Evidence map›Paper›PMID 28786406›Full record

ReviewThe American journal of gastroenterology2017

Hereditary Colorectal Polyposis and Cancer Syndromes: A Primer on Diagnosis and Management.

Priyanka Kanth, Jade Grimmett, Marjan Champine, Randall Burt, N Jewel Samadder

Abstract readReview
PubMed Publisher
In one paragraph

Review in The American journal of gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Mosaicism in Patients With Colorectal Cancer or Polyposis Syndromes: A Systematic Review.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2020
    Pooled it
  5. Trial
  6. Trial
  7. Review
  8. Review
  9. Article
  10. Analysis ofFrontiers in oncology · 2026
    Article
  11. Article
  12. Article
  13. Article
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  15. Review
  16. Review
  17. A Haplotype GWAS in Syndromic Familial Colorectal Cancer.International journal of molecular sciences · 2025
    Article
  18. Review
  19. Chemopreventive strategies for sporadic colorectal cancer: a narrative review.Translational gastroenterology and hepatology · 2025
    Review
  20. Article

37 more citing papers are in PubMed but not listed here.

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

5 authors.

Priyanka KanthDepartment of Medicine (Gastroenterology), University of Utah, Salt Lake City, Utah, USA.
Jade GrimmettHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Marjan ChampineHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Randall BurtDepartment of Medicine (Gastroenterology), University of Utah, Salt Lake City, Utah, USA.
N Jewel SamadderDepartment of Medicine (Gastroenterology), University of Utah, Salt Lake City, Utah, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the fourth most common cancer amongst men and women. Between 3 and 6% of all CRCs are attributed to well-defined inherited syndromes, including Lynch syndrome, familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), and several hamartomatous polyposis conditions. Identification of these patients through family history and appropriate genetic testing can provide estimates of cancer risk that inform appropriate cancer screening, surveillance and/or preventative interventions. This narrative review examines the hereditary colorectal cancer and polyposis syndromes, their genetic basis, clinical management, and evidence supporting cancer screening.

Indexed as

Adenomatous Polyposis ColiColorectal Neoplasms, Hereditary NonpolyposisDisease ManagementEarly Detection of CancerGenetic Predisposition to DiseaseGenetic TestingHumansMedical History Taking

Identifiers

PMID28786406

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.