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List of works by Maria Sabater-Lleal

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

scientific article published on 13 May 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

scientific article published on 18 June 2008

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

scientific article

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

scientific article published on 27 July 2016

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

scientific article published in August 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

scientific article published on 01 December 2018

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

scientific article published on 01 January 2007

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 26 September 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

scientific article published on 16 June 2020

Functional analysis of the genetic variability in the F7 gene promoter

scientific article published on 09 February 2007

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

scientific article

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

scientific article

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

scientific article published in November 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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 4 January 2017

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

scientific article published on 01 November 2019

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

scientific article published on 16 November 2005

Human genetic evidence for involvement of CD137 in atherosclerosis

scientific article

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

scientific article

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

scientific article

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

scientific article published on 01 August 2012

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

scientific article

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

scientific article

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

scientific article (publication date: 17 September 2013)

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

scientific article published in 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

scientific article

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

scientific article

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

scientific article published on 02 January 2020

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

scientific article published on 28 July 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

scientific article

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

scientific article published in January 2008

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

scientific article

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

scientific article

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

scientific article published in October 2005

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

scientific article published in December 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

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

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