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 *

251 related articles for article (PubMed ID: 28229460)

  • 21. PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.
    Verma A; Lucas A; Verma SS; Zhang Y; Josyula N; Khan A; Hartzel DN; Lavage DR; Leader J; Ritchie MD; Pendergrass SA
    Am J Hum Genet; 2018 Apr; 102(4):592-608. PubMed ID: 29606303
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. HCLC-FC: A novel statistical method for phenome-wide association studies.
    Liang X; Cao X; Sha Q; Zhang S
    PLoS One; 2022; 17(11):e0276646. PubMed ID: 36350801
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS.
    Dey R; Schmidt EM; Abecasis GR; Lee S
    Am J Hum Genet; 2017 Jul; 101(1):37-49. PubMed ID: 28602423
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Phenome-Wide Association Study of Polygenic Risk Score for Alzheimer's Disease in Electronic Health Records.
    Fu M; ; ; Chang TS
    Front Aging Neurosci; 2022; 14():800375. PubMed ID: 35370621
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phenome-wide association study (PheWAS) of colorectal cancer risk SNP effects on health outcomes in UK Biobank.
    Zhang X; Li X; He Y; Law PJ; Farrington SM; Campbell H; Tomlinson IPM; Houlston RS; Dunlop MG; Timofeeva M; Theodoratou E
    Br J Cancer; 2022 Mar; 126(5):822-830. PubMed ID: 34912076
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association of Interleukin 6 Receptor Variant With Cardiovascular Disease Effects of Interleukin 6 Receptor Blocking Therapy: A Phenome-Wide Association Study.
    Cai T; Zhang Y; Ho YL; Link N; Sun J; Huang J; Cai TA; Damrauer S; Ahuja Y; Honerlaw J; Huang J; Costa L; Schubert P; Hong C; Gagnon D; Sun YV; Gaziano JM; Wilson P; Cho K; Tsao P; O'Donnell CJ; Liao KP;
    JAMA Cardiol; 2018 Sep; 3(9):849-857. PubMed ID: 30090940
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Research progress in the methodology used in phenome-wide association studies].
    Jiang FY; Wang LJ; Sun J; Yu LL; Zhou X; Zhu YM; Li X
    Zhonghua Liu Xing Bing Xue Za Zhi; 2022 Jul; 43(7):1154-1161. PubMed ID: 35856214
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Polygenic Liability to Depression Is Associated With Multiple Medical Conditions in the Electronic Health Record: Phenome-wide Association Study of 46,782 Individuals.
    Fang Y; Fritsche LG; Mukherjee B; Sen S; Richmond-Rakerd LS
    Biol Psychiatry; 2022 Dec; 92(12):923-931. PubMed ID: 35965108
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. 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]  

  • 34. Genomic and Phenomic Research in the 21st Century.
    Hebbring S
    Trends Genet; 2019 Jan; 35(1):29-41. PubMed ID: 30342790
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks.
    Fritsche LG; Patil S; Beesley LJ; VandeHaar P; Salvatore M; Ma Y; Peng RB; Taliun D; Zhou X; Mukherjee B
    Am J Hum Genet; 2020 Nov; 107(5):815-836. PubMed ID: 32991828
    [TBL] [Abstract][Full Text] [Related]  

  • 36. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
    Verma A; Verma SS; Pendergrass SA; Crawford DC; Crosslin DR; Kuivaniemi H; Bush WS; Bradford Y; Kullo I; Bielinski SJ; Li R; Denny JC; Peissig P; Hebbring S; De Andrade M; Ritchie MD; Tromp G
    BMC Med Genomics; 2016 Aug; 9 Suppl 1(Suppl 1):32. PubMed ID: 27535653
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb.
    Fritsche LG; Beesley LJ; VandeHaar P; Peng RB; Salvatore M; Zawistowski M; Gagliano Taliun SA; Das S; LeFaive J; Kaleba EO; Klumpner TT; Moser SE; Blanc VM; Brummett CM; Kheterpal S; Abecasis GR; Gruber SB; Mukherjee B
    PLoS Genet; 2019 Jun; 15(6):e1008202. PubMed ID: 31194742
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Contrasting Association Results between Existing PheWAS Phenotype Definition Methods and Five Validated Electronic Phenotypes.
    Leader JB; Pendergrass SA; Verma A; Carey DJ; Hartzel DN; Ritchie MD; Kirchner HL
    AMIA Annu Symp Proc; 2015; 2015():824-32. PubMed ID: 26958218
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies.
    Mitchell SL; Hall JB; Goodloe RJ; Boston J; Farber-Eger E; Pendergrass SA; Bush WS; Crawford DC
    BioData Min; 2014; 7():6. PubMed ID: 24731735
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.