Evidence map›Paper›PMID 9345111›Full record

ArticleAmerican journal of human genetics1997

"Mistakes happen": somatic mutation and disease.

F Qian, G G Germino

Abstract read
In one paragraph

Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Polycystic kidney disease: In danger of being X-rated?Proceedings of the National Academy of Sciences of the United States of America · 2001
    Review
  12. Article
  13. Interindividual variation in mitotic recombination.American journal of human genetics · 1999
    Article
  14. Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  15. Article
  16. Review
  17. 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

2 authors.

F QianDepartment of Medicine, Division of Nephrology, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2196, USA.
G G Germino

Funding

Novel Approach to the Molecular Genetics of PKD1R37DK048006 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI GERMINO, GREGORY G. · 2004 to 2009
$2.6M
NOVEL APPROACH TO THE MOLECULAR GENETICS OF PKD1R01DK048006 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI GERMINO, GREGORY G · 1994 to 2003
$1.6M
NIDDK NIH HHS DK48006
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome AberrationsChromosome DisordersGenetic Diseases, InbornHumansLoss of HeterozygosityModels, GeneticMutationNeurofibromatosesPolycystic Kidney, Autosomal DominantTuberous Sclerosis

Identifiers

PMID9345111
PMCPMC1716042

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.