BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 35763490)

  • 1. Genotype imputation and polygenic score estimation in northwestern Russian population.
    Kolosov N; Rezapova V; Rotar O; Loboda A; Freylikhman O; Melnik O; Sergushichev A; Stevens C; Voortman T; Kostareva A; Konradi A; Daly MJ; Artomov M
    PLoS One; 2022; 17(6):e0269434. PubMed ID: 35763490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype imputation performance of three reference panels using African ancestry individuals.
    Vergara C; Parker MM; Franco L; Cho MH; Valencia-Duarte AV; Beaty TH; Duggal P
    Hum Genet; 2018 Apr; 137(4):281-292. PubMed ID: 29637265
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels.
    Zhou W; Fritsche LG; Das S; Zhang H; Nielsen JB; Holmen OL; Chen J; Lin M; Elvestad MB; Hveem K; Abecasis GR; Kang HM; Willer CJ
    Genet Epidemiol; 2017 Dec; 41(8):744-755. PubMed ID: 28861891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
    Huerta-Chagoya A; Schroeder P; Mandla R; Deutsch AJ; Zhu W; Petty L; Yi X; Cole JB; Udler MS; Dornbos P; Porneala B; DiCorpo D; Liu CT; Li JH; Szczerbiński L; Kaur V; Kim J; Lu Y; Martin A; Eizirik DL; Marchetti P; Marselli L; Chen L; Srinivasan S; Todd J; Flannick J; Gubitosi-Klug R; Levitsky L; Shah R; Kelsey M; Burke B; Dabelea DM; Divers J; Marcovina S; Stalbow L; Loos RJF; Darst BF; Kooperberg C; Raffield LM; Haiman C; Sun Q; McCormick JB; Fisher-Hoch SP; Ordoñez ML; Meigs J; Baier LJ; González-Villalpando C; González-Villalpando ME; Orozco L; García-García L; Moreno-Estrada A; ; Aguilar-Salinas CA; Tusié T; Dupuis J; Ng MCY; Manning A; Highland HM; Cnop M; Hanson R; Below J; Florez JC; Leong A; Mercader JM
    Diabetologia; 2023 Jul; 66(7):1273-1288. PubMed ID: 37148359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Imputation of genotypes from low density (50,000 markers) to high density (700,000 markers) of cows from research herds in Europe, North America, and Australasia using 2 reference populations.
    Pryce JE; Johnston J; Hayes BJ; Sahana G; Weigel KA; McParland S; Spurlock D; Krattenmacher N; Spelman RJ; Wall E; Calus MP
    J Dairy Sci; 2014 Mar; 97(3):1799-811. PubMed ID: 24472132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools.
    Sariya S; Lee JH; Mayeux R; Vardarajan BN; Reyes-Dumeyer D; Manly JJ; Brickman AM; Lantigua R; Medrano M; Jimenez-Velazquez IZ; Tosto G
    Front Genet; 2019; 10():239. PubMed ID: 31001313
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort.
    Privé F; Aschard H; Carmi S; Folkersen L; Hoggart C; O'Reilly PF; Vilhjálmsson BJ
    Am J Hum Genet; 2022 Jan; 109(1):12-23. PubMed ID: 34995502
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comprehensive evaluation of imputation performance in African Americans.
    Chanda P; Yuhki N; Li M; Bader JS; Hartz A; Boerwinkle E; Kao WH; Arking DE
    J Hum Genet; 2012 Jul; 57(7):411-21. PubMed ID: 22648186
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.
    Pistis G; Porcu E; Vrieze SI; Sidore C; Steri M; Danjou F; Busonero F; Mulas A; Zoledziewska M; Maschio A; Brennan C; Lai S; Miller MB; Marcelli M; Urru MF; Pitzalis M; Lyons RH; Kang HM; Jones CM; Angius A; Iacono WG; Schlessinger D; McGue M; Cucca F; Abecasis GR; Sanna S
    Eur J Hum Genet; 2015 Jul; 23(7):975-83. PubMed ID: 25293720
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A comprehensive evaluation of polygenic score and genotype imputation performances of human SNP arrays in diverse populations.
    Nguyen DT; Tran TTH; Tran MH; Tran K; Pham D; Duong NT; Nguyen Q; Vo NS
    Sci Rep; 2022 Oct; 12(1):17556. PubMed ID: 36266455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype imputation for Han Chinese population using Haplotype Reference Consortium as reference.
    Lin Y; Liu L; Yang S; Li Y; Lin D; Zhang X; Yin X
    Hum Genet; 2018 Jul; 137(6-7):431-436. PubMed ID: 29855708
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population.
    Levi H; Elkon R; Shamir R
    Bioinformatics; 2024 Feb; 40(2):. PubMed ID: 38265251
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multi-generational imputation of single nucleotide polymorphism marker genotypes and accuracy of genomic selection.
    Toghiani S; Aggrey SE; Rekaya R
    Animal; 2016 Jul; 10(7):1077-85. PubMed ID: 27076192
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype-imputation accuracy across worldwide human populations.
    Huang L; Li Y; Singleton AB; Hardy JA; Abecasis G; Rosenberg NA; Scheet P
    Am J Hum Genet; 2009 Feb; 84(2):235-50. PubMed ID: 19215730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Imputation accuracy across global human populations.
    Cahoon JL; Rui X; Tang E; Simons C; Langie J; Chen M; Lo YC; Chiang CWK
    Am J Hum Genet; 2024 May; 111(5):979-989. PubMed ID: 38604166
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigating the accuracy of imputing autosomal variants in Nellore cattle using the ARS-UCD1.2 assembly of the bovine genome.
    Hermisdorff IDC; Costa RB; de Albuquerque LG; Pausch H; Kadri NK
    BMC Genomics; 2020 Nov; 21(1):772. PubMed ID: 33167856
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide polygenic score to predict chronic kidney disease across ancestries.
    Khan A; Turchin MC; Patki A; Srinivasasainagendra V; Shang N; Nadukuru R; Jones AC; Malolepsza E; Dikilitas O; Kullo IJ; Schaid DJ; Karlson E; Ge T; Meigs JB; Smoller JW; Lange C; Crosslin DR; Jarvik GP; Bhatraju PK; Hellwege JN; Chandler P; Torvik LR; Fedotov A; Liu C; Kachulis C; Lennon N; Abul-Husn NS; Cho JH; Ionita-Laza I; Gharavi AG; Chung WK; Hripcsak G; Weng C; Nadkarni G; Irvin MR; Tiwari HK; Kenny EE; Limdi NA; Kiryluk K
    Nat Med; 2022 Jul; 28(7):1412-1420. PubMed ID: 35710995
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome.
    Lert-Itthiporn W; Suktitipat B; Grove H; Sakuntabhai A; Malasit P; Tangthawornchaikul N; Matsuda F; Suriyaphol P
    BMC Med Genet; 2018 Feb; 19(1):23. PubMed ID: 29439659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polygenic scoring accuracy varies across the genetic ancestry continuum.
    Ding Y; Hou K; Xu Z; Pimplaskar A; Petter E; Boulier K; Privé F; Vilhjálmsson BJ; Olde Loohuis LM; Pasaniuc B
    Nature; 2023 Jun; 618(7966):774-781. PubMed ID: 37198491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analyzing the Korean reference genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population.
    Hwang MY; Choi NH; Won HH; Kim BJ; Kim YJ
    Front Genet; 2022; 13():1008646. PubMed ID: 36506321
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.