BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 29779949)

  • 1. Disease Heritability Inferred from Familial Relationships Reported in Medical Records.
    Polubriaginof FCG; Vanguri R; Quinnies K; Belbin GM; Yahi A; Salmasian H; Lorberbaum T; Nwankwo V; Li L; Shervey MM; Glowe P; Ionita-Laza I; Simmerling M; Hripcsak G; Bakken S; Goldstein D; Kiryluk K; Kenny EE; Dudley J; Vawdrey DK; Tatonetti NP
    Cell; 2018 Jun; 173(7):1692-1704.e11. PubMed ID: 29779949
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The use of electronic health records for psychiatric phenotyping and genomics.
    Smoller JW
    Am J Med Genet B Neuropsychiatr Genet; 2018 Oct; 177(7):601-612. PubMed ID: 28557243
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Text Mining for Precision Medicine: Bringing Structure to EHRs and Biomedical Literature to Understand Genes and Health.
    Simmons M; Singhal A; Lu Z
    Adv Exp Med Biol; 2016; 939():139-166. PubMed ID: 27807747
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Applying family analyses to electronic health records to facilitate genetic research.
    Huang X; Elston RC; Rosa GJ; Mayer J; Ye Z; Kitchner T; Brilliant MH; Page D; Hebbring SJ
    Bioinformatics; 2018 Feb; 34(4):635-642. PubMed ID: 28968884
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A method for cohort selection of cardiovascular disease records from an electronic health record system.
    Abrahão MTF; Nobre MRC; Gutierrez MA
    Int J Med Inform; 2017 Jun; 102():138-149. PubMed ID: 28495342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program.
    Cronin RM; Halvorson AE; Springer C; Feng X; Sulieman L; Loperena-Cortes R; Mayo K; Carroll RJ; Chen Q; Ahmedani BK; Karnes J; Korf B; O'Donnell CJ; Qian J; Ramirez AH
    J Am Med Inform Assoc; 2021 Mar; 28(4):695-703. PubMed ID: 33404595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Large-Scale Discovery of Disease-Disease and Disease-Gene Associations.
    Gligorijevic D; Stojanovic J; Djuric N; Radosavljevic V; Grbovic M; Kulathinal RJ; Obradovic Z
    Sci Rep; 2016 Aug; 6():32404. PubMed ID: 27578529
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Missing heritability of complex diseases: Enlightenment by genetic variants from intermediate phenotypes.
    Blanco-Gómez A; Castillo-Lluva S; Del Mar Sáez-Freire M; Hontecillas-Prieto L; Mao JH; Castellanos-Martín A; Pérez-Losada J
    Bioessays; 2016 Jul; 38(7):664-73. PubMed ID: 27241833
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Estimating Heritability from Nuclear Family and Pedigree Data.
    Bochud M
    Methods Mol Biol; 2017; 1666():195-210. PubMed ID: 28980247
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Optimizing research in symptomatic uterine fibroids with development of a computable phenotype for use with electronic health records.
    Hoffman SR; Vines AI; Halladay JR; Pfaff E; Schiff L; Westreich D; Sundaresan A; Johnson LS; Nicholson WK
    Am J Obstet Gynecol; 2018 Jun; 218(6):610.e1-610.e7. PubMed ID: 29432754
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detecting Familial Aggregation.
    Naj AC; Beaty TH
    Methods Mol Biol; 2017; 1666():133-169. PubMed ID: 28980245
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human Facial Shape and Size Heritability and Genetic Correlations.
    Cole JB; Manyama M; Larson JR; Liberton DK; Ferrara TM; Riccardi SL; Li M; Mio W; Klein OD; Santorico SA; Hallgrímsson B; Spritz RA
    Genetics; 2017 Feb; 205(2):967-978. PubMed ID: 27974501
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RAD-sequencing for estimating genomic relatedness matrix-based heritability in the wild: A case study in roe deer.
    Gervais L; Perrier C; Bernard M; Merlet J; Pemberton JM; Pujol B; Quéméré E
    Mol Ecol Resour; 2019 Sep; 19(5):1205-1217. PubMed ID: 31058463
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Semi-supervised learning of the electronic health record for phenotype stratification.
    Beaulieu-Jones BK; Greene CS;
    J Biomed Inform; 2016 Dec; 64():168-178. PubMed ID: 27744022
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic evaluation with major genes and polygenic inheritance when some animals are not genotyped using gene content multiple-trait BLUP.
    Legarra A; Vitezica ZG
    Genet Sel Evol; 2015 Nov; 47():89. PubMed ID: 26576649
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Marker-based estimation of heritability in immortal populations.
    Kruijer W; Boer MP; Malosetti M; Flood PJ; Engel B; Kooke R; Keurentjes JJ; van Eeuwijk FA
    Genetics; 2015 Feb; 199(2):379-98. PubMed ID: 25527288
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Using big data to improve cardiovascular care and outcomes in China: a protocol for the CHinese Electronic health Records Research in Yinzhou (CHERRY) Study.
    Lin H; Tang X; Shen P; Zhang D; Wu J; Zhang J; Lu P; Si Y; Gao P
    BMJ Open; 2018 Feb; 8(2):e019698. PubMed ID: 29440217
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genes and environment].
    Feingold J
    J Soc Biol; 2000; 194(1):5-8. PubMed ID: 11107542
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.