Evidence map›Paper›PMID 33432855›Full record

ReviewOphthalmic genetics2021

The evolving role of genetics in ophthalmology.

Natario L Couser, Brian P Brooks, Arlene V Drack, Suma P Shankar

Open access · greenAbstract readReview
In one paragraph

Review in Ophthalmic genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 29% 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.

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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

4 authors at 4 institutions in 1 country.

Natario L CouserDepartments of Ophthalmology & Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.ORCID 0000-0001-8713-2097
Brian P BrooksOphthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-1916-7551
Arlene V DrackDepartment of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-8195-8426
Suma P ShankarDepartments of Pediatrics & Ophthalmology, University of California Davis, Sacramento, CA, USA.ORCID 0000-0001-7100-5691
National Institutes of Health · USUniversity of California, Davis · USUniversity of Iowa · USVirginia Commonwealth University · US

Funding

National Ophthalmic Disease Genotyping and Phenotyping Network - eyeGENEZICEY000478 · NEI · NATIONAL EYE INSTITUTE · PI GOETZ, KERRY · 2009 to 2025
$14.8M
Intramural NIH HHS ZIC EY000478
6 · The paper itself

Abstract

Advances in molecular genetics over the past three decades have helped identify a substantial number of genetic variants causing inherited eye diseases that can be identified rapidly by appropriate genetic tests in a clinically useful window. With this progression of knowledge, the roles of genetics and ophthalmology in patient care have become increasingly intertwined, and the necessity for subspecialists in the field of ophthalmic genetics is of paramount importance. As a result of continual medical specialization, technological progress in genetics and knowledge garnered by over a century and a half of cataloguing eye pathology, ophthalmic genetics has become an emerging subspecialty within ophthalmology. By virtue of its rapidly changing advances, genetics and genomics serves a large role within ophthalmology, and subspecialists with the same level of detailed and broad knowledge as any other ophthalmology subspecialty are now required in order to meet the growing needs of the expanding population.

Indexed as

Eye DiseasesGenomicsHumansOphthalmologygene therapyInherited retinal diseaseocular genetics training programophthalmic genetics fellowshipOphthalmology subspecialist

Identifiers

PMID33432855
PMCPMC11512516
OpenAlexW3120113717

What OpenQuestion holds

Textmetadata
LicenceTDM
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.