Lista de obras - Luca A Lotta - Dominio Público Uruguay

A Systematic Review of Biomarkers and Risk of Incident Type 2 Diabetes: An Overview of Epidemiological, Prediction and Aetiological Research Literature

artículo científico publicado en 2016

A cross-platform approach identifies genetic regulators of human metabolism and health

scientific article published on 07 January 2021

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

artículo científico publicado en 2010

Addressing the complexity of cardiovascular disease by design

artículo científico publicado en 2011

Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis

artículo científico publicado en 2016

Association of a single nucleotide polymorphism of the NPR3 gene promoter with early onset ischemic stroke in an Italian cohort

artículo científico publicado en 2012

Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study

artículo científico publicado en 2015

B and T lymphocytes in acquired Thrombotic Thrombocytopenic Purpura during disease remission

article published in 2011

Case report: use of thienopyridines in a patient with acquired idiopathic thrombotic thrombocytopenic purpura

artículo científico publicado en 2012

Common genetic variants highlight the role of insulin resistance and body fat distribution in type 2 diabetes, independent of obesity

artículo científico publicado en 2014

Definitions of Metabolic Health and Risk of Future Type 2 Diabetes in BMI Categories: A Systematic Review and Network Meta-analysis

artículo científico publicado en 2015

Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

artículo científico publicado en 2010

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

Drop of residual plasmatic activity of ADAMTS13 to undetectable levels during acute disease in a patient with adult-onset congenital thrombotic thrombocytopenic purpura

artículo científico publicado en 2012

Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism

artículo científico publicado en 2010

Elevated Plasma Levels of 3-Hydroxyisobutyric Acid Are Associated With Incident Type 2 Diabetes

artículo científico publicado en 2017

Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk Study

scientific article published on 10 September 2019

Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

artículo científico publicado en 2015

FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients

artículo científico publicado en 2014

Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease

artículo científico publicado en 2016

Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis

artículo científico publicado en 2016

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

artículo científico publicado en 2018

Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease

scientific article published on 22 September 2020

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

scientific article published on 09 January 2020

Genome-wide association studies in atherothrombosis

scientific article published on 16 December 2009

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase.

artículo científico publicado en 2017

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

artículo científico publicado en 2012

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.

artículo científico publicado en 2016

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

artículo científico publicado en 2017

Measurement and prevalence of circulating ADAMTS13-specific immune complexes in autoimmune thrombotic thrombocytopenic purpura.

artículo científico publicado en 2014

Measurement of anti-ADAMTS13 neutralizing autoantibodies: a comparison between CBA and FRET assays

artículo científico publicado en 2012

Next-Generation Sequencing and In Vitro Expression Study of ADAMTS13 Single Nucleotide Variants in Deep Vein Thrombosis

artículo científico publicado en 2016

Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis.

artículo científico publicado en 2013

No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic stroke

artículo científico publicado en 2010

Non-invasive tool for foetal sex determination in early gestational age.

artículo científico publicado en 2011

PCSK9 inhibition and type 2 diabetes

artículo científico publicado en 2017

Pathogenesis and treatment of acquired idiopathic thrombotic thrombocytopenic purpura ⬇️

artículo científico publicado el 1 de septiembre de 2010

Plasma ADAMTS-13 levels and the risk of myocardial infarction: an individual patient data meta-analysis.

artículo científico publicado en 2015

Plasma Mannose Levels Are Associated with Incident Type 2 Diabetes and Cardiovascular Disease

artículo científico publicado en 2017

Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations

artículo científico publicado en 2020

Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission.

artículo científico publicado en 2011

Pregnancy complications in acquired thrombotic thrombocytopenic purpura: a case-control study.

artículo científico publicado en 2014

Preoperative hematocrit concentration and the risk of stroke in patients undergoing isolated coronary-artery bypass grafting

artículo científico publicado en 2013

Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects.

artículo científico publicado en 2013

Prothrombin Mutation Conveying Antithrombin Resistance ⬇️

artículo científico publicado el 13 de septiembre de 2012

Raised haematocrit concentration and the risk of death and vascular complications after major surgery.

artículo científico publicado en 2013

Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura

artículo científico publicado en 2012

Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis

artículo científico publicado en 2016

Smoking and the risk of mortality and vascular and respiratory events in patients undergoing major surgery

artículo científico publicado en 2013

The association between circulating 25-hydroxyvitamin D metabolites and type 2 diabetes in European populations: A meta-analysis and Mendelian randomisation analysis

scientific article published on 16 October 2020

The emerging concept of residual ADAMTS13 activity in ADAMTS13-deficient thrombotic thrombocytopenic purpura

artículo científico publicado en 2013

Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes

artículo científico publicado en 2015

Treatment of chronic hepatitis C with pegylated interferon-α in a patient with recurrent autoimmune thrombotic thrombocytopenic purpura.

artículo científico publicado en 2012

Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients

artículo científico publicado en 2016

Lista de obras de Luca A Lotta

A Systematic Review of Biomarkers and Risk of Incident Type 2 Diabetes: An Overview of Epidemiological, Prediction and Aetiological Research Literature

A cross-platform approach identifies genetic regulators of human metabolism and health

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

Addressing the complexity of cardiovascular disease by design

Association Between Low-Density Lipoprotein Cholesterol-Lowering Genetic Variants and Risk of Type 2 Diabetes: A Meta-analysis

Association of a single nucleotide polymorphism of the NPR3 gene promoter with early onset ischemic stroke in an Italian cohort

Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study

B and T lymphocytes in acquired Thrombotic Thrombocytopenic Purpura during disease remission

Case report: use of thienopyridines in a patient with acquired idiopathic thrombotic thrombocytopenic purpura

Common genetic variants highlight the role of insulin resistance and body fat distribution in type 2 diabetes, independent of obesity

Definitions of Metabolic Health and Risk of Future Type 2 Diabetes in BMI Categories: A Systematic Review and Network Meta-analysis

Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Drop of residual plasmatic activity of ADAMTS13 to undetectable levels during acute disease in a patient with adult-onset congenital thrombotic thrombocytopenic purpura

Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism

Elevated Plasma Levels of 3-Hydroxyisobutyric Acid Are Associated With Incident Type 2 Diabetes

Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk Study

Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients

Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease

Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Genome-wide association studies in atherothrombosis

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase.

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance.

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

Measurement and prevalence of circulating ADAMTS13-specific immune complexes in autoimmune thrombotic thrombocytopenic purpura.

Measurement of anti-ADAMTS13 neutralizing autoantibodies: a comparison between CBA and FRET assays

Next-Generation Sequencing and In Vitro Expression Study of ADAMTS13 Single Nucleotide Variants in Deep Vein Thrombosis

Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis.

No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic stroke

Non-invasive tool for foetal sex determination in early gestational age.

PCSK9 inhibition and type 2 diabetes

Pathogenesis and treatment of acquired idiopathic thrombotic thrombocytopenic purpura ⬇️

Plasma ADAMTS-13 levels and the risk of myocardial infarction: an individual patient data meta-analysis.

Plasma Mannose Levels Are Associated with Incident Type 2 Diabetes and Cardiovascular Disease

Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations

Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission.

Pregnancy complications in acquired thrombotic thrombocytopenic purpura: a case-control study.

Preoperative hematocrit concentration and the risk of stroke in patients undergoing isolated coronary-artery bypass grafting

Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects.

Prothrombin Mutation Conveying Antithrombin Resistance ⬇️

Raised haematocrit concentration and the risk of death and vascular complications after major surgery.

Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura

Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis

Smoking and the risk of mortality and vascular and respiratory events in patients undergoing major surgery

The association between circulating 25-hydroxyvitamin D metabolites and type 2 diabetes in European populations: A meta-analysis and Mendelian randomisation analysis

The emerging concept of residual ADAMTS13 activity in ADAMTS13-deficient thrombotic thrombocytopenic purpura

Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes

Treatment of chronic hepatitis C with pegylated interferon-α in a patient with recurrent autoimmune thrombotic thrombocytopenic purpura.

Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients