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.
132 related articles for article (PubMed ID: 33565109)
1. A Bayesian hierarchically structured prior for rare-variant association testing. Yang Y; Basu S; Zhang L Genet Epidemiol; 2021 Jun; 45(4):413-424. PubMed ID: 33565109 [TBL] [Abstract][Full Text] [Related]
2. A Bayesian hierarchically structured prior for gene-based association testing with multiple traits in genome-wide association studies. Yang Y; Basu S; Zhang L Genet Epidemiol; 2022 Feb; 46(1):63-72. PubMed ID: 34787916 [TBL] [Abstract][Full Text] [Related]
3. A Bayesian hierarchical variable selection prior for pathway-based GWAS using summary statistics. Yang Y; Basu S; Zhang L Stat Med; 2020 Mar; 39(6):724-739. PubMed ID: 31777110 [TBL] [Abstract][Full Text] [Related]
4. Testing rare variants for association with diseases: a Bayesian marker selection approach. Zhang L; Pei YF; Hai R; Lin Y; Deng HW Ann Hum Genet; 2012 Jan; 76(1):74-85. PubMed ID: 22034989 [TBL] [Abstract][Full Text] [Related]
5. Bayesian detection of causal rare variants under posterior consistency. Liang F; Xiong M PLoS One; 2013; 8(7):e69633. PubMed ID: 23922764 [TBL] [Abstract][Full Text] [Related]
6. Dynamic Bayesian testing of sets of variants in complex diseases. Zhang Y; Ghosh S; Hakonarson H Genetics; 2014 Nov; 198(3):867-78. PubMed ID: 25217050 [TBL] [Abstract][Full Text] [Related]
7. Bayesian model comparison for rare-variant association studies. Venkataraman GR; DeBoever C; Tanigawa Y; Aguirre M; Ioannidis AG; Mostafavi H; Spencer CCA; Poterba T; Bustamante CD; Daly MJ; Pirinen M; Rivas MA Am J Hum Genet; 2021 Dec; 108(12):2354-2367. PubMed ID: 34822764 [TBL] [Abstract][Full Text] [Related]
8. Incorporating model uncertainty in detecting rare variants: the Bayesian risk index. Quintana MA; Berstein JL; Thomas DC; Conti DV Genet Epidemiol; 2011 Nov; 35(7):638-49. PubMed ID: 22009789 [TBL] [Abstract][Full Text] [Related]
9. A Bayesian Gene-Based Genome-Wide Association Study Analysis of Osteosarcoma Trio Data Using a Hierarchically Structured Prior. Yang Y; Basu S; Mirabello L; Spector L; Zhang L Cancer Inform; 2018; 17():1176935118775103. PubMed ID: 29844655 [TBL] [Abstract][Full Text] [Related]
10. Part 1. Statistical Learning Methods for the Effects of Multiple Air Pollution Constituents. Coull BA; Bobb JF; Wellenius GA; Kioumourtzoglou MA; Mittleman MA; Koutrakis P; Godleski JJ Res Rep Health Eff Inst; 2015 Jun; (183 Pt 1-2):5-50. PubMed ID: 26333238 [TBL] [Abstract][Full Text] [Related]
11. A Bayesian Partitioning Model for the Detection of Multilocus Effects in Case-Control Studies. Ray D; Li X; Pan W; Pankow JS; Basu S Hum Hered; 2015; 79(2):69-79. PubMed ID: 26044550 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. A novel association test for rare variants based on algebraic statistics. Meng J; Zhu W; Li C; Jon K J Theor Biol; 2020 May; 493():110228. PubMed ID: 32135159 [TBL] [Abstract][Full Text] [Related]
14. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Lee S; Emond MJ; Bamshad MJ; Barnes KC; Rieder MJ; Nickerson DA; ; Christiani DC; Wurfel MM; Lin X Am J Hum Genet; 2012 Aug; 91(2):224-37. PubMed ID: 22863193 [TBL] [Abstract][Full Text] [Related]
15. A fast algorithm for Bayesian multi-locus model in genome-wide association studies. Duan W; Zhao Y; Wei Y; Yang S; Bai J; Shen S; Du M; Huang L; Hu Z; Chen F Mol Genet Genomics; 2017 Aug; 292(4):923-934. PubMed ID: 28534238 [TBL] [Abstract][Full Text] [Related]
16. Bayesian meta-analysis across genome-wide association studies of diverse phenotypes. Trochet H; Pirinen M; Band G; Jostins L; McVean G; Spencer CCA Genet Epidemiol; 2019 Jul; 43(5):532-547. PubMed ID: 30920090 [TBL] [Abstract][Full Text] [Related]
17. Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis. Yan Q; Tiwari HK; Yi N; Lin WY; Gao G; Lou XY; Cui X; Liu N Genet Epidemiol; 2014 Jul; 38(5):447-56. PubMed ID: 24849109 [TBL] [Abstract][Full Text] [Related]
18. Powerful rare variant association testing in a copula-based joint analysis of multiple phenotypes. Konigorski S; Yilmaz YE; Janke J; Bergmann MM; Boeing H; Pischon T Genet Epidemiol; 2020 Jan; 44(1):26-40. PubMed ID: 31732979 [TBL] [Abstract][Full Text] [Related]
19. A novel bayesian graphical model for genome-wide multi-SNP association mapping. Zhang Y Genet Epidemiol; 2012 Jan; 36(1):36-47. PubMed ID: 22127647 [TBL] [Abstract][Full Text] [Related]
20. A fast and efficient approach for gene-based association studies of ordinal phenotypes. Li N; Chen L; Zhou Y; Wei Q Stat Appl Genet Mol Biol; 2023 Jan; 22(1):. PubMed ID: 36724206 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]