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A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies

Bioinformatics, 2007-04, Vol.23 (8), p.1038-1039

2007

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A new algorithm for haplotype‐based association analysis: the Stochastic‐EM algorithm

Annals of human genetics, 2004-03, Vol.68 (2), p.165-177

2004

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Is there still room for additional common susceptibility alleles for venous thromboembolism?

Journal of thrombosis and haemostasis, 2016-09, Vol.14 (9), p.1798-1802

2016

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Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles‐NImes prediction model

Journal of thrombosis and haemostasis, 2014-02, Vol.12 (2), p.138-146

2014

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Association of plasminogen activator inhibitor (PAI)-1 (SERPINE1) SNPs with myocardial infarction, plasma PAI-1, and metabolic parameters: the HIFMECH study

Arteriosclerosis, thrombosis, and vascular biology, 2007-10, Vol.27 (10), p.2250

2007

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Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

Journal of molecular medicine (Berlin, Germany), 2008-10, Vol.86 (10), p.1153-1161

2008

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No prognostic role of a GWAS-derived genetic risk score in renal outcomes for patients from French cohorts with type 1 and type 2 diabetes

Diabetes & metabolism, 2019-10, Vol.45 (5), p.494-497

2019

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Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm

European journal of human genetics : EJHG, 2004-11, Vol.12 (11), p.971-974

2004

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Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk

Scientific reports, 2017-04, Vol.7 (1), p.45507-45507, Article 45507

2017

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Specific haplotypes of the P-selectin gene are associated with myocardial infarction

Human molecular genetics, 2002-08, Vol.11 (17), p.2015-2023

2002

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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation

Scientific reports, 2019-03, Vol.9 (1), p.3750-3750, Article 3750

2019

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A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2671-2679

2010

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

Journal of thrombosis and haemostasis, 2012-08, Vol.10 (8), p.1693-1695

2012

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Familial Aggregation of Metabolic Syndrome Indicators in Portuguese Families

BioMed research international, 2013-01, Vol.2013, p.314823-7

2013

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Impact on venous thrombosis risk of newly discovered gene variants associated with FVIII and VWF plasma levels

Journal of thrombosis and haemostasis, 2011-01, Vol.9 (1), p.229-231

2011

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Current knowledge on the genetics of incident venous thrombosis

Journal of thrombosis and haemostasis, 2013-06, Vol.11, p.111-121

2013

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Lessons from genome‐wide association studies in venous thrombosis

Journal of thrombosis and haemostasis, 2011-07, Vol.9, p.258-264

2011

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Metabolic determinants are much more important than genetic polymorphisms in determining the PAI-1 activity and antigen plasma concentrations: a family study with part of the Stanislas Cohort

Arteriosclerosis, thrombosis, and vascular biology, 1998-01, Vol.18 (1), p.84

1998

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Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

International journal of epidemiology, 2015-04, Vol.44 (2), p.578-586

2015

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Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study

Clinical genetics, 2017-01, Vol.91 (1), p.131-136

2017

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TAFI gene haplotypes, TAFI plasma levels and future risk of coronary heart disease: the PRIME Study

Journal of thrombosis and haemostasis, 2005-07, Vol.3 (7), p.1503-1510

2005

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Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism

Journal of thrombosis and haemostasis, 2016-10, Vol.14 (10), p.1960-1970

2016

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SELPLG Gene Polymorphisms in Relation to Plasma SELPLG Levels and Coronary Artery Disease

Annals of human genetics, 2003-11, Vol.67 (6), p.504-511

2003

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A systems-approach reveals human nestin is an endothelial-enriched, angiogenesis-independent intermediate filament protein

Scientific reports, 2018-10, Vol.8 (1), p.14668-15, Article 14668

2018

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A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies

A new algorithm for haplotype‐based association analysis: the Stochastic‐EM algorithm

Is there still room for additional common susceptibility alleles for venous thromboembolism?

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

Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles‐NImes prediction model

Association of plasminogen activator inhibitor (PAI)-1 (SERPINE1) SNPs with myocardial infarction, plasma PAI-1, and metabolic parameters: the HIFMECH study

Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

No prognostic role of a GWAS-derived genetic risk score in renal outcomes for patients from French cohorts with type 1 and type 2 diabetes

Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm

Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk

Specific haplotypes of the P-selectin gene are associated with myocardial infarction

Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation

A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

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

Familial Aggregation of Metabolic Syndrome Indicators in Portuguese Families

Impact on venous thrombosis risk of newly discovered gene variants associated with FVIII and VWF plasma levels

Current knowledge on the genetics of incident venous thrombosis

Lessons from genome‐wide association studies in venous thrombosis

Metabolic determinants are much more important than genetic polymorphisms in determining the PAI-1 activity and antigen plasma concentrations: a family study with part of the Stanislas Cohort

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study

TAFI gene haplotypes, TAFI plasma levels and future risk of coronary heart disease: the PRIME Study

Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism

SELPLG Gene Polymorphisms in Relation to Plasma SELPLG Levels and Coronary Artery Disease

A systems-approach reveals human nestin is an endothelial-enriched, angiogenesis-independent intermediate filament protein

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