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Journal Abstract Search

584 related items for PubMed ID: 21496265

  • 1. SNP-based pathway enrichment analysis for genome-wide association studies.
    Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.
    BMC Bioinformatics; 2011 Apr 15; 12():99. PubMed ID: 21496265
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  • 2. Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.
    Uimari O, Rahmioglu N, Nyholt DR, Vincent K, Missmer SA, Becker C, Morris AP, Montgomery GW, Zondervan KT.
    Hum Reprod; 2017 Apr 01; 32(4):780-793. PubMed ID: 28333195
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  • 3. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs.
    Schork AJ, Thompson WK, Pham P, Torkamani A, Roddey JC, Sullivan PF, Kelsoe JR, O'Donovan MC, Furberg H, Tobacco and Genetics Consortium, Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, Schork NJ, Andreassen OA, Dale AM.
    PLoS Genet; 2013 Apr 01; 9(4):e1003449. PubMed ID: 23637621
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  • 4. Pathway analysis of a genome-wide association study in schizophrenia.
    Lee YH, Kim JH, Song GG.
    Gene; 2013 Aug 01; 525(1):107-15. PubMed ID: 23644028
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  • 5. Pathway analysis of genome-wide association studies for Parkinson's disease.
    Song GG, Lee YH.
    Mol Biol Rep; 2013 Mar 01; 40(3):2599-607. PubMed ID: 23238920
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  • 7. Uncovering networks from genome-wide association studies via circular genomic permutation.
    Cabrera CP, Navarro P, Huffman JE, Wright AF, Hayward C, Campbell H, Wilson JF, Rudan I, Hastie ND, Vitart V, Haley CS.
    G3 (Bethesda); 2012 Sep 01; 2(9):1067-75. PubMed ID: 22973544
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  • 10. Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.
    Adewuyi EO, Mehta D, International Endogene Consortium (IEC), 23andMe Research Team, Nyholt DR.
    Hum Reprod; 2022 Jan 28; 37(2):366-383. PubMed ID: 35472084
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  • 11. Searching joint association signals in CATIE schizophrenia genome-wide association studies through a refined integrative network approach.
    Jia P, Zhao Z.
    BMC Genomics; 2012 Jan 28; 13 Suppl 6(Suppl 6):S15. PubMed ID: 23134571
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  • 13. 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 Jan 28; 13 Suppl 1(Suppl 1):S3. PubMed ID: 23566118
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  • 16. Leveraging existing GWAS summary data of genetically correlated and uncorrelated traits to improve power for a new GWAS.
    Xue H, Wu C, Pan W.
    Genet Epidemiol; 2020 Oct 28; 44(7):717-732. PubMed ID: 32677173
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  • 17. ICSNPathway: identify candidate causal SNPs and pathways from genome-wide association study by one analytical framework.
    Zhang K, Chang S, Cui S, Guo L, Zhang L, Wang J.
    Nucleic Acids Res; 2011 Jul 28; 39(Web Server issue):W437-43. PubMed ID: 21622953
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  • 18. e-GRASP: an integrated evolutionary and GRASP resource for exploring disease associations.
    Karim S, NourEldin HF, Abusamra H, Salem N, Alhathli E, Dudley J, Sanderford M, Scheinfeldt LB, Chaudhary AG, Al-Qahtani MH, Kumar S.
    BMC Genomics; 2016 Oct 17; 17(Suppl 9):770. PubMed ID: 27766955
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