BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 36777178)

  • 1. The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank.
    Johnson R; Ding Y; Bhattacharya A; Knyazev S; Chiu A; Lajonchere C; Geschwind DH; Pasaniuc B
    Cell Genom; 2023 Jan; 3(1):100243. PubMed ID: 36777178
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.
    Johnson R; Ding Y; Venkateswaran V; Bhattacharya A; Boulier K; Chiu A; Knyazev S; Schwarz T; Freund M; Zhan L; Burch KS; Caggiano C; Hill B; Rakocz N; Balliu B; Denny CT; Sul JH; Zaitlen N; Arboleda VA; Halperin E; Sankararaman S; Butte MJ; ; Lajonchere C; Geschwind DH; Pasaniuc B
    Genome Med; 2022 Sep; 14(1):104. PubMed ID: 36085083
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Scalable and Robust Regression Methods for Phenome-Wide Association Analysis on Large-Scale Biobank Data.
    Bi W; Lee S
    Front Genet; 2021; 12():682638. PubMed ID: 34211504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.
    Zhou W; Kanai M; Wu KH; Rasheed H; Tsuo K; Hirbo JB; Wang Y; Bhattacharya A; Zhao H; Namba S; Surakka I; Wolford BN; Lo Faro V; Lopera-Maya EA; Läll K; Favé MJ; Partanen JJ; Chapman SB; Karjalainen J; Kurki M; Maasha M; Brumpton BM; Chavan S; Chen TT; Daya M; Ding Y; Feng YA; Guare LA; Gignoux CR; Graham SE; Hornsby WE; Ingold N; Ismail SI; Johnson R; Laisk T; Lin K; Lv J; Millwood IY; Moreno-Grau S; Nam K; Palta P; Pandit A; Preuss MH; Saad C; Setia-Verma S; Thorsteinsdottir U; Uzunovic J; Verma A; Zawistowski M; Zhong X; Afifi N; Al-Dabhani KM; Al Thani A; Bradford Y; Campbell A; Crooks K; de Bock GH; Damrauer SM; Douville NJ; Finer S; Fritsche LG; Fthenou E; Gonzalez-Arroyo G; Griffiths CJ; Guo Y; Hunt KA; Ioannidis A; Jansonius NM; Konuma T; Lee MTM; Lopez-Pineda A; Matsuda Y; Marioni RE; Moatamed B; Nava-Aguilar MA; Numakura K; Patil S; Rafaels N; Richmond A; Rojas-Muñoz A; Shortt JA; Straub P; Tao R; Vanderwerff B; Vernekar M; Veturi Y; Barnes KC; Boezen M; Chen Z; Chen CY; Cho J; Smith GD; Finucane HK; Franke L; Gamazon ER; Ganna A; Gaunt TR; Ge T; Huang H; Huffman J; Katsanis N; Koskela JT; Lajonchere C; Law MH; Li L; Lindgren CM; Loos RJF; MacGregor S; Matsuda K; Olsen CM; Porteous DJ; Shavit JA; Snieder H; Takano T; Trembath RC; Vonk JM; Whiteman DC; Wicks SJ; Wijmenga C; Wright J; Zheng J; Zhou X; Awadalla P; Boehnke M; Bustamante CD; Cox NJ; Fatumo S; Geschwind DH; Hayward C; Hveem K; Kenny EE; Lee S; Lin YF; Mbarek H; Mägi R; Martin HC; Medland SE; Okada Y; Palotie AV; Pasaniuc B; Rader DJ; Ritchie MD; Sanna S; Smoller JW; Stefansson K; van Heel DA; Walters RG; Zöllner S; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; Martin AR; Willer CJ; Daly MJ; Neale BM
    Cell Genom; 2022 Oct; 2(10):100192. PubMed ID: 36777996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Role of Electronic Health Records in Advancing Genomic Medicine.
    Linder JE; Bastarache L; Hughey JJ; Peterson JF
    Annu Rev Genomics Hum Genet; 2021 Aug; 22():219-238. PubMed ID: 34038146
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population.
    Verma A; Damrauer SM; Naseer N; Weaver J; Kripke CM; Guare L; Sirugo G; Kember RL; Drivas TG; Dudek SM; Bradford Y; Lucas A; Judy R; Verma SS; Meagher E; Nathanson KL; Feldman M; Ritchie MD; Rader DJ; For The Penn Medicine BioBank
    J Pers Med; 2022 Nov; 12(12):. PubMed ID: 36556195
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defining Phenotypes from Clinical Data to Drive Genomic Research.
    Robinson JR; Wei WQ; Roden DM; Denny JC
    Annu Rev Biomed Data Sci; 2018 Jul; 1():69-92. PubMed ID: 34109303
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
    Joo YY; Pacheco JA; Thompson WK; Rasmussen-Torvik LJ; Rasmussen LV; Lin FTJ; Andrade M; Borthwick KM; Bottinger E; Cagan A; Carrell DS; Denny JC; Ellis SB; Gottesman O; Linneman JG; Pathak J; Peissig PL; Shang N; Tromp G; Veerappan A; Smith ME; Chisholm RL; Gawron AJ; Hayes MG; Kho AN
    PLoS One; 2023; 18(5):e0283553. PubMed ID: 37196047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine.
    Kember RL; Verma SS; Verma A; Xiao B; Lucas A; Kripke CM; Judy R; Chen J; Damrauer SM; Rader DJ; Ritchie MD
    Pac Symp Biocomput; 2024; 29():611-626. PubMed ID: 38160310
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
    Nagy R; Boutin TS; Marten J; Huffman JE; Kerr SM; Campbell A; Evenden L; Gibson J; Amador C; Howard DM; Navarro P; Morris A; Deary IJ; Hocking LJ; Padmanabhan S; Smith BH; Joshi P; Wilson JF; Hastie ND; Wright AF; McIntosh AM; Porteous DJ; Haley CS; Vitart V; Hayward C
    Genome Med; 2017 Mar; 9(1):23. PubMed ID: 28270201
    [TBL] [Abstract][Full Text] [Related]  

  • 14. mixWAS: An efficient distributed algorithm for mixed-outcomes genome-wide association studies.
    Li R; Benz L; Duan R; Denny JC; Hakonarson H; Mosley JD; Smoller JW; Wei WQ; Ritchie MD; Moore JH; Chen Y
    medRxiv; 2024 Jan; ():. PubMed ID: 38260403
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Extracting research-quality phenotypes from electronic health records to support precision medicine.
    Wei WQ; Denny JC
    Genome Med; 2015; 7(1):41. PubMed ID: 25937834
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison of phenomic profiles in the All of Us Research Program against the US general population and the UK Biobank.
    Zeng C; Schlueter DJ; Tran TC; Babbar A; Cassini T; Bastarache LA; Denny JC
    J Am Med Inform Assoc; 2024 Apr; 31(4):846-854. PubMed ID: 38263490
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic liability for substance use associated with medical comorbidities in electronic health records of African- and European-ancestry individuals.
    Hartwell EE; Merikangas AK; Verma SS; Ritchie MD; ; Kranzler HR; Kember RL
    Addict Biol; 2022 Jan; 27(1):e13099. PubMed ID: 34611967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The phenotype-genotype reference map: Improving biobank data science through replication.
    Bastarache L; Delozier S; Pandit A; He J; Lewis A; Annis AC; LeFaive J; Denny JC; Carroll RJ; Altman RB; Hughey JJ; Zawistowski M; Peterson JF
    Am J Hum Genet; 2023 Sep; 110(9):1522-1533. PubMed ID: 37607538
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.