UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

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

2007

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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.2250-2257

2007

Volltextzugriff (PDF)

Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design

BMC medical research methodology, 2023-04, Vol.23 (1), p.99-99, Article 99

2023

Volltextzugriff (PDF)

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

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

2002

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Familial Aggregation of Metabolic Syndrome Indicators in Portuguese Families

BioMed research international, 2013-01, Vol.2013 (2013), p.1-7

2013

Volltextzugriff (PDF)

Biological and genetic factors influencing plasma factor VIII levels in a healthy family population: results from the Stanislas cohort

British journal of haematology, 2005-01, Vol.128 (1), p.91-99

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease

Blood, 2020-07, Vol.136 (5), p.533-541

2020

Volltextzugriff (PDF)

Current knowledge on the genetics of incident venous thrombosis

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

2013

Volltextzugriff (PDF)

Lessons from genome‐wide association studies in venous thrombosis

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

2011

Volltextzugriff (PDF)

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.84-91

1998

Volltextzugriff (PDF)

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

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

2015

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

1 – 25 von 125

Suche als RSS-Feed

Aktive Filter

ThemaLife Sciences & Biomedicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(125)
Mit Volltextzugriff
(106)

Publikationsform

Artikel
(125)

Sprache

Englisch
(125)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

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

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

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

Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design

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

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

Biological and genetic factors influencing plasma factor VIII levels in a healthy family population: results from the Stanislas cohort

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

Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease

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

Aktive Filter

Suchergebnisse filtern