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 *

301 related articles for article (PubMed ID: 20435672)

  • 1. i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study.
    Zhang K; Cui S; Chang S; Zhang L; Wang J
    Nucleic Acids Res; 2010 Jul; 38(Web Server issue):W90-5. PubMed ID: 20435672
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 39(Web Server issue):W437-43. PubMed ID: 21622953
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SNPranker 2.0: a gene-centric data mining tool for diseases associated SNP prioritization in GWAS.
    Merelli I; Calabria A; Cozzi P; Viti F; Mosca E; Milanesi L
    BMC Bioinformatics; 2013; 14 Suppl 1(Suppl 1):S9. PubMed ID: 23369106
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 12():99. PubMed ID: 21496265
    [TBL] [Abstract][Full Text] [Related]  

  • 5. I-GSEA4GWAS v2: a web server for functional analysis of SNPs in trait-associated pathways identified from genome-wide association study.
    Zhang K; Chang S; Guo L; Wang J
    Protein Cell; 2015 Mar; 6(3):221-4. PubMed ID: 25407412
    [No Abstract]   [Full Text] [Related]  

  • 6. GSEA-SNP: applying gene set enrichment analysis to SNP data from genome-wide association studies.
    Holden M; Deng S; Wojnowski L; Kulle B
    Bioinformatics; 2008 Dec; 24(23):2784-5. PubMed ID: 18854360
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 2(9):1067-75. PubMed ID: 22973544
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Importance of SNP Dependency Correction and Association Integration for Gene Set Analysis in Genome-Wide Association Studies.
    Marczyk M; Macioszek A; Tobiasz J; Polanska J; Zyla J
    Front Genet; 2021; 12():767358. PubMed ID: 34956320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Performance Comparison of Two Gene Set Analysis Methods for Genome-wide Association Study Results: GSA-SNP vs i-GSEA4GWAS.
    Kwon JS; Kim J; Nam D; Kim S
    Genomics Inform; 2012 Jun; 10(2):123-7. PubMed ID: 23105940
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SNPsyn: detection and exploration of SNP-SNP interactions.
    Curk T; Rot G; Zupan B
    Nucleic Acids Res; 2011 Jul; 39(Web Server issue):W444-9. PubMed ID: 21576219
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SNPsnap: a Web-based tool for identification and annotation of matched SNPs.
    Pers TH; Timshel P; Hirschhorn JN
    Bioinformatics; 2015 Feb; 31(3):418-20. PubMed ID: 25316677
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity.
    Knoll N; Jarick I; Volckmar AL; Klingenspor M; Illig T; Grallert H; Gieger C; Wichmann HE; Peters A; Hebebrand J; Scherag A; Hinney A
    PLoS One; 2013; 8(2):e55884. PubMed ID: 23409076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GSA-SNP: a general approach for gene set analysis of polymorphisms.
    Nam D; Kim J; Kim SY; Kim S
    Nucleic Acids Res; 2010 Jul; 38(Web Server issue):W749-54. PubMed ID: 20501604
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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(Suppl 9):770. PubMed ID: 27766955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variable set enrichment analysis in genome-wide association studies.
    Yang W; de las Fuentes L; Dávila-Román VG; Charles Gu C
    Eur J Hum Genet; 2011 Aug; 19(8):893-900. PubMed ID: 21427759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies.
    Xu Z; Taylor JA
    Nucleic Acids Res; 2009 Jul; 37(Web Server issue):W600-5. PubMed ID: 19417063
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CandiSNPer: a web tool for the identification of candidate SNPs for causal variants.
    Schmitt AO; Assmus J; Bortfeldt RH; Brockmann GA
    Bioinformatics; 2010 Apr; 26(7):969-70. PubMed ID: 20172942
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PGMRA: a web server for (phenotype x genotype) many-to-many relation analysis in GWAS.
    Arnedo J; del Val C; de Erausquin GA; Romero-Zaliz R; Svrakic D; Cloninger CR; Zwir I
    Nucleic Acids Res; 2013 Jul; 41(Web Server issue):W142-9. PubMed ID: 23761451
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SNPpath: characterizing cattle SNPs by enriched pathway terms.
    Wang Q; Wang M; Yang Y; Pan Y
    Anim Sci J; 2012 Apr; 83(4):279-83. PubMed ID: 22515686
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Searching joint association signals in CATIE schizophrenia genome-wide association studies through a refined integrative network approach.
    Jia P; Zhao Z
    BMC Genomics; 2012; 13 Suppl 6(Suppl 6):S15. PubMed ID: 23134571
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.