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 *

124 related articles for article (PubMed ID: 9728890)

  • 21. Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies.
    Gourraud PA; Génin E; Cambon-Thomsen A
    Eur J Hum Genet; 2004 Oct; 12(10):805-12. PubMed ID: 15252420
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of probable genotyping errors by consideration of haplotypes.
    Becker T; Valentonyte R; Croucher PJ; Strauch K; Schreiber S; Hampe J; Knapp M
    Eur J Hum Genet; 2006 Apr; 14(4):450-8. PubMed ID: 16435001
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes.
    Morris AP
    Genet Epidemiol; 2005 Sep; 29(2):91-107. PubMed ID: 15940704
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Testing informative missingness in genetic studies using case-parent triads.
    Guo CY; Cupples LA; Yang Q
    Eur J Hum Genet; 2008 Aug; 16(8):992-1001. PubMed ID: 18337731
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.
    Cordell HJ; Barratt BJ; Clayton DG
    Genet Epidemiol; 2004 Apr; 26(3):167-85. PubMed ID: 15022205
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
    Liang L; Sun C; Liao XP; Xiao F; Chen XD; Huang SX; Tang XL; Wen GQ; Long ZG; Wang XY; Liu GX; Cheng S; Cai WW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):316-9. PubMed ID: 16767673
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Likelihoods and TDT for the case-parents design.
    Schaid DJ
    Genet Epidemiol; 1999; 16(3):250-60. PubMed ID: 10096688
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Quantifying bias due to allele misclassification in case-control studies of haplotypes.
    Govindarajulu US; Spiegelman D; Miller KL; Kraft P
    Genet Epidemiol; 2006 Nov; 30(7):590-601. PubMed ID: 16830341
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.
    Rohde K; Fuerst R
    Hum Mutat; 2001 Apr; 17(4):289-95. PubMed ID: 11295827
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Haplotypes vs single marker linkage disequilibrium tests: what do we gain?
    Akey J; Jin L; Xiong M
    Eur J Hum Genet; 2001 Apr; 9(4):291-300. PubMed ID: 11313774
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Relative-risk regression models using cases and their parents.
    Schaid DJ
    Genet Epidemiol; 1995; 12(6):813-8. PubMed ID: 8788014
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.
    Verpillat P; Bouley S; Campion D; Hannequin D; Dubois B; Belliard S; Puel M; Thomas-Antérion C; Agid Y; Brice A; Clerget-Darpoux F
    Eur J Hum Genet; 2001 Jun; 9(6):464-8. PubMed ID: 11436129
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Incorporating genotyping uncertainty in haplotype frequency estimation in pedigree studies.
    Zhu WS; Fung WK; Guo J
    Hum Hered; 2007; 64(3):172-81. PubMed ID: 17536211
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Likelihood-based disequilibrium mapping for two-marker haplotype data.
    Garner C; Slatkin M
    Theor Popul Biol; 2002 Mar; 61(2):153-61. PubMed ID: 11969387
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.
    Guo CY; DeStefano AL; Lunetta KL; Dupuis J; Cupples LA
    Hum Hered; 2005; 59(3):125-35. PubMed ID: 15867473
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A Monte Carlo approach for estimation of haplotype probabilities in half-sib families.
    Boettcher PJ; Pagnacco G; Stella A
    J Dairy Sci; 2004 Dec; 87(12):4303-10. PubMed ID: 15545394
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Relationship estimation in affected sib pair analysis of late-onset diseases.
    Göring HH; Ott J
    Eur J Hum Genet; 1997; 5(2):69-77. PubMed ID: 9195155
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HapSim: a simulation tool for generating haplotype data with pre-specified allele frequencies and LD coefficients.
    Montana G
    Bioinformatics; 2005 Dec; 21(23):4309-11. PubMed ID: 16188927
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The APL test: extension to general nuclear families and haplotypes and examination of its robustness.
    Chung RH; Hauser ER; Martin ER
    Hum Hered; 2006; 61(4):189-99. PubMed ID: 16877866
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Nonrandom segregation: uniformly most powerful test and related considerations.
    Majumder PP; Pal N
    Genet Epidemiol; 1987; 4(4):277-87. PubMed ID: 3478282
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.