GENTILINI, DAVIDE
 Distribuzione geografica
Continente #
NA - Nord America 1.438
AS - Asia 1.017
EU - Europa 997
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 4
AF - Africa 2
SA - Sud America 2
Totale 3.464
Nazione #
US - Stati Uniti d'America 1.433
CN - Cina 875
IE - Irlanda 510
IT - Italia 246
SG - Singapore 129
FI - Finlandia 74
DE - Germania 66
UA - Ucraina 23
RU - Federazione Russa 17
FR - Francia 13
BE - Belgio 12
GB - Regno Unito 10
SE - Svezia 8
CA - Canada 5
ES - Italia 5
GR - Grecia 5
EU - Europa 4
MY - Malesia 4
AU - Australia 3
IR - Iran 3
DK - Danimarca 2
IN - India 2
JP - Giappone 2
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
EG - Egitto 1
HK - Hong Kong 1
LU - Lussemburgo 1
LV - Lettonia 1
NL - Olanda 1
NZ - Nuova Zelanda 1
SA - Arabia Saudita 1
SI - Slovenia 1
VE - Venezuela 1
Totale 3.464
Città #
Dublin 510
Nanjing 242
Chandler 236
Ashburn 196
Boardman 151
Beijing 120
Princeton 90
Singapore 90
Lawrence 84
Nanchang 81
Jacksonville 79
Hebei 72
Medford 69
Shenyang 68
Changsha 65
Helsinki 61
Jiaxing 60
Shanghai 55
Wilmington 51
Hangzhou 31
Ann Arbor 26
Pavia 23
Houston 21
Milan 21
Tianjin 21
Fairfield 18
Washington 17
Woodbridge 13
Chieti 10
Guangzhou 10
Redwood City 10
Seattle 10
Norwalk 9
Brussels 8
Dallas 8
Los Angeles 8
New York 8
Santa Clara 8
Catanzaro 7
Mariglianella 7
Pescara 7
Rome 7
Brescia 6
Naples 6
Nuremberg 6
San Francisco 6
Falkenstein 5
Jinan 5
Ningbo 5
Zhengzhou 5
Des Moines 4
Florence 4
Leuven 4
Olgiate Olona 4
Turin 4
Bologna 3
Ferrara 3
Gunzenhausen 3
Muggiò 3
Piscataway 3
Seregno 3
Seri Kembangan 3
Taizhou 3
Thessaloniki 3
Toronto 3
Verona 3
Barcelona 2
Bari 2
Barletta 2
Borås 2
Buccinasco 2
Chicago 2
Clifton 2
Copenhagen 2
Cottbus 2
Francavilla Al Mare 2
Frankfurt am Main 2
Gorgonzola 2
Guanzate 2
Hefei 2
Montoro 2
Napoli 2
Orange 2
Palermo 2
Ponte San Pietro 2
Reading 2
Salerno 2
San Benedetto del Tronto 2
Tokyo 2
Venegono Inferiore 2
Zanica 2
Alessandria 1
Alghero 1
Aquila 1
Auckland 1
Belém 1
Benevento 1
Bitonto 1
Bollate 1
Buffalo 1
Totale 2.844
Nome #
Identificazione di microRNA circolanti specificatamente sovra espressi in corso di infarto miocardico acuto. 217
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis. 96
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 74
Genome Wide Association Studies using extreme blood pressure distribution identify variants in UMOD associated with hypertension 61
Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci 60
Can genetics predict risk for sudden cardiac death? The relentless search for the Holy Grail 59
Accelerated epigenetic aging in Down syndrome 58
Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approach 57
Characterization of the biological processes shaping the genetic structure of the Italian population 55
Antiphospholipid Antibodies and Infertility: A Gene Expression Study in Decidual Stromal Cells 51
Differences in Visceral Fat and Fat Bacterial Colonization between Ulcerative Colitis and Crohn's Disease. An In Vivo and In Vitro Study 50
Synergistic activity of everolimus and 5-aza-2′-deoxycytidine in medullary thyroid carcinoma cell lines 49
Age-dependent skewing of X chromosome inactivation appears delayed in centenarians' offspring. Is there a role for allelic imbalance in Healthy Aging and Longevity? 47
Acid Sensing Ion Channel 2: a new potential player in the pathophysiology of multiple sclerosis 47
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 46
Metronomic administration of zoledronic acid and taxotere combination in castration resistant prostate cancer patients. Phase I ZANTE trial 46
European genome-wide association study using extremes of blood pressure distribution: study design and methods. 45
Methylation of ELOVL2 gene as a new epigenetic marker of age 45
A frequent oligogenic involvement in congenital hypothyroidism 45
'Here comes the sun': Pigmentary traits and sun habits in women with endometriosis 44
Dissecting the Pre-Columbian genomic ancestry of Native Americans along the Andes-Amazonia divide 44
Erratum: A meta-analysis on age-associated changes in blood DNA methylation: results from an original analysis pipeline for Infinium 450k data 43
Pyk2 and Cyr61 at the cross-road of cAMP-dependent signalling in invasiveness and neuroendocrine differentiation of prostate cancer 43
Permanence of molecular features of obesity in subcutaneous adipose tissue of ex-obese subjects 40
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture 40
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring 40
Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS 40
Role of epigenetics in human aging and longevity: Genome-wide DNA methylation profile in centenarians and centenarians' offspring 39
Identification of a DNA methylation signature in blood cells from persons with Down Syndrome 39
Acceleration of leukocytes' epigenetic age as an early tumorand sex-specific marker of breast and colorectal cancer 39
Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females 39
Identification of upregulated microRNAs in the plasma of patients with acute myocardial infarction 38
Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor 38
Complex interplay between neutral and adaptive evolution shaped differential genomic background and disease susceptibility along the Italian peninsula 38
Heterogeneity of thyroid function and impact of peripheral thyroxine deiodination in centenarians and semi-supercentenarians: association with functional status and mortality 38
Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach 38
Epigenome wide association and stochastic epigenetic mutation analysis on cord blood of preterm birth 38
Immunomodulatory effects of VEGF: Clinical implications of VEGF-targeted therapy in human cancer 37
Integrated DNA methylation analysis identifies topographical and tumoral biomarkers in pilocytic astrocytomas 37
Early-life factors, in-utero exposures and endometriosis risk: a meta-analysis 37
Molecular Aging of Human Liver: An Epigenetic/Transcriptomic Signature 36
A rare familial case of endometriosis with very severe gynecological and obstetric complications: Novel genetic variants at a glance 36
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 36
PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival 36
One-year Mediterranean diet promotes epigenetic rejuvenation with country- and sex-specific effects: a pilot study from the NU-AGE project 36
An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis 36
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. 35
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 35
Endocannabinoid system regulates migration of endometrial stromal cells via cannabinoid receptor 1 through the activation of PI3K and ERK1/2 pathways 34
The endocannabinoid pathway and the female reproductive organs 34
Gene expression profiling in human corticotroph tumours reveals distinct, neuroendocrine profiles 34
Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis 33
Impact of demography and population dynamics on the genetic architecture of human longevity 33
Molecular and morphologic characterization of superficial-and deep-subcutaneous adipose tissue subdivisions in human obesity 32
Endometrial stromal cells from women with endometriosis reveal peculiar migratory behavior in response to ovarian steroids 31
Deregulated human glioma cell motility: Inhibitory effect of somatostatin 31
Surgical excision of ovarian endometriomas: Does it truly impair ovarian reserve? Long term anti-Müllerian hormone (AMH) changes after surgery 30
Pathogenic variants in STXBP1 and in genes for GABAa receptor subunities cause atypical rett/rett-like phenotypes 30
A pan-cancer approach to predict responsiveness to immune checkpoint inhibitors by machine learning 30
Replication and meta-analysis of previous genome-wide association studies confirm vezatin as the locus with the strongest evidence for association with endometriosis 29
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 28
The genetic legacy of the Yaghnobis: A witness of an ancient Eurasian ancestry in the historically reshuffled central Asian gene pool 28
NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis 28
Homozygosity haplotype and whole-exome sequencing analysis to identify potentially functional rare variants involved in multiple sclerosis among sardinian families 28
Gene expression profiling of peripheral blood mononuclear cells in endometriosis identifies genes altered in non-gynaecologic chronic inflammatory diseases 27
The vascular endothelial growth factor +405G>C polymorphism in endometriosis 27
Endometrial stromal progesterone receptor-A/progesterone receptor-B ratio: No difference between women with and without endometriosis 27
The genomic landscape of Nepalese Tibeto-Burmans reveals new insights into the recent peopling of Southern Himalayas 27
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy 27
PI3K/Akt And ERK1/2 signalling pathways are involved in endometrial cell migration induced by 17β-estradiol and growth factors 26
Article a new epigenetic model to stratify glioma patients according to their immunosuppressive state 26
Responders and non-responders to influenza vaccination: A DNA methylation approach on blood cells 25
Genetic diagnosis of endocrine diseases by NGS: Novel scenarios and unpredictable results and risks 25
Rationale and design of the CV-PREVITAL study: an Italian multiple cohort randomised controlled trial investigating innovative digital strategies in primary cardiovascular prevention 24
Plasminogen activator inhibitor-1 4G/5G polymorphism and susceptibility to endometriosis in the Italian population 24
Visceral adipocytes: Old actors in obesity and new protagonists in Crohn's disease? 24
Phenotypic overlap of Roberts and Baller-Gerold syndromes in two patients with craniosynostosis, limb reductions, and ESCO2 mutations 23
Hormonal therapy potentiates the effect of surgery on gene expression profile of peripheral blood mononuclear cells in patients affected by endometriosis 23
The selective vitamin D receptor agonist, elocalcitol, reduces endometriosis development in a mouse model by inhibiting peritoneal inflammation 22
Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset 20
Methylation alteration of SHANK1 as a predictive, diagnostic and prognostic biomarker for chronic lymphocytic leukemia 19
Genome-wide DNA methylation analysis of a cohort of 41 patients affected by oculo-auriculo-vertebral spectrum (OAVS) 19
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136 18
No association between frailty index and epigenetic clocks in Italian semi-supercentenarians 17
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects 15
The Association between Dysnatraemia during Hospitalisation and Post-COVID-19 Mental Fatigue 14
Extensive placental methylation profiling in normal pregnancies 14
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis 14
Statin use and long-term risk of recurrent intracerebral haemorrhage: the MUCH-Italy 13
Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome 13
The length of FOXE1 polyalanine tract in congenital hypothyroidism: Evidence for a pathogenic role from familial, molecular and cohort studies 13
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency 13
Soluble EMMPRIN levels discriminate aortic ectasia in marfan syndrome patients 12
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features 12
Germline NUP98 Variants in Two Siblings with a Rothmund-Thomson-Like Spectrum: Protein Functional Changes Predicted by Molecular Modeling 11
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis 11
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index 11
A meta-analysis on age-associated changes in blood DNA methylation: Results from an original analysis pipeline for Infinium 450k data 10
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny 10
Identification of gene expression in the brain causally linked to multiple sclerosis: a two-sample mendelian randomization approach 10
Totale 3.482
Categoria #
all - tutte 21.422
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 21.422


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020153 0 0 0 0 0 8 4 10 14 68 46 3
2020/2021135 5 5 2 5 10 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
2024/2025345 95 138 14 20 38 40 0 0 0 0 0 0
Totale 3.638