Evidence map›Paper›PMID 24913378›Full record

ReviewBest practice & research. Clinical gastroenterology2014

Genetic studies of Crohn's disease: past, present and future.

Jimmy Z Liu, Carl A Anderson

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in Best practice & research. Clinical gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03291743 (The Biologic Onset of Crohn's Disease), which is not on this map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
10.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03291743 naterminatednot on this mapstarted 2017, after this paper: background citation

The Biologic Onset of Crohn's Disease: A Screening Study in First Degree Relatives

TypeinterventionalSponsorCarilion ClinicRan2017 to 2022Enrolled38ConditionsCrohn Disease, Genetic Predisposition, IBDArmsCapsule endoscopy
3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Review
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  8. The role of goblet cells and mucus in intestinal homeostasis.Nature reviews. Gastroenterology & hepatology · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jimmy Z LiuThe Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK.
Carl A AndersonThe Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK. Electronic address: carl.anderson@sanger.ac.uk.
Wellcome Sanger Institute · GB

Funding

Wellcome TrustWellcome Trust 098051
6 · The paper itself

Abstract

The exact aetiology of Crohn's disease is unknown, though it is clear from early epidemiological studies that a combination of genetic and environmental risk factors contributes to an individual's disease susceptibility. Here, we review the history of gene-mapping studies of Crohn's disease, from the linkage-based studies that first implicated the NOD2 locus, through to modern-day genome-wide association studies that have discovered over 140 loci associated with Crohn's disease and yielded novel insights into the biological pathways underlying pathogenesis. We describe on-going and future gene-mapping studies that utilise next generation sequencing technology to pinpoint causal variants and identify rare genetic variation underlying Crohn's disease risk. We comment on the utility of genetic markers for predicting an individual's disease risk and discuss their potential for identifying novel drug targets and influencing disease management. Finally, we describe how these studies have shaped and continue to shape our understanding of the genetic architecture of Crohn's disease.

Indexed as

Genetic Predisposition to DiseaseCrohn DiseaseDisease SusceptibilityGenetic LinkageGenetic MarkersGenetic VariationGenome-Wide Association StudyGenomicsHumansNod2 Signaling Adaptor ProteinRisk FactorsTwin Studies as TopicGenetic MarkersNOD2 protein, humanNod2 Signaling Adaptor ProteinCrohn'sGeneticsGenomicsGenotypingSequencing

Identifiers

PMID24913378
PMCPMC4075408
OpenAlexW2022987102

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.