente #
EU - Europa 523
AS - Asia 80
NA - Nord America 62
AF - Africa 3
OC - Oceania 1
SA - Sud America 1
Totale 670
Nazione #
IT - Italia 361
US - Stati Uniti d'America 60
IE - Irlanda 57
FR - Francia 24
CZ - Repubblica Ceca 19
IN - India 18
DE - Germania 17
ID - Indonesia 17
VN - Vietnam 14
PL - Polonia 12
NL - Olanda 10
UA - Ucraina 8
TR - Turchia 7
SG - Singapore 5
HK - Hong Kong 4
JP - Giappone 4
KR - Corea 4
AT - Austria 3
IR - Iran 3
CH - Svizzera 2
FI - Finlandia 2
GB - Regno Unito 2
MX - Messico 2
PK - Pakistan 2
AU - Australia 1
BD - Bangladesh 1
BG - Bulgaria 1
BY - Bielorussia 1
DZ - Algeria 1
ES - Italia 1
HU - Ungheria 1
JO - Giordania 1
NG - Nigeria 1
RU - Federazione Russa 1
SE - Svezia 1
UY - Uruguay 1
ZA - Sudafrica 1
Totale 670
Città #
Messina 203
Dublin 56
Rome 18
Jakarta 16
Lago 16
Dong Ket 14
Warsaw 12
Mumbai 11
Ashburn 9
Padova 9
Boardman 7
Bremen 7
Ankara 5
Paris 5
Treviglio 5
Amsterdam 4
Bacoli 4
Jacksonville 4
Pavia 4
Torregrotta 4
Enna 3
Ispica 3
Milan 3
Parsippany 3
Ragusa 3
Vienna 3
Ahmedabad 2
Bologna 2
Brescia 2
Carini 2
Central 2
Council Bluffs 2
Frankfurt am Main 2
Gangnam-gu 2
Helsinki 2
Houston 2
Imphal 2
Islamabad 2
Landshut 2
Lexington 2
Mountain View 2
Nashville 2
Nicolosi 2
Osaka 2
Pozzo Di Gotto 2
Rochester 2
Siracusa 2
Zurich 2
Adelaide 1
Adrano 1
Ain Beida 1
Amman 1
Ann Arbor 1
Bedford 1
Bollebygd 1
Budapest 1
Buscate 1
Carmel 1
Carugate 1
Cernusco sul Naviglio 1
Charlotte 1
Chennai 1
Cork 1
Cuauhtemoc 1
Delhi 1
Dhaka 1
Eindhoven 1
Encino 1
Fleming Island 1
Francofonte 1
Genoa 1
Istanbul 1
Johannesburg 1
Kansas City 1
Kayseri 1
Kish 1
Lamezia Terme 1
Limbiate 1
Lipari 1
London 1
Merin 1
Mexico City 1
Milpitas 1
Mineo 1
Minsk 1
Montevideo 1
New Orleans 1
New York 1
Odesa 1
Oklahoma City 1
Pamplona 1
Perugia 1
Pescosolido 1
Piazza Armerina 1
Pontedera 1
Port Harcourt 1
Rejomulyo 1
Revere 1
Roubaix 1
Santa Venerina 1
Totale 527
Nome #
New omics approaches improving classification and personalized retinitis pigmentosa diagnosis, file de3e52b1-9ead-762d-e053-3705fe0a30e0 153
Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance, file de3e52b1-acc6-762d-e053-3705fe0a30e0 51
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions, file de3e52b1-3323-762d-e053-3705fe0a30e0 38
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study., file de3e52b0-639b-762d-e053-3705fe0a30e0 37
Novel Insights into RPGR Exon ORF15: Could G-Quadruplex Folding Lead to Challenging Sequencing?, file de3e52b3-ce0e-762d-e053-3705fe0a30e0 35
Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis?, file de3e52b1-3a1b-762d-e053-3705fe0a30e0 32
Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations, file de3e52b0-ad20-762d-e053-3705fe0a30e0 25
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study, file de3e52b0-fc5f-762d-e053-3705fe0a30e0 23
miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions, file de3e52b1-afa6-762d-e053-3705fe0a30e0 21
High-Throughput Sequencing to Detect Novel Likely Gene-Disrupting Variants in Pathogenesis of Sporadic Brain Arteriovenous Malformations, file de3e52b2-6a8b-762d-e053-3705fe0a30e0 20
Bioinformatic analysis of a “functional cluster” probably related to retinitis pigmentosa, file de3e52b3-4a5f-762d-e053-3705fe0a30e0 18
Investigating the role of imprinted genes in pediatric sporadic brain arteriovenous malformations, file de3e52b4-d181-762d-e053-3705fe0a30e0 17
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations, file de3e52af-f3ea-762d-e053-3705fe0a30e0 16
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, file de3e52b0-bb90-762d-e053-3705fe0a30e0 15
Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations, file de3e52b1-c53c-762d-e053-3705fe0a30e0 14
A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens, file de3e52b1-05f7-762d-e053-3705fe0a30e0 13
Gut-Brain Axis Cross-Talk and Limbic Disorders as BiologicalBasis of Secondary TMAU, file de3e52b4-e146-762d-e053-3705fe0a30e0 12
GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population, file de3e52b1-ac82-762d-e053-3705fe0a30e0 11
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype, file de3e52b2-a174-762d-e053-3705fe0a30e0 11
Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations, file 434ed9b9-77cc-4253-ac4d-fff70f8aab18 10
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation, file de3e52b0-9e3f-762d-e053-3705fe0a30e0 10
Down-expression of RHO gene in Egyptian patient with three regulative region variants could lead to retinitis punctata albescens phenotype, file de3e52b2-a175-762d-e053-3705fe0a30e0 10
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis, file de3e52b1-b0eb-762d-e053-3705fe0a30e0 8
null, file de3e52b2-cf07-762d-e053-3705fe0a30e0 6
Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms in Italian patients with sporadic cerebral cavernous malformations: a pilot study, file de3e52b3-3687-762d-e053-3705fe0a30e0 6
Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells, file de3e52b3-ad36-762d-e053-3705fe0a30e0 6
Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis, file de3e52b3-4a01-762d-e053-3705fe0a30e0 5
The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbert's Syndrome, file de3e52b3-97af-762d-e053-3705fe0a30e0 5
Nine differentially expressed genes from a post mortem study and their association with suicidal status in a sample of suicide completers, attempters and controls, file de3e52b0-cda6-762d-e053-3705fe0a30e0 4
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes, file de3e52b4-dfde-762d-e053-3705fe0a30e0 4
Two non-homologous co-regulated genes PDCD10 and SERPINI1: any possible related function?, file de3e52af-08b0-762d-e053-3705fe0a30e0 3
Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis, file de3e52b2-974a-762d-e053-3705fe0a30e0 3
N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells, file de3e52b4-c454-762d-e053-3705fe0a30e0 3
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations, file de3e52b3-6674-762d-e053-3705fe0a30e0 2
New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?, file de3e52b4-059f-762d-e053-3705fe0a30e0 2
Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells, file de3e52b4-0610-762d-e053-3705fe0a30e0 2
Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin, file de3e52b4-b8d2-762d-e053-3705fe0a30e0 2
Advances in Bioinformatics, Biostatistics and Omic Sciences, file de3e52b4-cc26-762d-e053-3705fe0a30e0 2
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling, file de3e52b4-cebe-762d-e053-3705fe0a30e0 2
Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline, file de3e52b5-1859-762d-e053-3705fe0a30e0 2
Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells, file a4316ffd-89d6-45b3-9520-815edc283c8e 1
Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis, file b2a7b645-8654-49fe-9580-96d9b165707f 1
Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration, file dc7ef7b9-cb3f-40b6-93ee-80051ab30d02 1
null, file de3e52b0-cb05-762d-e053-3705fe0a30e0 1
Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies, file de3e52b3-01ad-762d-e053-3705fe0a30e0 1
Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa, file de3e52b3-01af-762d-e053-3705fe0a30e0 1
Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa, file de3e52b3-0f4a-762d-e053-3705fe0a30e0 1
Association between three polymorphisms in RP1 hotspot region and risk of retinitis pigmentosa in Italian patients: A pilot study, file de3e52b3-2463-762d-e053-3705fe0a30e0 1
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, file de3e52b4-e2a5-762d-e053-3705fe0a30e0 1
Oxidative Stress and the Neurovascular Unit, file de3e52b4-ff8b-762d-e053-3705fe0a30e0 1
VARIANTS OF THE MOLECULAR CHAPERONE HSPA8 AND HSPA1A GENES IN TRIMETHYLAMINURIA: A PILOT STUDY, file de3e52b5-1ad9-762d-e053-3705fe0a30e0 1
Totale 670
Categoria #
all - tutte 1.659
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 1.659


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20193 0 0 0 0 0 0 0 0 0 1 1 1
2019/202064 3 0 1 0 1 0 0 0 7 17 26 9
2020/2021145 35 10 14 14 2 2 4 2 28 17 3 14
2021/2022113 2 2 4 37 3 1 17 12 11 6 11 7
2022/2023191 7 16 5 15 15 4 18 7 60 8 19 17
2023/2024110 4 9 10 13 8 5 19 16 17 9 0 0
Totale 670