相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
Heribert Schunkert et al.
CIRCULATION (2008)
Cox proportional hazards models have more statistical power than logistic regression models in cross-sectional genetic association studies
Jeroen B. van der Net et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Associations with myocardial infarction of six polymorphisms selected from a three-stage genome-wide association study
Benjamin D. Horne et al.
AMERICAN HEART JOURNAL (2007)
Genomewide association analysis of coronary artery disease
Nilesh J. Samani et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
A common variant on chromosome 9p21 affects the risk of myocardial infarction
Anna Helgadottir et al.
SCIENCE (2007)
A common allele on chromosome 9 associated with coronary heart disease
Ruth McPherson et al.
SCIENCE (2007)
Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations - CARE and WOSCOPS
Olga A. Iakoubova et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2006)
Relative risk for cardiovascular atherosclerotic events after smoking cessation: 6-9 years excess risk in individuals with familial hypercholesterolemia
Anneke Kramer et al.
BMC PUBLIC HEALTH (2006)
The regulation of INK4/ARF in cancer and aging
William Y. Kim et al.
CELL (2006)
A functional polymorphism in the glucocorticoid receptor gene and its relation to cardiovascular disease risk in familial hypercholesterolemia
Kristel C. M. C. Koeijvoets et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction
Dov Shiffman et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2006)
A prospective replication study of five gene variants previously associated with risk of myocardial infarction
R. Y. L. Zee et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2006)
Identification of four gene variants associated with myocardial infarction
D Shiffman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia
ACM Jansen et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2005)
Genetic association studies of complex traits: design and analysis issues
C Newton-Cheh et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2005)
Guidelines were developed for data collection from medical records for use in retrospective analyses
ACM Jansen et al.
JOURNAL OF CLINICAL EPIDEMIOLOGY (2005)
Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction
M Fischer et al.
CIRCULATION (2005)
The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients
ACM Jansen et al.
JOURNAL OF INTERNAL MEDICINE (2004)
Regulation of transcription by the heterogeneous nuclear ribonucleoprotein E1B-AP5 is mediated by complex formation with the novel bromodomain-containing protein BRD7
J Kzhyshkowska et al.
BIOCHEMICAL JOURNAL (2003)
Low-density lipoprotein receptor gene mutations and cardiovascular risk in a large genetic cascade screening population
MAW Umans-Eckenhausen et al.
CIRCULATION (2002)
Human C1qRp is identical with CD93 and the mNI-11 antigen but does not bind C1q
EP McGreal et al.
JOURNAL OF IMMUNOLOGY (2002)
The molecular basis of familial hypercholesterolemia in The Netherlands
SW Fouchier et al.
HUMAN GENETICS (2001)
Replication validity of genetic association studies
JPA Ioannidis et al.
NATURE GENETICS (2001)
Mortality over two centuries in large pedigree with familial hypercholesterolaemia: family tree mortality study
EJG Sijbrands et al.
BMJ-BRITISH MEDICAL JOURNAL (2001)
Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia
EJG Sijbrands et al.
ATHEROSCLEROSIS (2000)