Evidence map›Paper›PMID 26477493›Full record

ReviewSeminars in perinatology2015

Genomics in the neonatal nursery: Focus on ROP.

Mary Elizabeth Hartnett, C Michael Cotten

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in perinatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
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.

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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Systemic Cytokines in Retinopathy of Prematurity.Journal of personalized medicine · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. 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

2 authors at 2 institutions in 1 country.

Mary Elizabeth HartnettJohn A. Moran Eye Center, University of Utah, 65 Mario Capecchi Dr, Salt Lake City, Utah 84132. Electronic address: me.hartnett@hsc.utah.edu.
C Michael CottenDuke University Medical Center, Durham, NC.
Duke Medical Center · USUniversity of Utah · US

Funding

Endothelial Transmigration in Neovascular Age-related Macular DegenerationR01EY017011 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HARTNETT, MARY ELIZABETH RUTH · 2007 to 2025
$7.7M
Mechanisms of Angiogenesis of Retinopathy of PrematurityR01EY015130 · NEI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mary Elizabeth Ruth Hartnett · 2005 to 2026
$7.6M
NEI NIH HHS R01 EY015130NEI NIH HHS R01 EY017011
6 · The paper itself

Abstract

Retinopathy of prematurity (ROP) is a complex disease that is influenced by both genetic and environmental factors. Several small studies have found genetic variants in EPAS1, VEGF, SOD, and members of the WNT family in association with ROP. Design in genetic studies is challenging because of changing recommendations for the management of prematurity and ROP, the fact ROP is rare, and that availability of resources for managing premature infants can vary throughout the world. In addition, there is a shortage of ophthalmologists with the ability to diagnose and characterize severe ROP. Careful determination of the degree of prematurity is important when evaluating genetic studies. Controlling for significant epidemiologic factors and multiple comparisons is also important to consider when evaluating genetic studies. One large candidate gene study controlled for degree of prematurity, significant epidemiologic factors, and multiple comparisons and found variants within the intron of BDNF associated with severe ROP. Future studies using unbiased techniques to assess genetic risk are important as are in-depth study of BDNF through deep sequencing and associated mechanistic studies using appropriate experimental models.

Indexed as

Basic Helix-Loop-Helix ProteinsBrain-Derived Neurotrophic FactorEndothelial PAS Domain-Containing Protein 1FemaleGene-Environment InteractionGenetic Predisposition to DiseaseHumansInfantInfant, Low Birth WeightInfant, NewbornInfant, PrematureMaleNeonatal ScreeningPregnancyRetinopathy of PrematurityRetrospective StudiesBasic Helix-Loop-Helix ProteinsBDNF protein, humanBrain-Derived Neurotrophic FactorEndothelial PAS Domain-Containing Protein 1SOD1 protein, humanSuperoxide DismutaseSuperoxide Dismutase-1Vascular Endothelial Growth FactorsBDNFextremegeneticsROP

Identifiers

PMID26477493
PMCPMC4644692
OpenAlexW2132331009

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.