Detection of Parent-of-Origin Effects Based on Complete and Incomplete Nuclear Families with Multiple Affected Children
暂无分享,去创建一个
Ji-Yuan Zhou | Wing K. Fung | Yue-Qing Hu | W. Fung | Yue-Qing Hu | Shili Lin | Shili Lin | Ji-Yuan Zhou
[1] D. Allison,et al. Transmission-disequilibrium tests for quantitative traits. , 1997, American journal of human genetics.
[2] W. Fung,et al. The transmission disequilibrium test and imprinting effects test based on case‐parent pairs , 2007, Genetic epidemiology.
[3] Nicolas Produit,et al. Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization. , 2000, American journal of human genetics.
[4] R. Lewontin,et al. On measures of gametic disequilibrium. , 1988, Genetics.
[5] Yang Liu,et al. Monte Carlo pedigree disequilibrium test for markers on the X chromosome. , 2006, American journal of human genetics.
[6] Rodney C Samaco,et al. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. , 2005, Human molecular genetics.
[7] C R Weinberg,et al. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. , 1999, American journal of human genetics.
[8] J. Weissenbach,et al. Confinement of PGL, an Imprinted Gene Causing Hereditary Paragangliomas, to a 2-cM Interval on 11q22–q23 and Exclusion of DRD2 and NCAM as Candidate Genes , 1996, European journal of human genetics : EJHG.
[9] C. Amos,et al. Possible genomic imprinting of three human obesity-related genetic loci. , 2005, American journal of human genetics.
[10] I M Morison,et al. The imprinted gene and parent-of-origin effect database , 2001, Nucleic Acids Res..
[11] C R Weinberg,et al. Allowing for missing parents in genetic studies of case-parent triads. , 1999, American journal of human genetics.
[12] C. Weinberg,et al. Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent‐of‐origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available , 2007, Genetic epidemiology.
[13] W. Fung,et al. A simple method for detection of imprinting effects based on case–parents trios , 2007, Heredity.
[14] J. D. Baum,et al. An imprinted gene(s) for diabetes? , 1995, Nature Genetics.
[15] R C Elston,et al. Transmission/disequilibrium tests for quantitative traits , 2001, Genetic epidemiology.
[16] I. König,et al. A Statistical Approach to Genetic Epidemiology: Concepts and Applications , 2006 .
[17] W. Johnson,et al. Parental sex effect in spina bifida: a role for genomic imprinting? , 1992, American journal of medical genetics.
[18] G. Satten,et al. Informative missingness in genetic association studies: case-parent designs. , 2003, American journal of human genetics.
[19] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[20] M. Baur,et al. Detection of Parent-of-Origin Effects in Nuclear Families Using Haplotype Analysis , 2006, Human Heredity.
[21] E. Martin,et al. A test for linkage and association in general pedigrees: the pedigree disequilibrium test. , 2000, American journal of human genetics.
[22] W D Flanders,et al. Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT. , 1999, American journal of epidemiology.
[23] R. Jirtle,et al. Genomic imprinting: implications for human disease. , 1999, The American journal of pathology.
[24] C R Weinberg,et al. A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. , 1998, American journal of human genetics.