A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs

Loss-of-function mutation in ABCA1 and risk of Alzheimer's disease and cerebrovascular disease

(2015) Liv Tybjærg Nordestgaard et al.   Alzheimers & Dementia

Novel Association of the R230C Variant of the ABCA1 Gene with High Triglyceride Levels and Low High-density Lipoprotein Cholesterol Levels in Mexican School-age Children with High Prevalence of Obesity

(2015) Marco Alberto Gamboa-Meléndez et al.   ARCHIVES OF MEDICAL RESEARCH

Association Between theABCA1-565C/T Gene Promoter Polymorphism and Coronary Heart Disease Severity and Cholesterol Efflux in the Chinese Han Population

(2015) Li-Ping Qi et al.   Genetic Testing and Molecular Biomarkers

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

(2015) Jie Hu et al.   Journal of Neurodevelopmental Disorders

ABCA1rs4149313 Polymorphism and Susceptibility to Coronary Heart Disease: A Meta-Analysis

(2014) Shu-Li Fan et al.   ANNALS OF HUMAN GENETICS

Common Genetic Variants Contribute to Primary Hypertriglyceridemia Without Differences Between Familial Combined Hyperlipidemia and Isolated Hypertriglyceridemia

(2014) I. De Castro-Oros et al.   Circulation-Cardiovascular Genetics

The genetic architecture of the familial hyperlipidaemia syndromes

(2014) Philippa J. Talmud et al.   CURRENT OPINION IN LIPIDOLOGY

Feature ranking of type 1 diabetes susceptibility genes improves prediction of type 1 diabetes

(2014) Christiane Winkler et al.   DIABETOLOGIA

Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism

(2014) Tarek A. Abd El-Aziz et al.   Journal of Clinical Lipidology

Whole exome sequencing of familial hypercholesterolaemia patients negative forLDLR/APOB/PCSK9mutations

(2014) Marta Futema et al.   JOURNAL OF MEDICAL GENETICS

A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

(2014) Guanglin Cui et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A novel lipoprotein lipase gene missense mutation in Chinese patients with severe hypertriglyceridemia and pancreatitis

(2014) Tan-Zhou Chen et al.   Lipids in Health and Disease

The association of rs1149048 polymorphism in Matrilin-1(MATN1) gene with adolescent idiopathic scoliosis susceptibility: a meta-analysis

(2014) Hongqi Zhang et al.   MOLECULAR BIOLOGY REPORTS

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

(2014) Anna A Kashevarova et al.   Molecular Cytogenetics

Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci

(2014) Susan K. Service et al.   PLoS Genetics

Carrier frequencies of eleven mutations in eight genes associated with primary ciliary dyskinesia in the Ashkenazi Jewish population

(2014) Anastasia M. Fedick et al.   Molecular Genetics & Genomic Medicine

Evidence of a Polygenic Origin of Extreme High-Density Lipoprotein Cholesterol Levels

(2013) Mohammad Mahdi Motazacker et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

A low-frequency GLIS3 variant associated with resistance to Japanese type 1 diabetes

(2013) Takuya Awata et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci

(2013) Daphna Weissglas-Volkov et al.   JOURNAL OF MEDICAL GENETICS

Association of CETP Taq1B and -629C > A polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population

(2013) Yongjian Lu et al.   Lipids in Health and Disease

Common variants associated with plasma triglycerides and risk for coronary artery disease

(2013) Ron Do et al.   NATURE GENETICS

Discovery and refinement of loci associated with lipid levels

(2013) Cristen J Willer et al.   NATURE GENETICS

The Association of Common SNPs and Haplotypes in CETP Gene with HDL Cholesterol Levels in Latvian Population

(2013) Ilze Radovica et al.   PLoS One

A Genome Wide Association Study Identifies Common Variants Associated with Lipid Levels in the Chinese Population

(2013) Li Zhou et al.   PLoS One

Single heterozygote splice mutation in the ABCA1 gene is associated with diffuse atherosclerotic disease in a low high-density lipoprotein syndrome

(2012) Dimitrios Dimitroulis et al.   EUROPEAN HEART JOURNAL

Low-density lipoprotein receptor mutations generate synthetic genome-wide associations

(2012) Daniëlla M Oosterveer et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

(2012) Bryan Howie et al.   NATURE GENETICS

A Replication Study of GWAS-Derived Lipid Genes in Asian Indians: The Chromosomal Region 11q23.3 Harbors Loci Contributing to Triglycerides

(2012) Timothy R. Braun et al.   PLoS One

Genetic bases of hypertriglyceridemic phenotypes

(2011) Christopher T. Johansen et al.   CURRENT OPINION IN LIPIDOLOGY

A linear complexity phasing method for thousands of genomes

(2011) Olivier Delaneau et al.   NATURE METHODS

Effects of 16 Genetic Variants on Fasting Glucose and Type 2 Diabetes in South Asians: ADCY5 and GLIS3 Variants May Predispose to Type 2 Diabetes

(2011) Simon D. Rees et al.   PLoS One

GCTA: A Tool for Genome-wide Complex Trait Analysis

(2010) Jian Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Aging and Arterial Stiffness

(2010) Hae-Young Lee et al.   CIRCULATION JOURNAL

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

(2010) Christopher T Johansen et al.   NATURE GENETICS

Genotype imputation for genome-wide association studies

(2010) Jonathan Marchini et al.   NATURE REVIEWS GENETICS

Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people

(2009) Anna Murray et al.   EUROPEAN HEART JOURNAL

A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

(2009) Robert A. Hegele et al.   HUMAN MOLECULAR GENETICS

Purinergic contribution to small intestinal afferent hypersensitivity in a murine model of postinfectious bowel disease

(2009) w. rong et al.   NEUROGASTROENTEROLOGY AND MOTILITY

Ciliary defects and genetics of primary ciliary dyskinesia

(2009) Estelle Escudier et al.   Paediatric Respiratory Reviews

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

(2008) Yurii S Aulchenko et al.   NATURE GENETICS

Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events

(2008) Sekar Kathiresan et al.   NEW ENGLAND JOURNAL OF MEDICINE