Lista de obras - Maria Sabater-Lleal - Dominio Público Uruguay

A Genome-Wide Association Study Identifies KNG1 as a Genetic Determinant of Plasma Factor XI Level and Activated Partial Thromboplastin Time

article by Maria Sabater-Lleal et al published August 2012 in Arteriosclerosis, Thrombosis, and Vascular Biology

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

scientific article published on 14 January 2019

A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels

artículo científico publicado en 2008

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

artículo científico publicado en 2015

Analysis with the exome array identifies multiple new independent variants in lipid loci

artículo científico publicado en 2016

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

artículo científico publicado en 2012

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

artículo científico publicado en 2018

Clustering of individuals given SNPs similarity based on normalized mutual information: F7 SNPs in the GAIT sample

artículo científico publicado en 2007

Combined cis-regulator elements as important mechanism affecting FXII plasma levels

artículo científico publicado en 2009

Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease

artículo científico publicado en 2014

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

artículo científico publicado en 2017

Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.

artículo científico publicado en 2003

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

artículo científico publicado en 2016

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

scientific article published on 09 March 2022

Expression of microRNAs in human platelet-poor plasma: analysis of the factors affecting their expression and association with proximal genetic variants

artículo científico publicado en 2020

Functional analysis of the genetic variability in the F7 gene promoter

artículo científico publicado en 2007

Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain

artículo científico publicado en 2013

Genetic variants from lipid-related pathways and risk for incident myocardial infarction

artículo científico publicado en 2013

Genetically Determined FXI (Factor XI) Levels and Risk of Stroke

article

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

artículo científico publicado en 2016

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

artículo científico publicado en 2012

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

artículo científico publicado en 2014

Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels

artículo científico publicado en 2017

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

artículo científico publicado en 2019

Human F7 sequence is split into three deep clades that are related to FVII plasma levels

artículo científico publicado en 2005

Human genetic evidence for involvement of CD137 in atherosclerosis

artículo científico publicado en 2014

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

artículo científico publicado en 2012

Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes

scientific article published on 30 June 2019

Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism

artículo científico publicado en 2014

Lack of association of non-synonymous FUT2 and ALPL polymorphisms with venous thrombosis

artículo científico publicado en 2012

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease

artículo científico publicado en 2017

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

artículo científico publicado en 2022

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

artículo científico publicado en 2010

PCSK6 Is a Key Protease in the Control of Smooth Muscle Cell Function in Vascular Remodeling

artículo científico publicado en 2020

Phenotypic Modulation of Smooth Muscle Cells in Atherosclerosis Is Associated With Downregulation of LMOD1, SYNPO2, PDLIM7, PLN, and SYNM.

artículo científico publicado en 2016

Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors

scholarly article by M. Bruzelius et al published 12 January 2015 in Journal of Thrombosis and Haemostasis

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

artículo científico publicado en 2015

SNP sets selection under mutual information criterion, application to F7/FVII dataset

artículo científico publicado en 2008

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels

artículo científico publicado en 2009

Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease

artículo científico publicado en 2015

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus.

artículo científico publicado en 2005

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005.

artículo científico publicado en 2009

The TAGA Study: A Study of Factors Determining Aortic Diameter in Families at High Risk of Abdominal Aortic Aneurysm Reveal Two New Candidate Genes

scientific article published on 24 April 2020

The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function

scientific article published on 13 July 2020

Lista de obras de Maria Sabater-Lleal

A Genome-Wide Association Study Identifies KNG1 as a Genetic Determinant of Plasma Factor XI Level and Activated Partial Thromboplastin Time

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

Analysis with the exome array identifies multiple new independent variants in lipid loci

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

Associations of autozygosity with a broad range of human phenotypes

Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Clustering of individuals given SNPs similarity based on normalized mutual information: F7 SNPs in the GAIT sample

Combined cis-regulator elements as important mechanism affecting FXII plasma levels

Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Expression of microRNAs in human platelet-poor plasma: analysis of the factors affecting their expression and association with proximal genetic variants

Functional analysis of the genetic variability in the F7 gene promoter

Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain

Genetic variants from lipid-related pathways and risk for incident myocardial infarction

Genetically Determined FXI (Factor XI) Levels and Risk of Stroke

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

Human F7 sequence is split into three deep clades that are related to FVII plasma levels

Human genetic evidence for involvement of CD137 in atherosclerosis

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes

Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism

Lack of association of non-synonymous FUT2 and ALPL polymorphisms with venous thrombosis

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

PCSK6 Is a Key Protease in the Control of Smooth Muscle Cell Function in Vascular Remodeling

Phenotypic Modulation of Smooth Muscle Cells in Atherosclerosis Is Associated With Downregulation of LMOD1, SYNPO2, PDLIM7, PLN, and SYNM.

Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

SNP sets selection under mutual information criterion, application to F7/FVII dataset

Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels

Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus.

The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005.

The TAGA Study: A Study of Factors Determining Aortic Diameter in Families at High Risk of Abdominal Aortic Aneurysm Reveal Two New Candidate Genes

The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function

The power of genetic diversity in genome-wide association studies of lipids