Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Engel C, Rendek M, Assoumani J, Argilli E, Ariani F, Avice-Denizet AL, Bijlsma EK, Blanc P, Bruno LP, Callewaert B, Capra V, Carullo M, Chesneau B, Coppens S, Curry C, Dale B, Dahlen E, Delahaye-Duriez A, Denommé-Pichon AS, Demeer B, Dvořáková L, Fischer J, Geneviève D, Giacomini T, Handrup MM, Heron D, Hüning I, Iacomino M, Isidor B, Keren B, Kmoch S, Koolen DA, Kübler A, Laštůvková J, Le C, Levy J, Rizzo CL, Maitz S, Marlin S, Mignot C, Mirzaa G, Nagel I, Neuens S, Nosková L, Pao E, Pecková A, Plaisancie J, Porrmann J, Privitera F, Reis A, Renieri A, Rio M, Rippert A, Ryba L, Scala M, Schieving JH, Sherr EH, Shuen A, Sidlow R, Smol T, Soblet J, Striano P, Suri M, Syryn H, Tran Mau-Them F, Travessa AM, Van Gils J, Vasileiou G, Verseput JJA, Vilain C, Vincent-Delorme C, Vyhnálková E, Wakeling EL, Zacher P, Zara F, Kuentz P, Piard J

Open source

DOI: 10.1038/s41431-026-02087-w
Published: 2026 Apr 2
Container: European journal of human genetics : EJHG
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. 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
not scoredOpen access status: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
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:10.1038/s41431-026-02087-w,
  title = {Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.},
  author = {Engel C and Rendek M and Assoumani J and Argilli E and Ariani F and Avice-Denizet AL and Bijlsma EK and Blanc P and Bruno LP and Callewaert B and Capra V and Carullo M and Chesneau B and Coppens S and Curry C and Dale B and Dahlen E and Delahaye-Duriez A and Denommé-Pichon AS and Demeer B and Dvořáková L and Fischer J and Geneviève D and Giacomini T and Handrup MM and Heron D and Hüning I and Iacomino M and Isidor B and Keren B and Kmoch S and Koolen DA and Kübler A and Laštůvková J and Le C and Levy J and Rizzo CL and Maitz S and Marlin S and Mignot C and Mirzaa G and Nagel I and Neuens S and Nosková L and Pao E and Pecková A and Plaisancie J and Porrmann J and Privitera F and Reis A and Renieri A and Rio M and Rippert A and Ryba L and Scala M and Schieving JH and Sherr EH and Shuen A and Sidlow R and Smol T and Soblet J and Striano P and Suri M and Syryn H and Tran Mau-Them F and Travessa AM and Van Gils J and Vasileiou G and Verseput JJA and Vilain C and Vincent-Delorme C and Vyhnálková E and Wakeling EL and Zacher P and Zara F and Kuentz P and Piard J},
  year = {2026},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/s41431-026-02087-w},
  url = {https://doi.org/10.1038/s41431-026-02087-w}
}

RIS

TY  - JOUR
TI  - Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
AU  - Engel C
AU  - Rendek M
AU  - Assoumani J
AU  - Argilli E
AU  - Ariani F
AU  - Avice-Denizet AL
AU  - Bijlsma EK
AU  - Blanc P
AU  - Bruno LP
AU  - Callewaert B
AU  - Capra V
AU  - Carullo M
AU  - Chesneau B
AU  - Coppens S
AU  - Curry C
AU  - Dale B
AU  - Dahlen E
AU  - Delahaye-Duriez A
AU  - Denommé-Pichon AS
AU  - Demeer B
AU  - Dvořáková L
AU  - Fischer J
AU  - Geneviève D
AU  - Giacomini T
AU  - Handrup MM
AU  - Heron D
AU  - Hüning I
AU  - Iacomino M
AU  - Isidor B
AU  - Keren B
AU  - Kmoch S
AU  - Koolen DA
AU  - Kübler A
AU  - Laštůvková J
AU  - Le C
AU  - Levy J
AU  - Rizzo CL
AU  - Maitz S
AU  - Marlin S
AU  - Mignot C
AU  - Mirzaa G
AU  - Nagel I
AU  - Neuens S
AU  - Nosková L
AU  - Pao E
AU  - Pecková A
AU  - Plaisancie J
AU  - Porrmann J
AU  - Privitera F
AU  - Reis A
AU  - Renieri A
AU  - Rio M
AU  - Rippert A
AU  - Ryba L
AU  - Scala M
AU  - Schieving JH
AU  - Sherr EH
AU  - Shuen A
AU  - Sidlow R
AU  - Smol T
AU  - Soblet J
AU  - Striano P
AU  - Suri M
AU  - Syryn H
AU  - Tran Mau-Them F
AU  - Travessa AM
AU  - Van Gils J
AU  - Vasileiou G
AU  - Verseput JJA
AU  - Vilain C
AU  - Vincent-Delorme C
AU  - Vyhnálková E
AU  - Wakeling EL
AU  - Zacher P
AU  - Zara F
AU  - Kuentz P
AU  - Piard J
PY  - 2026
JO  - European journal of human genetics : EJHG
DO  - 10.1038/s41431-026-02087-w
UR  - https://doi.org/10.1038/s41431-026-02087-w
ER  -

APA

C, E., M, R., J, A., E, A., F, A., AL, A., EK, B., P, B., LP, B., B, C., V, C., M, C., B, C., S, C., C, C., B, D., E, D., A, D., AS, D., B, D., L, D., J, F., D, G., T, G., MM, H., D, H., I, H., M, I., B, I., B, K., S, K., DA, K., A, K., J, L., C, L., J, L., CL, R., S, M., S, M., C, M., G, M., I, N., S, N., L, N., E, P., A, P., J, P., J, P., F, P., A, R., A, R., M, R., A, R., L, R., M, S., JH, S., EH, S., A, S., R, S., T, S., J, S., P, S., M, S., H, S., F, T. M., AM, T., J, V. G., G, V., JJA, V., C, V., C, V., E, V., EL, W., P, Z., F, Z., P, K., & J, P. (2026). Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-026-02087-w

Source records

pubmed · retrieved 2026-09-27T09:29:25.502Z