BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 30042787)

  • 1. Application of Causal Inference to Genomic Analysis: Advances in Methodology.
    Hu P; Jiao R; Jin L; Xiong M
    Front Genet; 2018; 9():238. PubMed ID: 30042787
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bivariate Causal Discovery and Its Applications to Gene Expression and Imaging Data Analysis.
    Jiao R; Lin N; Hu Z; Bennett DA; Jin L; Xiong M
    Front Genet; 2018; 9():347. PubMed ID: 30233639
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-Wide Causation Studies of Complex Diseases.
    Jiao R; Chen X; Boerwinkle E; Xiong M
    J Comput Biol; 2022 Aug; 29(8):908-931. PubMed ID: 35451855
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
    DE LA Vega FM; Bustamante CD; Leal SM
    Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Some statistical consideration in transcriptome-wide association studies.
    Xue H; Pan W;
    Genet Epidemiol; 2020 Apr; 44(3):221-232. PubMed ID: 31821608
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Causal graph-based analysis of genome-wide association data in rheumatoid arthritis.
    Alekseyenko AV; Lytkin NI; Ai J; Ding B; Padyukov L; Aliferis CF; Statnikov A
    Biol Direct; 2011 May; 6():25. PubMed ID: 21592391
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Statistical methods for Mendelian randomization in genome-wide association studies: A review.
    Boehm FJ; Zhou X
    Comput Struct Biotechnol J; 2022; 20():2338-2351. PubMed ID: 35615025
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strengthening Causal Inference for Complex Disease Using Molecular Quantitative Trait Loci.
    Neumeyer S; Hemani G; Zeggini E
    Trends Mol Med; 2020 Feb; 26(2):232-241. PubMed ID: 31718940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Systems genetics: From GWAS to disease pathways.
    van der Sijde MR; Ng A; Fu J
    Biochim Biophys Acta; 2014 Oct; 1842(10):1903-1909. PubMed ID: 24798234
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Application of a Bayesian dominance model improves power in quantitative trait genome-wide association analysis.
    Bennewitz J; Edel C; Fries R; Meuwissen TH; Wellmann R
    Genet Sel Evol; 2017 Jan; 49(1):7. PubMed ID: 28088170
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regional heritability mapping and genome-wide association identify loci for complex growth, wood and disease resistance traits in Eucalyptus.
    Resende RT; Resende MD; Silva FF; Azevedo CF; Takahashi EK; Silva-Junior OB; Grattapaglia D
    New Phytol; 2017 Feb; 213(3):1287-1300. PubMed ID: 28079935
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults.
    Chen F; He J; Zhang J; Chen GK; Thomas V; Ambrosone CB; Bandera EV; Berndt SI; Bernstein L; Blot WJ; Cai Q; Carpten J; Casey G; Chanock SJ; Cheng I; Chu L; Deming SL; Driver WR; Goodman P; Hayes RB; Hennis AJ; Hsing AW; Hu JJ; Ingles SA; John EM; Kittles RA; Kolb S; Leske MC; Millikan RC; Monroe KR; Murphy A; Nemesure B; Neslund-Dudas C; Nyante S; Ostrander EA; Press MF; Rodriguez-Gil JL; Rybicki BA; Schumacher F; Stanford JL; Signorello LB; Strom SS; Stevens V; Van Den Berg D; Wang Z; Witte JS; Wu SY; Yamamura Y; Zheng W; Ziegler RG; Stram AH; Kolonel LN; Le Marchand L; Henderson BE; Haiman CA; Stram DO
    PLoS One; 2015; 10(6):e0131106. PubMed ID: 26125186
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evolutionary perspectives on polygenic selection, missing heritability, and GWAS.
    Uricchio LH
    Hum Genet; 2020 Jan; 139(1):5-21. PubMed ID: 31201529
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic Causal Inference Using Genome-Wide Association Study Data: Mendelian Randomization and Beyond.
    Walker VM; Zheng J; Gaunt TR; Smith GD
    Annu Rev Biomed Data Sci; 2022 Aug; 5():1-17. PubMed ID: 35363507
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Statistical power of transcriptome-wide association studies.
    He R; Xue H; Pan W;
    Genet Epidemiol; 2022 Dec; 46(8):572-588. PubMed ID: 35766062
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women.
    Verdiesen RMG; van der Schouw YT; van Gils CH; Verschuren WMM; Broekmans FJM; Borges MC; Gonçalves Soares AL; Lawlor DA; Eliassen AH; Kraft P; Sandler DP; Harlow SD; Smith JA; Santoro N; Schoemaker MJ; Swerdlow AJ; Murray A; Ruth KS; Onland-Moret NC
    Hum Reprod; 2022 May; 37(5):1069-1082. PubMed ID: 35274129
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization.
    Jiang L; Miao L; Yi G; Li X; Xue C; Li MJ; Huang H; Li M
    Am J Hum Genet; 2022 May; 109(5):838-856. PubMed ID: 35460606
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases.
    Li Y; Kellis M
    Nucleic Acids Res; 2016 Oct; 44(18):e144. PubMed ID: 27407109
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Disentangling molecular relationships with a causal inference test.
    Millstein J; Zhang B; Zhu J; Schadt EE
    BMC Genet; 2009 May; 10():23. PubMed ID: 19473544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies.
    He Z; Liu L; Belloy ME; Le Guen Y; Sossin A; Liu X; Qi X; Ma S; Gyawali PK; Wyss-Coray T; Tang H; Sabatti C; Candès E; Greicius MD; Ionita-Laza I
    Nat Commun; 2022 Nov; 13(1):7209. PubMed ID: 36418338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.