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 *

98 related articles for article (PubMed ID: 11037338)

  • 1. Sequential methods of analysis for genome scans.
    Province MA
    Adv Genet; 2001; 42():499-514. PubMed ID: 11037338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A single, sequential, genome-wide test to identify simultaneously all promising areas in a linkage scan.
    Province MA
    Genet Epidemiol; 2000 Dec; 19(4):301-22. PubMed ID: 11108641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. False positives and false negatives in genome scans.
    Rao DC; Gu C
    Adv Genet; 2001; 42():487-98. PubMed ID: 11037337
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MVQTLCIM: composite interval mapping of multivariate traits in a hybrid F
    Liu F; Tong C; Tao S; Wu J; Chen Y; Yao D; Li H; Shi J
    BMC Bioinformatics; 2017 Nov; 18(1):515. PubMed ID: 29169342
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stratified false discovery control for large-scale hypothesis testing with application to genome-wide association studies.
    Sun L; Craiu RV; Paterson AD; Bull SB
    Genet Epidemiol; 2006 Sep; 30(6):519-30. PubMed ID: 16800000
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
    Fisher SE; Francks C; Marlow AJ; MacPhie IL; Newbury DF; Cardon LR; Ishikawa-Brush Y; Richardson AJ; Talcott JB; Gayán J; Olson RK; Pennington BF; Smith SD; DeFries JC; Stein JF; Monaco AP
    Nat Genet; 2002 Jan; 30(1):86-91. PubMed ID: 11743577
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mapping the genetic architecture of complex traits in experimental populations.
    Yang J; Zhu J; Williams RW
    Bioinformatics; 2007 Jun; 23(12):1527-36. PubMed ID: 17459962
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reducing sample sizes in genome scans: group sequential study designs with futility stops.
    König IR; Schäfer H; Ziegler A; Müller HH
    Genet Epidemiol; 2003 Dec; 25(4):339-49. PubMed ID: 14639703
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A simple correction for multiple comparisons in interval mapping genome scans.
    Cheverud JM
    Heredity (Edinb); 2001 Jul; 87(Pt 1):52-8. PubMed ID: 11678987
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HEGESMA: genome search meta-analysis and heterogeneity testing.
    Zintzaras E; Ioannidis JP
    Bioinformatics; 2005 Sep; 21(18):3672-3. PubMed ID: 15955784
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Factors influencing the identification of major genes in a complex disease genome scan.
    Yang H; Wang Y; Goldstein DR; Li Z; Vora H; Cantor RM
    Genet Epidemiol; 1997; 14(6):933-8. PubMed ID: 9433603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. On the assessment of statistical significance in disease-gene discovery.
    Zhao LP; Prentice R; Shen F; Hsu L
    Am J Hum Genet; 1999 Jun; 64(6):1739-53. PubMed ID: 10330362
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.
    Rosenberger A; Sharma M; Müller-Myhsok B; Gasser T; Bickeböller H
    BMC Genet; 2007 Jul; 8():44. PubMed ID: 17605797
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relaxed significance criteria for linkage analysis.
    Chen L; Storey JD
    Genetics; 2006 Aug; 173(4):2371-81. PubMed ID: 16783025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Empirical genomewide significance levels established by whole genome simulations.
    Sawcer S; Jones HB; Judge D; Visser F; Compston A; Goodfellow PN; Clayton D
    Genet Epidemiol; 1997; 14(3):223-9. PubMed ID: 9181352
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CAT scans, PET scans, and genomic scans.
    Rao DC
    Genet Epidemiol; 1998; 15(1):1-18. PubMed ID: 9523207
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The impact of genotyping error on family-based analysis of quantitative traits.
    Abecasis GR; Cherny SS; Cardon LR
    Eur J Hum Genet; 2001 Feb; 9(2):130-4. PubMed ID: 11313746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
    Hoffmann K; Mattheisen M; Dahm S; Nürnberg P; Roe C; Johnson J; Cox NJ; Wichmann HE; Wienker TF; Schulze J; Schwarz PE; Lindner TH
    Diabetologia; 2007 Jul; 50(7):1418-22. PubMed ID: 17464498
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The lod score method.
    Rice JP; Saccone NL; Corbett J
    Adv Genet; 2001; 42():99-113. PubMed ID: 11037316
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.