Evidence map›Paper›PMID 26933242›Full record

ArticleCold Spring Harbor protocols2016

Using the Collaborative Cross to Study the Role of Genetic Diversity in Cancer-Related Phenotypes.

Karlyne M Reilly

Abstract read
In one paragraph

Article in Cold Spring Harbor protocols, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Disease Animal Models for Cancer Research.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  5. Article
  6. Article
  7. Optic Pathway Gliomas in Neurofibromatosis Type 1.Journal of child neurology · 2018
    Review
  8. Review
  9. 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

1 author.

Karlyne M ReillyMouse Cancer Genetics Program, National Cancer Institute, Frederick, Maryland 21702.

Funding

Identification of Modifier Gene of Tumors Associated with NF1 and AstrocytomaZ01BC010539 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI REILLY, KARLYNE · 2003 to 2008
$1.4M
Intramural NIH HHS Z01 BC010539
6 · The paper itself

Abstract

Human populations are genetically diverse and often a single mouse model can only represent a small subset of the human population. Studying genetic diversity directly can improve the predictive value of mouse models of cancer biology and research on the effects of carcinogens and therapeutics in humans. The collaborative cross is a panel of inbred mouse lines that captures 90% of the genetic diversity of the Mus musculus strain and can help identify regions of the genome that are responsible for variation in cancer phenotypes across the population. The appropriate procedure will depend on the mouse model used; here, three mouse cross designs are described as examples.

Indexed as

Crosses, GeneticGenetic VariationPhenotypeAnimalsMiceNeoplasms

Identifiers

PMID26933242
PMCPMC6713446

What OpenQuestion holds

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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.