Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
出版年份 2018 全文链接
标题
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
作者
关键词
-
出版物
Nature Communications
Volume 9, Issue 1, Pages -
出版商
Springer Nature
发表日期
2018-06-28
DOI
10.1038/s41467-018-04668-w
参考文献
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。- Lipoprotein(a) and the risk of cardiovascular disease in the European population: results from the BiomarCaRE consortium
- (2017) Christoph Waldeyer et al. EUROPEAN HEART JOURNAL
- A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms
- (2017) Salome Mack et al. JOURNAL OF LIPID RESEARCH
- Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis
- (2017) Danish Saleheen et al. Lancet Diabetes & Endocrinology
- Are Interactions between cis -Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?
- (2016) Alexandra E. Fish et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Lipoprotein(a)-cholesterol levels estimated by vertical auto profile correlate poorly with Lp(a) mass in hyperlipidemic subjects: Implications for clinical practice interpretation of Lp(a)-mediated risk
- (2016) Calvin Yeang et al. Journal of Clinical Lipidology
- Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels
- (2016) Connor A. Emdin et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
- (2016) Andrea Ganna et al. NATURE NEUROSCIENCE
- Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
- (2016) Johannes Kettunen et al. Nature Communications
- Unified representation of genetic variants
- (2015) Adrian Tan et al. BIOINFORMATICS
- An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data
- (2015) Goo Jun et al. GENOME RESEARCH
- Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels
- (2015) W. Lu et al. HUMAN MOLECULAR GENETICS
- Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study
- (2015) Jin Li et al. JOURNAL OF HUMAN GENETICS
- Integrative analysis of 111 reference human epigenomes
- (2015) Anshul Kundaje et al. NATURE
- The impact of low-frequency and rare variants on lipid levels
- (2015) Ida Surakka et al. NATURE GENETICS
- Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
- (2015) Po-Ru Loh et al. NATURE GENETICS
- Large multiallelic copy number variations in humans
- (2015) Robert E Handsaker et al. NATURE GENETICS
- ORegAnno 3.0: a community-driven resource for curated regulatory annotation
- (2015) Robert Lesurf et al. NUCLEIC ACIDS RESEARCH
- Sequence Variation within the KIV-2 Copy Number Polymorphism of the Human LPA Gene in African, Asian, and European Populations
- (2015) Asma Noureen et al. PLoS One
- Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
- (2014) Gina M. Peloso et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Common LPA Null Allele Associates With Lower Lipoprotein(a) Levels and Coronary Artery Disease Risk
- (2014) Theodosios Kyriakou et al. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
- Toward better understanding of artifacts in variant calling from high-coverage samples
- (2014) Heng Li BIOINFORMATICS
- Another explanation for apparent epistasis
- (2014) Andrew R. Wood et al. NATURE
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
- (2014) Elaine T. Lim et al. PLoS Genetics
- Discovery and refinement of loci associated with lipid levels
- (2013) Cristen J Willer et al. NATURE GENETICS
- Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data
- (2012) Goo Jun et al. AMERICAN JOURNAL OF HUMAN GENETICS
- zCall: a rare variant caller for array-based genotyping
- (2012) Jacqueline I. Goldstein et al. BIOINFORMATICS
- Lipoprotein(a) as a Potential Causal Genetic Risk Factor of Cardiovascular Disease
- (2012) Sotirios Tsimikas et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Improved whole-chromosome phasing for disease and population genetic studies
- (2012) Olivier Delaneau et al. NATURE METHODS
- Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
- (2011) Robert E Handsaker et al. NATURE GENETICS
- Single-Nucleotide Polymorphisms in LPA Explain Most of the Ancestry-Specific Variation in Lp(a) Levels in African Americans
- (2011) Rahul C. Deo et al. PLoS One
- Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
- (2010) William McLaren et al. BIOINFORMATICS
- METAL: fast and efficient meta-analysis of genomewide association scans
- (2010) C. J. Willer et al. BIOINFORMATICS
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
- (2010) Kiran Musunuru et al. NATURE
- Variance component model to account for sample structure in genome-wide association studies
- (2010) Hyun Min Kang et al. NATURE GENETICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians
- (2009) Matthew B. Lanktree et al. Circulation-Cardiovascular Genetics
- Thirty-five-year trends in cardiovascular risk factors in Finland
- (2009) E. Vartiainen et al. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
- Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
- (2009) Robert Clarke et al. NEW ENGLAND JOURNAL OF MEDICINE
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
- (2009) Bryan N. Howie et al. PLoS Genetics
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data
- (2008) Bingshan Li et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR
- (2008) Matthew B. Lanktree et al. JOURNAL OF LIPID RESEARCH
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now