| scholarly article | Q13442814 |
| P50 | author | Guodong Wu | Q84424876 |
| P2093 | author name string | Degui Zhi | |
| P2860 | cites work | Finding the missing heritability of complex diseases | Q22122198 |
| Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 | ||
| From genomics to chemical genomics: new developments in KEGG | Q24538628 | ||
| Targeted capture and massively parallel sequencing of 12 human exomes | Q24615381 | ||
| A map of human genome variation from population-scale sequencing | Q24617794 | ||
| A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals | Q24644474 | ||
| ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data | Q29547161 | ||
| The variant call format and VCFtools | Q29614172 | ||
| Personal genomes: The case of the missing heritability | Q29614582 | ||
| Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 | ||
| Evolution and functional impact of rare coding variation from deep sequencing of human exomes | Q29617587 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| GSEA-SNP: applying gene set enrichment analysis to SNP data from genome-wide association studies | Q33375904 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| Associations of IL6 polymorphisms with lung function decline and COPD. | Q33808582 | ||
| A new testing strategy to identify rare variants with either risk or protective effect on disease | Q33815362 | ||
| SNP-based pathway enrichment analysis for genome-wide association studies | Q33874378 | ||
| Leptin receptor polymorphisms and lung function decline in COPD | Q33917491 | ||
| Discovering statistically significant pathways in expression profiling studies | Q33943511 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| GSA-SNP: a general approach for gene set analysis of polymorphisms | Q33957397 | ||
| Genome-wide gene and pathway analysis. | Q34076975 | ||
| The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals | Q34154481 | ||
| Replication Strategies for Rare Variant Complex Trait Association Studies via Next-Generation Sequencing | Q34381743 | ||
| Principal-component analysis for assessment of population stratification in mitochondrial medical genetics | Q34544496 | ||
| Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level | Q35167237 | ||
| Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship | Q35197544 | ||
| Bayesian analysis of rare variants in genetic association studies | Q35435860 | ||
| Medical sequencing at the extremes of human body mass | Q35752505 | ||
| Using the gene ontology to scan multilevel gene sets for associations in genome wide association studies | Q35846303 | ||
| A powerful test for multiple rare variants association studies that incorporates sequencing qualities | Q35922896 | ||
| Estimation of effect size distribution from genome-wide association studies and implications for future discoveries | Q36191121 | ||
| Pathway-based approaches for analysis of genomewide association studies | Q36512103 | ||
| Exome sequencing and the genetic basis of complex traits | Q37056084 | ||
| Power of deep, all-exon resequencing for discovery of human trait genes | Q37129418 | ||
| Transforming growth factor-beta receptor-3 is associated with pulmonary emphysema | Q37343767 | ||
| Statistical analysis strategies for association studies involving rare variants | Q37799723 | ||
| Rare Variant Association Analysis Methods for Complex Traits | Q37806780 | ||
| Analysing biological pathways in genome-wide association studies | Q37810464 | ||
| Gene set analysis of genome-wide association studies: methodological issues and perspectives | Q37874759 | ||
| Methods for detecting and correcting for population stratification | Q37999301 | ||
| An evaluation of statistical approaches to rare variant analysis in genetic association studies | Q39941009 | ||
| Linkage strategies for genetically complex traits. I. Multilocus models | Q40623210 | ||
| An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people | Q43136367 | ||
| Trend tests for case-control studies of genetic markers: power, sample size and robustness | Q47180831 | ||
| Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish Family-Cancer Database | Q52041429 | ||
| Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance--a population-based twin study | Q54103713 | ||
| Design of the Lung Health Study: a randomized clinical trial of early intervention for chronic obstructive pulmonary disease | Q54243123 | ||
| Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants | Q57087763 | ||
| Transforming growth factor-beta1 polymorphisms, airway responsiveness and lung function decline in smokers | Q79312647 | ||
| P433 | issue | 5 | |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | 478-494 | |
| P577 | publication date | 2013-05-05 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Pathway-based approaches for sequencing-based genome-wide association studies | |
| P478 | volume | 37 |
| Q36226770 | A Data Fusion Approach to Enhance Association Study in Epilepsy. |
| Q47159542 | A Review of Pathway-Based Analysis Tools That Visualize Genetic Variants |
| Q47878052 | Alzheimer disease: modeling an Aβ-centered biological network |
| Q36068307 | An Optimal Bahadur-Efficient Method in Detection of Sparse Signals with Applications to Pathway Analysis in Sequencing Association Studies |
| Q90444258 | Gene-level genome-wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population |
| Q34429995 | Missing genetic risk in neural tube defects: can exome sequencing yield an insight? |
| Q39429370 | Pathway-based approach using hierarchical components of collapsed rare variants |
| Q38851955 | Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies |
| Q38293376 | Recent advances in systemic lupus erythematosus genetics in an Asian population |
| Q37222581 | Whole exome sequencing of extreme age-related macular degeneration phenotypes |
| Q40431321 | Whole-Exome Sequencing to Identify Novel Biological Pathways Associated With Infertility After Pelvic Inflammatory Disease |
| Q38955754 | gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels |
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