Literature DB >> 17953999

The potential role of epigenomic dysregulation in complex human disease.

Eli Hatchwell1, John M Greally.   

Abstract

One of the major challenges in genetics today is to understand the causes of complex genetic diseases. The genes involved in these disorders are thought to interact with poorly-defined environmental factors to exert their phenotypic effects. An emerging view is that epigenetics also plays a role in complex diseases. Here we review the evidence that epigenetic regulatory mediators can be influenced by several environmental factors, that variability of the epigenome can cause variation in phenotypes, and that epigenetic dysregulation can be heritable across generations. Assays that map epigenetic regulatory patterns across the whole genome have recently become available, which enable us to explore the epigenomic influences on complex diseases, thus offering new avenues for diagnostic biomarker development and therapeutic strategies.

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Year:  2007        PMID: 17953999     DOI: 10.1016/j.tig.2007.08.010

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  32 in total

Review 1.  Nutritional genomics: defining the dietary requirement and effects of choline.

Authors:  Steven H Zeisel
Journal:  J Nutr       Date:  2011-01-26       Impact factor: 4.798

2.  A longitudinal study of epigenetic variation in twins.

Authors:  Chloe Chung Yi Wong; Avshalom Caspi; Benjamin Williams; Ian W Craig; Renate Houts; Antony Ambler; Terrie E Moffitt; Jonathan Mill
Journal:  Epigenetics       Date:  2010-08-16       Impact factor: 4.528

Review 3.  Prospects for epigenetic epidemiology.

Authors:  Debra L Foley; Jeffrey M Craig; Ruth Morley; Craig A Olsson; Craig J Olsson; Terence Dwyer; Katherine Smith; Richard Saffery
Journal:  Am J Epidemiol       Date:  2009-01-12       Impact factor: 4.897

4.  Extreme methylation values of imprinted genes in human abortions and stillbirths.

Authors:  Galyna Pliushch; Eberhard Schneider; Daniela Weise; Nady El Hajj; Achim Tresch; Larissa Seidmann; Wiltrud Coerdt; Annette M Müller; Ulrich Zechner; Thomas Haaf
Journal:  Am J Pathol       Date:  2010-01-21       Impact factor: 4.307

5.  Heritable individual-specific and allele-specific chromatin signatures in humans.

Authors:  Ryan McDaniell; Bum-Kyu Lee; Lingyun Song; Zheng Liu; Alan P Boyle; Michael R Erdos; Laura J Scott; Mario A Morken; Katerina S Kucera; Anna Battenhouse; Damian Keefe; Francis S Collins; Huntington F Willard; Jason D Lieb; Terrence S Furey; Gregory E Crawford; Vishwanath R Iyer; Ewan Birney
Journal:  Science       Date:  2010-03-18       Impact factor: 47.728

Review 6.  Dark matters in AMD genetics: epigenetics and stochasticity.

Authors:  Leonard M Hjelmeland
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-03-01       Impact factor: 4.799

7.  Alternative transcription exceeds alternative splicing in generating the transcriptome diversity of cerebellar development.

Authors:  Sharmistha Pal; Ravi Gupta; Hyunsoo Kim; Priyankara Wickramasinghe; Valérie Baubet; Louise C Showe; Nadia Dahmane; Ramana V Davuluri
Journal:  Genome Res       Date:  2011-06-28       Impact factor: 9.043

Review 8.  In vivo epigenome editing and transcriptional modulation using CRISPR technology.

Authors:  Cia-Hin Lau; Yousin Suh
Journal:  Transgenic Res       Date:  2018-10-04       Impact factor: 2.788

9.  Identifying and mapping cell-type-specific chromatin programming of gene expression.

Authors:  Troels T Marstrand; John D Storey
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-27       Impact factor: 11.205

10.  Bisulfite-based epityping on pooled genomic DNA provides an accurate estimate of average group DNA methylation.

Authors:  Sophia J Docherty; Oliver S P Davis; Claire M A Haworth; Robert Plomin; Jonathan Mill
Journal:  Epigenetics Chromatin       Date:  2009-03-10       Impact factor: 4.954

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