Evidence map›Paper›PMID 37359372›Full record

ArticleFrontiers in genetics2023

Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations.

Giuseppe Giovanni Nardone, Beatrice Spedicati, Maria Pina Concas, Aurora Santin, Anna Morgan, Lorenzo Mazzetto, Maurizio Battaglia-Parodi, Giorgia Girotto

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Review
  3. Genetic drivers of progression in Alzheimer's disease are distinct from disease risk.medRxiv : the preprint server for health sciences · 2025
    Article
  4. 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 3 institutions in 1 country.

Giuseppe Giovanni NardoneDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Beatrice SpedicatiDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Maria Pina ConcasInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
Aurora SantinDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Anna MorganInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo", Trieste, Italy.
Lorenzo MazzettoDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Maurizio Battaglia-ParodiOphthalmology Department, Vita-Salute San Raffaele University, Milano, Italy.
Giorgia GirottoDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
IRCCS Materno Infantile Burlo Garofolo · ITUniversity of Trieste · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

color vision defectsDeutangenetic isolatesgenome wide association studypathway analysisProtanSilk RoadTritan

Identifiers

PMID37359372
PMCPMC10288324
OpenAlexW4380083640

What Socratic 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 Socratic graph.