Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center
Open Access
- 1 June 2020
- journal article
- research article
- Published by Elsevier BV in Gastroenterology
- Vol. 158 (8), 2208-2220
- https://doi.org/10.1053/j.gastro.2020.02.023
Abstract
No abstract availableFunding Information
- National Institutes of Health
This publication has 61 references indexed in Scilit:
- GEMINI: Integrative Exploration of Genetic Variation and Genome AnnotationsPLoS Computational Biology, 2013
- Host–microbe interactions have shaped the genetic architecture of inflammatory bowel diseaseNature, 2012
- VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencingGenome Research, 2012
- Pediatric modification of the Montreal classification for inflammatory bowel diseaseInflammatory Bowel Diseases, 2011
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataGenome Research, 2010
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataNucleic Acids Research, 2010
- Estimation of effect size distribution from genome-wide association studies and implications for future discoveriesNature Genetics, 2010
- Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 ReceptorThe New England Journal of Medicine, 2009
- The Sequence Alignment/Map format and SAMtoolsBioinformatics, 2009
- PAnnBuilder: an R package for assembling proteomic annotation dataBioinformatics, 2009