| scholarly article | Q13442814 |
| P2093 | author name string | Wei Pan | |
| Saonli Basu | |||
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| Some results on Tchebycheffian spline functions | Q56387244 | ||
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| Comprehensive Approach to Analyzing Rare Genetic Variants | Q33745005 | ||
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| So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests | Q36512128 | ||
| A powerful and flexible multilocus association test for quantitative traits | Q37149380 | ||
| Power comparisons between similarity-based multilocus association methods, logistic regression, and score tests for haplotypes | Q37172191 | ||
| Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility | Q37699224 | ||
| Genomic similarity and kernel methods II: methods for genomic information | Q37770382 | ||
| Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations | Q37770834 | ||
| Statistical analysis strategies for association studies involving rare variants | Q37799723 | ||
| Rare Variant Association Analysis Methods for Complex Traits | Q37806780 | ||
| A global test for groups of genes: testing association with a clinical outcome | Q38522319 | ||
| P433 | issue | 7 | |
| P921 | main subject | statistics | Q12483 |
| P304 | page(s) | 606-619 | |
| P577 | publication date | 2011-07-18 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Comparison of statistical tests for disease association with rare variants | |
| P478 | volume | 35 |
| Q41873773 | A Bayesian Hierarchical Model for Relating Multiple SNPs within Multiple Genes to Disease Risk |
| Q91867827 | A Family-Based Rare Haplotype Association Method for Quantitative Traits |
| Q40788285 | A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants. |
| Q40040125 | A Powerful Variant-Set Association Test Based on Chi-Square Distribution |
| Q40261222 | A combination test for detection of gene-environment interaction in cohort studies. |
| Q38597100 | A gene-based test of association through an orthogonal decomposition of genotype scores |
| Q54431091 | A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus. |
| Q37031565 | A geometric framework for evaluating rare variant tests of association |
| Q91379638 | A linear mixed model framework for gene-based gene-environment interaction tests in twin studies |
| Q37525404 | A method to incorporate prior information into score test for genetic association studies |
| Q47133696 | A non-threshold region-specific method for detecting rare variants in complex diseases. |
| Q35170645 | A permutation test for oligoset DNA pooling studies |
| Q34016536 | A powerful and adaptive association test for rare variants |
| Q38822421 | A powerful microbiome-based association test and a microbial taxa discovery framework for comprehensive association mapping. |
| Q35922896 | A powerful test for multiple rare variants association studies that incorporates sequencing qualities |
| Q35447555 | A robust GWSS method to simultaneously detect rare and common variants for complex disease |
| Q30578001 | A unified method for detecting secondary trait associations with rare variants: application to sequence data |
| Q30599570 | A variance component based multi-marker association test using family and unrelated data. |
| Q30578631 | A variational Bayes discrete mixture test for rare variant association |
| Q42639822 | Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants |
| Q41004097 | Adjustment for population stratification via principal components in association analysis of rare variants |
| Q52370685 | Advances in the Genetics of Hypertension: The Effect of Rare Variants. |
| Q93234377 | An optimal kernel-based U-statistic method for quantitative gene-set association analysis |
| Q47848108 | An optimum projection and noise reduction approach for detecting rare and common variants associated with complex diseases |
| Q38903902 | Are rare variants really independent? |
| Q37182574 | Assessing association between protein truncating variants and quantitative traits |
| Q35799275 | Assessing the Power of Exome Chips |
| Q39382116 | Associating rare genetic variants with human diseases |
| Q52318656 | Association analysis of multiple traits by an approach of combining P values. |
| Q30800931 | Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic |
| Q47352396 | Association detection between ordinal trait and rare variants based on adaptive combination of P values |
| Q51095276 | Bayesian latent variable collapsing model for detecting rare variant interaction effect in twin study. |
| Q36605794 | Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study |
| Q24627723 | Beyond the fourth wave of genome-wide obesity association studies |
| Q39604108 | Block-based association tests for rare variants using Kullback-Leibler divergence |
| Q37218511 | Boosting the Power of the Sequence Kernel Association Test by Properly Estimating Its Null Distribution |
| Q30879444 | Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data |
| Q37096365 | Comparison of haplotype-based statistical tests for disease association with rare and common variants |
| Q34559821 | Comparison of similarity-based tests and pooling strategies for rare variants |
| Q36386480 | Comparison of single-marker and multi-marker tests in rare variant association studies of quantitative traits. |
| Q41827728 | Comparison of statistical tests for group differences in brain functional networks |
| Q44102840 | Comparison of three summary statistics for ranking genes in genome-wide association studies. |
| Q37035863 | Conditioning adaptive combination of P-values method to analyze case-parent trios with or without population controls |
| Q50798327 | Detecting association of rare and common variants by adaptive combination of P-values. |
| Q36060594 | Detecting associations of rare variants with common diseases: collapsing or haplotyping? |
| Q41316117 | Detecting disease association signals with multiple genetic variants and covariates |
| Q30654520 | Detecting genomic clustering of risk variants from sequence data: cases versus controls. |
| Q42109315 | Detecting rare variant effects using extreme phenotype sampling in sequencing association studies |
| Q36506772 | Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
| Q38662558 | DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease |
| Q34471680 | Dynamic Bayesian testing of sets of variants in complex diseases |
| Q40536938 | Efficient unified rare variant association test by modeling the population genetic distribution in case-control studies. |
| Q37689468 | Evaluating the impact of genotype errors on rare variant tests of association |
| Q27499091 | Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes |
| Q39364566 | Exome Variant Analysis of Chronic Periodontitis in 2 Large Cohort Studies |
| Q37056084 | Exome sequencing and the genetic basis of complex traits |
| Q30587122 | Family-based association tests for sequence data, and comparisons with population-based association tests |
| Q35920852 | Filtering genetic variants and placing informative priors based on putative biological function. |
| Q40090917 | Generalization of Rare Variant Association Tests for Longitudinal Family Studies |
| Q47579970 | Genetic architecture: the shape of the genetic contribution to human traits and disease |
| Q38218925 | Genetic studies of Crohn's disease: past, present and future |
| Q33976828 | Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. |
| Q30869613 | Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data |
| Q36495251 | How the effects of aging and stresses of life are integrated in mortality rates: insights for genetic studies of human health and longevity |
| Q40813909 | How to make DNA methylome wide association studies more powerful |
| Q30846819 | Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model |
| Q34085279 | Identifying rare variants associated with hypertension using the C-alpha test |
| Q38705442 | Improving power for rare-variant tests by integrating external controls |
| Q38274665 | Imputation of rare variants in next-generation association studies |
| Q89645874 | Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analyses |
| Q47243152 | Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies. |
| Q30408390 | Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants |
| Q40283155 | Investigation of the role of TCF4 rare sequence variants in schizophrenia |
| Q34216699 | Joint rare variant association test of the average and individual effects for sequencing studies |
| Q37160445 | Kernel machine SNP-set testing under multiple candidate kernels |
| Q30932501 | Kullback-Leibler distance methods for detecting disease association with rare variants from sequencing data |
| Q34010750 | Longitudinal analysis is more powerful than cross-sectional analysis in detecting genetic association with neuroimaging phenotypes |
| Q33677747 | Longitudinal data analysis for rare variants detection with penalized quadratic inference function |
| Q38219242 | Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits |
| Q30841933 | Methods for collapsing multiple rare variants in whole-genome sequence data |
| Q30621608 | Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data |
| Q30376535 | Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense. |
| Q37485550 | On Robust Association Testing for Quantitative Traits and Rare Variants. |
| Q34149953 | On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing. |
| Q31065241 | Optimal tests for rare variant effects in sequencing association studies |
| Q36152947 | Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies |
| Q39084727 | PERCH: A Unified Framework for Disease Gene Prioritization |
| Q52602399 | Pathogenic Germline Variants in 10,389 Adult Cancers. |
| Q36437964 | Patterns and functional implications of rare germline variants across 12 cancer types |
| Q39759238 | Penalized regression approaches to testing for quantitative trait-rare variant association |
| Q30857114 | Performance of statistical methods on CHARGE targeted sequencing data |
| Q41908748 | Permutation testing in the presence of polygenic variation |
| Q36902678 | Phenotypic extremes in rare variant study designs |
| Q36910604 | Power Calculation of Multi-step Combined Principal Components with Applications to Genetic Association Studies |
| Q37646569 | Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes |
| Q31149258 | Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19. |
| Q34597952 | Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect. |
| Q51076379 | Rank-based tests for identifying multiple genetic variants associated with quantitative traits. |
| Q36063830 | Rare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus Level |
| Q42141782 | Rare genetic variants and treatment response: sample size and analysis issues |
| Q47563247 | Rare variant association analysis in case-parents studies by allowing for missing parental genotypes |
| Q37484322 | Rare variant association testing by adaptive combination of P-values |
| Q35133493 | Rare variants detection with kernel machine learning based on likelihood ratio test |
| Q26852733 | Rare-variant association analysis: study designs and statistical tests |
| Q38084443 | Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits |
| Q61445253 | Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico |
| Q36392512 | Region-based association tests for sequencing data on survival traits |
| Q42426913 | Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging |
| Q87405700 | Robust and powerful tests for rare variants using Fisher's method to combine evidence of association from two or more complementary tests |
| Q34255847 | SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations |
| Q37543773 | Searching for missing heritability: designing rare variant association studies |
| Q34778042 | SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies |
| Q36909285 | Sequence kernel association tests for the combined effect of rare and common variants |
| Q34057033 | Sequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study |
| Q33981063 | Sequencing studies in human genetics: design and interpretation. |
| Q55261515 | Set-Based Tests for the Gene-Environment Interaction in Longitudinal Studies. |
| Q42795627 | Some surprising twists on the road to discovering the contribution of rare variants to complex diseases |
| Q95819232 | Statistical Method Based on Bayes-Type Empirical Score Test for Assessing Genetic Association with Multilocus Genotype Data |
| Q38205106 | Statistical power and significance testing in large-scale genetic studies |
| Q28655423 | Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study |
| Q34737989 | Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation |
| Q42207015 | Targeted deep resequencing of ALOX5 and ALOX5AP in patients with diabetes and association of rare variants with leukotriene pathways |
| Q36522128 | Test for rare variants by environment interactions in sequencing association studies |
| Q30579877 | Testing for association with multiple traits in generalized estimation equations, with application to neuroimaging data |
| Q39883188 | Testing for polygenic effects in genome-wide association studies. |
| Q94948752 | The exhaustive genomic scan approach, with an application to rare-variant association analysis |
| Q36410191 | The genetics of sudden cardiac death |
| Q33613854 | The impact of rare and low-frequency genetic variants in common disease |
| Q35612748 | The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease |
| Q89848369 | Two-phase SSU and SKAT in genetic association studies |
| Q26828744 | Two-phase and family-based designs for next-generation sequencing studies |
| Q42161561 | Two-stage extreme phenotype sequencing design for discovering and testing common and rare genetic variants: efficiency and power |
| Q38227818 | Using population isolates in genetic association studies |
| Q39368271 | Utilising family-based designs for detecting rare variant disease associations |
| Q30813514 | Variant association tools for quality control and analysis of large-scale sequence and genotyping array data |
| Q35798977 | Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies |
| Q34151873 | Weighted selective collapsing strategy for detecting rare and common variants in genetic association study |
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