D. Bailetti

发表

Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.

S. Pascarella, T. Mazza, P. Marchetti, 2015, American journal of human genetics.

The 9p21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitus.

Hetal S. Shah, A. Doria, T. Hauser, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The 9 p 21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitus

Hetal S. Shah, A. Doria, T. Hauser, 2012 .

Circulating pro-neurotensin levels predict bodyweight gain and metabolic alterations in children.

O. Melander, J. Struck, S. Loche, 2020, Nutrition, metabolism, and cardiovascular diseases : NMCD.

The rs45454496 (E1813K) variant in the adiposity gene ANK2 doesn't associate with obesity in Southern European subjects

F. Leonetti, I. Barchetta, M. Cavallo, 2021 .

The Arg282Ser missense mutation in APOA5 gene determines a reduction of triglyceride and LDL-cholesterol in children, together with low serum levels of apolipoprotein A-V

A. Lenzi, S. Loche, I. Barchetta, 2017, Lipids in Health and Disease.

Joint effect of insulin signaling genes on all-cause mortality.

M. Copetti, A. Fontana, C. Zoccali, 2014, Atherosclerosis.

IRS1 G972R Missense Polymorphism Is Associated With Failure to Oral Antidiabetes Drugs in White Patients With Type 2 Diabetes From Italy

M. Copetti, L. Giusti, S. De Cosmo, 2014, Diabetes.

The SH2B1 obesity locus and abnormal glucose homeostasis: lack of evidence for association from a meta-analysis in individuals of European ancestry.

J. Florez, M. Copetti, N. Abate, 2013, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Variability in genes regulating vitamin D metabolism is associated with vitamin D levels in type 2 diabetes

M. Copetti, F. Leonetti, N. Napoli, 2018, Oncotarget.

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

A. Di Costanzo, F. Leonetti, I. Barchetta, 2022, International journal of molecular sciences.

Evaluation of Polygenic Determinants of Non-Alcoholic Fatty Liver Disease (NAFLD) By a Candidate Genes Resequencing Strategy

G. Giannini, A. Angeloni, A. Montali, 2018, Scientific Reports.

The IRS1 G972R polymorphism and glomerular filtration rate in patients with type 2 diabetes of European ancestry.

M. Copetti, A. Doria, F. Pellegrini, 2013, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Association of Apelin Levels in Overweight-obese Children with Pubertal Development, but Not with Insulin Sensitivity: 6.5 Years Follow up Evaluation

A. Lenzi, S. Loche, I. Barchetta, 2020 .

Reduced High-Density Lipoprotein Cholesterol Is an Independent Determinant of Altered Bone Quality in Women with Type 2 Diabetes

E. Romagnoli, I. Barchetta, M. Cavallo, 2023, International journal of molecular sciences.

The single-point insulin sensitivity estimator (SPISE) index is a strong predictor of abnormal glucose metabolism in overweight/obese children: a long-term follow-up study

S. Loche, I. Barchetta, M. Cavallo, 2021, Journal of Endocrinological Investigation.

Neurotensin Gene rs2234762 C>G Variant Associates with Reduced Circulating Pro-NT Levels and Predicts Lower Insulin Resistance in Overweight/Obese Children

O. Melander, I. Barchetta, M. Cavallo, 2023, International journal of molecular sciences.

ANGPTL4 gene E40K variation protects against obesity‐associated dyslipidemia in participants with obesity

A. Lenzi, F. Leonetti, D. Capoccia, 2018, Obesity science & practice.

Genetic Variant at the GLUL Locus Predicts All-Cause Mortality in Patients With Type 2 Diabetes

Hetal S. Shah, A. Doria, M. Pezzolesi, 2015, Diabetes.

The Arg282Ser missense mutation in APOA5 gene determines a reduction of triglyceride and LDL-cholesterol in children, together with low serum levels of apolipoprotein A-V

A. Lenzi, S. Loche, I. Barchetta, 2017, Lipids in Health and Disease.

The vitamin D receptor functional variant rs2228570 (C>T) does not associate with type 2 diabetes mellitus

A. Lenzi, F. Leonetti, D. Capoccia, 2017, Endocrine research.

Infrequent TRIB3 coding variants and coronary artery disease in type 2 diabetes.

M. Copetti, A. Fontana, G. Sesti, 2015, Atherosclerosis.

The "Sapienza University Mortality and Morbidity Event Rate (SUMMER) study in diabetes": Study protocol.

M. Copetti, F. Leonetti, S. De Cosmo, 2016, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Joint effect of insulin signaling genes on insulin secretion and glucose homeostasis.

Hetal S. Shah, M. Copetti, N. Abate, 2013, The Journal of clinical endocrinology and metabolism.

Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.

S. Pascarella, T. Mazza, P. Marchetti, 2015, American journal of human genetics.