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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 22710642)

  • 21. Shrinkage estimation for robust and efficient screening of single-SNP association from case-control genome-wide association studies.
    Luo S; Mukherjee B; Chen J; Chatterjee N
    Genet Epidemiol; 2009 Dec; 33(8):740-50. PubMed ID: 19434716
    [TBL] [Abstract][Full Text] [Related]  

  • 22. On the adjustment for covariates in genetic association analysis: a novel, simple principle to infer direct causal effects.
    Vansteelandt S; Goetgeluk S; Lutz S; Waldman I; Lyon H; Schadt EE; Weiss ST; Lange C
    Genet Epidemiol; 2009 Jul; 33(5):394-405. PubMed ID: 19219893
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A general framework for robust and efficient association analysis in family-based designs: quantitative and dichotomous phenotypes.
    Won S; Lange C
    Stat Med; 2013 Nov; 32(25):4482-98. PubMed ID: 23740776
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies.
    Hoggart CJ; Whittaker JC; De Iorio M; Balding DJ
    PLoS Genet; 2008 Jul; 4(7):e1000130. PubMed ID: 18654633
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A General and Robust Framework for Secondary Traits Analysis.
    Song X; Ionita-Laza I; Liu M; Reibman J; We Y
    Genetics; 2016 Apr; 202(4):1329-43. PubMed ID: 26896329
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comparison of weighting approaches for genetic risk scores in gene-environment interaction studies.
    Hüls A; Krämer U; Carlsten C; Schikowski T; Ickstadt K; Schwender H
    BMC Genet; 2017 Dec; 18(1):115. PubMed ID: 29246113
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes.
    Simcoe MJ; Weisschuh N; Wissinger B; Hysi PG; Hammond CJ
    JAMA Ophthalmol; 2020 Mar; 138(3):294-299. PubMed ID: 31999318
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Feature selection with interactions in logistic regression models using multivariate synergies for a GWAS application.
    Xu EL; Qian X; Yu Q; Zhang H; Cui S
    BMC Genomics; 2018 Mar; 19(Suppl 4):170. PubMed ID: 29589561
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A general framework for studying genetic effects and gene-environment interactions with missing data.
    Hu YJ; Lin DY; Zeng D
    Biostatistics; 2010 Oct; 11(4):583-98. PubMed ID: 20348396
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood.
    Rye MS; Warrington NM; Scaman ES; Vijayasekaran S; Coates HL; Anderson D; Pennell CE; Blackwell JM; Jamieson SE
    PLoS One; 2012; 7(10):e48215. PubMed ID: 23133572
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Adaptively weighted association statistics.
    LeBlanc M; Kooperberg C
    Genet Epidemiol; 2009 Jul; 33(5):442-52. PubMed ID: 19170133
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Simple and efficient analysis of disease association with missing genotype data.
    Lin DY; Hu Y; Huang BE
    Am J Hum Genet; 2008 Feb; 82(2):444-52. PubMed ID: 18252224
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Constrained maximum entropy models to select genotype interactions associated with censored failure times.
    Yang A; Miller D; Pan Q
    J Bioinform Comput Biol; 2018 Dec; 16(6):1840024. PubMed ID: 30567478
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An optimal dose-effect mode trend test for SNP genotype tables.
    Yamada R; Okada Y
    Genet Epidemiol; 2009 Feb; 33(2):114-27. PubMed ID: 18688846
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. A Comparative Study on Multifactor Dimensionality Reduction Methods for Detecting Gene-Gene Interactions with the Survival Phenotype.
    Lee S; Kim Y; Kwon MS; Park T
    Biomed Res Int; 2015; 2015():671859. PubMed ID: 26339630
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Detecting Gene-Environment Interactions for a Quantitative Trait in a Genome-Wide Association Study.
    Zhang P; Lewinger JP; Conti D; Morrison JL; Gauderman WJ
    Genet Epidemiol; 2016 Jul; 40(5):394-403. PubMed ID: 27230133
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comparison of prospective and retrospective methods for haplotype inference in case-control studies.
    Satten GA; Epstein MP
    Genet Epidemiol; 2004 Nov; 27(3):192-201. PubMed ID: 15372619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Robust Mantel-Haenszel test under genetic model uncertainty allowing for covariates in case-control association studies.
    Zang Y; Fung WK
    Genet Epidemiol; 2011 Nov; 35(7):695-705. PubMed ID: 22009791
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Testing Genetic Pleiotropy with GWAS Summary Statistics for Marginal and Conditional Analyses.
    Deng Y; Pan W
    Genetics; 2017 Dec; 207(4):1285-1299. PubMed ID: 28971959
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.