Evidence map›Paper›PMID 34445325›Full record

ArticleInternational journal of molecular sciences2021

Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in

Giancarlo Iarossi, Andrea Maria Coppè, Chiara Passarelli, Paolo Enrico Maltese, Lorenzo Sinibaldi, Alessandro Cappelli, Sarah Cetola, Antonio Novelli, Luca Buzzonetti

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

9 authors at 1 institution in 1 country.

Giancarlo IarossiDepartment of Ophthalmology, Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Andrea Maria CoppèDepartment of Ophthalmology, Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Chiara PassarelliTranslational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Paolo Enrico MalteseMAGI'S Lab s.r.l., 38068 Rovereto, Italy.ORCID 0000-0002-1974-4937
Lorenzo SinibaldiTranslational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Alessandro CappelliDepartment of Ophthalmology, Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Sarah CetolaTranslational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Antonio NovelliTranslational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.ORCID 0000-0002-9037-4297
Luca BuzzonettiDepartment of Ophthalmology, Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Bambino Gesù Children's Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blue cone monochromatism (BCM) is an X-linked recessive cone dysfunction disorder caused by mutations in the

Indexed as

AdultColor Vision DefectsEye ProteinsFovea CentralisHumansMaleMembrane GlycoproteinsMutationPedigreeRod OpsinsEye ProteinsGPR143 protein, humanlong-wavelength opsinMembrane GlycoproteinsRod Opsinsblue cone monochromatismfoveal hypoplasiaOPN1LW/OPN1MW gene clusterX-linked inheritance

Identifiers

PMID34445325
PMCPMC8395340
OpenAlexW3189246602

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.