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.
90 related articles for article (PubMed ID: 26784232)
21. Analysis of Sequence Data Under Multivariate Trait-Dependent Sampling. Tao R; Zeng D; Franceschini N; North KE; Boerwinkle E; Lin DY J Am Stat Assoc; 2015 Jun; 110(510):560-572. PubMed ID: 26366025 [TBL] [Abstract][Full Text] [Related]
22. Kullback-Leibler distance methods for detecting disease association with rare variants from sequencing data. Turkmen AS; Yan Z; Hu YQ; Lin S Ann Hum Genet; 2015 May; 79(3):199-208. PubMed ID: 25875492 [TBL] [Abstract][Full Text] [Related]
23. GMEPS: a fast and efficient likelihood approach for genome-wide mediation analysis under extreme phenotype sequencing. Liyanage JSS; Estepp JH; Srivastava K; Li Y; Mori M; Kang G Stat Appl Genet Mol Biol; 2022 Mar; 21(1):. PubMed ID: 35266368 [TBL] [Abstract][Full Text] [Related]
24. Detection of rare variant effects in association studies: extreme values, iterative regression, and a hybrid approach. Zhang Z; Sha Q; Wang X; Zhang S BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S112. PubMed ID: 22373188 [TBL] [Abstract][Full Text] [Related]
25. Statistical power of association using the extreme discordant phenotype design. Zhang G; Nebert DW; Chakraborty R; Jin L Pharmacogenet Genomics; 2006 Jun; 16(6):401-13. PubMed ID: 16708049 [TBL] [Abstract][Full Text] [Related]
26. Comparison of statistical approaches to rare variant analysis for quantitative traits. Chen H; Hendricks AE; Cheng Y; Cupples AL; Dupuis J; Liu CT BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S113. PubMed ID: 22373209 [TBL] [Abstract][Full Text] [Related]
27. Are quantitative trait-dependent sampling designs cost-effective for analysis of rare and common variants? Yilmaz YE; Bull SB BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S111. PubMed ID: 22373146 [TBL] [Abstract][Full Text] [Related]
28. Test Gene-Environment Interactions for Multiple Traits in Sequencing Association Studies. Zhang J; Sha Q; Hao H; Zhang S; Gao XR; Wang X Hum Hered; 2019; 84(4-5):170-196. PubMed ID: 32417835 [TBL] [Abstract][Full Text] [Related]
29. Identifying rare and common variants with Bayesian variable selection. Oh C BMC Proc; 2016; 10(Suppl 7):379-384. PubMed ID: 27980665 [TBL] [Abstract][Full Text] [Related]
30. A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data. Liu DJ; Leal SM Eur J Hum Genet; 2012 Apr; 20(4):449-56. PubMed ID: 22166943 [TBL] [Abstract][Full Text] [Related]
31. Testing rare variants for hypertension using family-based tests with different weighting schemes. Wang X; Zhao X; Zhou J BMC Proc; 2016; 10(Suppl 7):233-237. PubMed ID: 27980642 [TBL] [Abstract][Full Text] [Related]
33. A novel statistical method for rare-variant association studies in general pedigrees. Zhu H; Wang Z; Wang X; Sha Q BMC Proc; 2016; 10(Suppl 7):193-196. PubMed ID: 27980635 [TBL] [Abstract][Full Text] [Related]
34. Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data. Derkach A; Lawless JF; Merico D; Paterson AD; Sun L BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S9. PubMed ID: 25519417 [TBL] [Abstract][Full Text] [Related]
35. Evaluation of the power and type I error of recently proposed family-based tests of association for rare variants. Hainline A; Alvarez C; Luedtke A; Greco B; Beck A; Tintle NL BMC Proc; 2014; 8(Suppl 1):S36. PubMed ID: 25519321 [TBL] [Abstract][Full Text] [Related]
36. Detecting association of rare and common variants by testing an optimally weighted combination of variants with longitudinal data. Wang S; Fang S; Sha Q; Zhang S BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S91. PubMed ID: 25519418 [TBL] [Abstract][Full Text] [Related]
38. Working in extreme settings. Caulfield A BMJ; 2016 Oct; 355():i3879. PubMed ID: 31055322 [No Abstract] [Full Text] [Related]
39. A Cautionary Note on the Effects of Population Stratification Under an Extreme Phenotype Sampling Design. Panarella M; Burkett KM Front Genet; 2019; 10():398. PubMed ID: 31130982 [TBL] [Abstract][Full Text] [Related]