Wednesday, July 18, 2012

Nature Reviews Genetics Contents August 2012 Volume 13 Number 8 pp 517 - 594

Nature Reviews Genetics

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TABLE OF CONTENTS
 
August 2012 Volume 13 Number 8Advertisement

Nature Reviews Genetics cover
Impact Factor 38.075 *
In this issue
Research Highlights
Reviews
Perspectives


Also this month
Article series:
Disease mechanisms
Study designs
Applications of next-generation sequencing
 Featured article:
Genetic architectures of psychiatric disorders: the emerging picture and its implications
Patrick F. Sullivan, Mark J. Daly & Michael O'Donovan



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September 19-22, 2012 - Potomac, MD, USA

Keynote Speakers: Francis Collins (National Institutes of Health, USA), Thomas Hudson (Ontario Institute for Cancer Research, Canada), Neil Risch (University of California, San Francisco, USA), Sarah Tishkoff (University of Pennsylvania School of Medicine, USA)

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RESEARCH HIGHLIGHTS

Top

Epigenetics: Detecting the dynamics and memory of heterochromatin
p517 | doi:10.1038/nrg3283
PDF


Alternative splicing: Proteomic rewiring through transcriptomic diversity
p518 | doi:10.1038/nrg3288
PDF


Small RNAs: piRNA surveillance in the C. elegans germline
p518 | doi:10.1038/nrg3289
PDF


DNA methylation: In vivo enzyme action
p520 | doi:10.1038/nrg3284
PDF


Cancer genomics: Indicators for drug response from sequencing
p520 | doi:10.1038/nrg3285
PDF


Telomeres: Stem cells, cancer and telomerase linked by WNT
p521 | doi:10.1038/nrg3286
PDF


Evolution: The birth of new genes
p521 | doi:10.1038/nrg3287
PDF



IN BRIEF

Development: Retroviruses as cell fate regulators | Microbiology: The Human Microbiome Project | Genetic interactions: Improved yield through interaction studies under different conditions | Gene regulation: Transcription factors slide to find binding sites in vivo | Ageing: Longevity by design | Gene expression: Transcriptional roles for DNA repair factors | Pathogen genomics: Within-host sequencing of malaria parasites | Evolutionary genomics: The genomic landscape of maize
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REVIEWS

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Computational tools for prioritizing candidate genes: boosting disease gene discovery
Yves Moreau & Léon-Charles Tranchevent
p523 | doi:10.1038/nrg3253
Various studies (such as genetic linkage or 'omics'-based approaches) generate large lists of candidate genes, of which only a minority may be biologically relevant for a phenotype or disease of interest. This Review discusses computational tools for gene prioritization, emphasizing key considerations for how biologists can incorporate these tools into their research, and it includes hands-on tutorials.
Abstract | Full Text | PDF | Supplementary information


Article series: Disease mechanisms
Genetic architectures of psychiatric disorders: the emerging picture and its implications
Patrick F. Sullivan, Mark J. Daly & Michael O'Donovan
p537 | doi:10.1038/nrg3240
This Review considers recent findings — from genome-wide association studies, structural variant studies and exome sequencing — about the genetics of nine psychiatric disorders. The authors evaluate the implications of our current picture of the genetic architectures of these conditions for future research strategies.
Abstract | Full Text | PDF | Supplementary information


Article series: Study designs
Studying and modelling dynamic biological processes using time-series gene expression data
Ziv Bar-Joseph, Anthony Gitter & Itamar Simon
p552 | doi:10.1038/nrg3244
Biological processes are inherently dynamic and therefore capturing data about gene expression at multiple time points can provide valuable insights into biological systems. This Review discusses experimental and analytical considerations for studies of gene expression dynamics, and the possibilities for integration with other data sets.
Abstract | Full Text | PDF


Article series: Applications of next-generation sequencing
De novo mutations in human genetic disease
Joris A. Veltman & Han G. Brunner
p565 | doi:10.1038/nrg3241
Recent family-based genomic studies are providing a window into the incidence of new mutations in human genomes. This Review discusses our understanding of various types of de novo mutation, including the determinants and consequences of their occurrence rates, and the challenges both for their detection and for linking them to disease pathogenesis.
Abstract | Full Text | PDF


Article series: Disease mechanisms
Genetics of osteoporosis from genome-wide association studies: advances and challenges
J. Brent Richards, Hou-Feng Zheng & Tim D. Spector
p576 | doi:10.1038/nrg3228
Genome-wide association studies have recently furthered the understanding of the genetics of osteoporosis. The authors here present the major findings from these studies, the pathways that have been highlighted in the progress of the disease and strategies for future diagnosis and therapy development.
Abstract | Full Text | PDF



 
PERSPECTIVES

Top
VIEWPOINT
The place of genetics in ageing research
Nir Barzilai, Leonard Guarente, Thomas B. L. Kirkwood, Linda Partridge, Thomas A. Rando & P. Eline Slagboom
p589 | doi:10.1038/nrg3290
Is ageing in our genes? In this Viewpoint, six experts present their views on the extent to which ageing is genetic and discuss future strategies for research into ageing and longevity.
Abstract | Full Text | PDF


Erratum: Transcriptome-wide N 6-methyladenosine analysis
Hannah Stower
p594 | doi:10.1038/nrg3292
Full Text | PDF

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