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 *

176 related articles for article (PubMed ID: 29304743)

  • 21. A powerful approach for association analysis incorporating imprinting effects.
    Xia F; Zhou JY; Fung WK
    Bioinformatics; 2011 Sep; 27(18):2571-7. PubMed ID: 21798962
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A statistical measure for the skewness of X chromosome inactivation based on family trios.
    Xu SQ; Zhang Y; Wang P; Liu W; Wu XB; Zhou JY
    BMC Genet; 2018 Dec; 19(1):109. PubMed ID: 30518319
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Likelihood Ratio Test for Excess Homozygosity at Marker Loci on X Chromosome.
    You XP; Zou QL; Li JL; Zhou JY
    PLoS One; 2015; 10(12):e0145032. PubMed ID: 26671781
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An efficient study design to test parent-of-origin effects in family trios.
    Yu X; Chen G; Feng R
    Genet Epidemiol; 2017 Nov; 41(7):587-598. PubMed ID: 28726280
    [TBL] [Abstract][Full Text] [Related]  

  • 25. X-APL: an improved family-based test of association in the presence of linkage for the X chromosome.
    Chung RH; Morris RW; Zhang L; Li YJ; Martin ER
    Am J Hum Genet; 2007 Jan; 80(1):59-68. PubMed ID: 17160894
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A genomic imprinting test for ordinal traits in pedigree data.
    Feng R; Zhang H
    Genet Epidemiol; 2008 Feb; 32(2):132-42. PubMed ID: 17922481
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An Efficient Bayesian Method for Estimating the Degree of the Skewness of X Chromosome Inactivation Based on the Mixture of General Pedigrees and Unrelated Females.
    Kong YF; Li SZ; Wang KW; Zhu B; Yuan YX; Li MK; Zhou JY
    Biomolecules; 2023 Mar; 13(3):. PubMed ID: 36979477
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers.
    Zhou JY; Lin S; Fung WK; Hu YQ
    Hum Hered; 2009; 67(2):116-27. PubMed ID: 19077428
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits.
    Belonogova NM; Axenovich TI; Aulchenko YS
    Eur J Hum Genet; 2010 Mar; 18(3):379-84. PubMed ID: 19809476
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A robust test for X-chromosome genetic association accounting for X-chromosome inactivation and imprinting.
    Zhang Y; Xu SQ; Liu W; Fung WK; Zhou JY
    Genet Res (Camb); 2020 Apr; 102():e2. PubMed ID: 32234109
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Bayesian oligogenic analysis of quantitative and qualitative traits in general pedigrees.
    Uimari P; Sillanpää MJ
    Genet Epidemiol; 2001 Nov; 21(3):224-42. PubMed ID: 11668579
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Haplotype association analyses in resources of mixed structure using Monte Carlo testing.
    Abo R; Wong J; Thomas A; Camp NJ
    BMC Bioinformatics; 2010 Dec; 11():592. PubMed ID: 21143908
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Parent-of-origin, imprinting, mitochondrial, and X-linked effects in traits related to alcohol dependence: presentation Group 18 of Genetic Analysis Workshop 14.
    Strauch K; Baur MP
    Genet Epidemiol; 2005; 29 Suppl 1():S125-32. PubMed ID: 16342190
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genomic imprinting and linkage test for quantitative-trait Loci in extended pedigrees.
    Shete S; Zhou X; Amos CI
    Am J Hum Genet; 2003 Oct; 73(4):933-8. PubMed ID: 13680523
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A powerful test of parent-of-origin effects for quantitative traits using haplotypes.
    Feng R; Wu Y; Jang GH; Ordovas JM; Arnett D
    PLoS One; 2011; 6(12):e28909. PubMed ID: 22174922
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Inferring haplotypes and parental genotypes in larger full sib-ships and other pedigrees with missing or erroneous genotype data.
    Nettelblad C
    BMC Genet; 2012 Oct; 13():85. PubMed ID: 23046532
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The parent-of-origin of the extra X chromosome may differentially affect psychopathology in Klinefelter syndrome.
    Bruining H; van Rijn S; Swaab H; Giltay J; Kates W; Kas MJ; van Engeland H; de Sonneville L
    Biol Psychiatry; 2010 Dec; 68(12):1156-62. PubMed ID: 21035791
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Imprinting detection by extending a regression-based QTL analysis method.
    Gorlova OY; Lei L; Zhu D; Weng SF; Shete S; Zhang Y; Li WD; Price RA; Amos CI
    Hum Genet; 2007 Sep; 122(2):159-74. PubMed ID: 17562082
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Powerful tests for association on quantitative trait loci incorporating imprinting effects.
    Xia F; Zhou JY; Fung WK
    J Hum Genet; 2013 Jun; 58(6):384-90. PubMed ID: 23552672
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing data.
    Yang Y; Wise CA; Gordon D; Finch SJ
    Hum Hered; 2008; 66(2):99-110. PubMed ID: 18382089
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.