172 related articles for article (PubMed ID: 29545466)
21. Rare variant association testing for next-generation sequencing data via hierarchical clustering.
Tachmazidou I; Morris A; Zeggini E
Hum Hered; 2012; 74(3-4):165-71. PubMed ID: 23594494
[TBL] [Abstract][Full Text] [Related]
22. Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method.
Yan Q; Weeks DE; Celedón JC; Tiwari HK; Li B; Wang X; Lin WY; Lou XY; Gao G; Chen W; Liu N
Genetics; 2015 Dec; 201(4):1329-39. PubMed ID: 26482791
[TBL] [Abstract][Full Text] [Related]
23. Leveraging Family History in Case-Control Analyses of Rare Variation.
Solis-Lemus CR; Fischer ST; Todor A; Liu C; Leslie EJ; Cutler DJ; Ghosh D; Epstein MP
Genetics; 2020 Feb; 214(2):295-303. PubMed ID: 31843756
[TBL] [Abstract][Full Text] [Related]
24. Bayesian analysis of rare variants in genetic association studies.
Yi N; Zhi D
Genet Epidemiol; 2011 Jan; 35(1):57-69. PubMed ID: 21181897
[TBL] [Abstract][Full Text] [Related]
25. A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data.
Wang P; Rahman M; Jin L; Xiong M
BMC Genomics; 2016 Nov; 17(1):881. PubMed ID: 27821073
[TBL] [Abstract][Full Text] [Related]
26. A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.
Broadaway KA; Cutler DJ; Duncan R; Moore JL; Ware EB; Jhun MA; Bielak LF; Zhao W; Smith JA; Peyser PA; Kardia SLR; Ghosh D; Epstein MP
Am J Hum Genet; 2016 Mar; 98(3):525-540. PubMed ID: 26942286
[TBL] [Abstract][Full Text] [Related]
27. A Novel Statistic for Global Association Testing Based on Penalized Regression.
Austin E; Shen X; Pan W
Genet Epidemiol; 2015 Sep; 39(6):415-26. PubMed ID: 26282998
[TBL] [Abstract][Full Text] [Related]
28. Rare variant association test with multiple phenotypes.
Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
[TBL] [Abstract][Full Text] [Related]
29. Semiparametric Allelic Tests for Mapping Multiple Phenotypes: Binomial Regression and Mahalanobis Distance.
Majumdar A; Witte JS; Ghosh S
Genet Epidemiol; 2015 Dec; 39(8):635-50. PubMed ID: 26493781
[TBL] [Abstract][Full Text] [Related]
30. Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.
Coombes B; Basu S; Guha S; Schork N
PLoS One; 2015; 10(10):e0139355. PubMed ID: 26436424
[TBL] [Abstract][Full Text] [Related]
31. A unified mixed-effects model for rare-variant association in sequencing studies.
Sun J; Zheng Y; Hsu L
Genet Epidemiol; 2013 May; 37(4):334-44. PubMed ID: 23483651
[TBL] [Abstract][Full Text] [Related]
32. A novel rare variants association test for binary traits in family-based designs via copulas.
Dossa HRG; Bureau A; Maziade M; Lakhal-Chaieb L; Oualkacha K
Stat Methods Med Res; 2023 Nov; 32(11):2096-2122. PubMed ID: 37832140
[TBL] [Abstract][Full Text] [Related]
33. A rare variant association test in family-based designs and non-normal quantitative traits.
Lakhal-Chaieb L; Oualkacha K; Richards BJ; Greenwood CM
Stat Med; 2016 Mar; 35(6):905-21. PubMed ID: 26420132
[TBL] [Abstract][Full Text] [Related]
34. Leveraging population information in family-based rare variant association analyses of quantitative traits.
Jiang Y; Ji Y; Sibley AB; Li YJ; Allen AS
Genet Epidemiol; 2017 Feb; 41(2):98-107. PubMed ID: 27917519
[TBL] [Abstract][Full Text] [Related]
35. Statistical properties of single-marker tests for rare variants.
Bigdeli TB; Neale BM; Neale MC
Twin Res Hum Genet; 2014 Jun; 17(3):143-50. PubMed ID: 24739319
[TBL] [Abstract][Full Text] [Related]
36. Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants.
Guey LT; Kravic J; Melander O; Burtt NP; Laramie JM; Lyssenko V; Jonsson A; Lindholm E; Tuomi T; Isomaa B; Nilsson P; Almgren P; Kathiresan S; Groop L; Seymour AB; Altshuler D; Voight BF
Genet Epidemiol; 2011 May; 35(4):236-46. PubMed ID: 21308769
[TBL] [Abstract][Full Text] [Related]
37. BinomiRare: A robust test of the association of a rare variant with a disease for pooled analysis and meta-analysis, with application to the HCHS/SOL.
Sofer T
Genet Epidemiol; 2017 Jul; 41(5):388-395. PubMed ID: 28393384
[TBL] [Abstract][Full Text] [Related]
38. Block-based association tests for rare variants using Kullback-Leibler divergence.
Zhu D; Hu YQ; Lin S
J Hum Genet; 2016 Nov; 61(11):965-975. PubMed ID: 27412875
[TBL] [Abstract][Full Text] [Related]
39. On the substructure controls in rare variant analysis: Principal components or variance components?
Luo Y; Maity A; Wu MC; Smith C; Duan Q; Li Y; Tzeng JY
Genet Epidemiol; 2018 Apr; 42(3):276-287. PubMed ID: 29280188
[TBL] [Abstract][Full Text] [Related]
40. Comparison of similarity-based tests and pooling strategies for rare variants.
Zakharov S; Salim A; Thalamuthu A
BMC Genomics; 2013 Jan; 14():50. PubMed ID: 23343094
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]