His primary areas of study are Genetics, Genome-wide association study, Immunology, Inflammatory bowel disease and Ulcerative colitis. His biological study deals with issues like IRGM, which deal with fields such as Interleukin-23 receptor. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Odds ratio, Genotyping, Case-control study and Locus.
His Locus research focuses on Candidate gene and how it connects with Genetic linkage, Genome, Human genome and Expression quantitative trait loci. His studies deal with areas such as Allele and NOD2 as well as Inflammatory bowel disease. His Ulcerative colitis research is multidisciplinary, incorporating elements of Crohn's disease and Diarrhea.
His main research concerns Genetics, Inflammatory bowel disease, Ulcerative colitis, Immunology and Crohn's disease. All of his Genetics and Genome-wide association study, Locus, Genetic association, Single-nucleotide polymorphism and Linkage disequilibrium investigations are sub-components of the entire Genetics study. Disease covers Richard H. Duerr research in Inflammatory bowel disease.
His Ulcerative colitis study combines topics in areas such as Odds ratio, Colitis, Primary sclerosing cholangitis, Genetic heterogeneity and Cohort. His Immunology research incorporates elements of Family aggregation, Genetic predisposition and NOD2. His studies examine the connections between Crohn's disease and genetics, as well as such issues in Gastroenterology, with regards to Ileal resection.
Richard H. Duerr mainly investigates Internal medicine, Gastroenterology, Crohn's disease, Ileal resection and Exome sequencing. He has researched Crohn's disease in several fields, including Post operative and Period. The Ileal resection study which covers Perioperative that intersects with Gene expression.
His work deals with themes such as Genome-wide association study, Immunology and Rare disease, which intersect with Exome sequencing. His Genome-wide association study study is concerned with the field of Genetics as a whole. His research on Rare disease also deals with topics like
The scientist’s investigation covers issues in Allele frequency, Genome-wide association study, Exome sequencing, Mixture model and Genetic variation. His Allele frequency study integrates concerns from other disciplines, such as Ashkenazi jews, Kinase activity, Immunology and LRRK2. His Genome-wide association study study frequently intersects with other fields, such as Haplotype.
His Mixture model research is multidisciplinary, incorporating perspectives in Transcriptome, Computational biology, Cluster analysis and Genomics. His Genetic variation study necessitates a more in-depth grasp of Genetics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Yasunori Ogura;Denise K. Bonen;Naohiro Inohara;Dan L. Nicolae.
Nature (2001)
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Luke Jostins;Stephan Ripke;Rinse K Weersma;Richard H Duerr.
Nature (2012)
A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene
Richard H. Duerr;Kent D. Taylor;Steven R. Brant;Steven R. Brant;John D. Rioux;John D. Rioux.
Science (2006)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett;Sarah Hansoul;Dan L. Nicolae;Judy H. Cho.
Nature Genetics (2008)
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Andre Franke;Dermot P B McGovern;Jeffrey C. Barrett;Kai Wang.
Nature Genetics (2010)
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
John D. Rioux;John D. Rioux;Ramnik J. Xavier;Kent D. Taylor;Mark S. Silverberg.
Nature Genetics (2007)
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Carl A. Anderson;Gabrielle Boucher;Charlie W. Lees;Andre Franke.
Nature Genetics (2011)
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Gosia Trynka;Karen A Hunt;Nicholas A Bockett;Jihane Romanos.
Nature Genetics (2011)
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.
Manuel A. Rivas;Manuel A. Rivas;Manuel A. Rivas;Mélissa Beaudoin;Agnes Gardet;Christine Stevens.
Nature Genetics (2011)
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.
Steven A McCarroll;Alan Huett;Petric Kuballa;Shannon D Chilewski.
Nature Genetics (2008)
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