Evidence map›Paper›PMID 34203883›Full record

ArticleInternational journal of molecular sciences2021

Novel

Vasily Smirnov, Olivier Grunewald, Jean Muller, Christina Zeitz, Carolin D Obermaier, Aurore Devos, Valérie Pelletier, Béatrice Bocquet, Camille Andrieu, Jean-Louis Bacquet and 10 more

Open access · goldAbstract read
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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Benign foveal retinal pigment epithelium hypopigmentation without functional loss : pediatric case series.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Article
  2. Article
  3. Tapetal-like sheen as a key phenotypical feature inAmerican journal of ophthalmology case reports · 2025
    Article
  4. Article
  5. Article
  6. Towards a Long-Read Sequencing Approach for the Molecular Diagnosis of RPGRInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Impaired glutamylation of RPGRProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. International journal of molecular sciences · 2021
    Observational
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

20 authors at 8 institutions in 4 countries.

Vasily SmirnovUniversité de Lille, Faculté de Médecine, 59037 Lille, France.
Olivier GrunewaldUniv. Lille, Inserm, CHU Lille, U1172-LilNCog-Lille Neuroscience & Cognition, 59045 Lille, France.ORCID 0000-0002-9845-948X
Jean MullerLaboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), INSERM U1112, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg UMRS_1112, 67000 Strasbourg, France.ORCID 0000-0002-7682-559X
Christina ZeitzSorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.ORCID 0000-0002-3510-1712
Carolin D ObermaierPraxis für Humangenetik Tuebingen & Center for Genomics and Transcriptomics, CeGaT GmbH, 72076 Tuebingen, Germany.
Aurore DevosUniv. Lille, CHU Lille, Service de Toxicologie et Génopathies, 59037 Lille, France.ORCID 0000-0003-0668-6771
Valérie PelletierCentre de Référence pour les Affections Rares en Génétique Ophtalmologiques, Hopitaux Universitaires de Strasbourg, 67000 Strasbourg, France.
Béatrice BocquetNational Reference Centre for Inherited Sensory Diseases, University of Montpellier, Montpellier University Hospital, Sensgene Care Network, ERN-EYE Network, 34295 Montpellier, France.ORCID 0000-0002-6369-4818
Camille AndrieuCentre Hospitalier National d'Ophtalmologie des Quinze-Vingts, INSERM-DHOS CIC 1423, 75012 Paris, France.
Jean-Louis BacquetCentre de Référence pour les Affections Rares en Génétique Ophtalmologiques, Hopitaux Universitaires de Strasbourg, 67000 Strasbourg, France.
Elodie LebredonchelUniv. Lille, CHU Lille, Service de Toxicologie et Génopathies, 59037 Lille, France.ORCID 0000-0001-5119-6005
Saddek Mohand-SaïdSorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
Sabine Defoort-DhellemmesCHU Lille, Service d'Exploration Fonctionnelle de la Vision et de Neuro-Ophtalmologie, Hôpital Salengro, 59037 Lille, France.
José-Alain SahelSorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
Hélène DollfusCentre de Référence pour les Affections Rares en Génétique Ophtalmologiques, Hopitaux Universitaires de Strasbourg, 67000 Strasbourg, France.
Xavier ZanlonghiService d'Ophtalmologie, CHU de Rennes, 35000 Rennes, France.
Isabelle AudoSorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.ORCID 0000-0003-0698-5309
Isabelle MeunierNational Reference Centre for Inherited Sensory Diseases, University of Montpellier, Montpellier University Hospital, Sensgene Care Network, ERN-EYE Network, 34295 Montpellier, France.
Elise Boulanger-ScemamaFondation Ophtalmologique Adolphe de Rothschild, 75019 Paris, France.
Claire-Marie DhaenensUniv. Lille, Inserm, CHU Lille, U1172-LilNCog-Lille Neuroscience & Cognition, 59045 Lille, France.
Inserm · FRCentre National de la Recherche Scientifique · FRHôpitaux Universitaires de Strasbourg · FRUniversité de Lille · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Rennes · FRFondation Ophtalmologique Adolphe de Rothschild · FRPraxis für Humangenetik Tübingen · DE

Funding

Fondation Fighting Blindness BR-GE-0619-0761-INSERMPHRC I 2013 HUS N° 5724Retina France 2019
6 · The paper itself

Abstract

Variants of the

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdultAgedCarrier ProteinsChildChromosome BreakpointsComputer SimulationCone-Rod DystrophiesDNA Copy Number VariationsElectroretinographyEye Diseases, HereditaryFemaleGenotypeHumansMaleCarrier ProteinsTTLL5 protein, humancone-rod dystrophyearly onset severe retinal dystrophylarge deletionnovel variantsTTLL5 gene

Identifiers

PMID34203883
PMCPMC8232641
OpenAlexW3169664767

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.