BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 38171363)

  • 21. ANNORE: genetic fine-mapping with functional annotation.
    Fisher V; Sebastiani P; Cupples LA; Liu CT
    Hum Mol Genet; 2021 Dec; 31(1):32-40. PubMed ID: 34302344
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Evaluating the Performance of Fine-Mapping Strategies at Common Variant GWAS Loci.
    van de Bunt M; Cortes A; ; Brown MA; Morris AP; McCarthy MI
    PLoS Genet; 2015; 11(9):e1005535. PubMed ID: 26406328
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. A practical view of fine-mapping and gene prioritization in the post-genome-wide association era.
    Broekema RV; Bakker OB; Jonkers IH
    Open Biol; 2020 Jan; 10(1):190221. PubMed ID: 31937202
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.
    Lu ZH; Zhu H; Knickmeyer RC; Sullivan PF; Williams SN; Zou F;
    Genet Epidemiol; 2015 Dec; 39(8):664-77. PubMed ID: 26515609
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The utility of the Laplace effect size prior distribution in Bayesian fine-mapping studies.
    Walters K; Cox A; Yaacob H
    Genet Epidemiol; 2021 Jun; 45(4):386-401. PubMed ID: 33410201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Quantitative trait nucleotide analysis using Bayesian model selection.
    Blangero J; Goring HH; Kent JW; Williams JT; Peterson CP; Almasy L; Dyer TD
    Hum Biol; 2005 Oct; 77(5):541-59. PubMed ID: 16596940
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Efficient weighting methods for genomic best linear-unbiased prediction (BLUP) adapted to the genetic architectures of quantitative traits.
    Ren D; An L; Li B; Qiao L; Liu W
    Heredity (Edinb); 2021 Feb; 126(2):320-334. PubMed ID: 32980863
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A fast algorithm for Bayesian multi-locus model in genome-wide association studies.
    Duan W; Zhao Y; Wei Y; Yang S; Bai J; Shen S; Du M; Huang L; Hu Z; Chen F
    Mol Genet Genomics; 2017 Aug; 292(4):923-934. PubMed ID: 28534238
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fine-mapping of Parkinson's disease susceptibility loci identifies putative causal variants.
    Schilder BM; Raj T
    Hum Mol Genet; 2022 Mar; 31(6):888-900. PubMed ID: 34617105
    [TBL] [Abstract][Full Text] [Related]  

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

  • 32. Leveraging allelic imbalance to refine fine-mapping for eQTL studies.
    Zou J; Hormozdiari F; Jew B; Castel SE; Lappalainen T; Ernst J; Sul JH; Eskin E
    PLoS Genet; 2019 Dec; 15(12):e1008481. PubMed ID: 31834882
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification.
    Faye LL; Machiela MJ; Kraft P; Bull SB; Sun L
    PLoS Genet; 2013; 9(8):e1003609. PubMed ID: 23950724
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait.
    Chundru VK; Marioni RE; Prendergast JGD; Vallerga CL; Lin T; Beveridge AJ; ; Gratten J; Hume DA; Deary IJ; Wray NR; Visscher PM; McRae AF
    Genetics; 2019 Jul; 212(3):577-586. PubMed ID: 31040117
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fine-mapping genetic associations.
    Hutchinson A; Asimit J; Wallace C
    Hum Mol Genet; 2020 Sep; 29(R1):R81-R88. PubMed ID: 32744321
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Probabilistic colocalization of genetic variants from complex and molecular traits: promise and limitations.
    Hukku A; Pividori M; Luca F; Pique-Regi R; Im HK; Wen X
    Am J Hum Genet; 2021 Jan; 108(1):25-35. PubMed ID: 33308443
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans.
    Fatumo S; Chikowore T; Kalyesubula R; Nsubuga RN; Asiki G; Nashiru O; Seeley J; Crampin AC; Nitsch D; Smeeth L; Kaleebu P; Burgess S; Nyirenda M; Franceschini N; Morris AP; Tomlinson L; Newton R
    Hum Mol Genet; 2021 Jul; 30(16):1559-1568. PubMed ID: 33783510
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Conditional transcriptome-wide association study for fine-mapping candidate causal genes.
    Liu L; Yan R; Guo P; Ji J; Gong W; Xue F; Yuan Z; Zhou X
    Nat Genet; 2024 Feb; 56(2):348-356. PubMed ID: 38279040
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Stochastic search and joint fine-mapping increases accuracy and identifies previously unreported associations in immune-mediated diseases.
    Asimit JL; Rainbow DB; Fortune MD; Grinberg NF; Wicker LS; Wallace C
    Nat Commun; 2019 Jul; 10(1):3216. PubMed ID: 31324808
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.