Evidence map›Paper›PMID 22167527›Full record

GuidelineJournal of genetic counseling2012

Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.

Scott M Weissman, Randall Burt, James Church, Steve Erdman, Heather Hampel, Spring Holter, Kory Jasperson, Matt F Kalady, Joy Larsen Haidle, Henry T Lynch and 3 more

Abstract readPractice Guideline
PubMed Publisher
In one paragraph

Guideline in Journal of genetic counseling, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
7.5field-weighted citation impact, top 2% 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.

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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 131 citations in OpenAlex.

  1. Guideline
  2. American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2014
    Guideline
  3. Article
  4. Article
  5. Article
  6. Article
  7. Genes · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Somatic Tumor Profile Analysis in a Patient with GermlineJournal of personalized medicine · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Effective Identification of Lynch Syndrome in Gastroenterology Practice.Current treatment options in gastroenterology · 2019
    Review

5 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

13 authors at 10 institutions in 2 countries.

Scott M WeissmanCenter for Medical Genetics, NorthShore University HealthSystem, Evanston, IL, USA. sweissman@northshore.org
Randall Burt
James Church
Steve Erdman
Heather Hampel
Spring Holter
Kory Jasperson
Matt F Kalady
Joy Larsen Haidle
Henry T Lynch
Selvi Palaniappan
Paul E Wise
Leigha Senter
University of Utah · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USCleveland Clinic · USCreighton University · USMount Sinai Hospital · CANationwide Children's Hospital · USNorth Memorial Health Care · USNorthShore University HealthSystem · USNorthside Hospital · USVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying individuals who have Lynch syndrome (LS) involves a complex diagnostic work up that includes taking a detailed family history and a combination of various genetic and immunohistochemical tests. The National Society of Genetic Counselors (NSGC) and the Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC) have come together to publish this clinical practice testing guideline for the evaluation of LS. The purpose of this practice guideline is to provide guidance and a testing algorithm for LS as well as recommendations on when to offer testing. This guideline does not replace a consultation with a genetics professional. This guideline includes explanations in support of this and a summary of background data. While this guideline is not intended to serve as a review of LS, it includes a discussion of background information on LS, and cites a number of key publications which should be reviewed for a more in-depth understanding of LS. These guidelines are intended for genetic counselors, geneticists, gastroenterologists, surgeons, medical oncologists, obstetricians and gynecologists, nurses and other healthcare providers who evaluate patients for LS.

Indexed as

Genetic CounselingGenetic Predisposition to DiseaseGenetic TestingSocieties, MedicalAdaptor Proteins, Signal TransducingAdenosine TriphosphatasesAntigens, NeoplasmBase Pair MismatchCell Adhesion MoleculesColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisDNA-Binding ProteinsDNA MethylationDNA RepairDNA Repair EnzymesEpithelial Cell Adhesion MoleculeAdaptor Proteins, Signal TransducingAdenosine TriphosphatasesAntigens, NeoplasmBRAF protein, humanCell Adhesion MoleculesDNA-Binding ProteinsDNA Repair EnzymesEPCAM protein, humanEpithelial Cell Adhesion MoleculeMismatch Repair Endonuclease PMS2MLH1 protein, humanMutL Protein Homolog 1Nuclear ProteinsPMS2 protein, humanProto-Oncogene Proteins B-raf

Identifiers

PMID22167527
OpenAlexW2052700799

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.