BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 24786325)

  • 1. Disease risk factors identified through shared genetic architecture and electronic medical records.
    Li L; Ruau DJ; Patel CJ; Weber SC; Chen R; Tatonetti NP; Dudley JT; Butte AJ
    Sci Transl Med; 2014 Apr; 6(234):234ra57. PubMed ID: 24786325
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Systematic identification of risk factors for Alzheimer's disease through shared genetic architecture and electronic medical records.
    Li L; Ruau D; Chen R; Weber S; Butte AJ
    Pac Symp Biocomput; 2013; ():224-35. PubMed ID: 23424127
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR.
    Verma SS; Lucas AM; Lavage DR; Leader JB; Metpally R; Krishnamurthy S; Dewey F; Borecki I; Lopez A; Overton J; Penn J; Reid J; Pendergrass SA; Breitwieser G; Ritchie MD
    Pac Symp Biocomput; 2017; 22():533-544. PubMed ID: 27897004
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Investigation of multi-trait associations using pathway-based analysis of GWAS summary statistics.
    Pei G; Sun H; Dai Y; Liu X; Zhao Z; Jia P
    BMC Genomics; 2019 Feb; 20(Suppl 1):79. PubMed ID: 30712509
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A genome-wide association study of red blood cell traits using the electronic medical record.
    Kullo IJ; Ding K; Jouni H; Smith CY; Chute CG
    PLoS One; 2010 Sep; 5(9):. PubMed ID: 20927387
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Constraints on Biological Mechanism from Disease Comorbidity Using Electronic Medical Records and Database of Genetic Variants.
    Bagley SC; Sirota M; Chen R; Butte AJ; Altman RB
    PLoS Comput Biol; 2016 Apr; 12(4):e1004885. PubMed ID: 27115429
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.
    Li B; Veturi Y; Bradford Y; Verma SS; Verma A; Lucas AM; Haas DW; Ritchie MD
    Pac Symp Biocomput; 2019; 24():296-307. PubMed ID: 30864331
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Complex-disease networks of trait-associated single-nucleotide polymorphisms (SNPs) unveiled by information theory.
    Li H; Lee Y; Chen JL; Rebman E; Li J; Lussier YA
    J Am Med Inform Assoc; 2012; 19(2):295-305. PubMed ID: 22278381
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network.
    Pendergrass SA; Brown-Gentry K; Dudek S; Frase A; Torstenson ES; Goodloe R; Ambite JL; Avery CL; Buyske S; Bůžková P; Deelman E; Fesinmeyer MD; Haiman CA; Heiss G; Hindorff LA; Hsu CN; Jackson RD; Kooperberg C; Le Marchand L; Lin Y; Matise TC; Monroe KR; Moreland L; Park SL; Reiner A; Wallace R; Wilkens LR; Crawford DC; Ritchie MD
    PLoS Genet; 2013; 9(1):e1003087. PubMed ID: 23382687
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Common and Rare Variants Genetic Association Analysis of Cigarettes per Day Among Ever-Smokers in Chronic Obstructive Pulmonary Disease Cases and Controls.
    Lutz SM; Frederiksen B; Begum F; McDonald MN; Cho MH; Hobbs BD; Parker MM; DeMeo DL; Hersh CP; Ehringer MA; Young K; Jiang L; Foreman MG; Kinney GL; Make BJ; Lomas DA; Bakke P; Gulsvik A; Crapo JD; Silverman EK; Beaty TH; Hokanson JE;
    Nicotine Tob Res; 2019 May; 21(6):714-722. PubMed ID: 29767774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exploring the Genetic Patterns of Complex Diseases via the Integrative Genome-Wide Approach.
    Teng B; Yang C; Liu J; Cai Z; Wan X
    IEEE/ACM Trans Comput Biol Bioinform; 2016; 13(3):557-64. PubMed ID: 27295639
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of Genetic Variants in ARID5B, IKZF1 and CEBPE with Risk of Childhood de novo B-Lineage Acute Lymphoblastic Leukemia in India.
    Bhandari P; Ahmad F; Mandava S; Das BR
    Asian Pac J Cancer Prev; 2016; 17(8):3989-95. PubMed ID: 27644650
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Powerful and Adaptive Testing for Multi-trait and Multi-SNP Associations with GWAS and Sequencing Data.
    Kim J; Zhang Y; Pan W;
    Genetics; 2016 Jun; 203(2):715-31. PubMed ID: 27075728
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. A unifying framework for joint trait analysis under a non-infinitesimal model.
    Johnson R; Shi H; Pasaniuc B; Sankararaman S
    Bioinformatics; 2018 Jul; 34(13):i195-i201. PubMed ID: 29949958
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.