| scholarly article | Q13442814 |
| P50 | author | Suzanne M. Leal | Q67209642 |
| P2093 | author name string | Paul L Auer | |
| P2860 | cites work | An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 |
| Linkage analysis of quantitative traits: increased power by using selected samples. | Q40566766 | ||
| Low-coverage sequencing: implications for design of complex trait association studies | Q42596059 | ||
| Detecting association of rare and common variants by testing an optimally weighted combination of variants | Q47600019 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| A global reference for human genetic variation | Q25909434 | ||
| Rare-variant association analysis: study designs and statistical tests | Q26852733 | ||
| A method and server for predicting damaging missense mutations | Q27860835 | ||
| Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits | Q28239018 | ||
| Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel | Q28607364 | ||
| Pooled association tests for rare variants in exon-resequencing studies | Q28743126 | ||
| A new initiative on precision medicine | Q29615654 | ||
| A general framework for estimating the relative pathogenicity of human genetic variants | Q29615730 | ||
| Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project | Q30275850 | ||
| Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction | Q30301147 | ||
| Loss-of-function mutations in APOC3, triglycerides, and coronary disease | Q30408720 | ||
| Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks | Q30411387 | ||
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol | Q30411390 | ||
| Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis | Q30452653 | ||
| Variant association tools for quality control and analysis of large-scale sequence and genotyping array data | Q30813514 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| Proper analysis of secondary phenotype data in case-control association studies | Q33389080 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions | Q33728642 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| Defining the role of common variation in the genomic and biological architecture of adult human height | Q34441746 | ||
| The UK10K project identifies rare variants in health and disease | Q34494047 | ||
| Obama's Precision Medicine Initiative | Q35180917 | ||
| Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies | Q36152947 | ||
| A unified mixed-effects model for rare-variant association in sequencing studies | Q37088008 | ||
| Power of deep, all-exon resequencing for discovery of human trait genes | Q37129418 | ||
| Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps | Q37613798 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 395-396 | |
| P577 | publication date | 2017-01-25 | |
| P1433 | published in | European Journal of Human Genetics | Q2155433 |
| P1476 | title | From exomes to genomes: challenges and solutions in population-based genetic association studies | |
| P478 | volume | 25 |
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