نتایج جستجو برای: genetic studies

تعداد نتایج: 1925122  

Journal: :The Journal of Cell Biology 2004
William A. Wells

ytoplasmic structures are sites of active mammalian mRNA decay, according to Cougot et al. (page 31). The group had previously identified cytoplasmic foci that included two human mRNA decapping enzymes. They now add subunits of a deadenylase, exonuclease, and possible helicase to the list of proteins found at these sites. After inhibition of a 5 –3 exonuclease, poly(A) RNA accumulates at the sa...

Journal: :Genetic epidemiology 2009
Eric Jorgenson Mark Kvale John S Witte

Promising findings from genetic association studies are commonly presented with two distinct figures: one gives the association study results and the other indicates linkage disequilibrium (LD) between genetic markers in the region(s) of interest. Fully interpreting the results of such studies requires synthesizing the information in these figures, which is generally done in a subjective and un...

Journal: :Biometrics 2014
Xiaoquan Wen

Motivated by examples from genetic association studies, this article considers the model selection problem in a general complex linear model system and in a Bayesian framework. We discuss formulating model selection problems and incorporating context-dependent a priori information through different levels of prior specifications. We also derive analytic Bayes factors and their approximations to...

2012
Ron Do Sekar Kathiresan Gonçalo R. Abecasis

Genetic association and linkage studies can provide insights into complex disease biology, guiding the development of new diagnostic and therapeutic strategies. Over the past decade, genetic association studies have largely focused on common, easy to measure genetic variants shared between many individuals. These common variants typically have subtle functional consequence and translating the r...

2016
Romana Vulturar Adina Chiş Melinda Hambrich Beatrice Kelemen Loredana Ungureanu Andrei C. Miu

Population stratification of functional gene polymorphisms is a potential confounding factor in genetic association studies. The Val66Met (rs6265) single-nucleotide polymorphism in the brain-derived neurotrophic factor gene (BDNF) exhibits one of the highest variabilities in terms of allelic distribution between populations. The present study reports the distribution of BDNF Val66Met alleles in...

Journal: :Twin research : the official journal of the International Society for Twin Studies 2004
Jacqueline Wicks Susan A Treloar Nicholas G Martin

The aim of this study was to determine whether identity-by-descent (IBD) information for affected sib pairs (ASPs) can be used to select a sample of cases for a genetic case-control study which will provide more power for detecting association with loci in a known linkage region. By modeling the expected frequency of the disease allele in ASPs showing IBD sharing of 0, 1, or 2 alleles, and cons...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Augustine Kong Michael L Frigge Gudmar Thorleifsson Hreinn Stefansson Alexander I Young Florian Zink Gudrun A Jonsdottir Aysu Okbay Patrick Sulem Gisli Masson Daniel F Gudbjartsson Agnar Helgason Gyda Bjornsdottir Unnur Thorsteinsdottir Kari Stefansson

Epidemiological and genetic association studies show that genetics play an important role in the attainment of education. Here, we investigate the effect of this genetic component on the reproductive history of 109,120 Icelanders and the consequent impact on the gene pool over time. We show that an educational attainment polygenic score, POLYEDU, constructed from results of a recent study is as...

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