BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 33795679)

  • 21. An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.
    Wang L; Balmat TJ; Antonia AL; Constantine FJ; Henao R; Burke TW; Ingham A; McClain MT; Tsalik EL; Ko ER; Ginsburg GS; DeLong MR; Shen X; Woods CW; Hauser ER; Ko DC
    Genome Med; 2021 May; 13(1):83. PubMed ID: 34001247
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Searching Genome-Wide Multi-Locus Associations for Multiple Diseases Based on Bayesian Inference.
    Guo X; Zhang J; Cai Z; Du DZ; Pan Y
    IEEE/ACM Trans Comput Biol Bioinform; 2017; 14(3):600-610. PubMed ID: 26887006
    [TBL] [Abstract][Full Text] [Related]  

  • 23. PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics.
    Lee CH; Shi H; Pasaniuc B; Eskin E; Han B
    Am J Hum Genet; 2021 Jan; 108(1):36-48. PubMed ID: 33352115
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Methods for meta-analysis of multiple traits using GWAS summary statistics.
    Ray D; Boehnke M
    Genet Epidemiol; 2018 Mar; 42(2):134-145. PubMed ID: 29226385
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Simulating autosomal genotypes with realistic linkage disequilibrium and a spiked-in genetic effect.
    Shi M; Umbach DM; Wise AS; Weinberg CR
    BMC Bioinformatics; 2018 Jan; 19(1):2. PubMed ID: 29291710
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Enhancing the power to detect low-frequency variants in genome-wide screens.
    Lin CY; Xing G; Ku HC; Elston RC; Xing C
    Genetics; 2014 Apr; 196(4):1293-302. PubMed ID: 24496013
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prioritizing tests of epistasis through hierarchical representation of genomic redundancies.
    Cowman T; Koyutürk M
    Nucleic Acids Res; 2017 Aug; 45(14):e131. PubMed ID: 28605458
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies.
    Li Z; Li X; Liu Y; Shen J; Chen H; Zhou H; Morrison AC; Boerwinkle E; Lin X
    Am J Hum Genet; 2019 May; 104(5):802-814. PubMed ID: 30982610
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular genetic studies of complex phenotypes.
    Marian AJ
    Transl Res; 2012 Feb; 159(2):64-79. PubMed ID: 22243791
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data.
    Shi H; Kichaev G; Pasaniuc B
    Am J Hum Genet; 2016 Jul; 99(1):139-53. PubMed ID: 27346688
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Bivariate association analysis for quantitative traits using generalized estimation equation.
    Yang F; Tang Z; Deng H
    J Genet Genomics; 2009 Dec; 36(12):733-43. PubMed ID: 20129400
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genomic prediction based on selective linkage disequilibrium pruning of low-coverage whole-genome sequence variants in a pure Duroc population.
    Zhu D; Zhao Y; Zhang R; Wu H; Cai G; Wu Z; Wang Y; Hu X
    Genet Sel Evol; 2023 Oct; 55(1):72. PubMed ID: 37853325
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Model-based assessment of replicability for genome-wide association meta-analysis.
    McGuire D; Jiang Y; Liu M; Weissenkampen JD; Eckert S; Yang L; Chen F; ; Berg A; Vrieze S; Jiang B; Li Q; Liu DJ
    Nat Commun; 2021 Mar; 12(1):1964. PubMed ID: 33785739
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Exploiting Linkage Disequilibrium for Ultrahigh-Dimensional Genome-Wide Data with an Integrated Statistical Approach.
    Carlsen M; Fu G; Bushman S; Corcoran C
    Genetics; 2016 Feb; 202(2):411-26. PubMed ID: 26661113
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Scalable linkage-disequilibrium-based selective sweep detection: a performance guide.
    Alachiotis N; Pavlidis P
    Gigascience; 2016; 5():7. PubMed ID: 26862394
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genome-Wide Association Analyses of Equine Metabolic Syndrome Phenotypes in Welsh Ponies and Morgan Horses.
    Norton E; Schultz N; Geor R; McFarlane D; Mickelson J; McCue M
    Genes (Basel); 2019 Nov; 10(11):. PubMed ID: 31698676
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bridging heterogeneous mutation data to enhance disease gene discovery.
    Zhou K; Wang Y; Bretonnel Cohen K; Kim JD; Ma X; Shen Z; Meng X; Xia J
    Brief Bioinform; 2021 Sep; 22(5):. PubMed ID: 33847357
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new permutation strategy of pathway-based approach for genome-wide association study.
    Guo YF; Li J; Chen Y; Zhang LS; Deng HW
    BMC Bioinformatics; 2009 Dec; 10():429. PubMed ID: 20021635
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Improved detection of rare genetic variants for diseases.
    Zhang L; Pei YF; Li J; Papasian CJ; Deng HW
    PLoS One; 2010 Nov; 5(11):e13857. PubMed ID: 21079782
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.
    Adewuyi EO; Mehta D; ; ; Nyholt DR
    Hum Reprod; 2022 Jan; 37(2):366-383. PubMed ID: 35472084
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.