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1. Development and validation of a novel Barrett's oesophagus patient reported outcome measure (B-PROM)

2. Multi-Omic Analysis of Esophageal Adenocarcinoma Uncovers Candidate Therapeutic Targets and Cancer-Selective Posttranscriptional Regulation

5. Serial ctDNA detection using a personalized, tumor-informed assay in esophageal adenocarcinoma patients following resection

7. Dedicated service for Barrett’s oesophagus surveillance endoscopy yields higher dysplasia detection and guideline adherence in a non-tertiary setting in the UK: a 5-year comparative cohort study

8. Identification of Prognostic Phenotypes of Esophageal Adenocarcinoma in 2 Independent Cohorts

9. Pretreatment prediction of response to ursodeoxycholic acid in primary biliary cholangitis: development and validation of the UDCA Response Score

13. Author Correction: Authentication and characterisation of a new oesophageal adenocarcinoma cell line: MFD-1

16. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

17. Combined burden and functional impact tests for cancer driver discovery using DriverPower

18. Integrative pathway enrichment analysis of multivariate omics data

19. Pathway and network analysis of more than 2500 whole cancer genomes

20. Divergent mutational processes distinguish hypoxic and normoxic tumours

21. Genomic footprints of activated telomere maintenance mechanisms in cancer

25. P193 A dedicated Barrett’s oesophagus endoscopy service improves dysplasia detection and adherence to guidelines: 5-year experience

26. Rearrangement processes and structural variations show evidence of selection in oesophageal adenocarcinomas

28. Dedicated services for Barrett’s esophagus—a survey and service assessment of provision in United Kingdom hospitals

31. X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis

32. Serial circulating tumor DNA detection using a personalized, tumor-informed assay in esophageal adenocarcinoma patients following resection

33. British Society of Gastroenterology guidelines on the diagnosis and management of Barrettʼs oesophagus

34. P9 Outcomes from the UK purastat® registry: multicentre observational study of purastat® use in gastrointestinal bleeding

36. Multi-Omic Analysis of Esophageal Adenocarcinoma Uncovers Candidate Therapeutic Targets and Cancer-Selective Posttranscriptional Regulation

37. Repurposing of KLF5 activates a cell cycle signature during the progression from Barrett’s Oesophagus to Oesophageal Adenocarcinoma

39. Learning curves and the influence of procedural volume for the treatment of dysplastic Barrett’s esophagus

42. Tele-Monitoring of Cancer Patients’ Rhythms during Daily Life Identifies Actionable Determinants of Circadian and Sleep Disruption

43. Tu1020 OUTCOMES FROM THE UK PURASTAT REGISTRY – A MULTICENTRE PROSPECTIVE OBSERVATIONAL STUDY TO EVALUATE THE ROLE OF PURASTAT IN THE MANAGEMENT OF GASTROINTESTINAL BLEEDING (POPS)

44. Identification of Subtypes of Barrett’s Esophagus and Esophageal Adenocarcinoma Based on DNA Methylation Profiles and Integration of Transcriptome and Genome Data

46. Relevance of real-time teletransmission of physical activity, sleep, and circadian rhythms from gastrointestinal cancer (GIC) patients (pts) during daily routine (IDEAs, IRAS 233972).

47. Machine learning to predict early recurrence after oesophageal cancer surgery

50. Barrett’s oesophagus: a qualitative study of patient burden, care delivery experience and follow up needs:A qualitative study of patient burden, care delivery experience and follow-up needs

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