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

American journal of human genetics, 2015-07, Vol.97 (1), p.177-185

2015

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The Need to Increase Clinical Skills and Change the Genetic Testing Strategy for Monogenic Diabetes

Diabetes (New York, N.Y.), 2022-03, Vol.71 (3), p.379-380

2022

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A Haplotype at the Adiponectin Locus Is Associated With Obesity and Other Features of the Insulin Resistance Syndrome

Diabetes (New York, N.Y.), 2002-07, Vol.51 (7), p.2306-2312

2002

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Is There Really a Paradoxical Effect of Obesity on Mortality Rate in High-Risk Patients? It Is Time for Large Mendelian Randomization Studies

The American journal of cardiology, 2018-09, Vol.122 (5), p.910-910

2018

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Role of GALNT2 on Insulin Sensitivity, Lipid Metabolism and Fat Homeostasis

International journal of molecular sciences, 2022-01, Vol.23 (2), p.929

2022

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Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012

The journal of clinical endocrinology and metabolism, 2017-06, Vol.102 (6), p.1826-1834

2017

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On the emerging role of GALNT2 on intermediate metabolism and adipogenesis

Acta diabetologica, 2022-09, Vol.59 (9), p.1255-1256

2022

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Rare forms of monogenic diabetes in non-European individuals. First reports of CEL and RFX6 mutations from the Indian subcontinent

Acta diabetologica, 2024-08

2024

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GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Acta diabetologica, 2024, Vol.61 (8), p.1007-1013

2024

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GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling

International Journal of Obesity, 2019-12, Vol.43 (12), p.2448-2457

2019

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Correction: GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Acta diabetologica, 2024, Vol.61 (8), p.1015-1015

2024

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Early-Onset Diabetes in an Infant with a Novel Frameshift Mutation in LRBA

International journal of environmental research and public health, 2022-09, Vol.19 (17), p.11031

2022

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Morphological and molecular characterization of GALNT2-mediated adipogenesis

International Journal of Obesity, 2021-06, Vol.45 (6), p.1362-1366

2021

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A Serum Resistin and Multicytokine Inflammatory Pathway Is Linked With and Helps Predict All-cause Death in Diabetes

The journal of clinical endocrinology and metabolism, 2021-11, Vol.106 (11), p.e4350-e4359

2021

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Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia

The journal of clinical endocrinology and metabolism, 2022-03, Vol.107 (3), p.668-684

2022

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Development and Validation of a Predicting Model of All-Cause Mortality in Patients With Type 2 Diabetes

Diabetes care, 2013-09, Vol.36 (9), p.2830-2835

2013

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MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Acta diabetologica, 2023-01, Vol.60 (1), p.131-135

2023

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Correction to: MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Acta diabetologica, 2023-03, Vol.60 (3), p.459-459

2023

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Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients

Acta diabetologica, 2022-08, Vol.59 (8), p.1113-1116

2022

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STAT1 overexpression triggers aplastic anemia: a pilot study unravelling novel pathogenetic insights in bone marrow failure

Clinical and experimental medicine, 2023-10, Vol.23 (6), p.2687-2694

2023

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Role of Actionable Genes in Pursuing a True Approach of Precision Medicine in Monogenic Diabetes

Genes, 2022-01, Vol.13 (1), p.117

2022

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GALNT2 expression is reduced in patients with Type 2 diabetes: possible role of hyperglycemia

PloS one, 2013-07, Vol.8 (7), p.e70159-e70159

2013

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A Cluster of Three Single Nucleotide Polymorphisms in the 3′-Untranslated Region of Human Glycoprotein PC-1 Gene Stabilizes PC-1 mRNA and Is Associated With Increased PC-1 Protein Content and Insulin Resistance–Related Abnormalities

Diabetes (New York, N.Y.), 2001-08, Vol.50 (8), p.1952-1955

2001

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Serum resistin and kidney function: a family-based study in non-diabetic, untreated individuals

PloS one, 2012-06, Vol.7 (6), p.e38414-e38414

2012

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ENPP1 affects insulin action and secretion: evidences from in vitro studies

PloS one, 2011-05, Vol.6 (5), p.e19462

2011

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

The Need to Increase Clinical Skills and Change the Genetic Testing Strategy for Monogenic Diabetes

A Haplotype at the Adiponectin Locus Is Associated With Obesity and Other Features of the Insulin Resistance Syndrome

Is There Really a Paradoxical Effect of Obesity on Mortality Rate in High-Risk Patients? It Is Time for Large Mendelian Randomization Studies

Role of GALNT2 on Insulin Sensitivity, Lipid Metabolism and Fat Homeostasis

Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012

On the emerging role of GALNT2 on intermediate metabolism and adipogenesis

Rare forms of monogenic diabetes in non-European individuals. First reports of CEL and RFX6 mutations from the Indian subcontinent

GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling

Correction: GALNT2 expression is associated with glucose control and serum metabolites in patients with type 2 diabetes

Early-Onset Diabetes in an Infant with a Novel Frameshift Mutation in LRBA

Morphological and molecular characterization of GALNT2-mediated adipogenesis

A Serum Resistin and Multicytokine Inflammatory Pathway Is Linked With and Helps Predict All-cause Death in Diabetes

Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia

Development and Validation of a Predicting Model of All-Cause Mortality in Patients With Type 2 Diabetes

MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Correction to: MODY patients carrying mutation in syndromic diabetes genes. An Italian single-center experience

Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients

STAT1 overexpression triggers aplastic anemia: a pilot study unravelling novel pathogenetic insights in bone marrow failure

Role of Actionable Genes in Pursuing a True Approach of Precision Medicine in Monogenic Diabetes

GALNT2 expression is reduced in patients with Type 2 diabetes: possible role of hyperglycemia

A Cluster of Three Single Nucleotide Polymorphisms in the 3′-Untranslated Region of Human Glycoprotein PC-1 Gene Stabilizes PC-1 mRNA and Is Associated With Increased PC-1 Protein Content and Insulin Resistance–Related Abnormalities

Serum resistin and kidney function: a family-based study in non-diabetic, untreated individuals

ENPP1 affects insulin action and secretion: evidences from in vitro studies

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