Using Transcription Modules to Identify Expression Clusters Perturbed in Williams-Beuren Syndrome
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Using Transcription Modules to Identify Expression Clusters Perturbed in Williams-Beuren Syndrome
Authors
Keywords
-
Journal
PLoS Computational Biology
Volume 7, Issue 1, Pages e1001054
Publisher
Public Library of Science (PLoS)
Online
2011-01-21
DOI
10.1371/journal.pcbi.1001054
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- ExpressionView--an interactive viewer for modules identified in gene expression data
- (2010) A. Luscher et al. BIOINFORMATICS
- Modular analysis of gene expression data with R
- (2010) G. Csardi et al. BIOINFORMATICS
- Network properties of human disease genes with pleiotropic effects
- (2010) Sreenivas Chavali et al. BMC Systems Biology
- Transcriptome profile in Williams–Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits
- (2010) Anna Antonell et al. HUMAN GENETICS
- Williams–Beuren Syndrome
- (2010) Barbara R. Pober NEW ENGLAND JOURNAL OF MEDICINE
- Lack of nAChR Activity Depresses Cochlear Maturation and Up-Regulates GABA System Components: Temporal Profiling of Gene Expression in α9 Null Mice
- (2010) Sevin Turcan et al. PLoS One
- Is it Williams syndrome?GTF2IRD1implicated in visual-spatial construction andGTF2Iin sociability revealed by high resolution arrays
- (2009) L. Dai et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice
- (2009) Hong Hua Li et al. EMBO Molecular Medicine
- An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient
- (2009) Giovanni Battista Ferrero et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Copy number variants, diseases and gene expression
- (2009) C. N. Henrichsen et al. HUMAN MOLECULAR GENETICS
- Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile
- (2009) A. Antonell et al. JOURNAL OF MEDICAL GENETICS
- Segmental copy number variation shapes tissue transcriptomes
- (2009) Charlotte N Henrichsen et al. NATURE GENETICS
- Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11.23-q21.11
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A novel 2.43 Mb deletion of 7q11.22-q11.23
- (2008) Moira Blyth et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase
- (2008) Lucia Micale et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion
- (2008) I. Cusco et al. GENOME RESEARCH
- Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome
- (2008) Jessica Molina et al. HUMAN MOLECULAR GENETICS
- Hsp27 Protects against Ischemic Brain Injury via Attenuation of a Novel Stress-Response Cascade Upstream of Mitochondrial Cell Death Signaling
- (2008) R. A. Stetler et al. JOURNAL OF NEUROSCIENCE
- The promiscuous role of the epsilon subunit in GABAA receptor biogenesis
- (2008) Karen A. Bollan et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Hierarchical structure and the prediction of missing links in networks
- (2008) Aaron Clauset et al. NATURE
- Distribution and functional impact of DNA copy number variation in the rat
- (2008) Victor Guryev et al. NATURE GENETICS
- Use and misuse of the gene ontology annotations
- (2008) Seung Yon Rhee et al. NATURE REVIEWS GENETICS
- STRING 8--a global view on proteins and their functional interactions in 630 organisms
- (2008) L. J. Jensen et al. NUCLEIC ACIDS RESEARCH
- Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development
- (2008) B. Enkhmandakh et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Network properties of genes harboring inherited disease mutations
- (2008) I. Feldman et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started