BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 26661625)

  • 1. A new method for estimating effect size distribution and heritability from genome-wide association summary results.
    Zhang L; Shen YP; Hu WZ; Ran S; Lin Y; Lei SF; Zhang YH; Papasian CJ; Yi N; Pei YF
    Hum Genet; 2016 Feb; 135(2):171-84. PubMed ID: 26661625
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model.
    Holland D; Frei O; Desikan R; Fan CC; Shadrin AA; Smeland OB; Sundar VS; Thompson P; Andreassen OA; Dale AM
    PLoS Genet; 2020 May; 16(5):e1008612. PubMed ID: 32427991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability.
    Kutalik Z; Whittaker J; Waterworth D; ; Beckmann JS; Bergmann S
    Genet Epidemiol; 2011 Jul; 35(5):341-9. PubMed ID: 21465548
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio.
    Lin BD; Willemsen G; Fedko IO; Jansen R; Penninx B; de Geus E; Kluft C; Hottenga J; Boomsma DI
    Twin Res Hum Genet; 2017 Apr; 20(2):97-107. PubMed ID: 28193307
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SNP-based heritability estimation using a Bayesian approach.
    Krag K; Janss LL; Shariati MM; Berg P; Buitenhuis AJ
    Animal; 2013 Apr; 7(4):531-9. PubMed ID: 23177174
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mixture SNPs effect on phenotype in genome-wide association studies.
    Wang L; Shen H; Liu H; Guo G
    BMC Genomics; 2015 Feb; 16(1):3. PubMed ID: 25649116
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Single Nucleotide Polymorphism Heritability of Behavior Problems in Childhood: Genome-Wide Complex Trait Analysis.
    Pappa I; Fedko IO; Mileva-Seitz VR; Hottenga JJ; Bakermans-Kranenburg MJ; Bartels M; van Beijsterveldt CE; Jaddoe VW; Middeldorp CM; Rippe RC; Rivadeneira F; Tiemeier H; Verhulst FC; van IJzendoorn MH; Boomsma DI
    J Am Acad Child Adolesc Psychiatry; 2015 Sep; 54(9):737-44. PubMed ID: 26299295
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates.
    So HC; Xue X; Ma Z; Sham PC
    Int J Mol Sci; 2024 Jan; 25(2):. PubMed ID: 38279346
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A multi-SNP locus-association method reveals a substantial fraction of the missing heritability.
    Ehret GB; Lamparter D; Hoggart CJ; ; Whittaker JC; Beckmann JS; Kutalik Z
    Am J Hum Genet; 2012 Nov; 91(5):863-71. PubMed ID: 23122585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture.
    Hou K; Burch KS; Majumdar A; Shi H; Mancuso N; Wu Y; Sankararaman S; Pasaniuc B
    Nat Genet; 2019 Aug; 51(8):1244-1251. PubMed ID: 31358995
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Limitations of GCTA as a solution to the missing heritability problem.
    Krishna Kumar S; Feldman MW; Rehkopf DH; Tuljapurkar S
    Proc Natl Acad Sci U S A; 2016 Jan; 113(1):E61-70. PubMed ID: 26699465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.
    Li D; Kang H; Lee S; Won S
    Genes Genomics; 2020 Apr; 42(4):393-403. PubMed ID: 31902109
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Concepts, estimation and interpretation of SNP-based heritability.
    Yang J; Zeng J; Goddard ME; Wray NR; Visscher PM
    Nat Genet; 2017 Aug; 49(9):1304-1310. PubMed ID: 28854176
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Estimating heritability in pharmacogenetic studies.
    Marshall SL; Guennel T; Kohler J; Man M; Fossceco S
    Pharmacogenomics; 2013 Mar; 14(4):369-77. PubMed ID: 23438884
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals.
    Yang S; Liu Y; Jiang N; Chen J; Leach L; Luo Z; Wang M
    BMC Genomics; 2014 Jan; 15(1):13. PubMed ID: 24405759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reevaluation of SNP heritability in complex human traits.
    Speed D; Cai N; ; Johnson MR; Nejentsev S; Balding DJ
    Nat Genet; 2017 Jul; 49(7):986-992. PubMed ID: 28530675
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits.
    Evans LM; Tahmasbi R; Vrieze SI; Abecasis GR; Das S; Gazal S; Bjelland DW; de Candia TR; ; Goddard ME; Neale BM; Yang J; Visscher PM; Keller MC
    Nat Genet; 2018 May; 50(5):737-745. PubMed ID: 29700474
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Nature of Genetic Variation for Complex Traits Revealed by GWAS and Regional Heritability Mapping Analyses.
    Caballero A; Tenesa A; Keightley PD
    Genetics; 2015 Dec; 201(4):1601-13. PubMed ID: 26482794
    [TBL] [Abstract][Full Text] [Related]  

  • 19. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
    Zheng J; Erzurumluoglu AM; Elsworth BL; Kemp JP; Howe L; Haycock PC; Hemani G; Tansey K; Laurin C; ; Pourcain BS; Warrington NM; Finucane HK; Price AL; Bulik-Sullivan BK; Anttila V; Paternoster L; Gaunt TR; Evans DM; Neale BM
    Bioinformatics; 2017 Jan; 33(2):272-279. PubMed ID: 27663502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multi-breed genome-wide association study reveals novel loci associated with the weight of internal organs.
    He Y; Li X; Zhang F; Su Y; Hou L; Chen H; Zhang Z; Huang L
    Genet Sel Evol; 2015 Nov; 47():87. PubMed ID: 26576866
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.