BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 23255287)

  • 1. One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study.
    Machiela MJ; Chen C; Liang L; Diver WR; Stevens VL; Tsilidis KK; Haiman CA; Chanock SJ; Hunter DJ; Kraft P;
    Prostate; 2013 May; 73(7):677-89. PubMed ID: 23255287
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Performance of genotype imputation for low frequency and rare variants from the 1000 genomes.
    Zheng HF; Rong JJ; Liu M; Han F; Zhang XW; Richards JB; Wang L
    PLoS One; 2015; 10(1):e0116487. PubMed ID: 25621886
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effect of genome-wide genotyping and reference panels on rare variants imputation.
    Zheng HF; Ladouceur M; Greenwood CM; Richards JB
    J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification.
    Faye LL; Machiela MJ; Kraft P; Bull SB; Sun L
    PLoS Genet; 2013; 9(8):e1003609. PubMed ID: 23950724
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haplotype reference consortium panel: Practical implications of imputations with large reference panels.
    Iglesias AI; van der Lee SJ; Bonnemaijer PWM; Höhn R; Nag A; Gharahkhani P; Khawaja AP; Broer L; ; Foster PJ; Hammond CJ; Hysi PG; van Leeuwen EM; MacGregor S; Mackey DA; Mazur J; Nickels S; Uitterlinden AG; Klaver CCW; Amin N; van Duijn CM
    Hum Mutat; 2017 Aug; 38(8):1025-1032. PubMed ID: 28493391
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative.
    Liu EY; Buyske S; Aragaki AK; Peters U; Boerwinkle E; Carlson C; Carty C; Crawford DC; Haessler J; Hindorff LA; Marchand LL; Manolio TA; Matise T; Wang W; Kooperberg C; North KE; Li Y
    Genet Epidemiol; 2012 Feb; 36(2):107-17. PubMed ID: 22851474
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Replication of five prostate cancer loci identified in an Asian population--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3).
    Lindström S; Schumacher FR; Campa D; Albanes D; Andriole G; Berndt SI; Bueno-de-Mesquita HB; Chanock SJ; Diver WR; Ganziano JM; Gapstur SM; Giovannucci E; Haiman CA; Henderson B; Hunter DJ; Johansson M; Kolonel LN; Le Marchand L; Ma J; Stampfer M; Stevens VL; Trichopoulos D; Virtamo J; Willett WC; Yeager M; Hsing AW; Kraft P
    Cancer Epidemiol Biomarkers Prev; 2012 Jan; 21(1):212-6. PubMed ID: 22056501
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Improving accuracy of rare variant imputation with a two-step imputation approach.
    Kreiner-Møller E; Medina-Gomez C; Uitterlinden AG; Rivadeneira F; Estrada K
    Eur J Hum Genet; 2015 Mar; 23(3):395-400. PubMed ID: 24939589
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Imputation-based assessment of next generation rare exome variant arrays.
    Martin AR; Tse G; Bustamante CD; Kenny EE
    Pac Symp Biocomput; 2014; ():241-52. PubMed ID: 24297551
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.
    Wood AR; Perry JR; Tanaka T; Hernandez DG; Zheng HF; Melzer D; Gibbs JR; Nalls MA; Weedon MN; Spector TD; Richards JB; Bandinelli S; Ferrucci L; Singleton AB; Frayling TM
    PLoS One; 2013; 8(5):e64343. PubMed ID: 23696881
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data.
    Wu Y; Zheng Z; Visscher PM; Yang J
    Genome Biol; 2017 May; 18(1):86. PubMed ID: 28506277
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.
    Murabito JM; Rosenberg CL; Finger D; Kreger BE; Levy D; Splansky GL; Antman K; Hwang SJ
    BMC Med Genet; 2007 Sep; 8 Suppl 1(Suppl 1):S6. PubMed ID: 17903305
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait.
    Chundru VK; Marioni RE; Prendergast JGD; Vallerga CL; Lin T; Beveridge AJ; ; Gratten J; Hume DA; Deary IJ; Wray NR; Visscher PM; McRae AF
    Genetics; 2019 Jul; 212(3):577-586. PubMed ID: 31040117
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genome-wide pleiotropy scan for prostate cancer risk.
    Panagiotou OA; Travis RC; Campa D; Berndt SI; Lindstrom S; Kraft P; Schumacher FR; Siddiq A; Papatheodorou SI; Stanford JL; Albanes D; Virtamo J; Weinstein SJ; Diver WR; Gapstur SM; Stevens VL; Boeing H; Bueno-de-Mesquita HB; Barricarte Gurrea A; Kaaks R; Khaw KT; Krogh V; Overvad K; Riboli E; Trichopoulos D; Giovannucci E; Stampfer M; Haiman C; Henderson B; Le Marchand L; Gaziano JM; Hunter DJ; Koutros S; Yeager M; Hoover RN; ; Chanock SJ; Wacholder S; Key TJ; Tsilidis KK
    Eur Urol; 2015 Apr; 67(4):649-57. PubMed ID: 25277271
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Profile of common prostate cancer risk variants in an unscreened Romanian population.
    Iordache PD; Mates D; Gunnarsson B; Eggertsson HP; Sulem P; Guðmundsson J; Benónísdóttir S; Csiki IE; Rascu S; Radavoi D; Ursu R; Staicu C; Calota V; Voinoiu A; Jinga M; Rosoga G; Danau R; Sima SC; Badescu D; Suciu N; Radoi V; Manolescu A; Rafnar T; Halldórsson BV; Jinga V; Stefánsson K
    J Cell Mol Med; 2018 Mar; 22(3):1574-1582. PubMed ID: 29266682
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects.
    Sung YJ; Gu CC; Tiwari HK; Arnett DK; Broeckel U; Rao DC
    Genet Epidemiol; 2012 Jul; 36(5):508-16. PubMed ID: 22644746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Imputation-based genomic coverage assessments of current human genotyping arrays.
    Nelson SC; Doheny KF; Pugh EW; Romm JM; Ling H; Laurie CA; Browning SR; Weir BS; Laurie CC
    G3 (Bethesda); 2013 Oct; 3(10):1795-807. PubMed ID: 23979933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Performance of genotype imputation for rare variants identified in exons and flanking regions of genes.
    Li L; Li Y; Browning SR; Browning BL; Slater AJ; Kong X; Aponte JL; Mooser VE; Chissoe SL; Whittaker JC; Nelson MR; Ehm MG
    PLoS One; 2011; 6(9):e24945. PubMed ID: 21949800
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.