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 *

162 related articles for article (PubMed ID: 27248145)

  • 1. Evaluation of methodology for the analysis of 'time-to-event' data in pharmacogenomic genome-wide association studies.
    Syed H; Jorgensen AL; Morris AP
    Pharmacogenomics; 2016 Jun; 17(8):907-15. PubMed ID: 27248145
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SurvivalGWAS_Power: a user friendly tool for power calculations in pharmacogenetic studies with "time to event" outcomes.
    Syed H; Jorgensen AL; Morris AP
    BMC Bioinformatics; 2016 Dec; 17(1):523. PubMed ID: 27931206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SurvivalGWAS_SV: software for the analysis of genome-wide association studies of imputed genotypes with "time-to-event" outcomes.
    Syed H; Jorgensen AL; Morris AP
    BMC Bioinformatics; 2017 May; 18(1):265. PubMed ID: 28525968
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design.
    Staley JR; Jones E; Kaptoge S; Butterworth AS; Sweeting MJ; Wood AM; Howson JMM
    Eur J Hum Genet; 2017 Jun; 25(7):854-862. PubMed ID: 28594416
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An efficient and robust method for analyzing population pharmacokinetic data in genome-wide pharmacogenomic studies: a generalized estimating equation approach.
    Nagashima K; Sato Y; Noma H; Hamada C
    Stat Med; 2013 Nov; 32(27):4838-58. PubMed ID: 23852468
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Merging pharmacometabolomics with pharmacogenomics using '1000 Genomes' single-nucleotide polymorphism imputation: selective serotonin reuptake inhibitor response pharmacogenomics.
    Abo R; Hebbring S; Ji Y; Zhu H; Zeng ZB; Batzler A; Jenkins GD; Biernacka J; Snyder K; Drews M; Fiehn O; Fridley B; Schaid D; Kamatani N; Nakamura Y; Kubo M; Mushiroda T; Kaddurah-Daouk R; Mrazek DA; Weinshilboum RM
    Pharmacogenet Genomics; 2012 Apr; 22(4):247-53. PubMed ID: 22322242
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Power and sample size calculations for SNP association studies with censored time-to-event outcomes.
    Owzar K; Li Z; Cox N; Jung SH
    Genet Epidemiol; 2012 Sep; 36(6):538-48. PubMed ID: 22685040
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS.
    Irlmeier R; Hughey JJ; Bastarache L; Denny JC; Chen Q
    Bioinformatics; 2022 Apr; 38(8):2297-2306. PubMed ID: 35157022
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A conceptual framework for pharmacodynamic genome-wide association studies in pharmacogenomics.
    Wu R; Tong C; Wang Z; Mauger D; Tantisira K; Szefler SJ; Chinchilli VM; Israel E
    Drug Discov Today; 2011 Oct; 16(19-20):884-90. PubMed ID: 21920452
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prediction of a time-to-event trait using genome wide SNP data.
    Kim J; Sohn I; Son DS; Kim DH; Ahn T; Jung SH
    BMC Bioinformatics; 2013 Feb; 14():58. PubMed ID: 23418752
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.
    Dubé MP; Legault MA; Lemaçon A; Lemieux Perreault LP; Fouodjio R; Waters DD; Kouz S; Pinto FJ; Maggioni AP; Diaz R; Berry C; Koenig W; Lopez-Sendon J; Gamra H; Kiwan GS; Asselin G; Provost S; Barhdadi A; Sun M; Cossette M; Blondeau L; Mongrain I; Dubois A; Rhainds D; Bouabdallaoui N; Samuel M; de Denus S; L'Allier PL; Guertin MC; Roubille F; Tardif JC
    Circ Genom Precis Med; 2021 Apr; 14(2):e003183. PubMed ID: 33560138
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two-step hypothesis testing to detect gene-environment interactions in a genome-wide scan with a survival endpoint.
    Kawaguchi ES; Li G; Lewinger JP; Gauderman WJ
    Stat Med; 2022 Apr; 41(9):1644-1657. PubMed ID: 35075649
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methods for analysis in pharmacogenomics: lessons from the Pharmacogenetics Research Network Analysis Group.
    Srinivasan BS; Chen J; Cheng C; Conti D; Duan S; Fridley BL; Gu X; Haines JL; Jorgenson E; Kraja A; Lasky-Su J; Li L; Rodin A; Wang D; Province M; Ritchie MD
    Pharmacogenomics; 2009 Feb; 10(2):243-51. PubMed ID: 19207025
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies.
    Lu H; Wei Y; Jiang Z; Zhang J; Wang T; Huang S; Zeng P
    J Transl Med; 2021 Oct; 19(1):418. PubMed ID: 34627275
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application and interpretation of genome-wide association (GWA) studies for informing pharmacogenomic research - examples from the field of age-related macular degeneration.
    SanGiovanni JP; Rosen R; Kaushal S
    Curr Mol Med; 2014; 14(7):814-32. PubMed ID: 25109799
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fast Algorithms for Conducting Large-Scale GWAS of Age-at-Onset Traits Using Cox Mixed-Effects Models.
    He L; Kulminski AM
    Genetics; 2020 May; 215(1):41-58. PubMed ID: 32132097
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lymphoblastoid cell lines models of drug response: successes and lessons from this pharmacogenomic model.
    Jack J; Rotroff D; Motsinger-Reif A
    Curr Mol Med; 2014; 14(7):833-40. PubMed ID: 25109794
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ProbABEL package for genome-wide association analysis of imputed data.
    Aulchenko YS; Struchalin MV; van Duijn CM
    BMC Bioinformatics; 2010 Mar; 11():134. PubMed ID: 20233392
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methodological and statistical issues in pharmacogenomics.
    Peters BJ; Rodin AS; de Boer A; Maitland-van der Zee AH
    J Pharm Pharmacol; 2010 Feb; 62(2):161-6. PubMed ID: 20487194
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide algorithm for detecting CNV associations with diseases.
    Xu Y; Peng B; Fu Y; Amos CI
    BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.