Natalie J. Prescott
educated at: UCL Institute of Child Health, King's College London
occupation: researcher
Articles 55
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Streptococcus Salivarius: A Potential Salivary Biomarker for Orofacial Granulomatosis and Crohn's Disease?
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Association of genetic variants in CHEK2 with oesophageal squamous cell carcinoma in the South African Black population.
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Genetic and Inflammatory Biomarkers Classify Small Intestine Inflammation in Asymptomatic First-degree Relatives of Patients With Crohn's Disease
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Exome sequencing and genotyping identify a rare variant in NLRP7 gene associated with ulcerative colitis.
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Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer.
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Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.
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Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism
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Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.
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Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
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Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease
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Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis.
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Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes
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Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease.
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The unusual suspects--innate lymphoid cells as novel therapeutic targets in IBD.
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Defective macrophage handling of Escherichia coli in Crohn's disease
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Altered intestinal microbiota and blood T cell phenotype are shared by patients with Crohn's disease and their unaffected siblings.
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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
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Effect of communicating DNA based risk assessments for Crohn's disease on smoking cessation: randomised controlled trial
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Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population
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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
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Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
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Accuracy and differential bias in copy number measurement of CCL3L1 in association studies with three auto-immune disorders
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Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study
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Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa
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Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota.
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Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
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Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
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Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
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Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.
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Common variants at five new loci associated with early-onset inflammatory bowel disease
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Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Human - wd:Q30348902