Evidence map›Paper›PMID 8651273›Full record

ArticleAmerican journal of human genetics1996

The FRAXE Syndrome: is it time for routine screening?

W T Brown

Abstract readEditorial
In one paragraph

Article in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Autism spectrum disorder: FRAXE mutation, a rare etiology.Journal of autism and developmental disorders · 2015
    Article
  3. Article
  4. Article
  5. Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  6. Synaptic regulation of protein synthesis and the fragile X protein.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Review
  7. Chromosomal fragility and human genetic disorders.Indian journal of clinical biochemistry : IJCB · 2000
    Article
  8. FRAXA and FRAXE: the results of a five year survey.Journal of medical genetics · 2000
    Article
  9. Article
  10. Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  11. Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  12. Review
  13. FRAXE testing.American journal of human genetics · 1996
    Article
  14. Coverage of new genetic technologies: what matters to insurers?American journal of human genetics · 1996
    Article
  15. Review
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.

W T Brown

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Fragile X SyndromeGenetic TestingHumans

Identifiers

PMID8651273
PMCPMC1914605

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.