Evidence map›Paper›PMID 19654196›Full record

ReviewCMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne2009

Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model.

Henry T Lynch, Jane F Lynch, Thomas A Attard

Abstract readReview
In one paragraph

Review in CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–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

27 citing papers in PubMed.

  1. Trial
  2. Article
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  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
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  11. Review
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  14. Review
  15. Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description.International journal of hematology-oncology and stem cell research · 2017
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

3 authors.

Henry T LynchDepartment of Preventive Medicine and Public Health, Creighton University School of Medicine, Omaha, NE 68178, USA. htlynch@creighton.edu
Jane F Lynch
Thomas A Attard

Funding

EDRN--THE HEREDITARY CANCER CLINICAL CENTERU01CA086389 · NCI · CREIGHTON UNIVERSITY · PI LYNCH, HENRY T · 2000 to 2010
$6.2M
NCI NIH HHS 1U01 CA 86389NCI NIH HHS U01 CA086389
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Disease ManagementGenetic TestingAdaptor Proteins, Signal TransducingColorectal Neoplasms, Hereditary NonpolyposisDNA GlycosylasesGenetic Predisposition to DiseaseGerm-Line MutationHumansMutL Protein Homolog 1MutL ProteinsNeoplasm ProteinsNuclear ProteinsPedigreePractice Guidelines as TopicReferral and ConsultationAdaptor Proteins, Signal TransducingDNA GlycosylasesMLH1 protein, humanMutL Protein Homolog 1MutL ProteinsmutY adenine glycosylaseNeoplasm ProteinsNuclear ProteinsPMS1 protein, human

Identifiers

PMID19654196
PMCPMC2734205

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.