Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease
Authors
Keywords
Inflammatory bowel disease, Gene regulation, Genome-wide association studies, Copy number variation, Genetic loci, MAPK signaling cascades, Microarrays, Algorithms
Journal
PLoS One
Volume 14, Issue 6, Pages e0217846
Publisher
Public Library of Science (PLoS)
Online
2019-06-12
DOI
10.1371/journal.pone.0217846
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap
- (2019) Jüri Reimand et al. Nature Protocols
- Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
- (2017) Katrina M de Lange et al. NATURE GENETICS
- Dosage sensitivity is a major determinant of human copy number variant pathogenicity
- (2017) Alan M. Rice et al. Nature Communications
- Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci
- (2016) Hamid Reza Saadati et al. BMC Medical Genetics
- The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
- (2016) William J. Astle et al. CELL
- SAPCD2 Controls Spindle Orientation and Asymmetric Divisions by Negatively Regulating the Gαi-LGN-NuMA Ternary Complex
- (2016) Catherine W.N. Chiu et al. DEVELOPMENTAL CELL
- Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder
- (2016) Stephen J Mosca et al. JOURNAL OF MEDICAL GENETICS
- Analyzing and interpreting genome data at the network level with ConsensusPathDB
- (2016) Ralf Herwig et al. Nature Protocols
- Inflammatory Bowel Disease: A Canadian Burden of Illness Review
- (2016) Angela Rocchi et al. CANADIAN JOURNAL OF GASTROENTEROLOGY
- Nuclear termination of STAT3 signaling through SIPAR (STAT3-Interacting Protein As a Repressor)-dependent recruitment of T cell tyrosine phosphatase TC-PTP
- (2015) Fangli Ren et al. FEBS LETTERS
- A global reference for human genetic variation
- (2015) Richard A. Gibbs et al. NATURE
- Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
- (2015) Jimmy Z Liu et al. NATURE GENETICS
- Epidemiology and risk factors for IBD
- (2015) Ashwin N. Ananthakrishnan Nature Reviews Gastroenterology & Hepatology
- A copy number variation map of the human genome
- (2015) Mehdi Zarrei et al. NATURE REVIEWS GENETICS
- Clinically relevant copy number variations detected in cerebral palsy
- (2015) Maryam Oskoui et al. Nature Communications
- Clinical implications of copy number variations in autoimmune disorders
- (2015) Seon-Hee Yim et al. KOREAN JOURNAL OF INTERNAL MEDICINE
- Second-generation PLINK: rising to the challenge of larger and richer datasets
- (2015) Christopher C Chang et al. GigaScience
- Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes
- (2014) Abdul Noor et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Physiological functions of MTA family of proteins
- (2014) Nirmalya Sen et al. CANCER AND METASTASIS REVIEWS
- The Microbiome in Inflammatory Bowel Disease: Current Status and the Future Ahead
- (2014) Aleksandar D. Kostic et al. GASTROENTEROLOGY
- Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data
- (2014) G.-B. Chen et al. HUMAN MOLECULAR GENETICS
- A Genome-wide Small Interfering RNA (siRNA) Screen Reveals Nuclear Factor-κB (NF-κB)-independent Regulators of NOD2-induced Interleukin-8 (IL-8) Secretion
- (2014) Neil Warner et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
- (2013) Suk-Kyun Yang et al. GUT
- Plakins, a Versatile Family of Cytolinkers: Roles in Skin Integrity and in Human Diseases
- (2013) Jamal-Eddine Bouameur et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
- (2013) Virginie J M Verhoeven et al. NATURE GENETICS
- The Database of Genomic Variants: a curated collection of structural variation in the human genome
- (2013) Jeffrey R. MacDonald et al. NUCLEIC ACIDS RESEARCH
- Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
- (2012) Luke Jostins et al. NATURE
- Single Nucleotide Polymorphisms That Increase Expression of the Guanosine Triphosphatase RAC1 Are Associated With Ulcerative Colitis
- (2011) Aleixo M. Muise et al. GASTROENTEROLOGY
- Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
- (2011) Dalila Pinto et al. NATURE BIOTECHNOLOGY
- Cysteine-rich intestinal protein 2 (CRIP2) acts as a repressor of NF- B-mediated proangiogenic cytokine transcription to suppress tumorigenesis and angiogenesis
- (2011) A. K. L. Cheung et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Cytoscape 2.8: new features for data integration and network visualization
- (2010) M. E. Smoot et al. BIOINFORMATICS
- The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing
- (2010) Shivendra Kishore et al. HUMAN MOLECULAR GENETICS
- Multiple common variants for celiac disease influencing immune gene expression
- (2010) Patrick C A Dubois et al. NATURE GENETICS
- Association of Higher DEFB4 Genomic Copy Number With Crohn's Disease
- (2009) Robert W Bentley et al. AMERICAN JOURNAL OF GASTROENTEROLOGY
- Circos: An information aesthetic for comparative genomics
- (2009) M. Krzywinski et al. GENOME RESEARCH
- Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
- (2008) Steven A McCarroll et al. NATURE GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now