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 *

153 related articles for article (PubMed ID: 22859961)

  • 41. Group-combined P-values with applications to genetic association studies.
    Hu X; Zhang W; Zhang S; Ma S; Li Q
    Bioinformatics; 2016 Sep; 32(18):2737-43. PubMed ID: 27259542
    [TBL] [Abstract][Full Text] [Related]  

  • 42. An Adaptive Fisher's Combination Method for Joint Analysis of Multiple Phenotypes in Association Studies.
    Liang X; Wang Z; Sha Q; Zhang S
    Sci Rep; 2016 Oct; 6():34323. PubMed ID: 27694844
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Circadian pathway genetic variation and cancer risk: evidence from genome-wide association studies.
    Mocellin S; Tropea S; Benna C; Rossi CR
    BMC Med; 2018 Feb; 16(1):20. PubMed ID: 29455641
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A powerful method for combining P-values in genomic studies.
    Chen HS; Pfeiffer RM; Zhang S
    Genet Epidemiol; 2013 Dec; 37(8):814-9. PubMed ID: 23959976
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A powerful and adaptive association test for rare variants.
    Pan W; Kim J; Zhang Y; Shen X; Wei P
    Genetics; 2014 Aug; 197(4):1081-95. PubMed ID: 24831820
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Genomewide association mapping and pathway analysis of meat tenderness in Polled Nellore cattle.
    Castro LM; Rosa GJM; Lopes FB; Regitano LCA; Rosa AJM; Magnabosco CU
    J Anim Sci; 2017 May; 95(5):1945-1956. PubMed ID: 28727016
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Incorporating biological pathways via a Markov random field model in genome-wide association studies.
    Chen M; Cho J; Zhao H
    PLoS Genet; 2011 Apr; 7(4):e1001353. PubMed ID: 21490723
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Identification of additional loci associated with antibody response to Mycobacterium avium ssp. Paratuberculosis in cattle by GSEA-SNP analysis.
    Del Corvo M; Luini M; Stella A; Pagnacco G; Ajmone-Marsan P; Williams JL; Minozzi G
    Mamm Genome; 2017 Dec; 28(11-12):520-527. PubMed ID: 28864882
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data.
    Kang C; Yu H; Yi GS
    BMC Med Inform Decis Mak; 2013; 13 Suppl 1(Suppl 1):S3. PubMed ID: 23566118
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Genome-wide association studies with high-dimensional phenotypes.
    Marttinen P; Gillberg J; Havulinna A; Corander J; Kaski S
    Stat Appl Genet Mol Biol; 2013 Aug; 12(4):413-31. PubMed ID: 23759510
    [TBL] [Abstract][Full Text] [Related]  

  • 51. On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis.
    Peterson RE; Maes HH; Lin P; Kramer JR; Hesselbrock VM; Bauer LO; Nurnberger JI; Edenberg HJ; Dick DM; Webb BT
    BMC Genomics; 2014 May; 15(1):368. PubMed ID: 24884913
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A network-based conditional genetic association analysis of the human metabolome.
    Tsepilov YA; Sharapov SZ; Zaytseva OO; Krumsiek J; Prehn C; Adamski J; Kastenmüller G; Wang-Sattler R; Strauch K; Gieger C; Aulchenko YS
    Gigascience; 2018 Dec; 7(12):. PubMed ID: 30496450
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Gene set enrichment; a problem of pathways.
    Davies MN; Meaburn EL; Schalkwyk LC
    Brief Funct Genomics; 2010 Dec; 9(5-6):385-90. PubMed ID: 20861160
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The Bayesian lasso for genome-wide association studies.
    Li J; Das K; Fu G; Li R; Wu R
    Bioinformatics; 2011 Feb; 27(4):516-23. PubMed ID: 21156729
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Adaptive testing for multiple traits in a proportional odds model with applications to detect SNP-brain network associations.
    Kim J; Pan W;
    Genet Epidemiol; 2017 Apr; 41(3):259-277. PubMed ID: 28191669
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Powerful statistical method to detect disease-associated genes using publicly available genome-wide association studies summary data.
    Zhang J; Zhao Z; Guo X; Guo B; Wu B
    Genet Epidemiol; 2019 Dec; 43(8):941-951. PubMed ID: 31392781
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A network-based kernel machine test for the identification of risk pathways in genome-wide association studies.
    Freytag S; Manitz J; Schlather M; Kneib T; Amos CI; Risch A; Chang-Claude J; Heinrich J; Bickeböller H
    Hum Hered; 2013; 76(2):64-75. PubMed ID: 24434848
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Identifying SNP targeted pathways in partial epilepsies with genome-wide association study data.
    Bakir-Gungor B; Baykan B; Ugur İseri S; Tuncer FN; Sezerman OU
    Epilepsy Res; 2013 Jul; 105(1-2):92-102. PubMed ID: 23498093
    [TBL] [Abstract][Full Text] [Related]  

  • 59. PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.
    Ried JS; Döring A; Oexle K; Meisinger C; Winkelmann J; Klopp N; Meitinger T; Peters A; Suhre K; Wichmann HE; Gieger C
    Genet Epidemiol; 2012 Apr; 36(3):244-52. PubMed ID: 22714936
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Recently evolved human-specific methylated regions are enriched in schizophrenia signals.
    Banerjee N; Polushina T; Bettella F; Giddaluru S; Steen VM; Andreassen OA; Le Hellard S
    BMC Evol Biol; 2018 May; 18(1):63. PubMed ID: 29747567
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.