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 *

187 related articles for article (PubMed ID: 37425935)

  • 21. MESuSiE enables scalable and powerful multi-ancestry fine-mapping of causal variants in genome-wide association studies.
    Gao B; Zhou X
    Nat Genet; 2024 Jan; 56(1):170-179. PubMed ID: 38168930
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Comparison of two multi-trait association testing methods and sequence-based fine mapping of six additive QTL in Swiss Large White pigs.
    Nosková A; Mehrotra A; Kadri NK; Lloret-Villas A; Neuenschwander S; Hofer A; Pausch H
    BMC Genomics; 2023 Apr; 24(1):192. PubMed ID: 37038103
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomization.
    Liu L; Zeng P; Xue F; Yuan Z; Zhou X
    Am J Hum Genet; 2021 Feb; 108(2):240-256. PubMed ID: 33434493
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genome-wide fine-mapping improves identification of causal variants.
    Wu Y; Zheng Z; Thibaut L; Goddard ME; Wray NR; Visscher PM; Zeng J
    medRxiv; 2024 Aug; ():. PubMed ID: 39072021
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome-wide fine-mapping improves identification of causal variants.
    Wu Y; Zheng Z; Thibaut L; Goddard ME; Wray NR; Visscher PM; Zeng J
    Res Sq; 2024 Aug; ():. PubMed ID: 39149449
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An in-depth association analysis of genetic variants within nicotine-related loci: Meeting in middle of GWAS and genetic fine-mapping.
    Mo C; Ye Z; Pan Y; Zhang Y; Wu Q; Bi C; Liu S; Mitchell B; Kochunov P; Hong LE; Ma T; Chen S
    Mol Cell Neurosci; 2023 Dec; 127():103895. PubMed ID: 37634742
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hierarchical joint analysis of marginal summary statistics-Part I: Multipopulation fine mapping and credible set construction.
    Shen J; Jiang L; Wang K; Wang A; Chen F; Newcombe PJ; Haiman CA; Conti DV
    Genet Epidemiol; 2024 Sep; 48(6):241-257. PubMed ID: 38606643
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of potential genetic causal variants for obesity-related traits using statistical fine mapping.
    Gong R; Greenbaum J; Lin X; Du Y; Su KJ; Gong Y; Shen J; Deng HW
    Mol Genet Genomics; 2023 Nov; 298(6):1309-1319. PubMed ID: 37498361
    [TBL] [Abstract][Full Text] [Related]  

  • 29. CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
    Wang J; Huang D; Zhou Y; Yao H; Liu H; Zhai S; Wu C; Zheng Z; Zhao K; Wang Z; Yi X; Zhang S; Liu X; Liu Z; Chen K; Yu Y; Sham PC; Li MJ
    Nucleic Acids Res; 2020 Jan; 48(D1):D807-D816. PubMed ID: 31691819
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Improving polygenic prediction from summary data by learning patterns of effect sharing across multiple phenotypes.
    Kunkel D; Sørensen P; Shankar V; Morgante F
    bioRxiv; 2024 May; ():. PubMed ID: 38766136
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A multi-trait Bayesian method for mapping QTL and genomic prediction.
    Kemper KE; Bowman PJ; Hayes BJ; Visscher PM; Goddard ME
    Genet Sel Evol; 2018 Mar; 50(1):10. PubMed ID: 29571285
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Improving the coverage of credible sets in Bayesian genetic fine-mapping.
    Hutchinson A; Watson H; Wallace C
    PLoS Comput Biol; 2020 Apr; 16(4):e1007829. PubMed ID: 32282791
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.
    Kundu K; Tardaguila M; Mann AL; Watt S; Ponstingl H; Vasquez L; Von Schiller D; Morrell NW; Stegle O; Pastinen T; Sawcer SJ; Anderson CA; Walter K; Soranzo N
    Nat Genet; 2022 Mar; 54(3):251-262. PubMed ID: 35288711
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Integrate multiple traits to detect novel trait-gene association using GWAS summary data with an adaptive test approach.
    Guo B; Wu B
    Bioinformatics; 2019 Jul; 35(13):2251-2257. PubMed ID: 30476000
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Improved multi-ancestry fine-mapping identifies
    Lu Z; Wang X; Carr M; Kim A; Gazal S; Mohammadi P; Wu L; Gusev A; Pirruccello J; Kachuri L; Mancuso N
    medRxiv; 2024 Apr; ():. PubMed ID: 38699369
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Regression-based multi-trait QTL mapping using a structural equation model.
    Mi X; Eskridge K; Wang D; Baenziger PS; Campbell BT; Gill KS; Dweikat I; Bovaird J
    Stat Appl Genet Mol Biol; 2010; 9():Article38. PubMed ID: 21044042
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry.
    Kamiza AB; Touré SM; Zhou F; Soremekun O; Cissé C; Wélé M; Touré AM; Nashiru O; Corpas M; Nyirenda M; Crampin A; Shaffer J; Doumbia S; Zeggini E; Morris AP; Asimit JL; Chikowore T; Fatumo S
    Nat Commun; 2023 Sep; 14(1):5403. PubMed ID: 37669986
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identifying causal variants by fine mapping across multiple studies.
    LaPierre N; Taraszka K; Huang H; He R; Hormozdiari F; Eskin E
    PLoS Genet; 2021 Sep; 17(9):e1009733. PubMed ID: 34543273
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Significance Testing for Allelic Heterogeneity.
    Deng Y; Pan W
    Genetics; 2018 Sep; 210(1):25-32. PubMed ID: 29959179
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Bayesian mapping of quantitative trait loci for multiple complex traits with the use of variance components.
    Liu J; Liu Y; Liu X; Deng HW
    Am J Hum Genet; 2007 Aug; 81(2):304-20. PubMed ID: 17668380
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.