Incorporating information from markers in LD with test locus for detecting imprinting and maternal effects
Author:
Funder
Center for Selective C-H Functionalization, National Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/s41431-020-0590-3.pdf
Reference36 articles.
1. Lawson HA, Cheverud JM, Wolf JB. Genomic imprinting and parent-of-origin effects on complex traits. Nat Rev Genet. 2013;14:609–17.
2. Nousome D, Lupo PJ, Okcu MF, Scheurer ME. Maternal and offspring xenobiotic metabolism haplotypes and the risk of childhood acute lymphoblastic leukemia. Leuk Res. 2013;37:531–5.
3. Ferguson-Smith AC. Genome imprinting: the emergence of an epigenetic paradigm. Nat Rev. 2011;12:565–75.
4. Naumova AK, Croteau S. Mechanisms of epigenetic variation: polymorphic imprinting. Curr Genomics. 2004;5:417–29.
5. Hager R, Cheverud JM, Wolf JB. Maternal effects as the cause of parent-of-origin effects that mimic genomic imprinting. Genetics. 2008;178:1755–62.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Analysis of parent‐of‐origin effects for secondary phenotypes using case–control mother–child pair data;Genetic Epidemiology;2022-05-29
2. Covariate adjusted inference of parent‐of‐origin effects using case–control mother–child paired multilocus genotype data;Genetic Epidemiology;2021-08-23
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