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 *

489 related articles for article (PubMed ID: 27147087)

  • 1. Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.
    Denny JC; Bastarache L; Roden DM
    Annu Rev Genomics Hum Genet; 2016 Aug; 17():353-73. PubMed ID: 27147087
    [TBL] [Abstract][Full Text] [Related]  

  • 2. INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.
    Verma A; Leader JB; Verma SS; Frase A; Wallace J; Dudek S; Lavage DR; Van Hout CV; Dewey FE; Penn J; Lopez A; Overton JD; Carey DJ; Ledbetter DH; Kirchner HL; Ritchie MD; Pendergrass SA
    Pac Symp Biocomput; 2016; 21():168-79. PubMed ID: 26776183
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application of clinical text data for phenome-wide association studies (PheWASs).
    Hebbring SJ; Rastegar-Mojarad M; Ye Z; Mayer J; Jacobson C; Lin S
    Bioinformatics; 2015 Jun; 31(12):1981-7. PubMed ID: 25657332
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenome-wide association studies (PheWASs) for functional variants.
    Ye Z; Mayer J; Ivacic L; Zhou Z; He M; Schrodi SJ; Page D; Brilliant MH; Hebbring SJ
    Eur J Hum Genet; 2015 Apr; 23(4):523-9. PubMed ID: 25074467
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort.
    Schlauch KA; Read RW; Lombardi VC; Elhanan G; Metcalf WJ; Slonim AD; ; Grzymski JJ
    G3 (Bethesda); 2020 Feb; 10(2):645-664. PubMed ID: 31888951
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
    Zhao J; Cheng F; Jia P; Cox N; Denny JC; Zhao Z
    Genome Med; 2018 Jan; 10(1):7. PubMed ID: 29378629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative.
    Fritsche LG; Gruber SB; Wu Z; Schmidt EM; Zawistowski M; Moser SE; Blanc VM; Brummett CM; Kheterpal S; Abecasis GR; Mukherjee B
    Am J Hum Genet; 2018 Jun; 102(6):1048-1061. PubMed ID: 29779563
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electronic health records: the next wave of complex disease genetics.
    Wolford BN; Willer CJ; Surakka I
    Hum Mol Genet; 2018 May; 27(R1):R14-R21. PubMed ID: 29547983
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
    Joo YY; Pacheco JA; Thompson WK; Rasmussen-Torvik LJ; Rasmussen LV; Lin FTJ; Andrade M; Borthwick KM; Bottinger E; Cagan A; Carrell DS; Denny JC; Ellis SB; Gottesman O; Linneman JG; Pathak J; Peissig PL; Shang N; Tromp G; Veerappan A; Smith ME; Chisholm RL; Gawron AJ; Hayes MG; Kho AN
    PLoS One; 2023; 18(5):e0283553. PubMed ID: 37196047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Developing and evaluating pediatric phecodes (Peds-Phecodes) for high-throughput phenotyping using electronic health records.
    Grabowska ME; Van Driest SL; Robinson JR; Patrick AE; Guardo C; Gangireddy S; Ong HH; Feng Q; Carroll R; Kannankeril PJ; Wei WQ
    J Am Med Inform Assoc; 2024 Jan; 31(2):386-395. PubMed ID: 38041473
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.
    Weissenkampen JD; Jiang Y; Eckert S; Jiang B; Li B; Liu DJ
    Curr Protoc Hum Genet; 2019 Apr; 101(1):e83. PubMed ID: 30849219
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals.
    Verma A; Bang L; Miller JE; Zhang Y; Lee MTM; Zhang Y; Byrska-Bishop M; Carey DJ; Ritchie MD; Pendergrass SA; Kim D;
    Am J Hum Genet; 2019 Jan; 104(1):55-64. PubMed ID: 30598166
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of genetic and phenotypic heterogeneity of obstructive sleep apnea using electronic health records.
    Veatch OJ; Bauer CR; Keenan BT; Josyula NS; Mazzotti DR; Bagai K; Malow BA; Robishaw JD; Pack AI; Pendergrass SA
    BMC Med Genomics; 2020 Jul; 13(1):105. PubMed ID: 32711518
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery.
    Pendergrass SA; Ritchie MD
    Curr Genet Med Rep; 2015 Jun; 3(2):92-100. PubMed ID: 26146598
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
    Denny JC; Bastarache L; Ritchie MD; Carroll RJ; Zink R; Mosley JD; Field JR; Pulley JM; Ramirez AH; Bowton E; Basford MA; Carrell DS; Peissig PL; Kho AN; Pacheco JA; Rasmussen LV; Crosslin DR; Crane PK; Pathak J; Bielinski SJ; Pendergrass SA; Xu H; Hindorff LA; Li R; Manolio TA; Chute CG; Chisholm RL; Larson EB; Jarvik GP; Brilliant MH; McCarty CA; Kullo IJ; Haines JL; Crawford DC; Masys DR; Roden DM
    Nat Biotechnol; 2013 Dec; 31(12):1102-10. PubMed ID: 24270849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unravelling the human genome-phenome relationship using phenome-wide association studies.
    Bush WS; Oetjens MT; Crawford DC
    Nat Rev Genet; 2016 Mar; 17(3):129-45. PubMed ID: 26875678
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS.
    Bastarache L
    Annu Rev Biomed Data Sci; 2021 Jul; 4():1-19. PubMed ID: 34465180
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The challenges, advantages and future of phenome-wide association studies.
    Hebbring SJ
    Immunology; 2014 Feb; 141(2):157-65. PubMed ID: 24147732
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methodology in phenome-wide association studies: a systematic review.
    Wang L; Zhang X; Meng X; Koskeridis F; Georgiou A; Yu L; Campbell H; Theodoratou E; Li X
    J Med Genet; 2021 Nov; 58(11):720-728. PubMed ID: 34272311
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Maturation and application of phenome-wide association studies.
    Liu S; Crawford DC
    Trends Genet; 2022 Apr; 38(4):353-363. PubMed ID: 34991903
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.