List of works - Stefano Romeo

A case of severe occult ectopic adrenocorticotropin syndrome treated with retrograde venous adrenal ablation using ethanol.

scientific article published in December 2008

Alcohol consumption and alcohol problems after bariatric surgery in the Swedish obese subjects study

scientific article published on 31 May 2013

Altered glucose homeostasis is associated with increased serum apelin levels in type 2 diabetes mellitus

scientific article

Analysis of TBC1D4 in patients with severe insulin resistance.

scientific article published on 27 March 2010

Association between low C-peptide and low lumbar bone mineral density in postmenopausal women without diabetes

scientific article published on 24 January 2015

Association between the PNPLA3 (rs738409 C>G) variant and hepatocellular carcinoma: Evidence from a meta-analysis of individual participant data

scientific article

Association of FTO polymorphisms with early age of obesity in obese Italian subjects

scientific article published on 20 February 2012

Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis.

scientific article published on 13 October 2013

Bariatric surgery and prevention of type 2 diabetes in Swedish obese subjects

scientific article

Brachial artery diameter measurement: a tool to simplify non-invasive vascular assessment.

scientific article published on January 2012

Cardiovascular events after bariatric surgery in obese subjects with type 2 diabetes.

scientific article

Carotid and brachial arterial enlargement in postmenopausal women with hypertension

scientific article published on 01 February 2012

Clinical application of best practice guidelines for the genetic diagnosis of MODY2 and MODY3.

scientific article published on November 2010

Complete clinical remission and disappearance of liver metastases after treatment with somatostatin analogue in a 40-year-old woman with a malignant insulinoma positive for somatostatin receptors type 2.

scientific article published on 9 February 2006

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene

scientific article published on 01 July 2005

Corrigendum: PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease

scientific article published on 01 July 2015

DEPDC5 variants increase fibrosis progression in Europeans with chronic hepatitis C virus infection.

scientific article published on 30 October 2015

Don't forget to ask how mum and dad are doing

scientific article published on 01 April 2019

Editorial: new insights into the relationship between the intestine and non-alcoholic fatty liver-is "fatty gut" involved in disease progression?

scientific article published on August 2017

Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans

scientific article published on 5 September 2012

Evaluation of current eligibility criteria for bariatric surgery: diabetes prevention and risk factor changes in the Swedish obese subjects (SOS) study

scientific article published on 28 January 2013

Fat utilization and arterial hypertension in overweight/obese subjects

scientific article published on 02 July 2013

First on-line survey of an international multidisciplinary working group (MightyMedic) on current practice in diagnosis, therapy and follow-up of dyslipidemias.

scientific article published on May 2015

Gender difference in handgrip strength of Italian children aged 9 to 10 years

scientific article published on 19 February 2016

Genetic Factors in the Pathogenesis of Nonalcoholic Fatty Liver and Steatohepatitis

scientific article (publication date: 2015)

Genetic diagnosis of familial hypercholesterolaemia by targeted next-generation sequencing.

scientific article

Genetic variants in the MTHFR are not associated with fatty liver disease

scientific article published on 27 May 2020

Genetic variation in SULF2 is associated with postprandial clearance of triglyceride-rich remnant particles and triglyceride levels in healthy subjects

scientific article

HCC and liver disease risks in homozygous PNPLA3 p.I148M carriers approach monogenic inheritance

scientific article published on 02 January 2015

HSD17B13 as a promising therapeutic target against chronic liver disease

scientific article published on 01 April 2020

Hepatocellular carcinoma in nonalcoholic fatty liver: role of environmental and genetic factors.

scientific article

High Vegetable Fats Intake Is Associated with High Resting Energy Expenditure in Vegetarians.

scientific article published on 17 July 2015

Human resistin gene, obesity, and type 2 diabetes: mutation analysis and population study

scientific article published on 01 March 2002

Identification of sequence variants in the UBL5 (ubiquitin-like 5 or BEACON) gene in obese children by PCR-SSCP: no evidence for association with obesity.

scientific article published in December 2008

Individuals with Metabolically Healthy Overweight/Obesity Have Higher Fat Utilization than Metabolically Unhealthy Individuals

scientific article published on 4 January 2016

LPIAT1/MBOAT7 depletion increases triglyceride synthesis fueled by high phosphatidylinositol turnover

scientific article published on 06 April 2020

Lack of effect of apolipoprotein C3 polymorphisms on indices of liver steatosis, lipid profile and insulin resistance in obese Southern Europeans

scientific article

Liver transcriptomics highlights interleukin-32 as novel NAFLD-related cytokine and candidate biomarker

scientific article published on 30 January 2020

Long-term effect of bariatric surgery on liver enzymes in the Swedish Obese Subjects (SOS) study.

scientific article

MAFLD vs NAFLD: Let the contest begin!

scientific article published on 01 September 2020

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes.

scientific article published on 13 February 2009

Monitoring of Lipids, Enzymes, and Creatine Kinase in Patients on Lipid-Lowering Drug Therapy ⬇️

scientific article published on September 1, 2013

No association between polymorphism in PEMT (V175M) and hepatic triglyceride content in the Dallas Heart Study

scientific article published on 01 October 2006

Nutrients utilization in obese individuals with and without hypertriglyceridemia

scientific article published on 21 February 2014

Nutritional parameters predicting pressure ulcers and short-term mortality in patients with minimal conscious state as a result of traumatic and non-traumatic acquired brain injury.

scientific article

Osteoporosis in chronic inflammatory disease: the role of malnutrition.

scientific article published on 09 October 2012

PCSK9 rs11591147 R46L Loss-of-Function Variant Protects Against Liver Damage in Individuals with NAFLD

scientific article published on 22 October 2020

PNPLA 3I148M genetic variant associates with insulin resistance and baseline viral load in HCV genotype 2 but not in genotype 3 infection ⬇️

scientific article published on September 14, 2012

PNPLA3 148M Carriers with Inflammatory Bowel Diseases Have Higher Susceptibility to Hepatic Steatosis and Higher Liver Enzymes.

scientific article published on 09 September 2015

PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease.

scientific article published on 12 May 2015

PNPLA3 I148M (rs738409) genetic variant and age at onset of at-risk alcohol consumption are independent risk factors for alcoholic cirrhosis.

scientific article

PNPLA3 I148M (rs738409) genetic variant is associated with hepatocellular carcinoma in obese individuals

scientific article

PNPLA3 I148M Variant Influences Circulating Retinol in Adults with Nonalcoholic Fatty Liver Disease or Obesity

scientific article published in July 2015

PNPLA3 I148M polymorphism and progressive liver disease

scientific article

PNPLA3 I148M variant and hepatocellular carcinoma: a common genetic variant for a rare disease.

scientific article published on 16 January 2013

PNPLA3 genetic variation in alcoholic steatosis and liver disease progression

scientific article published on June 2015

PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells

scientific article

Paradoxical dissociation between hepatic fat content and de novo lipogenesis due to PNPLA3 sequence variant.

scientific article

Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant

scientific article

Patatin-like phospholipase domain containing 3 sequence variant and hepatocellular carcinoma

scientific article published on 01 May 2011

Patatin-like phospholipase domain-containing 3 (PNPLA3) I148M (rs738409) affects hepatic VLDL secretion in humans and in vitro

scientific article published on 06 August 2012

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

scientific article published on 25 February 2007

Postmenopausal women with carotid atherosclerosis: Potential role of the serum calcium levels

scientific article published on 07 March 2013

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

scientific article published on 15 December 2008

Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function

scientific article published on 22 December 2013

Reply

scientific article published on 03 July 2015

Reply

scientific article published on 28 July 2014

Reply to "Statin treatment for non-alcoholic steatohepatitis"

scientific article published on 08 October 2015

Reply: To PMID 25251399

scientific article published on 17 June 2015

Review article: the emerging role of genetics in precision medicine for patients with non-alcoholic steatohepatitis

scientific article published on 07 May 2020

Search for genetic variants in the p66Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease

scientific article

Search for genetic variants in the retinoid X receptor-gamma-gene by polymerase chain reaction-single-strand conformation polymorphism in patients with resistance to thyroid hormone without mutations in thyroid hormone receptor beta gene.

scientific article

Serum adiponectin is decreased in patients with familial combined hyperlipidemia and normolipaemic relatives and is influenced by lipid-lowering treatment.

scientific article published on 24 July 2009

Single-strand conformation polymorphism analysis of the glucose transporter gene GLUT1 in maturity-onset diabetes of the young.

scientific article published in June 2001

Statin use and non-alcoholic steatohepatitis in at risk individuals

scientific article

Stratification of Hepatocellular Carcinoma Patients Based on Acetate Utilization

scientific article published on 19 November 2015

Subclinical cardiovascular damage and fat utilization in overweight/obese individuals receiving the same dietary and pharmacological interventions

scientific article

The 148M allele of the PNPLA3 gene is associated with indices of liver damage early in life.

scientific article published on 27 April 2010

The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.

scientific article

The COBLL1 C allele is associated with lower serum insulin levels and lower insulin resistance in overweight and obese children

scientific article published on July 2013

The G-308A variant of the Tumor Necrosis Factor-alpha (TNF-alpha) gene is not associated with obesity, insulin resistance and body fat distribution

scientific article

The G972R variant of the insulin receptor substrate-1 (IRS-1) gene, body fat distribution and insulin-resistance.

scientific article published in March 2001

The G972R variant of the insulin receptor substrate-1 gene impairs insulin signaling and cell differentiation in 3T3L1 adipocytes; treatment with a PPARgamma agonist restores normal cell signaling and differentiation.

scientific article published on February 2006

The Gly482Ser missense mutation of the peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1 alpha) gene associates with reduced insulin sensitivity in normal and glucose-intolerant obese subjects

scientific article published on January 2005

The IRS1 rs2943641 variant and risk of future cancer among morbidly obese individuals

scientific article published on 15 February 2013

The MBOAT7-TMC4 Variant rs641738 Increases Risk of Nonalcoholic Fatty Liver Disease in Individuals of European Descent

scientific article published on 2 February 2016

The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levels

scientific article published on 22 February 2014

The TM6SF2 E167K genetic variant induces lipid biosynthesis and reduces apolipoprotein B secretion in human hepatic 3D spheroids

scientific article published on 12 August 2019

The adiponectin gene SNP+276G>T associates with early-onset coronary artery disease and with lower levels of adiponectin in younger coronary artery disease patients (age <or=50 years).

scientific article

The androgen receptor confers protection against diet-induced atherosclerosis, obesity, and dyslipidemia in female mice

scientific article published on 30 December 2014

The incidence of albuminuria after bariatric surgery and usual care in Swedish Obese Subjects (SOS): a prospective controlled intervention trial

scientific article

The link between nutritional parameters and bone mineral density in women: results of a screening programme for osteoporosis

scientific article published on 19 February 2014

The rs2294918 E434K variant modulates patatin-like phospholipase domain-containing 3 expression and liver damage

scientific article published on 14 January 2016

Transmembrane 6 superfamily member 2 gene E167K variant impacts on steatosis and liver damage in chronic hepatitis C patients

scientific article published on 6 May 2015

Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease

scientific article published in February 2015

Transmembrane-6 superfamily member 2 (TM6SF2) E167K variant increases susceptibility to hepatic steatosis in obese children

scientific article published on 13 October 2015

Type 1 hyperlipoproteinemia due to a novel deletion of exons 3 and 4 in the GPIHBP1 gene

scientific article published on 18 February 2014

Unravelling the pathogenesis of fatty liver disease: patatin-like phospholipase domain-containing 3 protein

scientific article published on June 2010

List of works by Stefano Romeo

A case of severe occult ectopic adrenocorticotropin syndrome treated with retrograde venous adrenal ablation using ethanol.

Alcohol consumption and alcohol problems after bariatric surgery in the Swedish obese subjects study

Altered glucose homeostasis is associated with increased serum apelin levels in type 2 diabetes mellitus

Analysis of TBC1D4 in patients with severe insulin resistance.

Association between low C-peptide and low lumbar bone mineral density in postmenopausal women without diabetes

Association between the PNPLA3 (rs738409 C>G) variant and hepatocellular carcinoma: Evidence from a meta-analysis of individual participant data

Association of FTO polymorphisms with early age of obesity in obese Italian subjects

Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis.

Bariatric surgery and prevention of type 2 diabetes in Swedish obese subjects

Brachial artery diameter measurement: a tool to simplify non-invasive vascular assessment.

Cardiovascular events after bariatric surgery in obese subjects with type 2 diabetes.

Carotid and brachial arterial enlargement in postmenopausal women with hypertension

Clinical application of best practice guidelines for the genetic diagnosis of MODY2 and MODY3.

Complete clinical remission and disappearance of liver metastases after treatment with somatostatin analogue in a 40-year-old woman with a malignant insulinoma positive for somatostatin receptors type 2.

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene

Corrigendum: PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease

DEPDC5 variants increase fibrosis progression in Europeans with chronic hepatitis C virus infection.

Don't forget to ask how mum and dad are doing

Editorial: new insights into the relationship between the intestine and non-alcoholic fatty liver-is "fatty gut" involved in disease progression?

Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans

Evaluation of current eligibility criteria for bariatric surgery: diabetes prevention and risk factor changes in the Swedish obese subjects (SOS) study

Fat utilization and arterial hypertension in overweight/obese subjects

First on-line survey of an international multidisciplinary working group (MightyMedic) on current practice in diagnosis, therapy and follow-up of dyslipidemias.

Gender difference in handgrip strength of Italian children aged 9 to 10 years

Genetic Factors in the Pathogenesis of Nonalcoholic Fatty Liver and Steatohepatitis

Genetic diagnosis of familial hypercholesterolaemia by targeted next-generation sequencing.

Genetic variants in the MTHFR are not associated with fatty liver disease

Genetic variation in SULF2 is associated with postprandial clearance of triglyceride-rich remnant particles and triglyceride levels in healthy subjects

HCC and liver disease risks in homozygous PNPLA3 p.I148M carriers approach monogenic inheritance

HSD17B13 as a promising therapeutic target against chronic liver disease

Hepatocellular carcinoma in nonalcoholic fatty liver: role of environmental and genetic factors.

High Vegetable Fats Intake Is Associated with High Resting Energy Expenditure in Vegetarians.

Human resistin gene, obesity, and type 2 diabetes: mutation analysis and population study

Identification of sequence variants in the UBL5 (ubiquitin-like 5 or BEACON) gene in obese children by PCR-SSCP: no evidence for association with obesity.

Individuals with Metabolically Healthy Overweight/Obesity Have Higher Fat Utilization than Metabolically Unhealthy Individuals

LPIAT1/MBOAT7 depletion increases triglyceride synthesis fueled by high phosphatidylinositol turnover

Lack of effect of apolipoprotein C3 polymorphisms on indices of liver steatosis, lipid profile and insulin resistance in obese Southern Europeans

Liver transcriptomics highlights interleukin-32 as novel NAFLD-related cytokine and candidate biomarker

Long-term effect of bariatric surgery on liver enzymes in the Swedish Obese Subjects (SOS) study.

MAFLD vs NAFLD: Let the contest begin!

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes.

Monitoring of Lipids, Enzymes, and Creatine Kinase in Patients on Lipid-Lowering Drug Therapy ⬇️

No association between polymorphism in PEMT (V175M) and hepatic triglyceride content in the Dallas Heart Study

Nutrients utilization in obese individuals with and without hypertriglyceridemia

Nutritional parameters predicting pressure ulcers and short-term mortality in patients with minimal conscious state as a result of traumatic and non-traumatic acquired brain injury.

Osteoporosis in chronic inflammatory disease: the role of malnutrition.

PCSK9 rs11591147 R46L Loss-of-Function Variant Protects Against Liver Damage in Individuals with NAFLD

PNPLA 3I148M genetic variant associates with insulin resistance and baseline viral load in HCV genotype 2 but not in genotype 3 infection ⬇️

PNPLA3 148M Carriers with Inflammatory Bowel Diseases Have Higher Susceptibility to Hepatic Steatosis and Higher Liver Enzymes.

PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease.

PNPLA3 I148M (rs738409) genetic variant and age at onset of at-risk alcohol consumption are independent risk factors for alcoholic cirrhosis.

PNPLA3 I148M (rs738409) genetic variant is associated with hepatocellular carcinoma in obese individuals

PNPLA3 I148M Variant Influences Circulating Retinol in Adults with Nonalcoholic Fatty Liver Disease or Obesity

PNPLA3 I148M polymorphism and progressive liver disease

PNPLA3 I148M variant and hepatocellular carcinoma: a common genetic variant for a rare disease.

PNPLA3 genetic variation in alcoholic steatosis and liver disease progression

PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells

Paradoxical dissociation between hepatic fat content and de novo lipogenesis due to PNPLA3 sequence variant.

Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant

Patatin-like phospholipase domain containing 3 sequence variant and hepatocellular carcinoma

Patatin-like phospholipase domain-containing 3 (PNPLA3) I148M (rs738409) affects hepatic VLDL secretion in humans and in vitro

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

Postmenopausal women with carotid atherosclerosis: Potential role of the serum calcium levels

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function

Reply

Reply

Reply to "Statin treatment for non-alcoholic steatohepatitis"

Reply: To PMID 25251399

Review article: the emerging role of genetics in precision medicine for patients with non-alcoholic steatohepatitis

Search for genetic variants in the p66Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular disease

Search for genetic variants in the retinoid X receptor-gamma-gene by polymerase chain reaction-single-strand conformation polymorphism in patients with resistance to thyroid hormone without mutations in thyroid hormone receptor beta gene.

Serum adiponectin is decreased in patients with familial combined hyperlipidemia and normolipaemic relatives and is influenced by lipid-lowering treatment.

Single-strand conformation polymorphism analysis of the glucose transporter gene GLUT1 in maturity-onset diabetes of the young.

Statin use and non-alcoholic steatohepatitis in at risk individuals

Stratification of Hepatocellular Carcinoma Patients Based on Acetate Utilization

Subclinical cardiovascular damage and fat utilization in overweight/obese individuals receiving the same dietary and pharmacological interventions

The 148M allele of the PNPLA3 gene is associated with indices of liver damage early in life.

The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.