Vincenzo Trischitta | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
All-cause mortality prediction models in type 2 diabetes: applicability in the early stage of disease	ACTA DIABETOLOGICA	2021
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
Correction to: Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation	JOURNAL OF THROMBOSIS AND THROMBOLYSIS	2021
The synergic association of hs-CRP and serum amyloid P component in predicting all-cause mortality in patients with type 2 diabetes	DIABETES CARE	2020
PPARA polymorphism influences the cardiovascular benefit of fenofibrate in type 2 diabetes: Findings from accord-lipid	DIABETES	2020
Moving toward the implementation of precision medicine needs highly discriminatory, validated, inexpensive, and easy-to-use prediction models	DIABETES CARE	2020
Association of the 1q25 Diabetes-Specific Coronary Heart Disease Locus With Alterations of the γ-Glutamyl Cycle and Increased Methylglyoxal Levels in Endothelial Cells	DIABETES	2020
Contribution of rare and common genetic variants to early-onset type 2 diabetes	DIABETOLOGIA	2020
Ruolo della variabilità genetica nel diabete tipo 2 (DT2) ad insorgenza precoce.	SID 2020	2020
Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do	CURRENT OPINION IN PHARMACOLOGY	2020
EstimatioN oF mORtality risk in type2 diabetiC patiEnts (ENFORCE): an inexpensive and parsimonious prediction model	THE JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM	2019
A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients	CARDIOVASCULAR DIABETOLOGY	2019
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	PLOS ONE	2019
Association of a homozygous GCK missense mutation with mild diabetes	MOLECULAR GENETICS & GENOMIC MEDICINE	2019
GALNT2 as a novel modulator of adipogenesis and adipocyte insulin signaling	INTERNATIONAL JOURNAL OF OBESITY	2019
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing	ACTA DIABETOLOGICA	2019
The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy	ACTA DIABETOLOGICA	2019
Serum amyloid component P improves the ability of C-reactive protein to predict all-cause mortality in patients with type 2 diabetes	DIABETOLOGIADIABETOLOGIA	2019
Unraveling the genetic background of early-onset type 2 diabetes: a step forward toward precision medicine	SIGU 2019	2019
Insights from Molecular Characterization of Adult Patients of Families with Multigenerational Diabetes Mellitus	DIABETES	2018

Progetti di Ricerca

Towards precision medicine: insights into the molecular pathogenesis of early-onset type 2 diabetes.

Gruppi di ricerca

Slowly progressive autoimmune diabetes: a clinical model for novel pathways of ß-cell protection