J. Soria

发表

Multivariable clinical-genetic risk model for predicting venous thromboembolic events in patients with cancer

C. Font, A. M. Muñoz Martín, I. Ortega, 2018, British Journal of Cancer.

Investigation of the fine structure of European populations with applications to disease association studies

S. Heath, L. Cardon, E. Génin, 2008, European Journal of Human Genetics.

The impact of sex on gene expression across human tissues

Ayellet V. Segrè, Stephane E. Castel, Ariel D. H. Gewirtz, 2020, Science.

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.

L. Almasy, L. Almasy, J. Blangero, 2000, American journal of human genetics.

Predictive Ability of a Clinical-Genetic Risk Score for Venous Thromboembolism in Northern and Southern European Populations

I. Ortega, E. Salas, J. Soria, 2021, TH Open.

The Central Role of KNG1 Gene as a Genetic Determinant of Coagulation Pathway-Related Traits: Exploring Metaphenotypes

J. Souto, J. Soria, A. Martinez-Perez, 2016, PloS one.

Acceptor splice site mutation in the invariant AG of intron 5 of the protein C gene, causing type I protein C deficiency

X. Estivill, J. Fontcuberta, J. Soria, 1993, Human Genetics.

Rapid detection of the 46C --> T polymorphism in the factor XII gene, a novel genetic risk factor for thrombosis, by melting peak analysis using fluorescence hybridization probes.

J. Fontcuberta, J. Soria, I. Tirado, 2003, Genetic testing.

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

J. Fontcuberta, M. Sabater-Lleal, J. Soria, 2003, Haematologica.

DNA Binding Site Characterization by Means of RÉnyi Entropy Measures on Nucleotide Transitions

P. Caminal, M. Vallverdu, P. Caminal, 2008, IEEE Transactions on NanoBioscience.

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

M. Sabater-Lleal, J. Souto, J. Soria, 2020, Epigenetics.

Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene.

J. Fontcuberta, J. Souto, J. Soria, 2001, Haematologica.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

J. Fontcuberta, J. Souto, J. Soria, 2001, Haematologica.

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

A. Folsom, Yuhuang Li, D. Trégouët, 2017, Human molecular genetics.

The prothrombin 20210A allele influences clinical manifestations of hemophilia A in patients with intron 22 inversion and without inhibitors.

M. Baiget, E. Tizzano, J. Fontcuberta, 2002, Haematologica.

TMAO and Gut Microbial-Derived Metabolites TML and γBB Are Not Associated with Thrombotic Risk in Patients with Venous Thromboembolism

M. Díaz-Ricart, S. Mojal, N. Rotllan, 2022, Journal of clinical medicine.

PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study.

D. Trégouët, M. Uhlén, J. Odeberg, 2016, Blood.

Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women

A. Buil, E. Arroyo-Pardo, A. M. Pérez-Granados, 2011, Nutrition & metabolism.

increases the risk for venous thrombosis A nonsense polymorphism in the protein Z-dependent protease inhibitor

J. González-Porras, V. Vicente, J. Souto, 2014 .

Cell type–specific genetic regulation of gene expression across human tissues

R. Guigó, G. Getz, M. Stephens, 2020, Science.

Prediction of Recurrent Pregnancy Loss by a New Thrombophilia Based Genetic Risk Score

J. Paramo, I. Ortega, E. Salas, 2018 .

Health in ultra endurance events: SUMMIT Lab® Project

E. Roca, J. Soria, P. Bogónez-Franco, 2016 .

A validated clinical-genetic score for assessing the risk of thrombosis in patients with COVID-19 receiving thromboprophylaxis

R. Antonijoan, J. Souto, J. Soria, 2022, Haematologica.

Ectopic Transcript Analysis Indicates that Allelic Exclusion is an Important Cause of Type I Protein C Deficiency in Patients with Nonsense and Frameshift Mutations in the PROC Gene

X. Estivill, D. Cooper, V. Kakkar, 1996, Thrombosis and Haemostasis.

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

P. Tsao, D. Gudbjartsson, U. Thorsteinsdóttir, 2012, Journal of the American College of Cardiology.

gene and associations with plasma FVIII activity levels A sequence variation scan of the coagulation factor VIII (FVIII) structural

L. Almasy, J. Blangero, A. Buil, 2009 .

A SEQUENCE VARIATION SCAN OF THE COAGULATION FACTOR ( F ) VIII STRUCTURAL GENE AND ASSOCIATIONS WITH PLASMA FVIII ACTIVITY ( FVIII : C ) LEVELS

L. Almasy, J. Blangero, A. Buil, 2007 .

A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.

L. Almasy, J. Blangero, A. Buil, 2007, Blood.

Salivary immunity and lower respiratory tract infections in non-elite marathon runners

E. Roca, J. Soria, L. Nescolarde, 2018, PloS one.

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

L. Almasy, A. Buil, J. Odeberg, 2012, Arteriosclerosis, thrombosis, and vascular biology.

Association after linkage analysis indicates that homozygosity for the 46C→T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis

J. Fontcuberta, J. Souto, J. Soria, 2004, Thrombosis and Haemostasis.

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

Andrew D. Johnson, C. Ward‐Caviness, O. Franco, 2019 .

Identiﬁcation of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study

L. Almasy, A. Buil, J. Peden, 2009 .

Multilocus Genetic Risk Scores for Venous Thromboembolism Risk Assessment

D. Trégouët, P. Morange, J. Vila, 2014, Journal of the American Heart Association.

The ABO blood group genotype and factor VIII levels as independent risk factors for venous thromboembolism

J. Fontcuberta, J. Soria, J. Mateo, 2005, Thrombosis and Haemostasis.

Clinical guidelines for the prevention, diagnosis and treatment of venous thromboembolism in sport

J. Soria, J. Souto, F. Drobnic, 2015 .

Cell type–specific genetic regulation of gene expression across human tissues

Stephane E. Castel, R. Guigó, G. Getz, 2019, Science.

Homozygosity of the T allele of the 46 C-->T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population.

J. Fontcuberta, J. Soria, J. Mateo, 2004, Haematologica.

SalaboMiner - A Biomedical Literature Mining Tool for Inferring the Genetics of Complex Diseases

Ricard Gavaldà, Alfonso Buil, José Manuel Soria, 2011, BIOINFORMATICS.

Short closure time values in PFA-100® are related to venous thrombotic risk. Results from the RETROVE Study.

J. Fontcuberta, J. Souto, J. Soria, 2018, Thrombosis Research.

The Relationship between Leukocyte Counts and Venous Thromboembolism: Results from RETROVE Study

J. Souto, J. Soria, J. Mateo, 2017 .

A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667t mutations, but belonging to an asymptomatic family.

J. Fontcuberta, J. Soria, C. Vallvé, 2000, Haematologica.

Antithrombin, protein C and protein S: Genome and transcriptome wide association studies identify 7 novel loci regulating plasma levels

D. A. Dobson, J. Pankow, D. Tregouet, 2022, medRxiv.

Prevalence and predisposition to deep vein thrombosis in professional male soccer players

J. Souto, J. Soria, X. Valle, 2021 .

Novel genes and sex differences in COVID-19 severity

Gloria L. Porras-Hurtado, M. Urioste, M. Buti, 2022, Human molecular genetics.

Homozygosity of the T Allele of the 46 C→T Polymorphism in the F12 Gene Is a Risk Factor for Ischemic Stroke in the Spanish Population

J. Martí-Fàbregas, J. Fontcuberta, J. Souto, 2004, Stroke.

Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G→A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency

X. Estivill, M. Morell, J. Soria, 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time.

L. Almasy, J. Blangero, J. Fontcuberta, 2000, Arteriosclerosis, thrombosis, and vascular biology.

Linkage and association analyses using families identified a locus affecting an osteoporosis-related trait.

G. Athanasiadis, J. Soria, L. Martin-Fernandez, 2014, Bone.

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis.

L. Almasy, J. Blangero, J. Fontcuberta, 2000, Blood.

Exploring correlation between bone metabolism markers and densitometric traits in extended families from Spain.

G. Athanasiadis, J. Soria, H. Brunel, 2016, Bone.

Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism

A. Brown, E. Dermitzakis, A. Viñuela, 2022, Thrombosis and Haemostasis.

Genetic determinants of normal variation in coagulation factor (F) IX levels: genome‐wide scan and examination of the FIX structural gene

L. Almasy, A. Buil, M. Lathrop, 2006, Journal of thrombosis and haemostasis : JTH.

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

L. Almasy, J. Blangero, A. Buil, 2010, Human molecular genetics.

Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection

M. Biasin, J. Soria, L. Real, 2015, Genes and Immunity.

lme4qtl: linear mixed models with flexible covariance structure for genetic studies of related individuals

Andrey Ziyatdinov, Hugues Aschard, Miquel Vázquez-Santiago, 2017, bioRxiv.

Genetic Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 Project

A. Hamsten, J. Souto, J. Soria, 2016, PloS one.

solarius: an R interface to SOLAR for variance component analysis in pedigrees

Andrey Ziyatdinov, Alexandre Perera-Lluna, Helena Brunel, 2015, bioRxiv.

Recurrent Miscarriage and Implantation Failure of Unknown Cause Studied by a Panel of Thrombophilia Conditions: Increased Frequency of FXIII Val34Leu Polymorphism

R. Matorras, J. Soria, M. Ferrando, 2019, Journal of reproduction & infertility.

Sex-Specific Regulation of Mitochondrial DNA Levels: Genome-Wide Linkage Analysis to Identify Quantitative Trait Loci

L. Almasy, J. Blangero, A. Buil, 2012, PloS one.

Molecular analysis of multiple genetic variants in Spanish FXII-deficient families

J. Fontcuberta, J. Soria, E. Martínez-Marchán, 2007, Haematologica.

A new gene-based association test for genome-wide association studies

A. Buil, P. Caminal, A. Perera-Lluna, 2009 .

Multiplex assay for genetic testing of thrombophilia: a method for routine clinical care

José Manuel Soria, Mónica López, R Cornudella, 2007, Journal of clinical laboratory analysis.

A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

L. Almasy, J. Blangero, A. Buil, 2003, Blood.

ThrombosisMolecular Basis of Disease

J. Fontcuberta, J. Soria, 2005 .

New approaches and future prospects for evaluating genetic risk of thrombosis.

J. Fontcuberta, J. Soria, 2005, Haematologica.

Aberrant RNA splicing of the protein C and protein S genes in healthy individuals.

X. Estivill, D. Cooper, V. Kakkar, 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Severe Homozygous Protein C Deficiency: Identification of a Splice Site Missense Mutation (184, Q → H) in Exon 7 of the Protein C Gene

X. Estivill, J. Fontcuberta, J. Soria, 1994, Thrombosis and Haemostasis.

A nonsense polymorphism in the protein Z-dependent protease inhibitor increases the risk for venous thrombosis.

J. González-Porras, J. Corral, V. Vicente, 2006, Blood.

Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children

J. Corral, V. Vicente, J. Soria, 2011, Haematologica.

Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis

J. Souto, J. Soria, F. Vidal, 2017, PloS one.

The Unravelling of the Genetic Architecture of Plasminogen Deficiency and its Relation to Thrombotic Disease

J. Soria, F. Vidal, L. Martin-Fernandez, 2016, Scientific Reports.

Age and gender effects on 15 platelet phenotypes in a Spanish population

Miquel Vázquez-Santiago, Andrey Ziyatdinov, Núria Pujol-Moix, 2016, Comput. Biol. Medicine.

Identification of a Plasma MicroRNA Profile Associated With Venous Thrombosis

J. Souto, J. Soria, A. Martinez-Perez, 2020, Arteriosclerosis, thrombosis, and vascular biology.

Affected pathways and transcriptional regulators in gene expression response to an ultra-marathon trail: Global and independent activity approaches

E. Roca, J. Soria, A. Perera, 2017, PloS one.

African-Americans Express Multiple Haplotypic Forms of the Wildtype Factor VIII (FVIII) Protein: A Possible Role for Pharmacogenetics in FVIII Inhibitor Development?.

L. Almasy, J. Soria, C. Doering, 2004 .

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

John D. Eicher, C. Ward‐Caviness, M. Fornage, 2019, Blood.

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

Andrew D. Johnson, C. Ward‐Caviness, M. Fornage, 2019, Circulation.

A Genome-Wide Association Study of the Protein C Anticoagulant Pathway

L. Almasy, A. Buil, M. Lathrop, 2011, PloS one.

A Genome Search for Genetic Determinants That Influence Plasma Fibrinogen Levels

L. Almasy, J. Blangero, A. Buil, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Platelet count and plateletcrit are associated with an increased risk of venous thrombosis in females. Results from the RETROVE study.

J. Fontcuberta, J. Souto, J. Soria, 2017, Thrombosis research.

Genetic determinants of platelet large-cell ratio, immature platelet fraction, and other platelet-related phenotypes.

J. Fontcuberta, J. Souto, J. Soria, 2015, Thrombosis research.

A Locus on Chromosome 2 Influences Levels of Tissue Factor Pathway Inhibitor: Results From the GAIT study

L. Almasy, A. Buil, M. Lathrop, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Heritability of Hemostasis Phenotypes and Their Correlation with Type 2 Diabetes Status in Mexican Americans

L. Almasy, L. Almasy, J. Blangero, 2005, Human biology.

Genomewide linkage analysis of soluble transferrin receptor plasma levels

L. Almasy, J. Blangero, A. Buil, 2005, Annals of Hematology.

Association of ABO haplotypes with the risk of venous thrombosis: impact on disease risks estimation.

Andrew D. Johnson, D. Chasman, D. Trégouët, 2020, Blood.

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

M. Sabater-Lleal, J. Soria, V. Plaza, 2020, Journal of clinical medicine.

The Genetic Component of Disorders of Coagulation and Thrombosis

J. Soria, 2009 .

Protein C Levels Are Regulated by a Quantitative Trait Locus on Chromosome 16: Results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project

L. Almasy, J. Blangero, A. Buil, 2004, Arteriosclerosis, thrombosis, and vascular biology.

A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q: Results From the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project

L. Almasy, J. Blangero, M. Lathrop, 2003, Arteriosclerosis, Thrombosis and Vascular Biology.

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.

J. Fontcuberta, J. Souto, J. Soria, 1999, Haematologica.

The F7 Gene and Clotting Factor VII Levels: Dissection of a Human Quantitative Trait Locus

Juan Carlos Souto, John Blangero, Maria Sabater-Lleal, 2006, Human biology.

Economic Analysis of Thrombo inCode, a Clinical–Genetic Function for Assessing the Risk of Venous Thromboembolism

P. Morange, J. Souto, E. Salas, 2015, Applied Health Economics and Health Policy.

Economic Analysis Of Thrombo Incode, A Clinical-Genetic Function For Assessing The Risk Of Venous Thromboembolism.

P. Morange, J. Souto, E. Salas, 2014, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.

Influence of Age, Gender and Lifestyle in Lymphocyte Subsets: Report from the Spanish Gait-2 Study

J. Fontcuberta, J. Soria, A. Martinez-Perez, 2012, Acta Haematologica.

Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism

A. Brown, E. Dermitzakis, A. Viñuela, 2022, Thrombosis and Haemostasis.

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

L. Almasy, A. Buil, M. Lathrop, 2013, Journal of thrombosis and haemostasis : JTH.

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

A. Brown, D. Hinds, E. Dermitzakis, 2016, Human molecular genetics.

Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk

A. Brown, E. Dermitzakis, A. Viñuela, 2022, Thrombosis and haemostasis.

A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project.

L. Almasy, J. Blangero, A. Buil, 2005, American journal of human genetics.

Identification of a Novel Quantitative Trait Nucleotype Related to Iron Status in a Calcium Channel Gene

A. Buil, E. Arroyo-Pardo, A. M. Pérez-Granados, 2013, Disease markers.

J. Fontcuberta, J. Souto, J. Soria, 2016, Blood cells, molecules & diseases.

A Clinical-Genetic Risk Score for Predicting Cancer-Associated Venous Thromboembolism: A Development and Validation Study Involving Two Independent Prospective Cohorts

C. Font, V. Pachón, V. Castellón, 2023, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Training-induced gene expression plasticity in cardiac function and neural regulation for ultra-trail runners

Alexandre Perera-Lluna, María Maqueda, Emma Roca, 2015, 2015 Computing in Cardiology Conference (CinC).

Genetic Contribution of Femoral Neck Bone Geometry to the Risk of Developing Osteoporosis: A Family-Based Study

G. Athanasiadis, J. Soria, J. Farrerons, 2016, PloS one.

Genetic and environmental factors influencing the human factor H plasma levels

L. Almasy, J. Blangero, A. Buil, 2004, Immunogenetics.

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

A. Hamsten, M. Sabater-Lleal, J. Soria, 2019, International journal of molecular sciences.

MISS: a non-linear methodology based on mutual information for genetic association studies in both population and sib-pairs analysis

Pere Caminal, Alexandre Perera-Lluna, Montserrat Vallverdú, 2010, Bioinform..

Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study.

L. Almasy, A. Buil, J. Peden, 2009, Blood.

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.

L. Almasy, A. Buil, S. Blankenberg, 2010, Blood.

Recurrence of the PROC gene mutation R178Q: Independent origins in Spanish protein C deficiency patients

X. Estivill, M. Morell, J. Soria, 1996, Human mutation.

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

L. Almasy, J. Blangero, J. Fontcuberta, 2010, Thrombosis research.

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

J. Blangero, A. Buil, M. Lathrop, 2008, Human Genetics.

A Locus on Chromosome 13 Influences Levels of TAFI Antigen in Healthy Mexican Americans

L. Almasy, J. Blangero, S. Cole, 2006, Human biology.

A genomewide study of body mass index and its genetic correlation with thromboembolic risk

A. Buil, J. Fontcuberta, J. Souto, 2014, Thrombosis and Haemostasis.

Functional analysis of the genetic variability in the F7 gene promoter.

José Manuel Soria, John Blangero, Laura Almasy, 2007, Atherosclerosis.

Heritability of Bone Mineral Density in a Multivariate Family-Based Study

G. Athanasiadis, J. Soria, J. Farrerons, 2014, Calcified Tissue International.

Plasma homocysteine and the genetics of cardiovascular disease.

J. Souto, J. Soria, 2006, Future cardiology.

The F7 Gene and Clotting Factor VII Levels: Dissection of a Human Quantitative Trait Locus

L. Almasy, J. Blangero, J. Fontcuberta, 2005, Human biology.

Heritability of Bone Mineral Density in a Multivariate Family-Based Study

G. Athanasiadis, J. Soria, J. Farrerons, 2014, Calcified Tissue International.

Update to Soria et al.'s “F7 Gene and Clotting Factor VII Levels” (2005): Genetic Determinants of Quantitative Traits in Thrombotic Disease

J. Soria, Itziar Arbesú, 2009, Human biology.

Genetic correlation between plasma levels of C4BP isoforms containing β chains and susceptibility to thrombosis

L. Almasy, J. Blangero, A. Buil, 2004, Journal of Medical Genetics.

Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties

L. Almasy, J. Blangero, J. Fontcuberta, 2002, Human Genetics.

A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease.

L. Almasy, J. Blangero, A. Buil, 2002, American journal of human genetics.

Incorporating genetic and clinical data into the prediction of thromboembolism risk in patients with lymphoma

I. Buño, E. Salas, J. Soria, 2021, Cancer medicine.

Floating Feature Selection for multiloci association of quantitative traits in sib-pairs analysis

Pere Caminal, Alexandre Perera-Lluna, Helena Brunel, 2008, 2008 8th IEEE International Conference on BioInformatics and BioEngineering.

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

L. Almasy, J. Blangero, J. Bertranpetit, 2006, Human Genetics.

Genetic determinants of cardiometabolic risk factors in rural families in Brazil

G. Velásquez-Melendez, R. Corrêa-Oliveira, J. Soria, 2016, American journal of human biology : the official journal of the Human Biology Council.

Impact of pre-admission antithrombotic therapy on disease severity and mortality in patients hospitalized for COVID-19

S. Mojal, R. Antonijoan, J. Soria, 2021, Journal of Thrombosis and Thrombolysis.

A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.

L. Almasy, A. Buil, J. Souto, 2014, Mitochondrion.

Thromboplastin-thrombomodulin-mediated Time and Serum Folate Levels Are Genetically Correlated with the Risk of Thromboembolic Disease: Results from the GAIT Project

L. Almasy, J. Blangero, J. Fontcuberta, 2002, Thrombosis and Haemostasis.

Heritability of plasma concentrations of activated protein C in a Spanish population

A. Buil, F. España, A. Estellés, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Genetic risk factors for thrombosis in a Basque population and its possible contribution to the analysis of a complex disease such as thrombophilia.

M. Tejada, M. Baiget, J. Fontcuberta, 2001, Haematologica.

Genetic determinants of 5-lipoxygenase pathway in a Spanish population and their relationship with cardiovascular risk.

A. Buil, J. Fontcuberta, J. Souto, 2012, Atherosclerosis.

Heritability of Thromboxane A2 and Prostaglandin E2 Biosynthetic Machinery in a Spanish Population

A. Buil, J. Fontcuberta, J. Souto, 2010, Arteriosclerosis, thrombosis, and vascular biology.

Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families

L. Almasy, J. Blangero, A. Buil, 2003, Immunogenetics.

Identification of Antithrombin-Modulating Genes. Role of LARGE, a Gene Encoding a Bifunctional Glycosyltransferase, in the Secretion of Proteins?

A. Buil, J. Corral, V. Vicente, 2013, PloS one.

Predicting individual risk of venous thrombosis.

J. Souto, J. Soria, 2012, Blood.

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

A. Buil, P. Caminal, M. Vallverdú, 2008, 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

C 4 BPB / C 4 BPA is a new susceptibility locus for venous thrombosis with unknown protein S – independent mechanism : results from genome-wide association and gene expression analyses followed by case-control studies

L. Almasy, A. Buil, S. Blankenberg, 2010 .

500 1 9 J U L Y 2 0 1 2 I V O L U M E 1 2 0 , N U M B E R 3 Blood

F. Geissmann, J. Souto, J. Soria, 2022 .

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.

R. Marioni, M. Fornage, L. Hou, 2023, medRxiv.

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Matthew A. Wiles, Ellen C. Smith, Jack D. Sanders, 2023, Nature.

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Matthew A. Wiles, Ellen C. Smith, Jack D. Sanders, 2023, Nature.

Hemostasis, Thrombosis, and Vascular Biology

J. Corral, V. Vicente, J. Fontcuberta, 2006 .

Cost-effectiveness of apixaban and rivaroxaban in thromboprophylaxis of cancer patients treated with chemotherapy in Spain.

E. Gallardo, J. Soria, A. Muñoz, 2023, Journal of medical economics.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

M. Margaglione, E. Grandone, J. Corral, 2005 .

A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

L. Almasy, A. Buil, M. Lathrop, 2003 .

Searching for master regulators of transcription in a human gene expression data set

L. Almasy, A. Buil, P. Caminal, 2007, BMC proceedings.

Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project.

L. Almasy, J. Blangero, A. Buil, 2003, Thrombosis and haemostasis.

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

L. Almasy, J. Blangero, J. Fontcuberta, 2000 .

Hemostasis, Thrombosis, and Vascular Biology Patients and Methods Subjects and Phenotypes Table 1. Results from the Linkage Analysis: Apcr with F5 Dna Variants, and Apcr Conditional on the Fvl Mutation

L. Almasy, J. Blangero, A. Buil, 2022 .

Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

J. Pankow, D. Trégouët, C. Sitlani, 2023, Arteriosclerosis, thrombosis, and vascular biology.

A second update on mapping the human genetic architecture of COVID-19

M. A. Hakim Newton, Jack D. Sanders, Jonathan H. Morgan, 2022, Nature.

A new gene-based association test for genome-wide association studies

A. Buil, P. Caminal, A. Perera-Lluna, 2009, BMC proceedings.

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Sebastian M. Armasu, Andrew D. Johnson, A. Reiner, 2022, medRxiv.

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

John D. Eicher, C. Ward‐Caviness, M. Fornage, 2019, Circulation.

Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism

D. Tregouet, M. Germain, Danny J. Smith, 2023, Blood advances.

Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels

L. Almasy, J. Blangero, A. Buil, 2008, European Journal of Human Genetics.