IRIS
GENTILINI, DAVIDE
 Distribuzione geografica
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Continente #
NA - Nord America 3.794
AS - Asia 3.171
EU - Europa 1.907
SA - Sud America 373
AF - Africa 103
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 4
Totale 9.363
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Nazione #
US - Stati Uniti d'America 3.712
CN - Cina 1.427
SG - Singapore 761
IE - Irlanda 516
HK - Hong Kong 404
IT - Italia 375
RU - Federazione Russa 322
BR - Brasile 278
VN - Vietnam 204
DE - Germania 168
FR - Francia 148
FI - Finlandia 102
IN - India 87
BD - Bangladesh 69
GB - Regno Unito 63
ZA - Sudafrica 54
AR - Argentina 42
CA - Canada 37
IQ - Iraq 33
PL - Polonia 31
UA - Ucraina 30
NL - Olanda 27
ES - Italia 22
SE - Svezia 22
PK - Pakistan 21
AT - Austria 19
MX - Messico 19
ID - Indonesia 18
JP - Giappone 17
VE - Venezuela 15
TR - Turchia 14
SA - Arabia Saudita 13
BE - Belgio 12
AE - Emirati Arabi Uniti 11
CO - Colombia 11
EC - Ecuador 11
JO - Giordania 11
UZ - Uzbekistan 11
AU - Australia 10
KR - Corea 9
LT - Lituania 8
PH - Filippine 8
EG - Egitto 7
GR - Grecia 7
LV - Lettonia 7
MA - Marocco 7
MY - Malesia 7
TN - Tunisia 7
AZ - Azerbaigian 6
DZ - Algeria 6
CL - Cile 5
CR - Costa Rica 5
IL - Israele 5
KZ - Kazakistan 5
LB - Libano 5
SY - Repubblica araba siriana 5
AL - Albania 4
BG - Bulgaria 4
EU - Europa 4
IR - Iran 4
JM - Giamaica 4
KE - Kenya 4
NP - Nepal 4
PA - Panama 4
PE - Perù 4
BO - Bolivia 3
CH - Svizzera 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
ET - Etiopia 3
SV - El Salvador 3
UY - Uruguay 3
BY - Bielorussia 2
HU - Ungheria 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LY - Libia 2
PS - Palestinian Territory 2
SN - Senegal 2
TT - Trinidad e Tobago 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BM - Bermuda 1
BS - Bahamas 1
BW - Botswana 1
CF - Repubblica Centrafricana 1
CM - Camerun 1
GA - Gabon 1
GE - Georgia 1
GW - Guinea-Bissau 1
HN - Honduras 1
KH - Cambogia 1
KY - Cayman, isole 1
LA - Repubblica Popolare Democratica del Laos 1
LS - Lesotho 1
LU - Lussemburgo 1
MD - Moldavia 1
MG - Madagascar 1
MK - Macedonia 1
Totale 9.351
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Città #
Dallas 644
Dublin 514
San Jose 485
Ashburn 437
Hong Kong 399
Singapore 397
Beijing 354
Nanjing 242
Chandler 236
Boardman 154
Lauterbourg 117
Princeton 90
Los Angeles 88
Ho Chi Minh City 87
Lawrence 84
Jacksonville 82
Nanchang 82
Hebei 72
Changsha 71
Medford 71
Shenyang 68
Council Bluffs 67
New York 67
Redondo Beach 67
Helsinki 66
Jiaxing 60
Buffalo 58
Shanghai 58
Moscow 53
Munich 53
Wilmington 51
Johannesburg 45
Milan 40
Hanoi 39
Santa Clara 39
Hangzhou 36
Orem 36
Pavia 34
São Paulo 34
The Dalles 30
Warsaw 29
Ann Arbor 26
Brooklyn 26
Nuremberg 26
Tianjin 26
Houston 24
Turku 23
Chennai 22
San Francisco 21
Guangzhou 19
Fairfield 18
Washington 18
Montreal 17
Tokyo 17
Chicago 16
Frankfurt am Main 16
Denver 15
Seattle 15
Baghdad 13
Rome 13
Woodbridge 13
Stockholm 12
Zhengzhou 12
Boston 11
Verona 11
Vienna 11
Atlanta 10
Chieti 10
Columbus 10
Manchester 10
Redwood City 10
Tashkent 10
Da Nang 9
Dhaka 9
Falkenstein 9
London 9
Norwalk 9
Amman 8
Belo Horizonte 8
Brussels 8
Catanzaro 8
Curitiba 8
Elk Grove Village 8
Naples 8
Phoenix 8
Rio de Janeiro 8
Amsterdam 7
Brescia 7
Florence 7
Lahore 7
Mariglianella 7
Pescara 7
Riga 7
Toronto 7
Baku 6
Caracas 6
Düsseldorf 6
Hyderabad 6
Jeddah 6
Jinan 6
Totale 6.446
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Nome #
Identificazione di microRNA circolanti specificatamente sovra espressi in corso di infarto miocardico acuto. 250
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 156
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis. 143
Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci 140
Acid Sensing Ion Channel 2: a new potential player in the pathophysiology of multiple sclerosis 126
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture 112
A frequent oligogenic involvement in congenital hypothyroidism 112
B Cells Isolated from Individuals Who Do Not Respond to the HBV Vaccine Are Characterized by Higher DNA Methylation-Estimated Aging Compared to Responders 111
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 107
Accelerated epigenetic aging in Down syndrome 105
Epigenome wide association and stochastic epigenetic mutation analysis on cord blood of preterm birth 104
Characterization of the biological processes shaping the genetic structure of the Italian population 103
Antiphospholipid Antibodies and Infertility: A Gene Expression Study in Decidual Stromal Cells 100
Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach 100
Genome Wide Association Studies using extreme blood pressure distribution identify variants in UMOD associated with hypertension 100
Age-dependent skewing of X chromosome inactivation appears delayed in centenarians' offspring. Is there a role for allelic imbalance in Healthy Aging and Longevity? 99
Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS 99
Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach 99
An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis 99
Dissecting the Pre-Columbian genomic ancestry of Native Americans along the Andes-Amazonia divide 97
Early-life factors, in-utero exposures and endometriosis risk: a meta-analysis 96
Acceleration of leukocytes' epigenetic age as an early tumorand sex-specific marker of breast and colorectal cancer 95
Differences in Visceral Fat and Fat Bacterial Colonization between Ulcerative Colitis and Crohn's Disease. An In Vivo and In Vitro Study 95
Metronomic administration of zoledronic acid and taxotere combination in castration resistant prostate cancer patients. Phase I ZANTE trial 94
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features 94
A pan-cancer approach to predict responsiveness to immune checkpoint inhibitors by machine learning 92
'Here comes the sun': Pigmentary traits and sun habits in women with endometriosis 90
Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail 89
One-year Mediterranean diet promotes epigenetic rejuvenation with country- and sex-specific effects: a pilot study from the NU-AGE project 88
The Association between Dysnatraemia during Hospitalisation and Post-COVID-19 Mental Fatigue 87
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 87
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis 87
Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females 87
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the IGF1R Gene 87
Rationale and design of the CV-PREVITAL study: an Italian multiple cohort randomised controlled trial investigating innovative digital strategies in primary cardiovascular prevention 86
A rare familial case of endometriosis with very severe gynecological and obstetric complications: Novel genetic variants at a glance 86
Complex interplay between neutral and adaptive evolution shaped differential genomic background and disease susceptibility along the Italian peninsula 86
Article a new epigenetic model to stratify glioma patients according to their immunosuppressive state 86
European genome-wide association study using extremes of blood pressure distribution: study design and methods. 85
Methylation of ELOVL2 gene as a new epigenetic marker of age 85
Synergistic activity of everolimus and 5-aza-2′-deoxycytidine in medullary thyroid carcinoma cell lines 84
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring 84
Identification of upregulated microRNAs in the plasma of patients with acute myocardial infarction 83
Pyk2 and Cyr61 at the cross-road of cAMP-dependent signalling in invasiveness and neuroendocrine differentiation of prostate cancer 82
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects 81
Identification of a DNA methylation signature in blood cells from persons with Down Syndrome 81
Heterogeneity of thyroid function and impact of peripheral thyroxine deiodination in centenarians and semi-supercentenarians: association with functional status and mortality 81
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 80
Impact of demography and population dynamics on the genetic architecture of human longevity 78
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation study 77
Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor 77
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. 77
Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas 76
Statin use and long-term risk of recurrent intracerebral haemorrhage: the MUCH-Italy 75
Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects 75
Erratum: A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data 75
Role of epigenetics in human aging and longevity: Genome-wide DNA methylation profile in centenarians and centenarians' offspring 74
Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset 74
Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosis 73
Homozygosity haplotype and whole-exome sequencing analysis to identify potentially functional rare variants involved in multiple sclerosis among sardinian families 73
Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome 72
Molecular Aging of Human Liver: An Epigenetic/Transcriptomic Signature 72
PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival 72
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index 71
Epigenetics of Autism Spectrum Disorders: A Multi-level Analysis Combining Epi-signature, Age Acceleration, Epigenetic Drift and Rare Epivariations Using Public Datasets 70
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 70
Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis 68
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy 68
Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis 67
Endometrial stromal progesterone receptor-A/progesterone receptor-B ratio: No difference between women with and without endometriosis 67
Pathogenic variants in STXBP1 and in genes for GABAa receptor subunities cause atypical rett/rett-like phenotypes 67
A meta-analysis on age-associated changes in blood DNA methylation: Results from an original analysis pipeline for Infinium 450k data 66
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis-like syndrome 66
NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis 65
Molecular and morphologic characterization of superficial-and deep-subcutaneous adipose tissue subdivisions in human obesity 64
Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles 64
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis 64
Endocannabinoid system regulates migration of endometrial stromal cells via cannabinoid receptor 1 through the activation of PI3K and ERK1/2 pathways 63
Immunomodulatory effects of VEGF: Clinical implications of VEGF-targeted therapy in human cancer 63
The genetic legacy of the Yaghnobis: A witness of an ancient Eurasian ancestry in the historically reshuffled central Asian gene pool 63
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 62
Surgical excision of ovarian endometriomas: Does it truly impair ovarian reserve? Long term anti-Müllerian hormone (AMH) changes after surgery 60
The vascular endothelial growth factor +405G>C polymorphism in endometriosis 60
The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas 60
Identification of gene expression in the brain causally linked to multiple sclerosis: a two-sample mendelian randomization approach 59
Genome-wide DNA methylation analysis of a cohort of 41 patients affected by oculo-auriculo-vertebral spectrum (OAVS) 59
No association between frailty index and epigenetic clocks in Italian semi-supercentenarians 59
Genetic diagnosis of endocrine diseases by NGS: Novel scenarios and unpredictable results and risks 58
Deregulated human glioma cell motility: Inhibitory effect of somatostatin 58
Meta-analysis of gene-level associations for rare variants based on single-variant statistics 57
Endometrial stromal cells from women with endometriosis reveal peculiar migratory behavior in response to ovarian steroids 56
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 56
Exploring the complexities of epigenetics in multiple sclerosis: A study involving meta-analysis of DNA methylation profiles, epigenetic drift, and rare epivariations 55
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study 55
Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations 55
Germline NUP98 Variants in Two Siblings with a Rothmund-Thomson-Like Spectrum: Protein Functional Changes Predicted by Molecular Modeling 54
Extensive placental methylation profiling in normal pregnancies 54
Extensive Placental Methylation Profiling in Normal Pregnancies 53
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136 53
Genomic adaptations to cereal‐based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry 52
Totale 8.181
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Categoria #
all - tutte 45.824
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 45.824
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 0 0 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
2025/20264.483 422 385 645 372 506 159 775 205 346 288 247 133
Totale 9.580