These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
170 related articles for article (PubMed ID: 29545466)
1. Reexamining Dis/Similarity-Based Tests for Rare-Variant Association with Case-Control Samples. Wang C; Tzeng JY; Wu PZ; Preisig M; Hsiao CK Genetics; 2018 May; 209(1):105-113. PubMed ID: 29545466 [TBL] [Abstract][Full Text] [Related]
2. Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico. Zhang X; Basile AO; Pendergrass SA; Ritchie MD BMC Bioinformatics; 2019 Jan; 20(1):46. PubMed ID: 30669967 [TBL] [Abstract][Full Text] [Related]
3. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants. Kinnamon DD; Hershberger RE; Martin ER PLoS One; 2012; 7(2):e30238. PubMed ID: 22363423 [TBL] [Abstract][Full Text] [Related]
4. Comparison of methods and sampling designs to test for association between rare variants and quantitative traits. Bacanu SA; Nelson MR; Whittaker JC Genet Epidemiol; 2011 May; 35(4):226-35. PubMed ID: 21370253 [TBL] [Abstract][Full Text] [Related]
5. Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples. Yan Q; Weeks DE; Tiwari HK; Yi N; Zhang K; Gao G; Lin WY; Lou XY; Chen W; Liu N Hum Hered; 2015; 80(3):126-38. PubMed ID: 27161037 [TBL] [Abstract][Full Text] [Related]
6. Comparison of common burden tests for genetic association studies of rare variants. Lin XQ; Liang R; Zhang JG; Pi LC; Chen SD; Liu L; Gao YH Yi Chuan; 2018 Feb; 40(2):162-169. PubMed ID: 29428909 [TBL] [Abstract][Full Text] [Related]
7. A powerful approach to test an optimally weighted combination of rare variants in admixed populations. Wang X; Zhang S; Li Y; Li M; Sha Q Genet Epidemiol; 2015 May; 39(4):294-305. PubMed ID: 25758547 [TBL] [Abstract][Full Text] [Related]
8. Trans-ethnic meta-analysis of rare variants in sequencing association studies. Shi J; Boehnke M; Lee S Biostatistics; 2021 Oct; 22(4):706-722. PubMed ID: 31883325 [TBL] [Abstract][Full Text] [Related]
10. Selection Probability for Rare Variant Association Studies. Lee G; Sun H J Comput Biol; 2017 May; 24(5):400-411. PubMed ID: 28281787 [TBL] [Abstract][Full Text] [Related]
11. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease. Persyn E; Karakachoff M; Le Scouarnec S; Le Clézio C; Campion D; Consortium FE; Schott JJ; Redon R; Bellanger L; Dina C PLoS One; 2017; 12(7):e0179364. PubMed ID: 28742119 [TBL] [Abstract][Full Text] [Related]
12. Robust and Powerful Affected Sibpair Test for Rare Variant Association. Lin KH; Zöllner S Genet Epidemiol; 2015 Jul; 39(5):325-33. PubMed ID: 25966809 [TBL] [Abstract][Full Text] [Related]
13. Two adaptive weighting methods to test for rare variant associations in family-based designs. Fang S; Sha Q; Zhang S Genet Epidemiol; 2012 Jul; 36(5):499-507. PubMed ID: 22674630 [TBL] [Abstract][Full Text] [Related]
14. Meta-analysis of Complex Diseases at Gene Level with Generalized Functional Linear Models. Fan R; Wang Y; Chiu CY; Chen W; Ren H; Li Y; Boehnke M; Amos CI; Moore JH; Xiong M Genetics; 2016 Feb; 202(2):457-70. PubMed ID: 26715663 [TBL] [Abstract][Full Text] [Related]
15. Likelihood ratio tests in rare variant detection for continuous phenotypes. Zeng P; Zhao Y; Liu J; Liu L; Zhang L; Wang T; Huang S; Chen F Ann Hum Genet; 2014 Sep; 78(5):320-32. PubMed ID: 25117149 [TBL] [Abstract][Full Text] [Related]
16. Methods for association analysis and meta-analysis of rare variants in families. Feng S; Pistis G; Zhang H; Zawistowski M; Mulas A; Zoledziewska M; Holmen OL; Busonero F; Sanna S; Hveem K; Willer C; Cucca F; Liu DJ; Abecasis GR Genet Epidemiol; 2015 May; 39(4):227-38. PubMed ID: 25740221 [TBL] [Abstract][Full Text] [Related]
17. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis. Chen R; Wei Q; Zhan X; Zhong X; Sutcliffe JS; Cox NJ; Cook EH; Li C; Chen W; Li B Bioinformatics; 2015 May; 31(9):1452-9. PubMed ID: 25568282 [TBL] [Abstract][Full Text] [Related]
18. Robust methods to detect disease-genotype association in genetic association studies: calculate p-values using exact conditional enumeration instead of simulated permutations or asymptotic approximations. Langaas M; Bakke Ø Stat Appl Genet Mol Biol; 2014 Dec; 13(6):675-92. PubMed ID: 25324457 [TBL] [Abstract][Full Text] [Related]
19. Rare variant association testing for multicategory phenotype. Bocher O; Marenne G; Saint Pierre A; Ludwig TE; Guey S; Tournier-Lasserve E; Perdry H; Génin E Genet Epidemiol; 2019 Sep; 43(6):646-656. PubMed ID: 31087445 [TBL] [Abstract][Full Text] [Related]
20. A new association test using haplotype similarity. Sha Q; Chen HS; Zhang S Genet Epidemiol; 2007 Sep; 31(6):577-93. PubMed ID: 17443704 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]