Evidence map›Paper›PMID 40371729›Full record

ArticleClinical genetics2025

Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.

Şenol Demir, Esra Arslan Ateş, Orkun Sevik, Bengisu Sözer, Tuğba Köse, Özlem Şahin, Ahmet Arman, Bilgen Bilge Geçkinli

Abstract read
In one paragraph

Article in Clinical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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.

Şenol DemirDepartment of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
Esra Arslan AteşDepartment of Medical Genetics, Istanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, Istanbul, Turkey.
Orkun SevikDepartment of Ophthalmology, School of Medicine, Marmara University, Istanbul, Turkey.ORCID 0000-0001-7130-4798
Bengisu SözerDepartment of Ophthalmology, School of Medicine, Marmara University, Istanbul, Turkey.
Tuğba KöseDepartment of Genetics and Bioengineering, Faculty of Engineering and Natural Sciences, Istanbul Bilgi University, Istanbul, Turkey.ORCID 0000-0001-9226-6444
Özlem ŞahinDepartment of Ophthalmology, School of Medicine, Marmara University, Istanbul, Turkey.
Ahmet ArmanDepartment of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
Bilgen Bilge GeçkinliDepartment of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited retinal dystrophies (IRDs) are genetic disorders characterized by retinal pigment epithelium or photoreceptor degeneration. Advances in molecular diagnostic technologies, particularly next-generation sequencing (NGS), have facilitated the identification of disease-causing variants; however, population-specific genetic data, especially for Turkish cohorts, remain limited. This study aims to investigate the genetic profile of IRD patients in a Turkish cohort and assess the diagnostic utility of NGS-based gene panel testing. A total of 94 patients diagnosed with IRDs were included in the study. Genomic DNA was extracted from the peripheral blood of patients who met the inclusion and exclusion criteria. NGS was performed to analyze 141 genes associated with IRDs, following current clinical guidelines and utilizing up-to-date variant databases. Among the 94 patients, 97 variants were identified in 70 patients (74%). Of these, 58 variants (59.79%) were classified as pathogenic and 39 variants (40.21%) as likely pathogenic. Additionally, 28 variants (28%) were novel and have not been previously reported in the literature. Our findings demonstrate that NGS is a powerful tool for the molecular diagnosis of IRDs and emphasizes the genetic diversity of IRDs in the Turkish population. The identification of novel variants also highlights the need for continued variant curation and population-specific studies to enhance diagnostic accuracy and genetic counseling.

Indexed as

Genetic Predisposition to DiseaseRetinal DystrophiesAdolescentAdultChildChild, PreschoolCohort StudiesFemaleGenetic Association StudiesGenetic TestingGenetic VariationHigh-Throughput Nucleotide SequencingHumansInfantMaleMiddle Agedinherited retinal dystrophiesIRDsnext‐generation sequencingretinitis pigmentosa

Identifiers

PMID40371729
PMCPMC12501730

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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.