Catalogo dei prodotti della ricerca

PRUDENTE, Sabrina
 Distribuzione geografica
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Continente #
NA - Nord America 3.640
EU - Europa 1.025
AS - Asia 675
AF - Africa 37
SA - Sud America 22
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 2
Totale 5.404
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Nazione #
US - Stati Uniti d'America 3.609
IT - Italia 397
SG - Singapore 278
CN - Cina 168
IN - India 165
SE - Svezia 158
UA - Ucraina 124
FI - Finlandia 82
DE - Germania 60
BG - Bulgaria 44
GB - Regno Unito 32
TG - Togo 31
CA - Canada 27
RU - Federazione Russa 20
IE - Irlanda 19
FR - Francia 17
NL - Olanda 17
AR - Argentina 16
MT - Malta 13
RO - Romania 13
ID - Indonesia 12
TW - Taiwan 11
BE - Belgio 8
HK - Hong Kong 8
TH - Thailandia 7
KR - Corea 6
KW - Kuwait 6
JP - Giappone 5
BR - Brasile 4
ES - Italia 4
HU - Ungheria 4
CH - Svizzera 3
EU - Europa 3
GR - Grecia 3
MX - Messico 3
DK - Danimarca 2
EG - Egitto 2
IR - Iran 2
PT - Portogallo 2
TR - Turchia 2
AM - Armenia 1
AU - Australia 1
CL - Cile 1
CZ - Repubblica Ceca 1
IQ - Iraq 1
LT - Lituania 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
PL - Polonia 1
SD - Sudan 1
TN - Tunisia 1
UZ - Uzbekistan 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 5.404
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Città #
Fairfield 670
Ashburn 286
Woodbridge 285
Houston 263
Cambridge 231
Seattle 229
Wilmington 213
Singapore 187
Ann Arbor 146
Chandler 143
Santa Clara 130
Beijing 119
Princeton 101
Rome 98
Lawrence 76
Plano 74
San Paolo di Civitate 73
Boston 60
Jacksonville 53
San Diego 50
Sofia 44
Millbury 33
Lomé 31
Bremen 30
Dearborn 27
Andover 25
New York 25
Falls Church 17
Dublin 16
Federal 16
Boardman 15
Helsinki 14
Napoli 14
Jakarta 12
London 12
Norwalk 12
Ottawa 12
Toronto 11
Le Casine-Perignano-Spinelli 10
Milan 10
Des Moines 9
Latina 9
Bologna 8
Falkenstein 8
Moscow 8
Guangzhou 6
Kunming 6
Kuwait City 6
Phoenix 6
Wakefield 6
Bangkok 5
Fremont 5
Stockholm 5
Waanrode 5
Bühl 4
Chongqing 4
Collecorvino 4
Debrecen 4
Msida 4
Redmond 4
Auburn Hills 3
Bern 3
Birkirkara 3
Brussels 3
Buffalo 3
Cesa 3
Domanico 3
Hefei 3
Islington 3
Messina 3
Naples 3
Palermo 3
Pisa 3
Pune 3
Redwood City 3
Rio de Janeiro 3
San Mateo 3
Southend 3
Tappahannock 3
Torre del Greco 3
Yonkers 3
Altomonte 2
Argelato 2
Arnsberg 2
Bra 2
Camisano 2
Capannelle 2
Central 2
Changsha 2
Chiaravalle Centrale 2
Chicago 2
Cinisello Balsamo 2
Copenhagen 2
Cordenons 2
Dallas 2
Fasano 2
Fontanellato 2
Geneva 2
Indiana 2
Istanbul 2
Totale 4.090
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Nome #
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies 143
Variability in genes regulating vitamin D metabolism is associated with vitamin D levels in type 2 diabetes 120
Mutazioni nel gene APPL1 e diabete mellito familiare dell’adulto 111
IRS1 G972R polymorphism and type 2 diabetes. a paradigm for the difficult ascertainment of the contribution to disease susceptibility of ‘low-frequency–low-risk’ variants 107
TRIB3 r84 variant is associated with impaired insulin-mediated nitric oxide production in human endothelial cells 88
The "Sapienza University Mortality and Morbidity Event Rate (SUMMER) study in diabetes": Study protocol 87
Mutations in APPL1 gene may contribute to familial diabetes mellitus 86
Glutamine to arginine substitution at amino acid 84 of mammalian tribbles homolog TRIB3 and ckd in whites with type 2 diabetes 86
ROCK2 and its alternatively spliced isoform ROCK2m positively control the maturation of the myogenic program 86
Pharmacogenetics of oral antidiabetes drugs: Evidence for diverse signals at the IRS1 locus 84
Infrequent TRIB3 coding variants and coronary artery disease in type 2 diabetes 83
A polymorphism at the IL6ST (gp130) locus is associated with traits of the metabolic syndrome 82
Loss-of-function mutations in appl1 in familial diabetes mellitus 81
The 9p21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitus 80
Pathogenic variants of MODY-genes in adult patients with early-onset type 2 diabetes 78
Exon scanning mutation analysis of the ATM gene in patients with ataxia-telangiectasia 77
ENPP1 gene, insulin resistance and related clinical outcomes 77
The ectonucleotide pyrophosphatase phosphodiesterase 1 (ENPP1) K121Q polymorphism modulates the beneficial effect of weight loss on fasting glucose in non-diabetic individuals 77
TRIB3 R84 variant affects glucose homeostasis by altering the interplay between insulin sensitivity and secretion 73
The PPARγ2 P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus 73
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing 73
IRS1 G972R missense polymorphism is associated with failure to oral antidiabetes drugs in white patients with type 2 diabetes from Italy 72
The IRS1 G972R polymorphism and glomerular filtration rate in patients with type 2 diabetes of European ancestry 71
Joint Effect of Insulin Signaling Genes on Insulin Secretion and Glucose Homeostasis 69
Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. 69
The common -866G/A polymorphism in the promoter region of the UCP-2 gene is associated with reduced risk of type 2 diabetes in Caucasians from Italy. 68
Some doubts about the mantra on the deleterious cardiovascular effects of sulfonylureas 68
Interaction between PPARγ2 variants and gender on the modulation of body weight 66
Identification and clinical characterization of adult patients with multigenerational diabetes mellitus 66
A genetic marker of hyperuricemia predicts cardiovascular events in a meta-analysis of three cohort studies in high risk patients 66
A functional variant of the adipocyte glycerol channel aquaporin 7 gene is associated with obesity and related metabolic abnormalities 65
The TRIB3 Q84R polymorphism and risk of early-onset type 2 diabetes 65
null 65
A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients 64
Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays 63
The SH2B1 obesity locus is associated with myocardial infarction in diabetic patients and with NO synthase activity in endothelial cells 63
The Mammalian Tribbles Homolog TRIB3, Glucose Homeostasis, and Cardiovascular Diseases 62
The TRIB3 Q84R polymorphism, insulin resistance and related metabolic alterations 62
The type 2 diabetes and insulin-resistance locus near IRS1 is a determinant of HDL cholesterol and triglycerides levels among diabetic subjects 62
Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation 62
Six novel ATM mutations in Italian patients with classical ataxia-telangiectasia. 61
Gain of function mutations in Malate Dehydrogenase 2 (MDH2) cause familial diabetes of the adulthood 61
The ENPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: evidence from an updated meta-analysis in 42,042 subjects 61
Insulin signaling regulating genes: effect on T2DM and cardiovascular risk. 60
The SH2B1 obesity locus and abnormal glucose homeostasis: Lack of evidence for association from a meta-analysis in individuals of European ancestry 60
Interaction of DIO2 T92A and PPARγ2 P12A polymorphisms in the modulation of metabolic syndrome. 60
Serum Resistin, Cardiovascular Disease and All-Cause Mortality in Patients with Type 2 Diabetes 60
The TRIB3 R84 variant is associated with increased carotid intima media thickness in vivo and with enhanced MAPK signalling in human endothelial cells. 60
Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes 59
Role of the ENPP1 K121Q Polymorphism on Glucose Homeostasis 59
Clinical worthlessness of genetic prediction of common forms of diabetes mellitus and related chronic complications: A position statement of the Italian Society of Diabetology 59
Heterogeneous effects of gene polymorphism on type 2 diabetes risk: lesson from the PPARγ2 Pro12Ala 58
The functional Q84R polymorphism of mammalian tribbles homolog TRB3 is associated with insulin resistance and related cardiovascular risk in Caucasian from Italy 57
Joint effect of insulin signaling genes on cardiovascular events and on whole body and endothelial insulin resistance 57
The K121Q polymorphism of the ENPP1/PC-1 gene is associated with insulin resistance/atherogenic phenotypes including earlier onset of type 2 diabetes and of myocardial infarction 56
The allelic variant of LAR gene promoter –127 bp T◊A is associated with reduced risk of obesity and other features related to insulin resistance. 56
ENPP1 affects insulin action and secretion: Evidences from in vitro studies 55
ENPP1 mRNA levels in white blood cells and prediction of metformin efficacy in type 2 diabetic patients: a preliminary evidence. 55
null 55
PPARA polymorphism influences the cardiovascular benefit of fenofibrate in type 2 diabetes: findings from accord-lipid 51
Analisi biochimica e molecolare di un nuovo caso di deficit di guanidinoacetato metiltrasferasi . 50
Genetic prediction of common diseases. Still no help for the clinical diabetologist! 50
Role of insulin resistance in kidney dysfunction: Insights into the mechanism and epidemiological evidence 49
The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy 48
Genetic variant at the GLUL locus predicts all-cause mortality in patients with type 2 diabetes. 47
The emerging role of TRIB3 as a gene affecting human insulin resistance and related clinical outcomes 46
Impact of the PPARγ2 Pro12Ala polymorphism and ACE inhibitor therapy on new-onset microalbuminuria in type 2 diabetes: evidence from Benedict 45
Aniridia ed epilessia: studio di una famiglia 44
Malate Dehydrogenase 2 (MDH2) as a New Diabetogene Causing Hyperglycemia in Families with Multigenerational Diabetes 43
Familial diabetes of adulthood: A bin of ignorance that needs to be addressed 42
Association of the 1q25 diabetes-specific coronary heart disease locus with slterations of the γ-glutamyl cycle and increased methylglyoxal levels in endothelial cells 42
Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do 41
Deep Resequencing of 9 Candidate Genes Identifies a Role for ARAP1 and IGF2BP2 in Modulating Insulin Secretion Adjusted for Insulin Resistance in Obese Southern Europeans 41
TWO NEW SEVERE MUTATIONS CAUSING GUANIDINOACETATE METHYLTRASFERASE DEFICIENCY. 40
Mutation of the ATM gene in Italy recovered through different methodological approaches 38
GALNT2 Expression Is Reduced in Patients with Type 2 Diabetes: Possible Role of Hyperglycemia 38
Clinical utility for monogenic diabetes molecular testing among patients with early-onset type 2 diabetes 38
Deep re-sequencing of 9 type 2 diabetes GWAS loci by comparison of extremes of dynamic indices of insulin secrection 37
Contribution of rare and common genetic variants to early-onset type 2 diabetes 37
ATM protein and p53-serine 15 phosphorylation in ataxia-telangiectasia (AT) patients and at heterozygotes 36
Proneness to cancer in italian Ataxia telangiectasia families 35
Gain of function of malate dehydrogenase 2 (MDH2) and familial hyperglycemia 34
Unraveling the genetic background of early-onset type 2 diabetes: a step forward toward precision medicine 33
The Q121/Q121 genotype of ENPP1/PC-1 is associated with lower BMI in non-diabetic Caucasians 33
The pleiotropic effect of the ENPP1 (PC-1) gene on insulin resistance, obesity and type 2 diabetes - Editorial 32
Expanding the Knowledge on the Spectrum of Familial Diabetes in Adult Patients 32
Ruolo della variabilità genetica nel diabete tipo 2 (DT2) ad insorgenza precoce. 32
The ENPP1 Q121 Variant Predicts Major Cardiovascular Events in High-Risk Individuals Evidence for Interaction With Obesity in Diabetic Patients 31
Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes 30
PPARγ2 P12A polymorphism and albuminuria in patients with type 2 diabetes: A meta-analysis of case-control studies 30
Molecular analysis of a new case of guanidinoacatate methyltransferase deficiency. 28
Comparison of Clinical Features and Mortality Rate of Adult Patients with Multigenerational Diabetes and of Patients with Type 2 Diabetes Mellitus 26
HISTOPATHOLOGIC FINDINGS IN A FETUS WITH PRENATALLY DIAGNOSED ATAXIA-TELANGIECTASIA 22
Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients 21
null 19
PAH ectopic transcript analysis as a complementary method to mutation screening in PKU patients. 18
Unusual Association of Scn2a Epileptic Encephalopathy with Severe Cortical Dysplasia Detected by Prenatal Mri 18
The rs12917707 polymorphism at the UMOD locus and glomerular filtration rate in individuals with type 2 diabetes: evidence of heterogeneity across two different European populations. 18
Insights from Molecular Characterization of Adult Patients of Families with Multigenerational Diabetes Mellitus 14
null 14
Totale 5.632
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Categoria #
all - tutte 17.081
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 17.081
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020901 0 0 0 0 0 157 171 159 146 140 73 55
2020/2021415 36 65 28 24 12 23 19 45 61 50 41 11
2021/20221.035 16 64 114 20 119 25 31 135 86 70 172 183
2022/2023801 172 214 28 95 67 70 13 24 67 13 24 14
2023/2024564 25 64 34 52 60 79 17 31 3 75 53 71
2024/2025494 42 58 66 70 156 102 0 0 0 0 0 0
Totale 5.651