Evidence map›Paper›PMID 18332328›Full record

ArticleArchives of ophthalmology (Chicago, Ill. : 1960)2008

Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE).

Brian P Brooks, Ian M Macdonald, Santa J Tumminia, Nizar Smaoui, Delphine Blain, Ajaina A Nezhuvingal, Paul A Sieving, National Ophthalmic Disease Genotyping Network (eyeGENE)

Registry-linked trialOpen access · greenAbstract readEditorial
PubMed Full text at PMC Publisher
In one paragraph

Article in Archives of ophthalmology (Chicago, Ill. : 1960), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01432847 (Generation of Induced Pluripotent Stem), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 15% 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.

NCT01432847 recruitingnot on this mapstarted 2011, after this paper: background citation

Generation of Induced Pluripotent Stem (iPS) Cell Lines From Somatic Cells of Participants With Eye Diseases and From Somatic Cells of Matched Controls

TypeobservationalSponsorNational Eye Institute (NEI)Ran2011Enrolled930ConditionsRetinal Disease, AMD, Retinal Degeneration, Retinitis Pigmentosa
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network.American journal of medical genetics. Part C, Seminars in medical genetics · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

8 authors at 1 institution in 1 country.

Brian P Brooks
Ian M Macdonald
Santa J Tumminia
Nizar Smaoui
Delphine Blain
Ajaina A Nezhuvingal
Paul A Sieving
National Ophthalmic Disease Genotyping Network (eyeGENE)
National Institutes of Health · US

Funding

National Ophthalmic Disease Genotyping and Phenotyping Network - eyeGENEZICEY000478 · NEI · NATIONAL EYE INSTITUTE · PI GOETZ, KERRY · 2009 to 2025
$14.8M
Preclinical and Clinical Development of Treatment for X-linked RetinoschisisZIADC000065 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI SIEVING, PAUL · 2009 to 2019
$5.7M
Intramural NIH HHS Z99 EY999999
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Databases, FactualMolecular Diagnostic TechniquesEye DiseasesGenomicsGenotypeHumansOphthalmologyUnited States

Identifiers

PMID18332328
PMCPMC2821692
OpenAlexW2095269478

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.