BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 36085083)

  • 1. 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]  

  • 2. Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles.
    Venkateswaran V; Boulier K; Ding Y; Johnson R; Bhattacharya A; Pasaniuc B
    Transl Psychiatry; 2024 Jan; 14(1):38. PubMed ID: 38238290
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Population structure and pharmacogenomic risk stratification in the United States.
    Nagar SD; Conley AB; Jordan IK
    BMC Biol; 2020 Oct; 18(1):140. PubMed ID: 33050895
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank.
    Hall JB; Dumitrescu L; Dilks HH; Crawford DC; Bush WS
    PLoS One; 2014; 9(6):e99161. PubMed ID: 24896101
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.
    Wei WQ; Bastarache LA; Carroll RJ; Marlo JE; Osterman TJ; Gamazon ER; Cox NJ; Roden DM; Denny JC
    PLoS One; 2017; 12(7):e0175508. PubMed ID: 28686612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Comparative Analysis of Genetic Ancestry and Admixture in the Colombian Populations of Chocó and Medellín.
    Conley AB; Rishishwar L; Norris ET; Valderrama-Aguirre A; Mariño-Ramírez L; Medina-Rivas MA; Jordan IK
    G3 (Bethesda); 2017 Oct; 7(10):3435-3447. PubMed ID: 28855283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Generalizability of PGS
    Shang H; Ding Y; Venkateswaran V; Boulier K; Kathuria-Prakash N; Malidarreh PB; Luber JM; Pasaniuc B
    HGG Adv; 2024 May; 5(3):100302. PubMed ID: 38704641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Additional impact of genetic ancestry over self-reported race/ethnicity to prevalence of KRAS mutations and allele-specific subtypes in non-small cell lung cancer.
    Wang X; Hou K; Ricciuti B; Alessi JV; Li X; Pecci F; Dey R; Luo J; Awad MM; Gusev A; Lin X; Johnson BE; Christiani DC
    HGG Adv; 2024 Jun; ():100320. PubMed ID: 38902927
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records.
    Kurreeman F; Liao K; Chibnik L; Hickey B; Stahl E; Gainer V; Li G; Bry L; Mahan S; Ardlie K; Thomson B; Szolovits P; Churchill S; Murphy SN; Cai T; Raychaudhuri S; Kohane I; Karlson E; Plenge RM
    Am J Hum Genet; 2011 Jan; 88(1):57-69. PubMed ID: 21211616
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS.
    Bastarache L
    Annu Rev Biomed Data Sci; 2021 Jul; 4():1-19. PubMed ID: 34465180
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Phenotype risk scores (PheRS) for pancreatic cancer using time-stamped electronic health record data: Discovery and validation in two large biobanks.
    Salvatore M; Beesley LJ; Fritsche LG; Hanauer D; Shi X; Mondul AM; Pearce CL; Mukherjee B
    J Biomed Inform; 2021 Jan; 113():103652. PubMed ID: 33279681
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ancestry effects on type 2 diabetes genetic risk inference in Hispanic/Latino populations.
    Chande AT; Rishishwar L; Conley AB; Valderrama-Aguirre A; Medina-Rivas MA; Jordan IK
    BMC Med Genet; 2020 Jun; 21(Suppl 2):132. PubMed ID: 32580712
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations.
    Bryc K; Velez C; Karafet T; Moreno-Estrada A; Reynolds A; Auton A; Hammer M; Bustamante CD; Ostrer H
    Proc Natl Acad Sci U S A; 2010 May; 107 Suppl 2(Suppl 2):8954-61. PubMed ID: 20445096
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.
    Rizig M; Bandres-Ciga S; Makarious MB; Ojo O; Crea PW; Abiodun O; Levine KS; Abubakar S; Achoru C; Vitale D; Adeniji O; Agabi O; Koretsky MJ; Agulanna U; Hall DA; Akinyemi R; Xie T; Ali M; Shamim EA; Ani-Osheku I; Padmanaban M; Arigbodi O; Standaert DG; Bello A; Dean M; Erameh C; Elsayed I; Farombi T; Okunoye O; Fawale M; Billingsley KJ; Imarhiagbe F; Jerez PA; Iwuozo E; Baker B; Komolafe M; Malik L; Nwani P; Daida K; Nwazor E; Miano-Burkhardt A; Nyandaiti Y; Fang ZH; Obiabo Y; Kluss JH; Odeniyi O; Hernandez D; Odiase F; Tayebi N; Ojini F; Sidranksy E; Onwuegbuzie G; D'Souza AM; Osaigbovo G; Berhe B; Osemwegie N; Reed X; Oshinaike O; Leonard H; Otubogun F; Alvarado CX; Oyakhire S; Ozomma S; Samuel S; Taiwo F; Wahab K; Zubair Y; Iwaki H; Kim JJ; Morris HR; Hardy J; Nalls M; Heilbron K; Norcliffe-Kaufmann L; ; Blauwendraat C; Houlden H; Singleton A; Okubadejo N
    medRxiv; 2023 May; ():. PubMed ID: 37398408
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank.
    James G; Reisberg S; Lepik K; Galwey N; Avillach P; Kolberg L; Mägi R; Esko T; Alexander M; Waterworth D; Loomis AK; Vilo J
    PLoS One; 2019; 14(4):e0215026. PubMed ID: 30978214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.