Whole exome sequencing unveils novel pathogenic variants in an Iranian cohort with retinal dystrophies: Implications for genetic diagnosis and counseling.
- DOI
- 10.1016/j.mcp.2026.102084
- Published
- 2026 Aug 20
- Container
- Molecular and cellular probes
- Publisher
- Not recorded
- Open access
- unknown
Credibility signals
limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1016/j.mcp.2026.102084,
title = {Whole exome sequencing unveils novel pathogenic variants in an Iranian cohort with retinal dystrophies: Implications for genetic diagnosis and counseling.},
author = {Alimoradi E and Salmaninejad A and Nejati P and Golestani S and Kamari M and Bahadori S and Azadi P and Ghafouri-Fard S and Alibakhshi R},
year = {2026},
journal = {Molecular and cellular probes},
doi = {10.1016/j.mcp.2026.102084},
url = {https://doi.org/10.1016/j.mcp.2026.102084}
}RIS
TY - JOUR TI - Whole exome sequencing unveils novel pathogenic variants in an Iranian cohort with retinal dystrophies: Implications for genetic diagnosis and counseling. AU - Alimoradi E AU - Salmaninejad A AU - Nejati P AU - Golestani S AU - Kamari M AU - Bahadori S AU - Azadi P AU - Ghafouri-Fard S AU - Alibakhshi R PY - 2026 JO - Molecular and cellular probes DO - 10.1016/j.mcp.2026.102084 UR - https://doi.org/10.1016/j.mcp.2026.102084 ER -
APA
E, A., A, S., P, N., S, G., M, K., S, B., P, A., S, G., & R, A. (2026). Whole exome sequencing unveils novel pathogenic variants in an Iranian cohort with retinal dystrophies: Implications for genetic diagnosis and counseling.. Molecular and cellular probes. https://doi.org/10.1016/j.mcp.2026.102084
Source records
- pubmed · retrieved 2026-09-26T13:14:36.990Z