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 *

179 related articles for article (PubMed ID: 36114182)

  • 1. Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks.
    Dey R; Zhou W; Kiiskinen T; Havulinna A; Elliott A; Karjalainen J; Kurki M; Qin A; ; Lee S; Palotie A; Neale B; Daly M; Lin X
    Nat Commun; 2022 Sep; 13(1):5437. PubMed ID: 36114182
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Fast and Accurate Method for Genome-wide Scale Phenome-wide G × E Analysis and Its Application to UK Biobank.
    Bi W; Zhao Z; Dey R; Fritsche LG; Mukherjee B; Lee S
    Am J Hum Genet; 2019 Dec; 105(6):1182-1192. PubMed ID: 31735295
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.
    Bi W; Fritsche LG; Mukherjee B; Kim S; Lee S
    Am J Hum Genet; 2020 Aug; 107(2):222-233. PubMed ID: 32589924
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
    Zhou W; Nielsen JB; Fritsche LG; Dey R; Gabrielsen ME; Wolford BN; LeFaive J; VandeHaar P; Gagliano SA; Gifford A; Bastarache LA; Wei WQ; Denny JC; Lin M; Hveem K; Kang HM; Abecasis GR; Willer CJ; Lee S
    Nat Genet; 2018 Sep; 50(9):1335-1341. PubMed ID: 30104761
    [TBL] [Abstract][Full Text] [Related]  

  • 5. UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.
    Zhao Z; Bi W; Zhou W; VandeHaar P; Fritsche LG; Lee S
    Am J Hum Genet; 2020 Jan; 106(1):3-12. PubMed ID: 31866045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Robust meta-analysis of biobank-based genome-wide association studies with unbalanced binary phenotypes.
    Dey R; Nielsen JB; Fritsche LG; Zhou W; Zhu H; Willer CJ; Lee S
    Genet Epidemiol; 2019 Jul; 43(5):462-476. PubMed ID: 30793809
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.
    McInnes G; Tanigawa Y; DeBoever C; Lavertu A; Olivieri JE; Aguirre M; Rivas MA
    Bioinformatics; 2019 Jul; 35(14):2495-2497. PubMed ID: 30520965
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Efficient mixed model approach for large-scale genome-wide association studies of ordinal categorical phenotypes.
    Bi W; Zhou W; Dey R; Mukherjee B; Sampson JN; Lee S
    Am J Hum Genet; 2021 May; 108(5):825-839. PubMed ID: 33836139
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study.
    Li X; Meng X; He Y; Spiliopoulou A; Timofeeva M; Wei WQ; Gifford A; Yang T; Varley T; Tzoulaki I; Joshi P; Denny JC; Mckeigue P; Campbell H; Theodoratou E
    PLoS Med; 2019 Oct; 16(10):e1002937. PubMed ID: 31626644
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.
    Córdova-Palomera A; Tcheandjieu C; Fries JA; Varma P; Chen VS; Fiterau M; Xiao K; Tejeda H; Keavney BD; Cordell HJ; Tanigawa Y; Venkataraman G; Rivas MA; Ré C; Ashley E; Priest JR
    Circ Genom Precis Med; 2020 Dec; 13(6):e003014. PubMed ID: 33125279
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.
    Tanigawa Y; Li J; Justesen JM; Horn H; Aguirre M; DeBoever C; Chang C; Narasimhan B; Lage K; Hastie T; Park CY; Bejerano G; Ingelsson E; Rivas MA
    Nat Commun; 2019 Sep; 10(1):4064. PubMed ID: 31492854
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Polygenic risk score-based phenome-wide association study of head and neck cancer across two large biobanks.
    Lee YC; Jung SH; Shivakumar M; Cha S; Park WY; Won HH; Eun YG; Biobank PM; Kim D
    BMC Med; 2024 Mar; 22(1):120. PubMed ID: 38486201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Genetic and Phenotypic Features of Schizophrenia in the UK Biobank.
    Legge SE; Pardiñas AF; Woolway G; Rees E; Cardno AG; Escott-Price V; Holmans P; Kirov G; Owen MJ; O'Donovan MC; Walters JTR
    JAMA Psychiatry; 2024 Jul; 81(7):681-690. PubMed ID: 38536179
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries.
    An U; Pazokitoroudi A; Alvarez M; Huang L; Bacanu S; Schork AJ; Kendler K; Pajukanta P; Flint J; Zaitlen N; Cai N; Dahl A; Sankararaman S
    Nat Genet; 2023 Dec; 55(12):2269-2276. PubMed ID: 37985819
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank.
    De Lillo A; D'Antona S; Pathak GA; Wendt FR; De Angelis F; Fuciarelli M; Polimanti R
    Hum Mol Genet; 2021 Jul; 30(15):1457-1467. PubMed ID: 33890984
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.