| scholarly article | Q13442814 |
| P2093 | author name string | Dan-Yu Lin | |
| Zheng-Zheng Tang | |||
| P2860 | cites work | Are rare variants responsible for susceptibility to complex diseases? | Q22337172 |
| Genome-wide association studies for complex traits: consensus, uncertainty and challenges | Q24550632 | ||
| Meta-analysis in clinical trials | Q27860779 | ||
| Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes | Q28680760 | ||
| Pooled association tests for rare variants in exon-resequencing studies | Q28743126 | ||
| Generating samples under a Wright-Fisher neutral model of genetic variation | Q29547168 | ||
| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants | Q29547210 | ||
| Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels | Q29547214 | ||
| Evolution and functional impact of rare coding variation from deep sequencing of human exomes | Q29617587 | ||
| NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy | Q29617901 | ||
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol | Q30411390 | ||
| Heterogeneity in meta-analyses of genome-wide association investigations | Q33297003 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| Extending DerSimonian and Laird's methodology to perform multivariate random effects meta-analyses | Q33437753 | ||
| Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups | Q33701819 | ||
| Testing for an unusual distribution of rare variants | Q33847792 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution | Q34142739 | ||
| Interpreting meta-analyses of genome-wide association studies | Q34187048 | ||
| On the relative efficiency of using summary statistics versus individual-level data in meta-analysis | Q34437384 | ||
| Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies | Q35136958 | ||
| A general framework for detecting disease associations with rare variants in sequencing studies | Q35204927 | ||
| Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies | Q36152947 | ||
| Required sample size and nonreplicability thresholds for heterogeneous genetic associations | Q36392953 | ||
| Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms | Q36477625 | ||
| Haplotype-based association analysis via variance-components score test. | Q36492182 | ||
| MASS: meta-analysis of score statistics for sequencing studies | Q36985001 | ||
| General framework for meta-analysis of rare variants in sequencing association studies | Q37010430 | ||
| Quantitative trait analysis in sequencing studies under trait-dependent sampling | Q37049572 | ||
| Meta-analysis of gene-level associations for rare variants based on single-variant statistics | Q37083452 | ||
| Power of deep, all-exon resequencing for discovery of human trait genes | Q37129418 | ||
| Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design? | Q37377502 | ||
| Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL. | Q37389540 | ||
| Meta-analysis of gene-level tests for rare variant association | Q37610893 | ||
| Meta-analysis methods for genome-wide association studies and beyond | Q38105261 | ||
| A method of moments estimator for random effect multivariate meta-analysis | Q39855140 | ||
| An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 | ||
| An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people | Q43136367 | ||
| Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: case-control study and meta-analysis. | Q46014654 | ||
| Novel rare mutations and promoter haplotypes in ABCA1 contribute to low-HDL-C levels. | Q46805420 | ||
| A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). | Q51928874 | ||
| P433 | issue | 5 | |
| P921 | main subject | meta-analysis | Q815382 |
| P304 | page(s) | 389-401 | |
| P577 | publication date | 2014-05-05 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Meta-analysis of sequencing studies with heterogeneous genetic associations | |
| P478 | volume | 38 |
| Q41242738 | A novel random effect model for GWAS meta-analysis and its application to trans-ethnic meta-analysis |
| Q35489723 | A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing |
| Q91919712 | An adaptive test for meta-analysis of rare variant association studies |
| Q38843404 | Discovery of rare variants for complex phenotypes. |
| Q36071282 | Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models |
| Q91315232 | General retrospective mega-analysis framework for rare variant association tests |
| Q38744262 | Integrative gene set enrichment analysis utilizing isoform-specific expression |
| Q37143043 | Meta-Analysis of Rare Variant Association Tests in Multiethnic Populations |
| Q48157613 | Meta-analysis approaches to combine multiple gene set enrichment studies |
| Q40816303 | Meta-analysis for Discovering Rare-Variant Associations: Statistical Methods and Software Programs |
| Q92228662 | Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits |
| Q96171658 | Multi-trait analysis of rare-variant association summary statistics using MTAR |
| Q36280271 | PreMeta: a tool to facilitate meta-analysis of rare-variant associations |
| Q90281013 | Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes |
| Q90663950 | Rare-variant collapsing analyses for complex traits: guidelines and applications |
| Q38386637 | SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations |
| Q92669095 | Subset testing and analysis of multiple phenotypes |
| Q28383497 | Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations |
| Q91639265 | metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies |
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