IRIS
GENTILINI, DAVIDE
 Distribuzione geografica
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Continente #
NA - Nord America 2.865
AS - Asia 2.538
EU - Europa 1.668
SA - Sud America 258
AF - Africa 32
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 7.370
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Nazione #
US - Stati Uniti d'America 2.807
CN - Cina 1.339
SG - Singapore 624
IE - Irlanda 514
HK - Hong Kong 355
RU - Federazione Russa 318
IT - Italia 313
BR - Brasile 221
DE - Germania 157
FI - Finlandia 94
VN - Vietnam 68
GB - Regno Unito 56
CA - Canada 31
PL - Polonia 31
FR - Francia 27
UA - Ucraina 27
IN - India 26
SE - Svezia 21
NL - Olanda 20
AT - Austria 18
ES - Italia 18
AR - Argentina 16
MX - Messico 16
BD - Bangladesh 15
JP - Giappone 15
BE - Belgio 12
ZA - Sudafrica 12
ID - Indonesia 11
IQ - Iraq 10
PK - Pakistan 9
KR - Corea 8
AE - Emirati Arabi Uniti 7
GR - Grecia 7
LT - Lituania 7
VE - Venezuela 7
LV - Lettonia 6
SA - Arabia Saudita 6
TR - Turchia 6
EG - Egitto 5
AU - Australia 4
AZ - Azerbaigian 4
EU - Europa 4
IL - Israele 4
IR - Iran 4
JO - Giordania 4
LB - Libano 4
MA - Marocco 4
MY - Malesia 4
AL - Albania 3
CO - Colombia 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
EC - Ecuador 3
KZ - Kazakistan 3
PA - Panama 3
TN - Tunisia 3
UY - Uruguay 3
BG - Bulgaria 2
BO - Bolivia 2
BY - Bielorussia 2
CH - Svizzera 2
CL - Cile 2
DZ - Algeria 2
HU - Ungheria 2
JM - Giamaica 2
KG - Kirghizistan 2
NP - Nepal 2
PS - Palestinian Territory 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
CM - Camerun 1
CR - Costa Rica 1
ET - Etiopia 1
HN - Honduras 1
KE - Kenya 1
KY - Cayman, isole 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LY - Libia 1
MK - Macedonia 1
MM - Myanmar 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
PY - Paraguay 1
SI - Slovenia 1
TH - Thailandia 1
UG - Uganda 1
Totale 7.370
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Città #
Dallas 637
Dublin 513
Hong Kong 353
Beijing 340
Ashburn 300
Singapore 296
Nanjing 242
Chandler 236
Boardman 151
Princeton 90
Lawrence 84
Nanchang 82
Jacksonville 79
Los Angeles 78
Hebei 72
Changsha 71
Medford 70
Shenyang 68
Redondo Beach 67
Helsinki 65
Jiaxing 60
Shanghai 56
Moscow 53
Munich 52
Buffalo 51
Wilmington 51
New York 43
Milan 37
Hangzhou 35
Ho Chi Minh City 35
Pavia 34
The Dalles 30
Warsaw 29
São Paulo 27
Ann Arbor 26
Nuremberg 26
Tianjin 26
Brooklyn 24
Houston 24
Guangzhou 19
Santa Clara 19
Fairfield 18
San Francisco 17
Washington 17
Turku 16
Chicago 15
Montreal 15
Tokyo 15
Seattle 14
Woodbridge 13
Denver 12
Stockholm 12
Zhengzhou 12
Chennai 11
Boston 10
Chieti 10
Columbus 10
Redwood City 10
Vienna 10
Falkenstein 9
Norwalk 9
Atlanta 8
Brussels 8
Elk Grove Village 8
Hanoi 8
Johannesburg 8
Naples 8
Orem 8
Rio de Janeiro 8
Belo Horizonte 7
Catanzaro 7
Florence 7
Frankfurt am Main 7
London 7
Mariglianella 7
Pescara 7
Rome 7
Verona 7
Brescia 6
Council Bluffs 6
Curitiba 6
Düsseldorf 6
Jinan 6
Newark 6
Ningbo 6
Phoenix 6
Riga 6
Toronto 6
Amsterdam 5
Bologna 5
Manchester 5
New Delhi 5
Amman 4
Baghdad 4
Baku 4
Charlotte 4
Da Nang 4
Des Moines 4
Dhaka 4
Jakarta 4
Totale 5.145
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Nome #
Identificazione di microRNA circolanti specificatamente sovra espressi in corso di infarto miocardico acuto. 236
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 132
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis. 126
Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci 110
Acid Sensing Ion Channel 2: a new potential player in the pathophysiology of multiple sclerosis 105
Accelerated epigenetic aging in Down syndrome 98
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 95
A frequent oligogenic involvement in congenital hypothyroidism 92
Antiphospholipid Antibodies and Infertility: A Gene Expression Study in Decidual Stromal Cells 92
Characterization of the biological processes shaping the genetic structure of the Italian population 90
Age-dependent skewing of X chromosome inactivation appears delayed in centenarians' offspring. Is there a role for allelic imbalance in Healthy Aging and Longevity? 88
An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis 88
Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach 87
Acceleration of leukocytes' epigenetic age as an early tumorand sex-specific marker of breast and colorectal cancer 85
Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS 84
Genome Wide Association Studies using extreme blood pressure distribution identify variants in UMOD associated with hypertension 84
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture 83
'Here comes the sun': Pigmentary traits and sun habits in women with endometriosis 81
Epigenome wide association and stochastic epigenetic mutation analysis on cord blood of preterm birth 80
Differences in Visceral Fat and Fat Bacterial Colonization between Ulcerative Colitis and Crohn's Disease. An In Vivo and In Vitro Study 79
European genome-wide association study using extremes of blood pressure distribution: study design and methods. 78
Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail 78
Early-life factors, in-utero exposures and endometriosis risk: a meta-analysis 77
Metronomic administration of zoledronic acid and taxotere combination in castration resistant prostate cancer patients. Phase I ZANTE trial 76
Methylation of ELOVL2 gene as a new epigenetic marker of age 75
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring 75
A pan-cancer approach to predict responsiveness to immune checkpoint inhibitors by machine learning 74
Synergistic activity of everolimus and 5-aza-2′-deoxycytidine in medullary thyroid carcinoma cell lines 73
A rare familial case of endometriosis with very severe gynecological and obstetric complications: Novel genetic variants at a glance 73
Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach 73
Article a new epigenetic model to stratify glioma patients according to their immunosuppressive state 73
Pyk2 and Cyr61 at the cross-road of cAMP-dependent signalling in invasiveness and neuroendocrine differentiation of prostate cancer 72
Identification of a DNA methylation signature in blood cells from persons with Down Syndrome 71
The Association between Dysnatraemia during Hospitalisation and Post-COVID-19 Mental Fatigue 70
Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas 70
Erratum: A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data 69
Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females 68
Complex interplay between neutral and adaptive evolution shaped differential genomic background and disease susceptibility along the Italian peninsula 67
One-year Mediterranean diet promotes epigenetic rejuvenation with country- and sex-specific effects: a pilot study from the NU-AGE project 67
Heterogeneity of thyroid function and impact of peripheral thyroxine deiodination in centenarians and semi-supercentenarians: association with functional status and mortality 67
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis 66
Identification of upregulated microRNAs in the plasma of patients with acute myocardial infarction 66
Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor 65
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features 65
Rationale and design of the CV-PREVITAL study: an Italian multiple cohort randomised controlled trial investigating innovative digital strategies in primary cardiovascular prevention 64
Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects 64
Multifactorial analysis of the stochastic epigenetic variability in cord blood confirmed an impact of common behavioral and environmental factors but not of in vitro conception. 64
Dissecting the Pre-Columbian genomic ancestry of Native Americans along the Andes-Amazonia divide 64
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the IGF1R Gene 64
Impact of demography and population dynamics on the genetic architecture of human longevity 63
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects 62
Is the pain just physical? The role of psychological distress, quality of life, and autistic traits in ehlers–danlos syndrome, an internet-based survey in italy 61
B Cells Isolated from Individuals Who Do Not Respond to the HBV Vaccine Are Characterized by Higher DNA Methylation-Estimated Aging Compared to Responders 60
Role of epigenetics in human aging and longevity: Genome-wide DNA methylation profile in centenarians and centenarians' offspring 60
Effects of human recombinant type I IFNs (IFN-α2b and IFN-β1a) on growth and migration of primary endometrial stromal cells from women with deeply infiltrating endometriosis: A preliminary study 60
Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis 58
Molecular Aging of Human Liver: An Epigenetic/Transcriptomic Signature 58
PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival 58
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index 57
Pathogenic variants in STXBP1 and in genes for GABAa receptor subunities cause atypical rett/rett-like phenotypes 57
Immunomodulatory effects of VEGF: Clinical implications of VEGF-targeted therapy in human cancer 56
Molecular and morphologic characterization of superficial-and deep-subcutaneous adipose tissue subdivisions in human obesity 56
Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis 56
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation study 55
Surgical excision of ovarian endometriomas: Does it truly impair ovarian reserve? Long term anti-Müllerian hormone (AMH) changes after surgery 55
Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles 55
Homozygosity haplotype and whole-exome sequencing analysis to identify potentially functional rare variants involved in multiple sclerosis among sardinian families 55
Statin use and long-term risk of recurrent intracerebral haemorrhage: the MUCH-Italy 53
Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset 53
Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome 52
Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosis 52
Endocannabinoid system regulates migration of endometrial stromal cells via cannabinoid receptor 1 through the activation of PI3K and ERK1/2 pathways 52
Interferon-inducible genes, TNF-related apoptosis-inducing ligand (TRAIL) and interferon inducible protein 27 (IFI27) are negatively regulated in leiomyomas: Implications for a role of the interferon pathway in leiomyoma development 51
NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis 51
The genetic legacy of the Yaghnobis: A witness of an ancient Eurasian ancestry in the historically reshuffled central Asian gene pool 50
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy 50
A meta-analysis on age-associated changes in blood DNA methylation: Results from an original analysis pipeline for Infinium 450k data 49
Endometrial stromal cells from women with endometriosis reveal peculiar migratory behavior in response to ovarian steroids 49
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis 49
The endocannabinoid pathway and the female reproductive organs 48
Deregulated human glioma cell motility: Inhibitory effect of somatostatin 48
No association between frailty index and epigenetic clocks in Italian semi-supercentenarians 48
Genetic diagnosis of endocrine diseases by NGS: Novel scenarios and unpredictable results and risks 47
Endometrial stromal progesterone receptor-A/progesterone receptor-B ratio: No difference between women with and without endometriosis 47
Epigenetics of Autism Spectrum Disorders: A Multi-level Analysis Combining Epi-signature, Age Acceleration, Epigenetic Drift and Rare Epivariations Using Public Datasets 46
The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas 46
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 46
The vascular endothelial growth factor +405G>C polymorphism in endometriosis 45
Visceral adipocytes: Old actors in obesity and new protagonists in Crohn's disease? 44
Genome-wide DNA methylation analysis of a cohort of 41 patients affected by oculo-auriculo-vertebral spectrum (OAVS) 44
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis-like syndrome 44
Investigating the Epigenetic Landscape of Major Depressive Disorder: A Genome-Wide Meta-Analysis of DNA Methylation Data, Including New Insights into Stochastic Epigenetic Mutations and Epivariations 43
Extensive Placental Methylation Profiling in Normal Pregnancies 43
Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations 43
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136 42
Gene expression profiling of peripheral blood mononuclear cells in endometriosis identifies genes altered in non-gynaecologic chronic inflammatory diseases 42
PI3K/Akt And ERK1/2 signalling pathways are involved in endometrial cell migration induced by 17β-estradiol and growth factors 42
Meta-analysis of gene-level associations for rare variants based on single-variant statistics 41
Germline NUP98 Variants in Two Siblings with a Rothmund-Thomson-Like Spectrum: Protein Functional Changes Predicted by Molecular Modeling 41
The length of FOXE1 polyalanine tract in congenital hypothyroidism: Evidence for a pathogenic role from familial, molecular and cohort studies 41
Totale 6.627
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Categoria #
all - tutte 39.024
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 39.024
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021108 0 0 0 0 0 16 3 53 26 6 3 1
2021/2022331 11 0 6 3 4 3 6 21 23 5 49 200
2022/20231.010 145 82 19 43 48 58 0 24 531 3 38 19
2023/2024627 35 68 35 45 52 129 12 47 2 18 76 108
2024/20251.804 95 138 14 20 38 97 76 123 425 101 252 425
2025/20262.463 422 385 645 372 506 133 0 0 0 0 0 0
Totale 7.560