Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. - Wikidata - wikimedia - TriplyDB

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.

http://www.wikidata.org/entity/Q30411390

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CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits Insights into blood lipids from rare variant discovery Rare-variant association analysis: study designs and statistical tests Genetic and epigenetic factors influencing chronic kidney disease Next-generation gene discovery for variants of large impact on lipid traits Insights from exome sequencing for endocrine disorders Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.Association of exome sequences with plasma C-reactive protein levels in >9000 participants.Whole Exome Sequencing in Atrial Fibrillation.Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data.Likelihood-based complex trait association testing for arbitrary depth sequencing data.Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.Review: High-performance computing to detect epistasis in genome scale data sets.Genetic Architecture of Familial Hypercholesterolaemia.The impact of rare and low-frequency genetic variants in common disease The impact of population demography and selection on the genetic architecture of complex traits.Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.Detecting association of rare and common variants based on cross-validation prediction error.Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.Meta-analysis of sequencing studies with heterogeneous genetic associations A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.Genetic variant in folate homeostasis is associated with lower warfarin dose in African Americans.PRIMUS: rapid reconstruction of pedigrees from genome-wide estimates of identity by descent.The UK10K project identifies rare variants in health and disease Genetic association analysis under complex survey sampling: the Hispanic Community Health Study/Study of Latinos.Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study.Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.Rare variant association studies: considerations, challenges and opportunities.Polycyclic aromatic hydrocarbons: from metabolism to lung cancer.The importance of an integrated analysis of clinical, molecular, and functional data for the genetic diagnosis of familial hypercholesterolemia.Glucokinase regulatory protein: complexity at the crossroads of triglyceride and glucose metabolism.PaPI: pseudo amino acid composition to score human protein-coding variants.Causal Inference in the Age of Decision Medicine.A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.Dissecting the genetic determinants of hemostasis and thrombosis Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.

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Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.

http://www.wikidata.org/entity/Q30411390

description

2014 nî lūn-bûn

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2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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type

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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Whole-exome sequencing identif ...... sociated with LDL cholesterol.

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J.AJHG.2014.01.010

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American Journal of Human Genetics

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Aaron Isaacs

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Adolfo Correa

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Alexander P Reiner

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Alisa Manning

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Chenyi Xue

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Chris Bizon

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Christie M Ballantyne

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Christina L Wassel

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Christopher J O'Donnell

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Christopher S Carlson

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P2860

Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption.

Biological, clinical and population relevance of 95 loci for blood lipids

Fast and accurate short read alignment with Burrows-Wheeler transform

Genome-wide association study of biochemical traits in Korcula Island, Croatia

PLINK: a tool set for whole-genome association and population-based linkage analyses

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

The Sequence Alignment/Map format and SAMtools

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

Discovery and refinement of loci associated with lipid levels.

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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10.1016/J.AJHG.2014.01.010

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Thomas Meitinger

Vilmundur Gudnason

Sekar Kathiresan

Eric Boerwinkle

Cornelia M. van Duijn

Charles Kooperberg

Caroline Hayward

André Uitterlinden

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2014-02-01T00:00:00Z

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