Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval.

Condell A, Zhang E, Sikora T, Massey S, Van Bergen NJ, Wang M, Simons C, Bell KM, Hock DH, Stroud DA, Francis D, Gold WA, Delatycki MB, Christodoulou J, Kaur S

Open source

DOI: 10.1111/cge.70213
Published: 2026 Oct
Container: Clinical genetics
Publisher: Not recorded
Open access: yes

Credibility signals

limited evidence Score 45/100 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. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
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. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1111/cge.70213,
  title = {Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval.},
  author = {Condell A and Zhang E and Sikora T and Massey S and Van Bergen NJ and Wang M and Simons C and Bell KM and Hock DH and Stroud DA and Francis D and Gold WA and Delatycki MB and Christodoulou J and Kaur S},
  year = {2026},
  journal = {Clinical genetics},
  doi = {10.1111/cge.70213},
  url = {https://doi.org/10.1111/cge.70213}
}

RIS

TY  - JOUR
TI  - Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval.
AU  - Condell A
AU  - Zhang E
AU  - Sikora T
AU  - Massey S
AU  - Van Bergen NJ
AU  - Wang M
AU  - Simons C
AU  - Bell KM
AU  - Hock DH
AU  - Stroud DA
AU  - Francis D
AU  - Gold WA
AU  - Delatycki MB
AU  - Christodoulou J
AU  - Kaur S
PY  - 2026
JO  - Clinical genetics
DO  - 10.1111/cge.70213
UR  - https://doi.org/10.1111/cge.70213
ER  -

APA

A, C., E, Z., T, S., S, M., NJ, V. B., M, W., C, S., KM, B., DH, H., DA, S., D, F., WA, G., MB, D., J, C., & S, K. (2026). Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval.. Clinical genetics. https://doi.org/10.1111/cge.70213

Source records

pubmed · retrieved 2026-09-24T23:08:15.582Z