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 *

156 related articles for article (PubMed ID: 39085219)

  • 21. Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits.
    Song W; Shi Y; Lin GN
    Elife; 2024 Apr; 12():. PubMed ID: 38639992
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes.
    Chung W; Chen J; Turman C; Lindstrom S; Zhu Z; Loh PR; Kraft P; Liang L
    Nat Commun; 2019 Feb; 10(1):569. PubMed ID: 30718517
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A resource-efficient tool for mixed model association analysis of large-scale data.
    Jiang L; Zheng Z; Qi T; Kemper KE; Wray NR; Visscher PM; Yang J
    Nat Genet; 2019 Dec; 51(12):1749-1755. PubMed ID: 31768069
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel method for multiple phenotype association studies based on genotype and phenotype network.
    Cao X; Zhang S; Sha Q
    PLoS Genet; 2024 May; 20(5):e1011245. PubMed ID: 38728360
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deriving GWAS summary estimates for paternal smoking in UK biobank: a GWAS by subtraction.
    Woolf B; Sallis HM; Munafò MR; Gill D
    BMC Res Notes; 2023 Jul; 16(1):159. PubMed ID: 37518004
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.
    Rocheleau G; Forrest IS; Duffy Á; Bafna S; Dobbyn A; Verbanck M; Won HH; Jordan DM; Do R
    Commun Biol; 2022 Aug; 5(1):849. PubMed ID: 35987940
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries.
    An U; Pazokitoroudi A; Alvarez M; Huang L; Bacanu S; Schork AJ; Kendler K; Pajukanta P; Flint J; Zaitlen N; Cai N; Dahl A; Sankararaman S
    Nat Genet; 2023 Dec; 55(12):2269-2276. PubMed ID: 37985819
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Controlling for background genetic effects using polygenic scores improves the power of genome-wide association studies.
    Bennett D; O'Shea D; Ferguson J; Morris D; Seoighe C
    Sci Rep; 2021 Oct; 11(1):19571. PubMed ID: 34599249
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Extreme-phenotype genome-wide association study (XP-GWAS): a method for identifying trait-associated variants by sequencing pools of individuals selected from a diversity panel.
    Yang J; Jiang H; Yeh CT; Yu J; Jeddeloh JA; Nettleton D; Schnable PS
    Plant J; 2015 Nov; 84(3):587-96. PubMed ID: 26386250
    [TBL] [Abstract][Full Text] [Related]  

  • 30. FiMAP: A fast identity-by-descent mapping test for biobank-scale cohorts.
    Chen H; Naseri A; Zhi D
    PLoS Genet; 2023 Dec; 19(12):e1011057. PubMed ID: 38039339
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fine-scale population structure in the UK Biobank: implications for genome-wide association studies.
    Cook JP; Mahajan A; Morris AP
    Hum Mol Genet; 2020 Sep; 29(16):2803-2811. PubMed ID: 32691046
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Robust meta-analysis of biobank-based genome-wide association studies with unbalanced binary phenotypes.
    Dey R; Nielsen JB; Fritsche LG; Zhou W; Zhu H; Willer CJ; Lee S
    Genet Epidemiol; 2019 Jul; 43(5):462-476. PubMed ID: 30793809
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identifying loci affecting trait variability and detecting interactions in genome-wide association studies.
    Young AI; Wauthier FL; Donnelly P
    Nat Genet; 2018 Nov; 50(11):1608-1614. PubMed ID: 30323177
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection.
    Schoech AP; Jordan DM; Loh PR; Gazal S; O'Connor LJ; Balick DJ; Palamara PF; Finucane HK; Sunyaev SR; Price AL
    Nat Commun; 2019 Feb; 10(1):790. PubMed ID: 30770844
    [TBL] [Abstract][Full Text] [Related]  

  • 35. SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.
    Mägi R; Suleimanov YV; Clarke GM; Kaakinen M; Fischer K; Prokopenko I; Morris AP
    BMC Bioinformatics; 2017 Jan; 18(1):25. PubMed ID: 28077070
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Using Genetic Marginal Effects to Study Gene-Environment Interactions with GWAS Data.
    Verhulst B; Pritikin JN; Clifford J; Prom-Wormley E
    Behav Genet; 2021 May; 51(3):358-373. PubMed ID: 33899139
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Conditional analysis of multiple quantitative traits based on marginal GWAS summary statistics.
    Deng Y; Pan W
    Genet Epidemiol; 2017 Jul; 41(5):427-436. PubMed ID: 28464407
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
    Galván-Femenía I; Obón-Santacana M; Piñeyro D; Guindo-Martinez M; Duran X; Carreras A; Pluvinet R; Velasco J; Ramos L; Aussó S; Mercader JM; Puig L; Perucho M; Torrents D; Moreno V; Sumoy L; de Cid R
    J Med Genet; 2018 Nov; 55(11):765-778. PubMed ID: 30166351
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Regularized quantile regression applied to genome-enabled prediction of quantitative traits.
    Nascimento M; E Silva FF; de Resende MD; Cruz CD; Nascimento AC; Viana JM; Azevedo CF; Barroso LM
    Genet Mol Res; 2017 Mar; 16(1):. PubMed ID: 28340274
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new test for trait mean and variance detects unreported loci for blood-pressure variation.
    Breeyear JH; Mautz BS; Keaton JM; Hellwege JN; Torstenson ES; Liang J; Bray MJ; Giri A; Warren HR; Munroe PB; Velez Edwards DR; Zhu X; Li C; Edwards TL
    Am J Hum Genet; 2024 May; 111(5):954-965. PubMed ID: 38614075
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.