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 *

156 related articles for article (PubMed ID: 24949630)

  • 1. Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations.
    Mosley JD; Van Driest SL; Weeke PE; Delaney JT; Wells QS; Bastarache L; Roden DM; Denny JC
    PLoS One; 2014; 9(6):e100322. PubMed ID: 24949630
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data.
    Mosley JD; Van Driest SL; Larkin EK; Weeke PE; Witte JS; Wells QS; Karnes JH; Guo Y; Bastarache L; Olson LM; McCarty CA; Pacheco JA; Jarvik GP; Carrell DS; Larson EB; Crosslin DR; Kullo IJ; Tromp G; Kuivaniemi H; Carey DJ; Ritchie MD; Denny JC; Roden DM
    PLoS One; 2013; 8(12):e81503. PubMed ID: 24349080
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.
    Ritchie MD; Denny JC; Crawford DC; Ramirez AH; Weiner JB; Pulley JM; Basford MA; Brown-Gentry K; Balser JR; Masys DR; Haines JL; Roden DM
    Am J Hum Genet; 2010 Apr; 86(4):560-72. PubMed ID: 20362271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.
    de Haan HG; van Hylckama Vlieg A; Lotta LA; Gorski MM; Bucciarelli P; Martinelli I; Baglin TP; Peyvandi F; Rosendaal FR;
    J Thromb Haemost; 2018 Dec; 16(12):2432-2441. PubMed ID: 30168256
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.
    Wood AR; Tuke MA; Nalls M; Hernandez D; Gibbs JR; Lin H; Xu CS; Li Q; Shen J; Jun G; Almeida M; Tanaka T; Perry JR; Gaulton K; Rivas M; Pearson R; Curran JE; Johnson MP; Göring HH; Duggirala R; Blangero J; Mccarthy MI; Bandinelli S; Murray A; Weedon MN; Singleton A; Melzer D; Ferrucci L; Frayling TM
    Hum Mol Genet; 2015 Mar; 24(5):1504-12. PubMed ID: 25378555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology.
    Shen F; Peng S; Fan Y; Wen A; Liu S; Wang Y; Wang L; Liu H
    J Biomed Inform; 2019 Aug; 96():103246. PubMed ID: 31255713
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiscale modeling of the causal functional roles of nsSNPs in a genome-wide association study: application to hypoxia.
    Xie L; Ng C; Ali T; Valencia R; Ferreira BL; Xue V; Tanweer M; Zhou D; Haddad GG; Bourne PE; Xie L
    BMC Genomics; 2013; 14 Suppl 3(Suppl 3):S9. PubMed ID: 23819581
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome bioinformatic analysis of nonsynonymous SNPs.
    Burke DF; Worth CL; Priego EM; Cheng T; Smink LJ; Todd JA; Blundell TL
    BMC Bioinformatics; 2007 Aug; 8():301. PubMed ID: 17708757
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heritable genotype contrast mining reveals novel gene associations specific to autism subgroups.
    Spencer M; Takahashi N; Chakraborty S; Miles J; Shyu CR
    J Biomed Inform; 2018 Jan; 77():50-61. PubMed ID: 29197649
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotype prediction of non-synonymous single-nucleotide polymorphisms in human ATP-binding cassette transporter genes.
    Wang LL; Liu YH; Meng LL; Li CG; Zhou SF
    Basic Clin Pharmacol Toxicol; 2011 Feb; 108(2):94-114. PubMed ID: 20849526
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The use of a DNA biobank linked to electronic medical records to characterize pharmacogenomic predictors of tacrolimus dose requirement in kidney transplant recipients.
    Birdwell KA; Grady B; Choi L; Xu H; Bian A; Denny JC; Jiang M; Vranic G; Basford M; Cowan JD; Richardson DM; Robinson MP; Ikizler TA; Ritchie MD; Stein CM; Haas DW
    Pharmacogenet Genomics; 2012 Jan; 22(1):32-42. PubMed ID: 22108237
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.
    Wood AR; Perry JR; Tanaka T; Hernandez DG; Zheng HF; Melzer D; Gibbs JR; Nalls MA; Weedon MN; Spector TD; Richards JB; Bandinelli S; Ferrucci L; Singleton AB; Frayling TM
    PLoS One; 2013; 8(5):e64343. PubMed ID: 23696881
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia.
    Carrera N; Arrojo M; Sanjuán J; Ramos-Ríos R; Paz E; Suárez-Rama JJ; Páramo M; Agra S; Brenlla J; Martínez S; Rivero O; Collier DA; Palotie A; Cichon S; Nöthen MM; Rietschel M; Rujescu D; Stefansson H; Steinberg S; Sigurdsson E; St Clair D; Tosato S; Werge T; Stefansson K; González JC; Valero J; Gutiérrez-Zotes A; Labad A; Martorell L; Vilella E; Carracedo Á; Costas J
    Biol Psychiatry; 2012 Jan; 71(2):169-77. PubMed ID: 22078303
    [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. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract.
    Wang Z; Huang C; Lv H; Zhang M; Li X
    PLoS One; 2020; 15(1):e0227859. PubMed ID: 31935276
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation and application of summary statistic imputation to discover new height-associated loci.
    Rüeger S; McDaid A; Kutalik Z
    PLoS Genet; 2018 May; 14(5):e1007371. PubMed ID: 29782485
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.