BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 23762230)

  • 1. Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
    McDavid A; Crane PK; Newton KM; Crosslin DR; McCormick W; Weston N; Ehrlich K; Hart E; Harrison R; Kukull WA; Rottscheit C; Peissig P; Stefanski E; McCarty CA; Zuvich RL; Ritchie MD; Haines JL; Denny JC; Schellenberg GD; de Andrade M; Kullo I; Li R; Mirel D; Crenshaw A; Bowen JD; Li G; Tsuang D; McCurry S; Teri L; Larson EB; Jarvik GP; Carlson CS
    PLoS One; 2013; 8(6):e63481. PubMed ID: 23762230
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A GWAS Study on Liver Function Test Using eMERGE Network Participants.
    Namjou B; Marsolo K; Lingren T; Ritchie MD; Verma SS; Cobb BL; Perry C; Kitchner TE; Brilliant MH; Peissig PL; Borthwick KM; Williams MS; Grafton J; Jarvik GP; Holm IA; Harley JB
    PLoS One; 2015; 10(9):e0138677. PubMed ID: 26413716
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
    Zheng NS; Feng Q; Kerchberger VE; Zhao J; Edwards TL; Cox NJ; Stein CM; Roden DM; Denny JC; Wei WQ
    J Am Med Inform Assoc; 2020 Nov; 27(11):1675-1687. PubMed ID: 32974638
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
    Stanaway IB; Hall TO; Rosenthal EA; Palmer M; Naranbhai V; Knevel R; Namjou-Khales B; Carroll RJ; Kiryluk K; Gordon AS; Linder J; Howell KM; Mapes BM; Lin FTJ; Joo YY; Hayes MG; Gharavi AG; Pendergrass SA; Ritchie MD; de Andrade M; Croteau-Chonka DC; Raychaudhuri S; Weiss ST; Lebo M; Amr SS; Carrell D; Larson EB; Chute CG; Rasmussen-Torvik LJ; Roy-Puckelwartz MJ; Sleiman P; Hakonarson H; Li R; Karlson EW; Peterson JF; Kullo IJ; Chisholm R; Denny JC; Jarvik GP; ; Crosslin DR
    Genet Epidemiol; 2019 Feb; 43(1):63-81. PubMed ID: 30298529
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.
    Ritchie MD; Verma SS; Hall MA; Goodloe RJ; Berg RL; Carrell DS; Carlson CS; Chen L; Crosslin DR; Denny JC; Jarvik G; Li R; Linneman JG; Pathak J; Peissig P; Rasmussen LV; Ramirez AH; Wang X; Wilke RA; Wolf WA; Torstenson ES; Turner SD; McCarty CA
    Mol Vis; 2014; 20():1281-95. PubMed ID: 25352737
    [TBL] [Abstract][Full Text] [Related]  

  • 6. LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.
    Goldstein JA; Weinstock JS; Bastarache LA; Larach DB; Fritsche LG; Schmidt EM; Brummett CM; Kheterpal S; Abecasis GR; Denny JC; Zawistowski M
    PLoS Genet; 2020 Nov; 16(11):e1009077. PubMed ID: 33175840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genome-wide association study of polycystic ovary syndrome identified from electronic health records.
    Zhang Y; Ho K; Keaton JM; Hartzel DN; Day F; Justice AE; Josyula NS; Pendergrass SA; Actkins K; Davis LK; Velez Edwards DR; Holohan B; Ramirez A; Stanaway IB; Crosslin DR; Jarvik GP; Sleiman P; Hakonarson H; Williams MS; Lee MTM
    Am J Obstet Gynecol; 2020 Oct; 223(4):559.e1-559.e21. PubMed ID: 32289280
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit.
    Pendergrass SA; Verma SS; Holzinger ER; Moore CB; Wallace J; Dudek SM; Huggins W; Kitchner T; Waudby C; Berg R; McCarty CA; Ritchie MD
    Pac Symp Biocomput; 2013; ():147-58. PubMed ID: 23424120
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
    Ritchie MD; Denny JC; Zuvich RL; Crawford DC; Schildcrout JS; Bastarache L; Ramirez AH; Mosley JD; Pulley JM; Basford MA; Bradford Y; Rasmussen LV; Pathak J; Chute CG; Kullo IJ; McCarty CA; Chisholm RL; Kho AN; Carlson CS; Larson EB; Jarvik GP; Sotoodehnia N; ; Manolio TA; Li R; Masys DR; Haines JL; Roden DM
    Circulation; 2013 Apr; 127(13):1377-85. PubMed ID: 23463857
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Opportunities for drug repositioning from phenome-wide association studies.
    Rastegar-Mojarad M; Ye Z; Kolesar JM; Hebbring SJ; Lin SM
    Nat Biotechnol; 2015 Apr; 33(4):342-5. PubMed ID: 25850054
    [No Abstract]   [Full Text] [Related]  

  • 11. Disease genetics: phenome-wide association studies go large.
    Flintoft L
    Nat Rev Genet; 2014 Jan; 15(1):2. PubMed ID: 24322724
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Translating genome wide association study results to associations among common diseases: in silico study with an electronic medical record.
    Anand V; Rosenman MB; Downs SM
    Int J Med Inform; 2013 Sep; 82(9):864-74. PubMed ID: 23743324
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide study of resistant hypertension identified from electronic health records.
    Dumitrescu L; Ritchie MD; Denny JC; El Rouby NM; McDonough CW; Bradford Y; Ramirez AH; Bielinski SJ; Basford MA; Chai HS; Peissig P; Carrell D; Pathak J; Rasmussen LV; Wang X; Pacheco JA; Kho AN; Hayes MG; Matsumoto M; Smith ME; Li R; Cooper-DeHoff RM; Kullo IJ; Chute CG; Chisholm RL; Jarvik GP; Larson EB; Carey D; McCarty CA; Williams MS; Roden DM; Bottinger E; Johnson JA; de Andrade M; Crawford DC
    PLoS One; 2017; 12(2):e0171745. PubMed ID: 28222112
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.
    Palmer MR; Kim DS; Crosslin DR; Stanaway IB; Rosenthal EA; Carrell DS; Cronkite DJ; Gordon A; Du X; Li YK; Williams MS; Weng C; Feng Q; Li R; Pendergrass SA; Hakonarson H; Fasel D; Sohn S; Sleiman P; Handelman SK; Speliotes E; Kullo IJ; Larson EB; ; Jarvik GP
    Genet Epidemiol; 2021 Feb; 45(1):4-15. PubMed ID: 32964493
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
    Gottesman O; Kuivaniemi H; Tromp G; Faucett WA; Li R; Manolio TA; Sanderson SC; Kannry J; Zinberg R; Basford MA; Brilliant M; Carey DJ; Chisholm RL; Chute CG; Connolly JJ; Crosslin D; Denny JC; Gallego CJ; Haines JL; Hakonarson H; Harley J; Jarvik GP; Kohane I; Kullo IJ; Larson EB; McCarty C; Ritchie MD; Roden DM; Smith ME; Böttinger EP; Williams MS;
    Genet Med; 2013 Oct; 15(10):761-71. PubMed ID: 23743551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Electronic medical records for genetic research: results of the eMERGE consortium.
    Kho AN; Pacheco JA; Peissig PL; Rasmussen L; Newton KM; Weston N; Crane PK; Pathak J; Chute CG; Bielinski SJ; Kullo IJ; Li R; Manolio TA; Chisholm RL; Denny JC
    Sci Transl Med; 2011 Apr; 3(79):79re1. PubMed ID: 21508311
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Semi-supervised validation of multiple surrogate outcomes with application to electronic medical records phenotyping.
    Hong C; Liao KP; Cai T
    Biometrics; 2019 Mar; 75(1):78-89. PubMed ID: 30267536
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mining the ultimate phenome repository.
    Shah NH
    Nat Biotechnol; 2013 Dec; 31(12):1095-7. PubMed ID: 24316646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.
    Glessner JT; Li J; Desai A; Palmer M; Kim D; Lucas AM; Chang X; Connolly JJ; Almoguera B; Harley JB; Jarvik GP; Ritchie MD; Sleiman PMA; Roden DM; Crosslin D; Hakonarson H
    Int J Cardiol; 2020 Jan; 298():107-113. PubMed ID: 31447229
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.