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June 2017 Volume 18 Number 6 | Advertisement | ||||||||||||||||||||||||||||||||||||
In this issue Research Highlights Reviews
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REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Article series: Disease mechanisms Genetics of coronary artery disease: discovery, biology and clinical translation Amit V. Khera & Sekar Kathiresan p331 | doi:10.1038/nrg.2016.160 The past decade has seen tremendous progress in understanding the genetic architecture of coronary artery disease (CAD). Khera and Kathiresan review research efforts that have improved our understanding of the genetic drivers of CAD, and discuss the promises and challenges of integrating genetic information into routine clinical practice. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Article series: Single-cell omics Scaling by shrinking: empowering single-cell 'omics' with microfluidic devices Sanjay M. Prakadan, Alex K. Shalek & David A. Weitz p345 | doi:10.1038/nrg.2017.15 As the genetic and phenotypic heterogeneities among cells become more appreciated, there is increasing demand for technologies that facilitate high-throughput and high-efficiency single-cell 'omic' analyses in miniaturized and automated formats. This Review discusses the diverse microfluidic methodologies — with a primary focus on valve-, droplet- and nanowell-based platforms — for characterization of the genomes, epigenomes, transcriptomes and proteomes of single cells, and addresses technical considerations and future opportunities. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Article series: Translational genetics Autism genetics: opportunities and challenges for clinical translation Jacob A. S. Vorstman, Jeremy R. Parr, Daniel Moreno-De-Luca, Richard J. L. Anney, John I. Nurnberger Jr & Joachim F. Hallmayer p362 | doi:10.1038/nrg.2017.4 Various large studies have provided unprecedented insights into the genetics of autism spectrum disorders (ASDs). This Review discusses the challenges and opportunities of translating genetic and biological insights into clinical progress for ASDs, in areas including genetic testing, ASD classification, genetic counselling, comorbidities and therapeutics. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
Article series: Modes of transcriptional regulation The X chromosome in space Teddy Jegu, Eric Aeby & Jeannie T. Lee p377 | doi:10.1038/nrg.2017.17 Three-dimensional genome organization can shape gene expression by facilitating interactions between regulatory elements. The authors review the process of X-chromosome inactivation with a focus on chromatin organization and subnuclear localization of the active and inactive X chromosomes, as well as the potential roles of long non-coding RNAs. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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