IRIS
CIRILLO, Grazia
 Distribuzione geografica
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Continente #
NA - Nord America 571
EU - Europa 502
AS - Asia 144
AF - Africa 3
OC - Oceania 1
SA - Sud America 1
Totale 1.222
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Nazione #
US - Stati Uniti d'America 570
IE - Irlanda 251
CN - Cina 91
IT - Italia 57
GB - Regno Unito 53
DE - Germania 38
SG - Singapore 37
UA - Ucraina 31
GR - Grecia 22
FR - Francia 17
BE - Belgio 11
FI - Finlandia 10
SE - Svezia 10
TR - Turchia 7
KR - Corea 6
IN - India 3
DZ - Algeria 2
BR - Brasile 1
CZ - Repubblica Ceca 1
MA - Marocco 1
MX - Messico 1
NL - Olanda 1
NZ - Nuova Zelanda 1
Totale 1.222
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Città #
Dublin 251
Chandler 131
Jacksonville 65
Ann Arbor 61
Ashburn 38
Beijing 37
Princeton 25
Roxbury 25
Bremen 20
New York 20
Singapore 20
Medford 18
Caserta 13
Munich 13
Brussels 11
Washington 10
Boardman 9
Cambridge 8
Nanjing 8
Wilmington 8
Woodbridge 8
Des Moines 7
Napoli 7
Seoul 6
Hangzhou 5
Jinan 4
Milan 4
Changchun 3
Mountain View 3
Ningbo 3
Shenyang 3
Arzano 2
Haikou 2
Hebei 2
Hyderabad 2
Kunming 2
Lappeenranta 2
Naples 2
Redwood City 2
Alghero 1
Amsterdam 1
Andover 1
Avellino 1
Aversa 1
Büdingen 1
Clifton 1
Frankfurt am Main 1
Grafing 1
Gragnano 1
Guangzhou 1
Helsinki 1
Jiaxing 1
Jinhua 1
London 1
Los Angeles 1
Miami 1
Nanchang 1
Prague 1
Pune 1
Qingdao 1
Rockville 1
Santa Clara 1
Shanghai 1
Shaoxing 1
São Paulo 1
Taizhou 1
Tianjin 1
Torre Annunziata 1
Zhengzhou 1
Totale 890
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Nome #
Novel association between the nonsynonymous A803G polymorphism of the N-acetyltransferase 2 gene and impaired glucose homeostasis in obese children and adolescents 65
Nonalcoholic fatty liver disease and eGFR levels could be linked by the PNPLA3 I148M polymorphism in children with obesity 62
The TM6SF2 E167K variant in HIV/HCV coinfection predicts severe liver fibrosis and, only for patients with HCV genotype non 3 severe steatosis. 61
A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene 61
MKRN3 levels in girls with central precocious puberty and correlation with sexual hormone levels: a pilot study 61
Congenital Solitary Kidney from Birth to Adulthood 59
Patatin-Like Phospholipase Domain-Containing 3 I148M Variant Is Associated with Liver Steatosis and Fat Distribution in Chronic Hepatitis B 58
Impact of PNPLA3 variants on liver histology of 168 patients with HIV infection and chronic hepatitis C. 56
The TM6SFZ 8167K variant is an independent predictor of severe liver steatosis in chronic hepatitis C 48
No effect of MTP polymorphisms on PNPLA3 in HCV-correlated steatosis 48
Acute kidney injury and renal tubular damage in children with type 1 diabetes mellitus onset 46
PNPLA3 I148M variant is associated with liver steatosis and fat distribution in chronic hepatitis B 42
Pediatric non-alcoholic fatty liver disease: current perspectives on diagnosis and management 39
PNPLA3 I148M polymorphism influences renal function in children with obesity and prediabetes 39
Early menarche is associated with insulin-resistance and non-alcoholic fatty liver disease in adolescents with obesity 37
Response to Letter by Speeckaert M., et al 37
The Membrane-bound O-Acyltransferase7 rs641738 Variant in Pediatric Nonalcoholic Fatty Liver Disease 36
MKRN3 Levels in Girls with Central Precocious Puberty during GnRHa Treatment: A Longitudinal Study 36
The rs72613567: TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children 36
The Role of Inflammation on Vitamin D Levels in a Cohort of Pediatric Patients With Inflammatory Bowel Disease 35
Pediatric non-alcoholic fatty liver disease and kidney function: Effect of HSD17B13 variant 32
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype 31
TM6SF2 E167K variant predicts severe liver fibrosis for human immunodeficiency/hepatitis C virus co-infected patients, and severe steatosis only for a non-3 hepatitis C virus genotype 31
Waist-to-height ratio is more strongly associated than other weight-related anthropometric measures with metabolic variables 31
When a secondary form of pediatric non-alcoholic fatty liver disease should be suspected? 28
Growth Hormone Receptor (GHR) 6Ω Pseudoexon Activation: a Novel Cause of Severe Growth Hormone Insensitivity 25
Transmembrane 6 superfamily member 2 167K allele improves renal function in children with obesity 24
Circulating levels of DLK1 and glucose homeostasis in girls with obesity: A pilot study 24
null 23
MKRN3 role in regulating pubertal onset: the state of art of functional studies 22
Impact of intrauterine growth restriction on cerebral and renal oxygenation and perfusion during the first 3 days after birth 21
MKRN3 circulating levels in Prader-Willi syndrome: a pilot study 18
NAFLD and renal function in children: is there a genetic link? 17
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations 9
The TM6SF2 E167 K variant is an independent predictor of severe liver steatosis in chronic hepatitis C. 8
LSS rs2254524 Increases the Risk of Hypertension in Children and Adolescents with Obesity 2
Whole-Blood Gene Expression Profile After Hypoxic-Ischemic Encephalopathy 2
The lncOb rs10487505 polymorphism impairs insulin sensitivity and glucose tolerance in children and adolescents with obesity 2
Totale 1.312
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Categoria #
all - tutte 6.807
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 6.807
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202095 0 0 0 0 15 1 31 10 7 16 13 2
2020/2021140 6 3 8 7 28 7 28 9 6 12 25 1
2021/2022195 6 4 2 8 59 3 11 4 7 26 10 55
2022/2023469 33 24 18 16 55 40 0 21 239 3 8 12
2023/2024246 14 7 17 15 70 48 13 7 10 1 10 34
2024/202524 4 8 10 2 0 0 0 0 0 0 0 0
Totale 1.312