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 *

319 related articles for article (PubMed ID: 22309429)

  • 41. Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.
    Ma C; Boehnke M; Lee S;
    Genet Epidemiol; 2015 Nov; 39(7):499-508. PubMed ID: 26454253
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A gene based combination test using GWAS summary data.
    Zhang J; Liang X; Gonzales S; Liu J; Gao XR; Wang X
    BMC Bioinformatics; 2023 Jan; 24(1):2. PubMed ID: 36597047
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Detecting rare variants for complex traits using family and unrelated data.
    Zhu X; Feng T; Li Y; Lu Q; Elston RC
    Genet Epidemiol; 2010 Feb; 34(2):171-87. PubMed ID: 19847924
    [TBL] [Abstract][Full Text] [Related]  

  • 44. On Robust Association Testing for Quantitative Traits and Rare Variants.
    Wei P; Cao Y; Zhang Y; Xu Z; Kwak IY; Boerwinkle E; Pan W
    G3 (Bethesda); 2016 Dec; 6(12):3941-3950. PubMed ID: 27678522
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Joint Analysis of Multiple Traits in Rare Variant Association Studies.
    Wang Z; Wang X; Sha Q; Zhang S
    Ann Hum Genet; 2016 May; 80(3):162-71. PubMed ID: 26990300
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detecting association of rare and common variants based on cross-validation prediction error.
    Yang X; Wang S; Zhang S; Sha Q
    Genet Epidemiol; 2017 Apr; 41(3):233-243. PubMed ID: 28176359
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. 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]  

  • 49. 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]  

  • 50. Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.
    Lin YC; Hsieh AR; Hsiao CL; Wu SJ; Wang HM; Lian IeB; Fann CS
    J Biomed Sci; 2014 Aug; 21(1):88. PubMed ID: 25175702
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Using prior information from humans to prioritize genes and gene-associated variants for complex traits in livestock.
    Raymond B; Yengo L; Costilla R; Schrooten C; Bouwman AC; Hayes BJ; Veerkamp RF; Visscher PM
    PLoS Genet; 2020 Sep; 16(9):e1008780. PubMed ID: 32925905
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A variational Bayes discrete mixture test for rare variant association.
    Logsdon BA; Dai JY; Auer PL; Johnsen JM; Ganesh SK; Smith NL; Wilson JG; Tracy RP; Lange LA; Jiao S; Rich SS; Lettre G; Carlson CS; Jackson RD; O'Donnell CJ; Wurfel MM; Nickerson DA; Tang H; Reiner AP; Kooperberg C;
    Genet Epidemiol; 2014 Jan; 38(1):21-30. PubMed ID: 24482836
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies.
    van der Sluis S; Posthuma D; Dolan CV
    PLoS Genet; 2013; 9(1):e1003235. PubMed ID: 23359524
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A nonparametric method to test for associations between rare variants and multiple traits.
    Zhou Y; Cheng Y; Zhu W; Zhou Q
    Genet Res (Camb); 2016; 98():e1. PubMed ID: 27159928
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The admixture maximum likelihood test to test for association between rare variants and disease phenotypes.
    Tyrer JP; Guo Q; Easton DF; Pharoah PD
    BMC Bioinformatics; 2013 Jun; 14():177. PubMed ID: 23738568
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Family-based association tests for rare variants with censored traits.
    Qi W; Allen AS; Li YJ
    PLoS One; 2019; 14(1):e0210870. PubMed ID: 30682063
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. [Family-based association tests for rare variants].
    Chen X; Wang SY; Xue EC; Wang XH; Peng HX; Fan M; Wang MY; Wu YQ; Qin XY; Li J; Wu T; Zhu J; Li ZP; Zhou DF; Chen YH; Hu Y
    Zhonghua Liu Xing Bing Xue Za Zhi; 2022 Sep; 43(9):1497-1502. PubMed ID: 36117360
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Optimal tests for rare variant effects in sequencing association studies.
    Lee S; Wu MC; Lin X
    Biostatistics; 2012 Sep; 13(4):762-75. PubMed ID: 22699862
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.