ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes
- DOI
- 10.1016/j.isci.2026.115454
- Published
- 2026-05
- Container
- iScience
- Publisher
- Elsevier BV
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- supportingDOI registered: A matching record was returned by Crossref.
- supportingDOI resolves: A matching record was returned by Crossref.
- 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.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1016/j.isci.2026.115454,
title = {ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes},
author = {Venkateshwarlu Bandi and Myrrhe Venema and Iona Wallace and Merel O. Mol and Anita Nikoncuk and Rachel Schot and Marjon van Slegtenhorst and Emilia K. Bijlsma and Amjad Khan and Susan M. White and Rocio Rius and Martin B. Delatycki and Vinodh Narayanan and Kirby N. Swatek and Tahsin Stefan Barakat and Francisco Bustos},
year = {2026},
journal = {iScience},
doi = {10.1016/j.isci.2026.115454},
url = {https://doi.org/10.1016/j.isci.2026.115454}
}RIS
TY - JOUR TI - ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes AU - Venkateshwarlu Bandi AU - Myrrhe Venema AU - Iona Wallace AU - Merel O. Mol AU - Anita Nikoncuk AU - Rachel Schot AU - Marjon van Slegtenhorst AU - Emilia K. Bijlsma AU - Amjad Khan AU - Susan M. White AU - Rocio Rius AU - Martin B. Delatycki AU - Vinodh Narayanan AU - Kirby N. Swatek AU - Tahsin Stefan Barakat AU - Francisco Bustos PY - 2026 JO - iScience DO - 10.1016/j.isci.2026.115454 UR - https://doi.org/10.1016/j.isci.2026.115454 ER -
APA
Bandi, V., Venema, M., Wallace, I., Mol, M. O., Nikoncuk, A., Schot, R., Slegtenhorst, M. V., Bijlsma, E. K., Khan, A., White, S. M., Rius, R., Delatycki, M. B., Narayanan, V., Swatek, K. N., Barakat, T. S., & Bustos, F. (2026). ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes. iScience. https://doi.org/10.1016/j.isci.2026.115454
Source records
- crossref · retrieved 2026-09-26T03:27:21.896Z