Evidence map›Paper›PMID 9497271›Full record

ArticleAmerican journal of human genetics1998

The genetics of cataract: our vision becomes clearer.

J F Hejtmancik

Registry-linked trialAbstract readEditorial
In one paragraph

Article in American journal of human genetics, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00001609 (Clinical and Molecular Studies in Families With Congenital or Hereditary Cataracts), which is not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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.

NCT00001609 completednot on this map

Clinical and Molecular Studies in Families With Congenital or Hereditary Cataracts

TypeobservationalSponsorNational Eye Institute (NEI)Ran1996 to 2003Enrolled1,200ConditionsCataract, Congenital Anomaly
3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Article
  2. Article
  3. A Novel Mutation inOphthalmology science · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. A novel splice site mutation ofInternational journal of ophthalmology · 2017
    Article
  10. Associations betweenClinical ophthalmology (Auckland, N.Z.) · 2017
    Article
  11. A novel mutation of p.F32I inInternational journal of ophthalmology · 2016
    Article
  12. Molecular Genetics of Cataract.Progress in molecular biology and translational science · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Molecular genetic analysis of autosomal dominant late-onset cataract in a Chinese Family.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2010
    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

1 author.

J F Hejtmancik

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AgingCataractChromosome MappingCrystallinsHumansLens, CrystallineMutationCrystallins

Identifiers

PMID9497271
PMCPMC1376968

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.